- Winchester Building25 York StreetNew Haven, CT 06511
- 1 Long Wharf DriveNew Haven, CT 06511
Yong-Hui Jiang, MD, PhD
Biography
Yong-Hui Jiang, MD, PhD, chief of Medical Genetics, is trained in pediatrics and board certified in clinical genetics and medical biochemical genetics. He not only evaluates and treats rare and undiagnosed genetic diseases in infants through adults, but conducts basic and translational research.
“I joke with families that I am not just a specialist, but a super specialist because of my credentials and experience as a medical biochemical geneticist, one of two such physicians in the state, and we are both here at Yale,” says Dr. Jiang.
Adding lightness to what can be daunting medical appointments is one way Dr. Jiang connects with patients. Medical biochemical geneticists specialize in inherited metabolic conditions including inborn errors of metabolism. Inborn errors of metabolism (often diagnosed during standard screening at birth) are problems with how the body uses enzymes to digest proteins, fatty, and carbohydrates, which are important to the functions of all organs. Dr. Jiang also treats neurodevelopmental disorders such as Angelman’s, Prader-Willi, and Phelan-McDermid syndromes; and autism spectrum disorder.
“One of the challenges in my specialty is that the first job is to figure out what is going on. Sometimes, a family has been searching for a diagnosis for 10 years or more, and it is very rewarding to give them an answer,” Dr. Jiang says. “What motivates me, both in my clinical and research work, is developing treatments that will help them.”
Meanwhile, advances in clinical genetics continue at a rapid pace thanks to cutting-edge genetics testing technology at Yale and extensive experience on applying genome technology here, he notes. “The tools we have for reading your genome are now such better quality and lower cost,” he says. “There is a lot of hope of being able to evaluate and treat conditions to degrees that were not possible five years ago.”
Titles
- Professor of Genetics and Dorys McConnell Duberg Professor of Neuroscience; Chief of Medical Genetics
- Vice Chair, Dept. of Genetics, Genetics
- Chief of Medical Genetics, Genetics
Education & Training
- Medical Biochemical Genetics Training by Service PathwayBaylor College of Medicine (2008)
- Clinical Genetics and Genomics FellowBaylor College of Medicine (2007)
- Pediatric residentTexas Children's Hosital, Baylor College of Medicine (2005)
- PhDBaylor College of Medicine, Molecular and Human Genetics (1999)
- MDFormer Shanghai Medical Univeristy/Current Shanghai Medical College of Fudan University (1987)
Languages Spoken
- 官話 / 官话 (Chinese-Mandarin)
- English
Additional Information
- Yale Faculty Innovation Award: Yale University (2024)
- Yale Faculty Innovation Award : Yale University (2023)
- Cure Angelman Discovery Award 2022: Foundation for Angelman Syndrome Therapeutics (2022), (2023)
- No. 1 of top 10 autism research project: Autism Speaks (2020)
- NIH (2019 - Present): Standing Member
- Foundation for Angelman Syndrome Therapeuics (2014 - Present): Committee Member
- Hendry C, Zhou J, Jiang YH. Applying the FDA’s plausible mechanism guidance across the rare disease landscape. Nature Genetics 2026 DOI: 10.1038/s41588-026-02750-4.
- Sun J, Nie Z, Wu F, Lai F, Chen S, Wang Y, Jiang Y. Highly sensitive fluorescent lateral flow immunoassay based on core–shell PS@Dip@SiO2 microspheres for SARS-CoV-2 IgG detection. Microchimica Acta 2026, 193: 571. PMID: 42517932, DOI: 10.1007/s00604-026-08296-w.
- Zhang J, Wang Y, Ye X, Peng Y, Hou Y, Li Y, Jiang Y. One-Pot Synthesis of Soft, Shape-Stable and Conductive Phase Change Hydrogels. New Journal Of Chemistry 2026, 50: 11568-11576. DOI: 10.1039/d5nj04824a.
- Tong C, Li C, Jacq A, Nie X, Guy C, Suh J, Wong R, Merlin C, Menet J, Jiang Y. Single-cell Multiomic and Spatiotemporal Dissection of the Liver Circadian Clock. Genomics Proteomics & Bioinformatics 2026, qzag050. PMID: 42360761, DOI: 10.1093/gpbjnl/qzag050.
- Li Y, Zhang Y, Zhou Y, Zhou X, Liu H, Lu L, Chen J, Zhang J, Huang X, Yang X, Qian D, Jiang Y. Comparative study of three viscosity-enhancing strategies for chitosan-alginate composite hydrogels. The Journal Of Adhesion 2026, ahead-of-print: 1-19. DOI: 10.1080/00218464.2026.2691431.
- Yuan S, Shi Q, Zhao H, Guo K, Jiang Y, Zhang Y. Emerging gene-edited dog models for autism spectrum disorder. Genomic Psychiatry 2026, 1-7. DOI: 10.61373/gp026p.0036.
- Hou Y, Cao W, Peng Y, Huang J, Li Y, Jiang Y. Investigation of silicone hydrogel contact lenses functionalized with hollow silica nanoparticles for drug loading. New Journal Of Chemistry 2026, 50: 9823-9833. DOI: 10.1039/d6nj00915h.
- Nie Y, Zhao Z, Chen X, Wang F, Huang J, Jiang Y. Tunable Polymer-Brush Interfaces on Magnetic Beads Enable Enhanced Chemiluminescence Immunoassay. Langmuir 2026, 42: 17162-17174. PMID: 42234452, DOI: 10.1021/acs.langmuir.6c02340.
- Chen X, Nie Y, Zhao Z, Wang F, Huang J, Jiang Y. Tunable dendritic Fe3O4@mSiO2-Ni2+ core-shell magnetic nanospheres for selective enrichment of histidine-rich proteins. Talanta 2026, 307: 129774. PMID: 41962442, DOI: 10.1016/j.talanta.2026.129774.
- Qiao S, Wang S, Kim K, Jo S, Jiang Y. Inflammation increases the penetrance of behavioral impairment in Shank3 haploinsufficiency mice — can it explain the behavioral regression in Autism? Molecular Psychiatry 2026, 31: 4369-4385. PMID: 41882256, PMCID: PMC13364677, DOI: 10.1038/s41380-026-03534-2.
- Ashokkumar M, Ge R, Cooper-Volkheimer A, Margolis D, Li Q, Jiang Y, Murdoch D, Browne E. Single cell multiomic analysis of the impact of Delta-9-tetrahydrocannabinol on HIV infected CD4 T cells. Journal Of Cannabis Research 2026, 8: 52. PMID: 41782037, PMCID: PMC13069807, DOI: 10.1186/s42238-026-00412-0.
- Abdelhamed Z, Dykas D, DiAdamo A, Chai H, Ma D, Spencer-Mazon M, Jiang Y, Wen J, Bale A, Li P, Zhang H. Concomitant Chromosomal and Molecular Aberrations in Trisomy 8 Mosaicism and Associated Compound Phenotypes: Report of Three Cases and Review of Literature. Case Reports In Genetics 2026, 2026: 4494577. PMID: 41624216, PMCID: PMC12855162, DOI: 10.1155/crig/4494577.
- Knee K, Weeber E, Armstrong N, Stoub R, Copping N, Bailus B, Jiang Y, Berry-Kravis E, Berent A. Rodent Models and How They Define Potential Human Benefit: A Translational Review for Angelman Syndrome. 2026 DOI: 10.65856/ffkj4964.
- Wei L, Du X, Qiao Z, Yang B, Long S, Jiang Y, Wang Y, Wang H. Microstructural White Matter Alterations in Angelman Syndrome: A Fixel‐Based Analysis. Autism Research 2025, 19: e70160. PMID: 41437736, DOI: 10.1002/aur.70160.
- Chen X, Nie Y, Fan W, Zhao Z, Wang Z, Jiang Y. Yolk-shell magnetic hydrogel Fe3O4@P(DVB-co-MAA)@Ag composite microspheres for enhanced catalytic reduction of nitroaromatics. Colloids And Surfaces A Physicochemical And Engineering Aspects 2025, 727: 138336. DOI: 10.1016/j.colsurfa.2025.138336.
- Folkes O, Donahue M, Wang S, Negrón-Moreno P, Oo N, Qiao S, Wang X, Jiang Y. Deficiency of Shank3 in the nucleus accumbens reveals a loss of social-specific motivation. Communications Biology 2025, 8: 1569. PMID: 41238633, PMCID: PMC12618580, DOI: 10.1038/s42003-025-08942-8.
- Nie Z, Sun J, Wu F, Lai F, Yang X, Chen S, Wang Y, Jiang Y. Preparation of Fe3O4@PMAA-N protein magnetic beads for antibody detection of SARS-CoV-2 based on indirect ELISA smartphone visual strategy. Microchimica Acta 2025, 192: 785. PMID: 41175250, DOI: 10.1007/s00604-025-07646-4.
- Coulter A, Tong C, Ni Y, Jiang Y. distQTL: distribution quantitative trait loci identification by population-scale single-cell data. NAR Genomics And Bioinformatics 2025, 7: lqaf155. PMID: 41323105, PMCID: PMC12661327, DOI: 10.1093/nargab/lqaf155.
- Zhang Q, Yamanaka H, Li P, Li Y, Luo T, Xia M, Liu T, Liu X, Lu Q, Yang B, He F, Du K, Shu Y, Peng B, Jiang Y, Wang Y. Haploinsufficiency of brain‐specific kinase BRSK1 causes epilepsy and neurodevelopmental disorders. Epilepsia 2025, 66: 5033-5054. PMID: 41035394, PMCID: PMC12779330, DOI: 10.1111/epi.18621.
- Ye X, Peng Y, Hou Y, Huang J, Cao W, Jiang Y. pH‐Responsive Polyacrylic Acid Hydrogels Cross‐Linked with Functionalized Collagen Peptide for Controlled Drug Release. ChemistrySelect 2025, 10 DOI: 10.1002/slct.202503021.
- Wang S, Cheng Y, Lim J, Jang M, Forrest E, Kim Y, Donahue M, Jo S, Qiao S, Lee D, Hong J, Xiong Y, Jin J, Wang S, Jiang Y. Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome. Nature Communications 2025, 16: 6125. PMID: 40610428, PMCID: PMC12229668, DOI: 10.1038/s41467-025-61156-8.
- Zhao H, Jiang Y, Zhang Y. Gene-Edited Canines as Emerging Models for Studies on Mental Disorders. National Science Review 2025, nwaf263. DOI: 10.1093/nsr/nwaf263.
- Gui L, Jiang Y, Wang J. Aggregating dependent signals with heavy-tailed combination tests. Biometrika 2025, 112: asaf038. PMID: 41169946, PMCID: PMC12570179, DOI: 10.1093/biomet/asaf038.
- Fan W, Zhao Z, Chen X, Nie Y, Wang Z, Jiang Y. Stable and Controllable Magnetic Functionalization of Polymer Microspheres via Covalent Layer-by-Layer Assembly. Langmuir 2025, 41: 14300-14310. PMID: 40445872, DOI: 10.1021/acs.langmuir.5c01372.
- Yuan S, Pang C, Wu L, Yi L, Guo K, Jiang Y, Zhang Y, Han S. Autism-like atypical face processing in Shank3 mutant dogs. Science Advances 2025, 11: eadu3793. PMID: 40173245, PMCID: PMC11963970, DOI: 10.1126/sciadv.adu3793.
- Lyu W, Li Y, Yao A, Tan Q, Zhang R, Zhao J, Guo K, Jiang Y, Tian R, Zhang Y. Oxytocin improves maternal licking behavior deficits in autism-associated Shank3 mutant dogs. Translational Psychiatry 2025, 15: 76. PMID: 40050270, PMCID: PMC11885833, DOI: 10.1038/s41398-025-03296-5.
- Kim Y, Kim M, Kim S, Lee R, Ujihara Y, Marquez-Wilkins E, Jiang Y, Yang E, Kim H, Lee C, Park C, Kim I. Endothelial SHANK3 regulates tight junctions in the neonatal mouse blood-brain barrier through β-Catenin signaling. Nature Communications 2025, 16: 1407. PMID: 39915488, PMCID: PMC11802743, DOI: 10.1038/s41467-025-56720-1.
- Zeng J, Xu Q, Nie Y, Han X, Jiang Y. Preparation and properties of silicone hydrogel contact lens based on PDMS-PU macromer. Colloid And Polymer Science 2025, 303: 793-804. DOI: 10.1007/s00396-025-05379-7.
- Weideman A, Wang R, Ibrahim J, Jiang Y. Canopy2: Tumor Phylogeny Inference by Bulk DNA and Single-Cell RNA Sequencing. Statistics In Biosciences 2025, 18: 68-110. PMID: 41694548, PMCID: PMC12904911, DOI: 10.1007/s12561-024-09466-1.
- Liao J, Yan W, Zhang Y, Berhane K, Chen W, Yang Z, Qiu C, Ge Y, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Zhang J, Huang G, Chen Z. Associations of preconception air pollution exposure with growth trajectory in young children: A prospective cohort study. Environmental Research 2024, 267: 120665. PMID: 39706320, PMCID: PMC11878012, DOI: 10.1016/j.envres.2024.120665.
- Chu X, Dou X, Yu J, Zhou J, Ma D, Miao M, Hu S, Sun K, Zhu S, Liu Q, Zhang X, Jiang Y, Wang Z. Synthesis of Polymers via Cancer Cell Metabolism-Mediated Controlled Radical Polymerization and Application in Engineering of Cell Surface. Biomacromolecules 2024, 26: 238-247. PMID: 39689279, DOI: 10.1021/acs.biomac.4c01020.
- Zhu S, Du D, Zhao Z, Chu X, Su D, Yu S, Tao T, Jiang Y, Wang Z. Fabrication of functional interface on magnetic beads via various amino acids and their application in chemiluminescent immunoassay as carrier. Colloids And Surfaces B Biointerfaces 2024, 245: 114364. PMID: 39527882, DOI: 10.1016/j.colsurfb.2024.114364.
- Shi Q, Wu L, Ren B, Guo K, Jiang Y, Zhang Y, Hu L. Impaired tactile processing in autism-associated Shank3 mutant dogs: neural mechanism and intervention. Science Bulletin 2024, 70: 483-487. PMID: 39294081, DOI: 10.1016/j.scib.2024.09.011.
- Liao J, Zhang Y, Yang Z, Chen W, Qiu C, Kiros B, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Zhang J, Yan W, Huang G, Chen Z. Association of Preconception Air Pollution Exposure with Growth Trajectory in Children. ISEE Conference Abstracts 2024, 2024 DOI: 10.1289/isee.2024.0146.
- Gao Y, Shonai D, Trn M, Zhao J, Soderblom E, Garcia-Moreno S, Gersbach C, Wetsel W, Dawson G, Velmeshev D, Jiang Y, Sloofman L, Buxbaum J, Soderling S. Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions. Nature Communications 2024, 15: 6801. PMID: 39122707, PMCID: PMC11316102, DOI: 10.1038/s41467-024-51037-x.
- Su D, Han J, Chen L, Zhu S, Jiang Y, Wang Z. Fabrication of dextran-grafted magnetic polymer microspheres with low nonspecific protein adsorption as carriers for chemiluminescence immunoassays. Colloids And Surfaces A Physicochemical And Engineering Aspects 2024, 694: 134115. DOI: 10.1016/j.colsurfa.2024.134115.
- Kose C, Lindsey-Boltz L, Sancar A, Jiang Y. Genome-wide analysis of transcription-coupled repair reveals novel transcription events in Caenorhabditis elegans. PLOS Genetics 2024, 20: e1011365. PMID: 39028758, PMCID: PMC11290646, DOI: 10.1371/journal.pgen.1011365.
- Xu Q, Zhao Z, Chen X, Fan W, Jiang Y. The Impact of Surface Modifier on Magnetic Nanoparticle Properties and Their Application in CD3+T Cell Separation. Langmuir 2024, 40: 15597-15609. PMID: 39024471, DOI: 10.1021/acs.langmuir.4c01332.
- Dalton G, Siecinski S, Nikolova V, Cofer G, Hornburg K, Qi Y, Johnson G, Jiang Y, Moy S, Gregory S. Transcriptome analysis identifies an ASD-Like phenotype in oligodendrocytes and microglia from C58/J amygdala that is dependent on sex and sociability. Behavioral And Brain Functions 2024, 20: 14. PMID: 38898502, PMCID: PMC11188533, DOI: 10.1186/s12993-024-00240-3.
- Lu X, Ni P, Suarez-Meade P, Ma Y, Forrest E, Wang G, Wang Y, Quiñones-Hinojosa A, Gerstein M, Jiang Y. Transcriptional determinism and stochasticity contribute to the complexity of autism-associated SHANK family genes. Cell Reports 2024, 43: 114376. PMID: 38900637, PMCID: PMC11328446, DOI: 10.1016/j.celrep.2024.114376.
- Nie Y, Xu Q, Wu D, Li J, Wang Z, Jiang Y, Lv Q, Jiang Y. Low-molecular-weight microspheres with soft-shell characteristics for remarkable signal enhancement in LOCI applications. Colloids And Surfaces A Physicochemical And Engineering Aspects 2024, 691: 133883. DOI: 10.1016/j.colsurfa.2024.133883.
- Wang S, Xiong Y, Jang M, Park K, Donahue M, Velez J, Jin J, Jiang Y. Newly developed oral bioavailable EHMT2 inhibitor as a potential epigenetic therapy for Prader-Willi syndrome. Molecular Therapy 2024, 32: 2662-2675. PMID: 38796700, PMCID: PMC11405540, DOI: 10.1016/j.ymthe.2024.05.034.
- Ashokkumar M, Mei W, Peterson J, Harigaya Y, Murdoch D, Margolis D, Kornfein C, Oesterling A, Guo Z, Rudin C, Jiang Y, Browne E. Integrated Single-cell Multiomic Analysis of HIV Latency Reversal Reveals Novel Regulators of Viral Reactivation. Genomics Proteomics & Bioinformatics 2024, 22: qzae003. PMID: 38902848, PMCID: PMC11189801, DOI: 10.1093/gpbjnl/qzae003.
- Su K, Ma Y, Zhou M, Liu Y, Li C, Jiang Y, Wu Q, Peng G, Wang Y, Fan S. De novo missense variants of UNC13A are implicated in epileptic encephalopathies and neurodevelopmental disorders. Genes & Diseases 2024, 12: 101315. PMID: 39634123, PMCID: PMC11615879, DOI: 10.1016/j.gendis.2024.101315.
- Lu X, Ng K, Pinto e Vairo F, Collins J, Cohn R, Riley K, Agre K, Gavrilova R, Klee E, Rosenfeld J, Jiang Y. Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European Journal Of Human Genetics 2024, 32: 879-883. PMID: 38702431, PMCID: PMC11219747, DOI: 10.1038/s41431-024-01576-0.
- Li J, Zhang P, Xu Q, Nie Y, Shao S, Wang Z, Jiang Y. Preparation of dyed polymer microspheres by a physical–chemical dual-binding method and their application in lateral flow immunoassay. Analytical Methods 2024, 16: 2033-2043. PMID: 38497428, DOI: 10.1039/d3ay02279j.
- DiAdamo A, Chai H, Chong M, Wang G, Wen J, Jiang Y, Li P. Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages. Global Medical Genetics 2024, 11: 123-131. PMID: 38560483, PMCID: PMC10980555, DOI: 10.1055/s-0044-1785227.
- Han J, Lv Q, Su D, Chen L, Zhu S, Liu Q, Jiang Y, Li X, Jiang Y, Wang Z. Polymer Microspheres Copolymerized with Deep Red Fluorescent Molecules as a Label for Lateral Flow Immunochromatography. Langmuir 2024, 40: 6971-6979. PMID: 38517386, DOI: 10.1021/acs.langmuir.3c04033.
- Lu X, Jiang Y. Intrathecal Injection of Newborn Mouse for Genome Editing and Drug Delivery. Journal Of Visualized Experiments 2024 PMID: 38526075, DOI: 10.3791/65761.
- Wu D, Xu Q, Nie Y, Jiang W, Wang Z, Jiang Y. Synergistic Fabrication of Magnetic Hypercrosslinked Porous P(VBC-DVB-AA)@Fe3O4 Microspheres for Removal of Cationic Dye. Journal Of Inorganic And Organometallic Polymers And Materials 2024, 34: 2746-2761. DOI: 10.1007/s10904-024-03009-3.
- Godse S, Brumer E, Kizilirmak T, Canapari C, Silva C, Morotti R, Jiang Y, Jeffries L, Chen L, Panacherry S. When lungs and weights tell different stories. Pediatric Pulmonology 2024, 59: 1047-1059. PMID: 38353400, DOI: 10.1002/ppul.26832.
- Xu Q, Nie Y, Wu D, Li J, Zeng J, Wang Z, Jiang Y. Anisotropic Magnetic Polymeric Particles with a Controllable Structure via Seeded Emulsion Polymerization. Langmuir 2024, 40: 3677-3690. PMID: 38343282, DOI: 10.1021/acs.langmuir.3c03379.
- Zhu F, Shi Q, Jiang Y, Zhang Y, Zhao H. Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs. Molecular Autism 2024, 15: 9. PMID: 38297387, PMCID: PMC10829216, DOI: 10.1186/s13229-024-00587-4.
- Yang Z, Liao J, Zhang Y, Lin Y, Ge Y, Chen W, Qiu C, Berhane K, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Chen Z, Huang G, Zhang J. Critical windows of greenness exposure during preconception and gestational periods in association with birthweight outcomes. Environmental Research Health 2023, 2: 015001. PMID: 38022394, PMCID: PMC10647935, DOI: 10.1088/2752-5309/ad0aa6.
- Nie Y, Man H, Shao S, Wang Y, Wang Z, Jiang Y. The influence of water on size of the monodisperse polystyrene microspheres prepared by dispersion polymerization. Journal Of Applied Polymer Science 2023, 141 DOI: 10.1002/app.54813.
- Liao J, Zhang Y, Yang Z, Qiu C, Chen W, Zhang J, Berhane K, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Huang G, Chen Z. Identifying critical windows of air pollution exposure during preconception and gestational period on birthweight: a prospective cohort study. Environmental Health 2023, 22: 71. PMID: 37858139, PMCID: PMC10585741, DOI: 10.1186/s12940-023-01022-6.
- Liao J, Zhang Y, Yang Z, Qiu C, Chen W, Zhang J, Berhane K, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Huang G, Chen Z. Identifying Critical Windows of Air Pollution Exposure during Preconception and Gestational Period on Birthweight. ISEE Conference Abstracts 2023, 2023 DOI: 10.1289/isee.2023.fp-236.
- Tian R, Li Y, Zhao H, Lyu W, Zhao J, Wang X, Lu H, Xu H, Ren W, Tan Q, Shi Q, Wang G, Zhang Y, Lai L, Mi J, Jiang Y, Zhang Y. Modeling SHANK3-associated autism spectrum disorder in Beagle dogs via CRISPR/Cas9 gene editing. Molecular Psychiatry 2023, 28: 3739-3750. PMID: 37848710, DOI: 10.1038/s41380-023-02276-9.
- Wang S, Jiang Y. Novel epigenetic molecular therapies for imprinting disorders. Molecular Psychiatry 2023, 28: 3182-3193. PMID: 37626134, PMCID: PMC10618104, DOI: 10.1038/s41380-023-02208-7.
- Xu Q, Jiang W, Bu F, Wang Z, Jiang Y. Magnetic Dendritic Polymer Nanospheres for High-Performance Separation of Histidine-Rich Proteins. ACS Applied Materials & Interfaces 2023, 15: 30837-30848. PMID: 37332160, DOI: 10.1021/acsami.3c05475.
- Contestabile A, Casarotto G, Musardo S, Espinosa P, Maltese F, Jiang Y, Bellone C, Glangetas C. Shank3 deficits in the anteromedial bed nucleus of the stria terminalis trigger an anxiety phenotype in mice. European Journal Of Neuroscience 2023, 57: 1966-1979. PMID: 37165567, DOI: 10.1111/ejn.16043.
- Jiang W, Xu Q, Bu F, Wei Y, Wang Y, Wang Z, Jiang Y. Fabrication of Fe3O4@APF Magnetic Nanospheres with Tunable Core–Shell Structure: An Effective Carrier and Reducing Agent for Ag Nanoparticles. Journal Of Inorganic And Organometallic Polymers And Materials 2023, 33: 2562-2573. DOI: 10.1007/s10904-023-02704-x.
- Mann B, Zhang X, Bell N, Adefolaju A, Thang M, Dasari R, Kanchi K, Valdivia A, Yang Y, Buckley A, Lettry V, Quinsey C, Rauf Y, Kram D, Cassidy N, Vaziri C, Corcoran D, Rego S, Jiang Y, Graves L, Dunn D, Floyd S, Baldwin A, Hingtgen S, Satterlee A. A living ex vivo platform for functional, personalized brain cancer diagnosis. Cell Reports Medicine 2023, 4: 101042. PMID: 37192626, PMCID: PMC10313921, DOI: 10.1016/j.xcrm.2023.101042.
- Zhang J, Man H, Han X, Wang Z, Jiang Y. Facile preparation of magnetic P(MMA-co-GMA)@Fe3O4@PMAA microspheres using porous microsphere as templates for removal of methylene blue. Colloid And Polymer Science 2023, 301: 933-947. DOI: 10.1007/s00396-023-05099-w.
- Peng G, Zhou Q, Chai H, Wen J, Zhao H, Taylor H, Jiang Y, Li P. Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine 2023, 11: e2181. PMID: 37013615, PMCID: PMC10422064, DOI: 10.1002/mgg3.2181.
- Bu F, Xu Q, Jiang W, Wei Y, Wang Z, Jiang Y. Fabrication of magnetic Fe 3 O 4 @P(DVB- co -MAA) microspheres using hollow microspheres as templates for protein separation. New Journal Of Chemistry 2023, 47: 6176-6185. DOI: 10.1039/d3nj00069a.
- Li B, Zhao H, Tu Z, Yang W, Han R, Wang L, Luo X, Pan M, Chen X, Zhang J, Xu H, Guo X, Yan S, Yin P, Zhao Z, Liu J, Luo Y, Li Y, Yang Z, Zhang B, Tan Z, Xu H, Jiang T, Jiang Y, Li S, Zhang Y, Li X. CHD8 mutations increase gliogenesis to enlarge brain size in the nonhuman primate. Cell Discovery 2023, 9: 27. PMID: 36878905, PMCID: PMC9988832, DOI: 10.1038/s41421-023-00525-3.
- Hu W, Nie Y, Wang Y, Gao P, Jiang Y. Synthesis of inorganic/organic raspberry-like composite particles for superhydrophobic and superlipophilic coatings. Colloids And Surfaces A Physicochemical And Engineering Aspects 2023, 660: 130843. DOI: 10.1016/j.colsurfa.2022.130843.
- Li Y, Huang C, Duan A, Li M, Zhang X, Lu L, Yu L, Yu L, Liu P, Chen K, Jiang Y. A temperature-sensitive DNA-PNIPAAm hydrogel prepared by base pairing. Colloid And Polymer Science 2023, 301: 383-388. DOI: 10.1007/s00396-023-05071-8.
- Xing X, lv Q, Sun C, Song J, Chen Z, Jiang Y, Wang Y, Jiang Y, Wang Z. One-step preparation of PEG segment-functionalized polystyrene microspheres and their application as latex in LOCI. New Journal Of Chemistry 2023, 47: 3970-3977. DOI: 10.1039/d2nj05630e.
- Guan P, Lee J, Wang L, Lin K, Mei W, Chen L, Jiang Y. Destin2: Integrative and cross-modality analysis of single-cell chromatin accessibility data. Frontiers In Genetics 2023, 14: 1089936. PMID: 36873935, PMCID: PMC9981783, DOI: 10.3389/fgene.2023.1089936.
- Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y. Cortical and subcortical morphological alteration in Angelman syndrome. Journal Of Neurodevelopmental Disorders 2023, 15: 7. PMID: 36788499, PMCID: PMC9930225, DOI: 10.1186/s11689-022-09469-3.
- Chen Z, Yu J, Sun K, Song J, Chen L, Jiang Y, Wang Z. Rational design of a turn-on near-infrared fluorescence probe for the highly sensitive and selective monitoring of carboxylesterase 2 in living systems. Analyst 2023, 148: 876-887. PMID: 36661088, DOI: 10.1039/d2an01874h.
- Zhang L, Bang S, He Q, Matsuda M, Luo X, Jiang Y, Ji R. SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis. Frontiers In Immunology 2023, 14: 1124356. PMID: 36845137, PMCID: PMC9944123, DOI: 10.3389/fimmu.2023.1124356.
- Agarwal A, Zhao F, Jiang Y, Chen L. TIVAN-indel: a computational framework for annotating and predicting non-coding regulatory small insertions and deletions. Bioinformatics 2023, 39: btad060. PMID: 36707993, PMCID: PMC9900211, DOI: 10.1093/bioinformatics/btad060.
- Preparation and characterization of a form-stable phase change hydrogel for heat-protective clothingWang Y, Zhang J, Han X, Jiang Y. Preparation and characterization of a form-stable phase change hydrogel for heat-protective clothing. New Journal Of Chemistry 2023, 47: 1818-1824. DOI: 10.1039/d2nj05096j.
- Dai H, Zhu W, Yuan B, Walley N, Schoch K, Jiang Y, Phillips J, Jones M, Liu P, Murdock D, Burrage L, Lee B, Rosenfeld J, Xiao R, Network U. A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay. Human Mutation 2022, 43: 1816-1823. PMID: 36317458, PMCID: PMC9772143, DOI: 10.1002/humu.24497.
- Yang X, Zhang P, Xing X, lv Q, Jiang Y, Jiang Y, Wang Z. Improving the fluorescence intensity of lanthanide-doped microspheres via incorporation of lauryl methacrylate: Synthesis and their application in C-reactive protein detection. Colloids And Surfaces A Physicochemical And Engineering Aspects 2022, 653: 130065. DOI: 10.1016/j.colsurfa.2022.130065.
- Thaler R, Khani F, Sturmlechner I, Dehghani SS, Denbeigh JM, Zhou X, Pichurin O, Dudakovic A, Jerez SS, Zhong J, Lee JH, Natarajan R, Kalajzic I, Jiang YH, Deyle DR, Paschalis EP, Misof BM, Ordog T, van Wijnen AJ. Vitamin C epigenetically controls osteogenesis and bone mineralization. Nature Communications 2022, 13: 5883. PMID: 36202795, PMCID: PMC9537512, DOI: 10.1038/s41467-022-32915-8.
- Wei Y, Chen L, Jiang Y. Self-healing polyacrylamide (PAAm) gels at room temperature based on complementary guanine and cytosine base pairs. Soft Matter 2022, 18: 7394-7401. PMID: 36125115, DOI: 10.1039/d2sm00933a.
- Wei Y, Du Q, Wang Y, Gao P, Wang Z, Jiang Y. Two-dimensional cellulose acetate membrane-supported mesoporous silica nanosheets for efficient nanosize-based molecules separation. Journal Of Molecular Liquids 2022, 363: 119827. DOI: 10.1016/j.molliq.2022.119827.
- Jiang Y, Harigaya Y, Zhang Z, Zhang H, Zang C, Zhang N. Nonparametric single-cell multiomic characterization of trio relationships between transcription factors, target genes, and cis-regulatory regions. Cell Systems 2022, 13: 737-751.e4. PMID: 36055233, PMCID: PMC9509445, DOI: 10.1016/j.cels.2022.08.004.
- Gao P, Wei Y, Xu Q, Jiang Y. A cysteine-induced one-pot synthesis of Au nanoparticle chains with tuneable NIR absorption and application in photothermal-chemo cancer therapy. New Journal Of Chemistry 2022, 46: 16359-16369. DOI: 10.1039/d2nj02339c.
- Al‐Ali S, Jeffries L, Faustino EVS, Ji W, Mis E, Konstantino M, Zerillo C, Jiang Y, Spencer‐Manzon M, Bale A, Zhang H, McGlynn J, McGrath JM, Tremblay T, Brodsky NN, Lucas CL, Pierce R, Deniz E, Khokha MK, Lakhani SA. A retrospective cohort analysis of the Yale pediatric genomics discovery program. American Journal Of Medical Genetics Part A 2022, 188: 2869-2878. PMID: 35899841, PMCID: PMC9474639, DOI: 10.1002/ajmg.a.62918.
- Wei L, Du X, Yang Z, Ding M, Yang B, Wang J, Long S, Qiao Z, Jiang Y, Wang Y, Wang H. Disrupted Topological Organization of White Matter Network in Angelman Syndrome. Journal Of Magnetic Resonance Imaging 2022, 57: 1212-1221. PMID: 35856797, DOI: 10.1002/jmri.28360.
- Man H, Nie Y, Shao S, Wang Y, Wang Z, Jiang Y. Fabrication of Fe 3 O 4 @poly(methyl methacrylate- co -glycidyl methacrylate) microspheres via miniemulsion polymerization using porous microspheres as templates for removal of cationic dyes. New Journal Of Chemistry 2022, 46: 13442-13453. DOI: 10.1039/d2nj01440h.
- Wang R, Jiang Y. Copy Number Variation Detection by Single-Cell DNA Sequencing with SCOPE. Methods In Molecular Biology 2022, 2493: 279-288. PMID: 35751822, DOI: 10.1007/978-1-0716-2293-3_18.
- Hong H, Zhao Z, Huang X, Guo C, Zhao H, Wang GD, Zhang YP, Zhao JP, Shi J, Wu QF, Jiang YH, Wang Y, Li LM, Du Z, Zhang YQ, Xiong Y. Comparative Proteome and Cis-Regulatory Element Analysis Reveals Specific Molecular Pathways Conserved in Dog and Human Brains. Molecular & Cellular Proteomics 2022, 21: 100261. PMID: 35738554, PMCID: PMC9304787, DOI: 10.1016/j.mcpro.2022.100261.
- Wang R, Lin D, Jiang Y. EPIC: Inferring relevant cell types for complex traits by integrating genome-wide association studies and single-cell RNA sequencing. PLOS Genetics 2022, 18: e1010251. PMID: 35709291, PMCID: PMC9242467, DOI: 10.1371/journal.pgen.1010251.
- Yang-Li D, Fei-Hong L, Hui-Wen Z, Ming-Sheng M, Xiao-Ping L, Li L, Yi W, Qing Z, Yong-Hui J, Chao-Chun Z. Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China. Orphanet Journal Of Rare Diseases 2022, 17: 221. PMID: 35698200, PMCID: PMC9195308, DOI: 10.1186/s13023-022-02302-z.
- Kim S, Kim YE, Song I, Ujihara Y, Kim N, Jiang YH, Yin HH, Lee TH, Kim IH. Neural circuit pathology driven by Shank3 mutation disrupts social behaviors. Cell Reports 2022, 39: 110906. PMID: 35675770, PMCID: PMC9210496, DOI: 10.1016/j.celrep.2022.110906.
- Xu Q, Gao P, Wang Y, Jiang W, Wang Z, Jiang Y, Jiao Z. Using supercritical carbon dioxide to synthesize polymer nanospheres with an open hole on the surface and the application of spatially structured PS/P(DVB-co-MAA)@Fe3O4/TA@Ag nanocomposites. The Journal Of Supercritical Fluids 2022, 184: 105561. DOI: 10.1016/j.supflu.2022.105561.
- Wang S, Jiang Y. Epigenetic Epidemiology of Autism and Other Neurodevelopmental Disorders. 2022, 405-426. DOI: 10.1007/978-3-030-94475-9_17.
- Barish S, Senturk M, Schoch K, Minogue AL, Lopergolo D, Fallerini C, Harland J, Seemann JH, Stong N, Kranz PG, Kansagra S, Mikati MA, Jasien J, El-Dairi M, Galluzzi P, Acosta M, Adam M, Adams D, Agrawal P, Alejandro M, Alvey J, Amendola L, Andrews A, Ashley E, Azamian M, Bacino C, Bademci G, Baker E, Balasubramanyam A, Baldridge D, Bale J, Bamshad M, Barbouth D, Bayrak-Toydemir P, Beck A, Beggs A, Behrens E, Bejerano G, Bennet J, Berg-Rood B, Bernstein J, Berry G, Bican A, Bivona S, Blue E, Bohnsack J, Bonnenmann C, Bonner D, Botto L, Boyd B, Briere L, Brokamp E, Brown G, Burke E, Burrage L, Butte M, Byers P, Byrd W, Carey J, Carrasquillo O, Chang T, Chanprasert S, Chao H, Clark G, Coakley T, Cobban L, Cogan J, Coggins M, Cole F, Colley H, Cooper C, Cope H, Craigen W, Crouse A, Cunningham M, D'Souza P, Dai H, Dasari S, Davids M, Dayal J, Deardorff M, Dell'Angelica E, Dhar S, Dipple K, Doherty D, Dorrani N, Douine E, Draper D, Duncan L, Earl D, Eckstein D, Emrick L, Eng C, Esteves C, Estwick T, Falk M, Fernandez L, Ferreira C, Fieg E, Findley L, Fisher P, Fogel B, Forghani I, Fresard L, GahlIan-Glass W, Godfrey R, Golden-Grant K, Goldman A, Goldstein D, Grajewski A, Groden C, Gropman A, Gutierrez I, Hahn S, Hamid R, Hanchard N, Hassey K, Hayes N, High F, Hing A, Hisama F, Holm I, Hom J, Horike-Pyne M, Huang A, Huang Y, Isasi R, Jamal F, Jarvik G, Jarvik J, Jayadev S, Johnston J, Karaviti L, Kelley E, Kennedy J, Kiley D, Kohane I, Kohler J, Krakow D, Krasnewich D, Kravets E, Korrick S, Koziura M, Krier J, Lalani S, Lam B, Lam C, Lanpher B, Lanza I, Lau C, LeBlanc K, Lee B, Lee H, Levitt R, Lewis R, Lincoln S, Liu P, Liu X, Longo N, Loo S, Loscalzo J, Maas R, Macnamara E, MacRae C, Maduro V, Majcherska M, Mak B, Malicdan M, Mamounas L, Manolio T, Mao R, Maravilla K, Markello T, Marom R, Marth G, Martin B, Martin M, Martínez-Agosto J, Marwaha S, McCauley J, McConkie-Rosell A, McCormack C, McCray A, McGee E, Mefford H, Merritt J, Might M, Mirzaa G, Morava E, Moretti P, Morimoto M, Mulvihill J, Murdock D, Nakano-Okuno M, Nath A, Nelson S, Newman J, Nicholas S, Nickerson D, Nieves-Rodriguez S, Novacic D, Oglesbee D, Orengo J, Pace L, Pak S, Pallais J, Palmer C, Papp J, Parker N, Phillips III J, Posey J, Potocki L, Pusey B, Quinlan A, Raskind W, Raja A, Rao D, Renteria G, Reuter C, Rives L, Robertson A, Rodan L, Rosenfeld J, Rosenwasser N, Ruzhnikov M, Sacco R, Sampson J, Samson S, Saporta M, Scott C, Schaechter J, Schedl T, Schoch K, Scott D, Sharma P, Shashi V, Shin J, Signer R, Sillari C, Silverman E, Sinsheimer J, Sisco K, Smith E, Smith K, Solem E, Solnica-Krezel L, Spillmann R, Stoler J, StongJ N, Sullivan E, Sullivan K, Sun A, Sutton S, Sweetser D, Sybert V, Tabor H, Tamburro C, K-GTan Q, Tekin M, Telischi F, Thorson W, Tifft C, Toro C, Tran A, Tucker B, Urv T, Vanderver A, Velinder M, Viskochil D, Vogel T, Wahl C, Wallace S, Walley N, Walsh C, Walker M, Wambach J, Wan J, Wang L, Wangler M, Ward P, Wegner D, Wener M, Wenger T, Perry K, Westerfield M, Wheeler M, Whitlock J, Wolfe L, Woods J, Yamamoto S, Yang J, Yu G, Zastrow D, Zhao C, Zuchner S, Ariani F, Renieri A, Mari F, Wangler M, Arur S, Jiang Y, Yamamoto S, Shashi V, Bellen H. The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Human Molecular Genetics 2022, 31: 2934-2950. PMID: 35405010, PMCID: PMC9433733, DOI: 10.1093/hmg/ddac085.
- Shao S, Man H, Nie Y, Wang Y, Xu Q, Wang Z, Jiang Y. Preparation of fluorescence-encoded microbeads with large encoding capacities and application of suspension array technology. New Journal Of Chemistry 2022, 46: 6986-6994. DOI: 10.1039/d2nj00628f.
- Mague SD, Talbot A, Blount C, Walder-Christensen KK, Duffney LJ, Adamson E, Bey AL, Ndubuizu N, Thomas GE, Hughes DN, Grossman Y, Hultman R, Sinha S, Fink AM, Gallagher NM, Fisher RL, Jiang YH, Carlson DE, Dzirasa K. Brain-wide electrical dynamics encode individual appetitive social behavior. Neuron 2022, 110: 1728-1741.e7. PMID: 35294900, PMCID: PMC9126093, DOI: 10.1016/j.neuron.2022.02.016.
- Wen J, Chai H, Grommisch B, DiAdamo A, Dykas D, Ma D, Popa A, Zhao C, Spencer‐Manzon M, Jiang Y, McGrath J, Li P, Bale A, Zhang H. Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients. American Journal Of Medical Genetics Part A 2022, 188: 1728-1738. PMID: 35199448, DOI: 10.1002/ajmg.a.62693.
- Dong M, He Y, Jiang Y, Zou F. Joint Gene Network Construction by Single-Cell RNA Sequencing Data. Biometrics 2022, 79: 915-925. PMID: 35184277, PMCID: PMC10548400, DOI: 10.1111/biom.13645.
- Tzanoulinou S, Musardo S, Contestabile A, Bariselli S, Casarotto G, Magrinelli E, Jiang YH, Jabaudon D, Bellone C. Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism. Molecular Psychiatry 2022, 27: 2080-2094. PMID: 35022531, PMCID: PMC9126815, DOI: 10.1038/s41380-021-01427-0.
- Isidor B, Ebstein F, Hurst A, Vincent M, Bader I, Rudy NL, Cogne B, Mayr J, Brehm A, Bupp C, Warren K, Bacino CA, Gerard A, Ranells JD, Metcalfe KA, van Bever Y, Jiang YH, Mendelssohn BA, Cope H, Rosenfeld JA, Blackburn PR, Goodenberger ML, Kearney HM, Kennedy J, Scurr I, Szczaluba K, Ploski R, de Saint Martin A, Alembik Y, Piton A, Bruel AL, Thauvin-Robinet C, Strong A, Diderich KEM, Bourgeois D, Dahan K, Vignard V, Bonneau D, Colin E, Barth M, Camby C, Baujat G, Briceño I, Gómez A, Deb W, Conrad S, Besnard T, Bézieau S, Krüger E, Küry S, Stankiewicz P. Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype. Genetics In Medicine : Official Journal Of The American College Of Medical Genetics 2022, 24: 179-191. PMID: 34906456, DOI: 10.1016/j.gim.2021.09.005.
- Gao P, Sun S, Wang Y, Wei Y, Jiang Y. Biodegradable T2-phage-like Janus nanoparticles for actively-targeted and chemo-photothermal synergistic therapy. Chemical Engineering Journal 2022, 428: 131284. DOI: 10.1016/j.cej.2021.131284.
- Wang Y, Wei Y, Xu Q, Shao S, Man H, Nie Y, Wang Z, Jiang Y. Fabrication of Yolk–Shell Fe3O4@NiSiO3/Ni Microspheres for Efficient Purification of Histidine-Rich Proteins. Langmuir 2021, 37: 14167-14176. PMID: 34839664, DOI: 10.1021/acs.langmuir.1c02433.
- Tremblay MW, Green MV, Goldstein BM, Aldridge AI, Rosenfeld JA, Streff H, Tan WD, Craigen W, Bekheirnia N, Al Tala S, West AE, Jiang YH. Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human Molecular Genetics 2021, 31: 1430-1442. PMID: 34788807, PMCID: PMC9271223, DOI: 10.1093/hmg/ddab321.
- Werner KM, Cox AJ, Qian E, Jain P, Ji W, Tikhonova I, Castaldi C, Bilguvar K, Knight J, Ferdinandusse S, Fawaz R, Jiang Y, Gallagher PG, Bizzarro M, Gruen JR, Bale A, Zhang H. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American Journal Of Medical Genetics Part A 2021, 188: 357-363. PMID: 34623748, PMCID: PMC8678290, DOI: 10.1002/ajmg.a.62520.
- Liu Z, Ruter D, Quigley K, Tanke N, Jiang Y, Bautch V. Single-Cell RNA Sequencing Reveals Endothelial Cell Transcriptome Heterogeneity Under Homeostatic Laminar Flow. Arteriosclerosis Thrombosis And Vascular Biology 2021, 41: 2575-2584. PMID: 34433297, PMCID: PMC8454496, DOI: 10.1161/atvbaha.121.316797.
- Khayat M, Hu J, Jiang Y, Li H, Chander V, Dawood M, Hansen A, Li S, Friedman J, Cross L, Bijlsma E, Ruivenkamp C, Sansbury F, Innis J, O’Shea J, Meng Q, Rosenfeld J, McWalter K, Wangler M, Lupski J, Posey J, Murdock D, Gibbs R. AHDC1 missense mutations in Xia-Gibbs syndrome. Human Genetics And Genomics Advances 2021, 2: 100049. PMID: 34950897, PMCID: PMC8694554, DOI: 10.1016/j.xhgg.2021.100049.
- Zhang L, Qian Y, Li J, Zhou X, Xu H, Yan J, Xiang J, Yuan X, Sun B, Sisodia SS, Jiang YH, Cao X, Jing N, Lin A. BAD-mediated neuronal apoptosis and neuroinflammation contribute to Alzheimer's disease pathology. IScience 2021, 24: 102942. PMID: 34430820, PMCID: PMC8369003, DOI: 10.1016/j.isci.2021.102942.
- Zhao C, Chai H, Zhou Q, Wen J, Reddy U, Kastury R, Jiang Y, Mak W, Bale A, Zhang H, Li P. Exome Sequencing Analysis on Products of Conception: A Cohort Study to Evaluate Clinical Utility and Genetic Etiology for Pregnancy Loss. Obstetrical & Gynecological Survey 2021, 76: 468-469. DOI: 10.1097/01.ogx.0000791680.43228.b1.
- Xu Q, Wang Y, Gao P, Jiang Y. Preparation of “pomegranate”-like QD/SiO 2 /poly(St- co -MAA) fluorescent nanobeads in two steps to improve stability and biocompatibility. New Journal Of Chemistry 2021, 45: 10618-10625. DOI: 10.1039/d1nj00526j.
- Moss T, May M, Flanagan-Steet H, Caylor R, Jiang YH, McDonald M, Friez M, McConkie-Rosell A, Steet R. Severe multisystem pathology, metabolic acidosis, mitochondrial dysfunction, and early death associated with an X-linked AIFM1 variant. Molecular Case Studies 2021, 7: a006081. PMID: 34117073, PMCID: PMC8208043, DOI: 10.1101/mcs.a006081.
- Zhao C, Xie X, Ji W, Qi M, Zhou Q, Li M, Li P, Jiang Y, Zhang H. A review of consensus statements, practice resources, standards and guidelines for clinical applications of next-generation sequencing technologies in the United States. 中华医学遗传学杂志 2021, 38: 513-520. PMID: 34096016, DOI: 10.3760/cma.j.cn511374-20200924-00691.
- Moyon S, Frawley R, Marechal D, Huang D, Marshall-Phelps KLH, Kegel L, Bøstrand SMK, Sadowski B, Jiang YH, Lyons DA, Möbius W, Casaccia P. TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice. Nature Communications 2021, 12: 3359. PMID: 34099715, PMCID: PMC8185117, DOI: 10.1038/s41467-021-23735-3.
- Wei Y, An S, Sun S, Jiang Y. Photo-polymerized and thermal-polymerized silicon hydrogels with different surface microstructure and wettability. Colloids And Surfaces A Physicochemical And Engineering Aspects 2021, 618: 126284. DOI: 10.1016/j.colsurfa.2021.126284.
- Wang Y, Jiang Y, Yao B, Huang K, Liu Y, Wang Y, Qin X, Saykin A, Chen L. WEVar: a novel statistical learning framework for predicting noncoding regulatory variants. Briefings In Bioinformatics 2021, 22: bbab189. PMID: 34021560, PMCID: PMC8574971, DOI: 10.1093/bib/bbab189.
- Ma Y, Zhou H, Li C, Zou X, Luo X, Wu L, Li T, Chen X, Mao M, Huang Y, Li E, An Y, Zhang L, Wang T, Xu X, Yan W, Jiang Y, Wang Y. Differential Metabolites in Chinese Autistic Children: A Multi-Center Study Based on Urinary 1H-NMR Metabolomics Analysis. Frontiers In Psychiatry 2021, 12: 624767. PMID: 34045978, PMCID: PMC8144639, DOI: 10.3389/fpsyt.2021.624767.
- Yan W, Siegert RJ, Zhou H, Zou X, Wu L, Luo X, Li T, Huang Y, Guan H, Chen X, Mao M, Xia K, Zhang L, Li E, Li C, Zhang X, Zhou Y, Shih A, Fombonne E, Zheng Y, Han J, Sun Z, Jiang YH, Wang Y. Psychometric properties of the Chinese Parent Version of the Autism Spectrum Rating Scale: Rasch analysis. Autism 2021, 25: 1872-1884. PMID: 33845648, PMCID: PMC8548063, DOI: 10.1177/13623613211004054.
- Wang Y, Wei Y, Gao P, Sun S, Du Q, Wang Z, Jiang Y. Preparation of Fe3O4@PMAA@Ni Microspheres towards the Efficient and Selective Enrichment of Histidine-Rich Proteins. ACS Applied Materials & Interfaces 2021, 13: 11166-11176. PMID: 33635047, DOI: 10.1021/acsami.0c19734.
- Li Y, Sun S, Gao P, Zhang M, Fan C, Lu Q, Li C, Chen C, Lin B, Jiang Y. A tough chitosan-alginate porous hydrogel prepared by simple foaming method. Journal Of Solid State Chemistry 2021, 294: 121797. DOI: 10.1016/j.jssc.2020.121797.
- Jiang Y, Li W, Lindsey-Boltz L, Yang Y, Li Y, Sancar A. Super hotspots and super coldspots in the repair of UV-induced DNA damage in the human genome. Journal Of Biological Chemistry 2021, 296: 100581. PMID: 33771559, PMCID: PMC8081918, DOI: 10.1016/j.jbc.2021.100581.
- Liu C, Li D, Yang H, Li H, Xu Q, Zhou B, Hu C, Li C, Wang Y, Qiao Z, Jiang YH, Xu X. Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling. Progress In Neurobiology 2020, 200: 101985. PMID: 33388374, PMCID: PMC8572121, DOI: 10.1016/j.pneurobio.2020.101985.
- Wang T, Wang J, Ma Y, Zhou H, Ding D, Li C, Du X, Jiang YH, Wang Y, Long S, Li S, Lu G, Chen W, Zhou Y, Zhou S, Wang Y. High genetic burden in 163 Chinese children with status epilepticus. Seizure 2020, 84: 40-46. PMID: 33278787, DOI: 10.1016/j.seizure.2020.10.032.
- Du Q, Zhang C, Sun S, Wang Y, Liu H, Wei Y, Jiang Y. Magnetically Superamphiphobic Nanoparticles for Magnetic Response Surface Preparation. Langmuir 2020, 36: 14318-14323. PMID: 33205988, DOI: 10.1021/acs.langmuir.0c02582.
- Zhao C, Chai H, Zhou Q, Wen J, Reddy UM, Kastury R, Jiang Y, Mak W, Bale AE, Zhang H, Li P. Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss. Genetics In Medicine 2020, 23: 435-442. PMID: 33100332, DOI: 10.1038/s41436-020-01008-6.
- Wang Y, Gao P, Wei Y, Jin Y, Sun S, Wang Z, Jiang Y. Silver nanoparticles decorated magnetic polymer composites (Fe3O4@PS@Ag) as highly efficient reusable catalyst for the degradation of 4-nitrophenol and organic dyes. Journal Of Environmental Management 2020, 278: 111473. PMID: 33120097, DOI: 10.1016/j.jenvman.2020.111473.
- Sun S, Xiao Q, Ye C, Jiang Y. Biomacromolecular fluorescent nanoparticles co-assembled by bovine serum albumin and DNA segments for living cell imaging. Colloids And Surfaces A Physicochemical And Engineering Aspects 2020, 603: 125255. DOI: 10.1016/j.colsurfa.2020.125255.
- Zhou H, Lin Y, Zhao W, Teng Y, Cui Y, Wang T, Li C, Jiang YH, Zhang JJ, Wang Y. The role of Hipk2-p53 pathways in arsenic-induced autistic behaviors: A translational study from rats to humans. Environmental Pollution 2020, 267: 115568. PMID: 33254717, DOI: 10.1016/j.envpol.2020.115568.
- Kishnani S, Riley K, Mikati M, Jiang Y. Phenotypic Variability of an Inherited Pathogenic Variant in CIC Gene: A New Case Report in Two-Generation Family and Literature Review. Journal Of Pediatric Neurology 2020, 19: 193-201. DOI: 10.1055/s-0040-1714070.
- Hulbert SW, Wang X, Gbadegesin SO, Xu Q, Xu X, Jiang Y. A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination. Autism Research 2020, 13: 1685-1697. PMID: 32815320, PMCID: PMC7780289, DOI: 10.1002/aur.2353.
- Mei W, Jiang Z, Chen Y, Chen L, Sancar A, Jiang Y. Genome-wide circadian rhythm detection methods: systematic evaluations and practical guidelines. Briefings In Bioinformatics 2020, 22: bbaa135. PMID: 32672832, PMCID: PMC8138819, DOI: 10.1093/bib/bbaa135.
- Zhou H, Xu X, Yan W, Zou X, Wu L, Luo X, Li T, Huang Y, Guan H, Chen X, Mao M, Xia K, Zhang L, Li E, Ge X, Zhang L, Li C, Zhang X, Zhou Y, Ding D, Shih A, Fombonne E, Zheng Y, Han J, Sun Z, Jiang YH, Wang Y. Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years. Neuroscience Bulletin 2020, 36: 961-971. PMID: 32607739, PMCID: PMC7475160, DOI: 10.1007/s12264-020-00530-6.
- Wang Y, Bhattacharya T, Jiang Y, Qin X, Wang Y, Liu Y, Saykin A, Chen L. A novel deep learning method for predictive modeling of microbiome data. Briefings In Bioinformatics 2020, 22: bbaa073. PMID: 32406914, PMCID: PMC13017428, DOI: 10.1093/bib/bbaa073.
- Xiao Q, Sun S, Cheraga N, Wu K, Jiang Y, Huang N. Highly sensitive hair springs to measure the contraction force of engineered cardiac tissues. Materials Horizons 2020, 7: 1327-1330. DOI: 10.1039/c9mh01712g.
- Schoch K, Tan Q, Stong N, Deak KL, McConkie-Rosell A, McDonald MT, Network U, Goldstein D, Jiang Y, Shashi V. Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses. Genetics In Medicine 2020, 22: 1269-1275. PMID: 32366967, PMCID: PMC7335342, DOI: 10.1038/s41436-020-0781-x.
- Wang R, Lin D, Jiang Y. SCOPE: A Normalization and Copy-Number Estimation Method for Single-Cell DNA Sequencing. Cell Systems 2020, 10: 445-452.e6. PMID: 32437686, PMCID: PMC7250054, DOI: 10.1016/j.cels.2020.03.005.
- Wang Y, Shi L, Jin Y, Sun S, Gao P, Wei Y, Wang Z, Jiang Y. Surface-initiated polymerization for the preparation of magnetic polymer composites. Polymer Chemistry 2020, 11: 1797-1805. DOI: 10.1039/c9py01744e.
- Bey AL, Gorman MP, Gallentine W, Kohlenberg TM, Frankovich J, Jiang YH, Van Haren K. Subacute Neuropsychiatric Syndrome in Girls With SHANK3 Mutations Responds to Immunomodulation. PEDIATRICS 2020, 145: e20191490. PMID: 32015180, PMCID: PMC7802010, DOI: 10.1542/peds.2019-1490.
- Zhang C, Li Y, Sun S, Kalulu M, Wang Y, Zhou X, Wang X, Du Q, Jiang Y. Novel magnetic and flame-retardant superhydrophobic sponge for solar-assisted high-viscosity oil/water separation. Progress In Organic Coatings 2020, 139: 105369. DOI: 10.1016/j.porgcoat.2019.105369.
- Dong M, Thennavan A, Urrutia E, Li Y, Perou C, Zou F, Jiang Y. SCDC: bulk gene expression deconvolution by multiple single-cell RNA sequencing references. Briefings In Bioinformatics 2020, 22: 416-427. PMID: 31925417, PMCID: PMC7820884, DOI: 10.1093/bib/bbz166.
- An P, Gu D, Gao Z, Fan F, Jiang Y, Sun B. Hypoxia-augmented and photothermally-enhanced ferroptotic therapy with high specificity and efficiency. Journal Of Materials Chemistry B 2020, 8: 78-87. PMID: 31769461, DOI: 10.1039/c9tb02268f.
- Sun S, Xiao Q, Wei J, Wei Y, Wang Y, Gao P, Jiang Y. Bioinspired DNA self-assembly for targeted cancer cell imaging and drug delivery. Colloids And Surfaces A Physicochemical And Engineering Aspects 2020, 585: 124182. DOI: 10.1016/j.colsurfa.2019.124182.
- Sun A, Yuan Q, Fukuda M, Yu W, Yan H, Lim G, Nai M, D'Agostino G, Tran H, Itahana Y, Wang D, Lokman H, Itahana K, Lim S, Tang J, Chang Y, Zhang M, Cook S, Rackham O, Lim C, Tan E, Ng H, Lim K, Jiang Y, Je H. Potassium channel dysfunction in human neuronal models of Angelman syndrome. Science 2019, 366: 1486-1492. PMID: 31857479, PMCID: PMC7735558, DOI: 10.1126/science.aav5386.
- Sun S, Cheraga N, Jiang H, Xiao Q, Gao P, Wang Y, Wei Y, Wang X, Jiang Y. Bioinspired DNA nanocockleburs for targeted delivery of doxorubicin. Colloids And Surfaces B Biointerfaces 2019, 186: 110733. PMID: 31864113, DOI: 10.1016/j.colsurfb.2019.110733.
- Zhou X, Sun S, Zhang C, Wang X, Li Y, Jiang Y. Facile fabrication of durable superamphiphobic PET fabrics. Journal Of Coatings Technology And Research 2019, 17: 711-718. DOI: 10.1007/s11998-019-00289-0.
- Wang Y, Sun S, Shi L, Gao P, Wei Y, Zhang C, Jiang Y. Synthesis of Fe3O4@SiO2-PHEMA via redox of H2O2 and Fe2+ for efficient removal of Cu2+ from aqueous solution. Journal Of Molecular Liquids 2019, 296: 111865. DOI: 10.1016/j.molliq.2019.111865.
- Huh R, Yang Y, Jiang Y, Shen Y, Li Y. SAME-clustering: Single-cell Aggregated Clustering via Mixture Model Ensemble. Nucleic Acids Research 2019, 48: 86-95. PMID: 31777938, PMCID: PMC6943136, DOI: 10.1093/nar/gkz959.
- Zhao H, Wang Q, Yan T, Zhang Y, Xu H, Yu H, Tu Z, Guo X, Jiang Y, Li X, Zhou H, Zhang Y. Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates. Translational Psychiatry 2019, 9: 267. PMID: 31636273, PMCID: PMC6803711, DOI: 10.1038/s41398-019-0608-1.
- McConkie‐Rosell A, Schoch K, Sullivan J, Cope H, Spillmann R, Palmer C, Pena L, Jiang Y, Daniels N, Walley N, Tan K, Network U, Hooper S, Shashi V. The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease. Clinical Genetics 2019, 96: 521-531. PMID: 31448412, PMCID: PMC6983919, DOI: 10.1111/cge.13635.
- Wang X, Zhang C, Sun S, Kalulu M, Chen L, Zhou X, Jiang Y. Durable superhydrophobic coating based on inorganic/organic double-network polysiloxane and functionalized nanoparticles. Colloids And Surfaces A Physicochemical And Engineering Aspects 2019, 578: 123550. DOI: 10.1016/j.colsurfa.2019.06.016.
- Chen L, Peng H, Wei Y, Wang X, Jin Y, Liu H, Jiang Y. Self‐Healing Properties of PDMS Elastomers via Guanine and Cytosine Base Pairs. Macromolecular Chemistry And Physics 2019, 220 DOI: 10.1002/macp.201900280.
- Yang R, Walder-Christensen KK, Lalani S, Yan H, García-Prieto ID, Álvarez S, Fernández-Jaén A, Speltz L, Jiang YH, Bennett V. Neurodevelopmental mutation of giant ankyrin-G disrupts a core mechanism for axon initial segment assembly. Proceedings Of The National Academy Of Sciences Of The United States Of America 2019, 116: 19717-19726. PMID: 31451636, PMCID: PMC6765234, DOI: 10.1073/pnas.1909989116.
- Holt RJ, Young RM, Crespo B, Ceroni F, Curry CJ, Bellacchio E, Bax DA, Ciolfi A, Simon M, Fagerberg CR, van Binsbergen E, De Luca A, Memo L, Dobyns WB, Mohammed AA, Clokie SJH, Seco C, Jiang YH, Sørensen KP, Andersen H, Sullivan J, Powis Z, Chassevent A, Smith-Hicks C, Petrovski S, Antoniadi T, Shashi V, Gelb BD, Wilson SW, Gerrelli D, Tartaglia M, Chassaing N, Calvas P, Ragge NK. De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. American Journal Of Human Genetics 2019, 105: 640-657. PMID: 31402090, PMCID: PMC6731360, DOI: 10.1016/j.ajhg.2019.07.005.
- Wang SE, Jiang YH. Potential of Epigenetic Therapy for Prader-Willi Syndrome. Trends In Pharmacological Sciences 2019, 40: 605-608. PMID: 31353046, DOI: 10.1016/j.tips.2019.07.002.
- Yang R, Walder-Christensen KK, Kim N, Wu D, Lorenzo DN, Badea A, Jiang YH, Yin HH, Wetsel WC, Bennett V. ANK2 autism mutation targeting giant ankyrin-B promotes axon branching and ectopic connectivity. Proceedings Of The National Academy Of Sciences Of The United States Of America 2019, 116: 15262-15271. PMID: 31285321, PMCID: PMC6660793, DOI: 10.1073/pnas.1904348116.
- Mansour M, Haupt S, Chan A, Godde N, Rizzitelli A, Loi S, Caramia F, Deb S, Takano E, Bishton M, Johnstone C, Monahan B, Levav-Cohen Y, Jiang Y, Yap A, Fox S, Bernard O, Anderson R, Haupt Y. Retraction: The E3-ligase E6AP Represses Breast Cancer Metastasis via Regulation of ECT2-Rho Signaling. Cancer Research 2019, 79: 3008-3008. PMID: 31160311, DOI: 10.1158/0008-5472.can-19-1133.
- Environmentally safe, durable and transparent superhydrophobic coating prepared by one-step sprayingZhang C, Kalulu M, Sun S, Jiang P, Zhou X, Wei Y, Jiang Y. Environmentally safe, durable and transparent superhydrophobic coating prepared by one-step spraying. Colloids And Surfaces A Physicochemical And Engineering Aspects 2019, 570: 147-155. DOI: 10.1016/j.colsurfa.2019.03.015.
- Li Z, Lin J, Sibley A, Truong T, Chua K, Jiang Y, McCarthy J, Kroetz D, Allen A, Owzar K. Efficient estimation of grouped survival models. BMC Bioinformatics 2019, 20: 269. PMID: 31138120, PMCID: PMC6540566, DOI: 10.1186/s12859-019-2899-x.
- Cheng K, Zhang Y, Li Y, Gao Z, Chen F, Sun K, An P, Sun C, Jiang Y, Sun B. A novel pH-responsive hollow mesoporous silica nanoparticle (HMSN) system encapsulating doxorubicin (DOX) and glucose oxidase (GOX) for potential cancer treatment. Journal Of Materials Chemistry B 2019, 7: 3291-3302. DOI: 10.1039/c8tb03198c.
- Abdelnour E, Gallentine W, McDonald M, Sachdev M, Jiang YH, Mikati MA. Corrigendum to “Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature” [Seizure 55 (February) (2018) 1–3]. Seizure 2019, 69: 305. PMID: 31072785, DOI: 10.1016/j.seizure.2019.04.014.
- Kalulu M, Oderinde O, Wei Y, Zhang C, Hussain I, Han X, Jiang Y. Robust solvent‐free fabrication and characterization of (polydimethylsiloxane‐co‐2‐hydroxyethylmethacrylate)/poly (ethylene glycol) methacrylate (PDMS‐HEMA)/PEGMA hydrogels. Polymers For Advanced Technologies 2019, 30: 1922-1932. DOI: 10.1002/pat.4623.
- Kim Y, Wang SE, Jiang YH. Epigenetic therapy of Prader–Willi syndrome. Translational Research 2019, 208: 105-118. PMID: 30904443, PMCID: PMC6527448, DOI: 10.1016/j.trsl.2019.02.012.
- Urrutia E, Chen L, Zhou H, Jiang Y. Destin: toolkit for single-cell analysis of chromatin accessibility. Bioinformatics 2019, 35: 3818-3820. PMID: 30821321, PMCID: PMC6761983, DOI: 10.1093/bioinformatics/btz141.
- Li W, Liu W, Kakoki A, Wang R, Adebali O, Jiang Y, Sancar A. Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells. Journal Of Biological Chemistry 2019, 294: 5914-5922. PMID: 30808711, PMCID: PMC6463700, DOI: 10.1074/jbc.ra119.007861.
- Dong M, Jiang Y. Single-Cell Allele-Specific Gene Expression Analysis. Methods In Molecular Biology 2019, 1935: 155-174. PMID: 30758826, DOI: 10.1007/978-1-4939-9057-3_11.
- Xia X, Wang X, Zhang W, Han X, Chen P, Jiang Y. Improving the wettability and antiprotein adsorption property of PDMS by swelling–deswelling approach. Journal Of Coatings Technology And Research 2019, 16: 353-361. DOI: 10.1007/s11998-018-0070-7.
- Tremblay MW, Jiang YH. DNA Methylation and Susceptibility to Autism Spectrum Disorder. Annual Review Of Medicine 2019, 70: 151-166. PMID: 30691368, PMCID: PMC6597259, DOI: 10.1146/annurev-med-120417-091431.
- Yimit A, Adebali O, Sancar A, Jiang Y. Differential damage and repair of DNA-adducts induced by anti-cancer drug cisplatin across mouse organs. Nature Communications 2019, 10: 309. PMID: 30659176, PMCID: PMC6338751, DOI: 10.1038/s41467-019-08290-2.
- Jiang YH, Huang T. The history and current status of medical genetics and genomics system in the United States. 中华医学遗传学杂志 2019, 36: 1-6. PMID: 30722085, DOI: 10.3760/cma.j.issn.1003-9406.2019.01.001.
- Murdock D, Jiang Y, Wangler M, Khayat M, Sabo A, Juusola J, McWalter K, Schatz K, Gunay-Aygun M, Gibbs R. Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition. Molecular Case Studies 2019, 5: a003608. PMID: 30622101, PMCID: PMC6549549, DOI: 10.1101/mcs.a003608.
- Machol K, Rousseau J, Ehresmann S, Garcia T, Nguyen TTM, Spillmann RC, Sullivan JA, Shashi V, Jiang YH, Stong N, Fiala E, Willing M, Pfundt R, Kleefstra T, Cho MT, McLaughlin H, Rosello Piera M, Orellana C, Martínez F, Caro-Llopis A, Monfort S, Roscioli T, Nixon CY, Buckley MF, Turner A, Jones WD, van Hasselt PM, Hofstede FC, van Gassen KLI, Brooks AS, van Slegtenhorst MA, Lachlan K, Sebastian J, Madan-Khetarpal S, Sonal D, Sakkubai N, Thevenon J, Faivre L, Maurel A, Petrovski S, Krantz ID, Tarpinian JM, Rosenfeld JA, Lee BH, Campeau PM. Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. American Journal Of Human Genetics 2019, 104: 164-178. PMID: 30580808, PMCID: PMC6323608, DOI: 10.1016/j.ajhg.2018.11.007.
- Xu Q, Liu YY, Wang X, Tan GH, Li HP, Hulbert SW, Li CY, Hu CC, Xiong ZQ, Xu X, Jiang YH. Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons. Molecular Autism 2018, 9: 65. PMID: 30574290, PMCID: PMC6299922, DOI: 10.1186/s13229-018-0244-2.
- Towers AJ, Tremblay MW, Chung L, Li XL, Bey AL, Zhang W, Cao X, Wang X, Wang P, Duffney LJ, Siecinski SK, Xu S, Kim Y, Kong X, Gregory S, Xie W, Jiang YH. Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders. JCI Insight 2018, 3: e120592. PMID: 30518695, PMCID: PMC6328031, DOI: 10.1172/jci.insight.120592.
- Sun S, Xiao Q, Zhou X, Wei Y, Shi L, Jiang Y. A bio-based environment-friendly membrane with facile preparation process for oil-water separation. Colloids And Surfaces A Physicochemical And Engineering Aspects 2018, 559: 18-22. DOI: 10.1016/j.colsurfa.2018.09.038.
- Jiang Y, Wang R, Urrutia E, Anastopoulos I, Nathanson K, Zhang N. CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing. Genome Biology 2018, 19: 202. PMID: 30477554, PMCID: PMC6260772, DOI: 10.1186/s13059-018-1578-y.
- Yang Y, Hu J, Selby C, Li W, Yimit A, Jiang Y, Sancar A. Single-nucleotide resolution analysis of nucleotide excision repair of ribosomal DNA in humans and mice. Journal Of Biological Chemistry 2018, 294: 210-217. PMID: 30413533, PMCID: PMC6322885, DOI: 10.1074/jbc.ra118.006121.
- Xu Q, Li CY, Wang Y, Li HP, Wu BB, Jiang YH, Xu X. Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature. BMC Medical Genomics 2018, 11: 92. PMID: 30352594, PMCID: PMC6199733, DOI: 10.1186/s12920-018-0421-3.
- Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencingWu J, Yu P, Jin X, Xu X, Li J, Li Z, Wang M, Wang T, Wu X, Jiang Y, Cai W, Mei J, Min Q, Xu Q, Zhou B, Guo H, Wang P, Zhou W, Hu Z, Li Y, Cai T, Wang Y, Xia K, Jiang YH, Sun ZS. Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing. Journal Of Genetics And Genomics 2018, 45: 527-538. PMID: 30392784, DOI: 10.1016/j.jgg.2018.09.002.
- Tu Z, Zhao H, Li B, Yan S, Wang L, Tang Y, Li Z, Bai D, Li C, Lin Y, Li Y, Liu J, Xu H, Guo X, Jiang YH, Zhang YQ, Li XJ. CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms. Human Molecular Genetics 2018, 28: 561-571. PMID: 30329048, PMCID: PMC6489410, DOI: 10.1093/hmg/ddy367.
- Hulbert SW, Bey AL, Jiang Y. Environmental enrichment has minimal effects on behavior in the Shank3 complete knockout model of autism spectrum disorder. Brain And Behavior 2018, 8: e01107. PMID: 30317697, PMCID: PMC6236244, DOI: 10.1002/brb3.1107.
- Chung C, Ha S, Kang H, Lee J, Um SM, Yan H, Yoo YE, Yoo T, Jung H, Lee D, Lee E, Lee S, Kim J, Kim R, Kwon Y, Kim W, Kim H, Duffney L, Kim D, Mah W, Won H, Mo S, Kim JY, Lim CS, Kaang BK, Boeckers TM, Chung Y, Kim H, Jiang YH, Kim E. Early Correction of N-Methyl-D-Aspartate Receptor Function Improves Autistic-like Social Behaviors in Adult Shank2 −/− Mice. Biological Psychiatry 2018, 85: 534-543. PMID: 30466882, PMCID: PMC6420362, DOI: 10.1016/j.biopsych.2018.09.025.
- Sun S, Xiao Q, Wang Y, Jiang Y. Roles of alcohol desolvating agents on the size control of bovine serum albumin nanoparticles in drug delivery system. Journal Of Drug Delivery Science And Technology 2018, 47: 193-199. DOI: 10.1016/j.jddst.2018.07.018.
- Walley NM, Pena LDM, Hooper SR, Cope H, Jiang YH, McConkie-Rosell A, Sanders C, Schoch K, Spillmann RC, Strong K, McCray AT, Mazur P, Esteves C, LeBlanc K, Undiagnosed Diseases Network, Wise AL, Shashi V. Characteristics of undiagnosed diseases network applicants: implications for referring providers. BMC Health Services Research 2018, 18: 652. PMID: 30134969, PMCID: PMC6106923, DOI: 10.1186/s12913-018-3458-2.
- Wang Y, Zeng C, Li J, Zhou Z, Ju X, Xia S, Li Y, Liu A, Teng H, Zhang K, Shi L, Bi C, Xie W, He X, Jia Z, Jiang Y, Cai T, Wu J, Xia K, Sun Z. PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior. Cell Reports 2018, 24: 2029-2041. PMID: 30134165, DOI: 10.1016/j.celrep.2018.07.061.
- Jiang P, Li Y, Zhang C, Zhou X, Jiang Y. Fabrication of a superamphiphobic coating by a simple and flexible method. Particuology 2018, 39: 33-39. DOI: 10.1016/j.partic.2017.09.004.
- Kalulu M, Zhang W, Xia X, Oderinde O, Jiang Y. Hydrophilic surface modification of polydimetylsiloxane‐co‐2‐hydroxyethylmethacrylate (PDMS‐HEMA) by Silwet L‐77 (heptamethyltrisiloxane) surface treatment. Polymers For Advanced Technologies 2018, 29: 2601-2611. DOI: 10.1002/pat.4373.
- Tan Q, Cope H, Spillmann RC, Stong N, Jiang YH, McDonald MT, Rothman JA, Butler MW, Frush DP, Lachman RS, Lee B, Bacino CA, Bonner MJ, McCall CM, Pendse AA, Walley N, Network U, Shashi V, Pena L, Alejandro M, Azamian M, Bacino C, Balasubramanyam A, Bostwick B, Burrage L, Chen S, Clark G, Craigen W, Dhar S, Emrick L, Goldman A, Hanchard N, Jamal F, Karaviti L, Lalani S, Lee B, Lewis R, Marom R, Moretti P, Murdock D, Nicholas S, Orange J, Orengo J, Posey J, Potocki L, Rosenfeld J, Samson S, Scott D, Tran A, Vogel T, Bellen H, Wangler M, Yamamoto S, Eng C, Muzny D, Ward P, Yang Y, Goldstein D, Stong N, Cope H, Jiang Y, McConkie-Rosell A, Pena L, Schoch K, Shashi V, Spillmann R, Sullivan J, Tan Q, Walley N, Aaron A, Beggs A, Berry G, Briere L, Cooper C, Donnell-Fink L, Fieg E, High F, Korrick S, Krier J, Lincoln S, Loscalzo J, Maas R, MacRae C, Pallais J, Rodan L, Silverman E, Stoler J, Sweetser D, Walker M, Walsh C, Esteves C, Glanton E, Holm I, Kohane I, McCray A, Might M, LeBlanc K, Bick D, Birch C, Boone B, Brown D, Dorset D, Jones A, Lazar J, Levy S, May T, Newberry J, Worthey E, Batzli G, Colley H, Dayal J, Eckstein D, Gould S, Howerton E, Krasnewich D, Mamounas L, Manolio T, Mulvihill J, Urv T, Wise A, Brush M, Gourdine J, Haendel M, Koeller D, Kyle J, Metz T, Waters K, Webb-Robertson B, Ashley E, Bernstein J, Bonner D, Coakley T, Davidson J, Dries A, Enns G, Fernandez L, Fisher P, Friedman N, Hom J, Huang Y, Kohler J, Majcherska M, Marwaha S, McCormack C, Merker J, Reuter C, Sampson J, Smith K, Waggott D, Wheeler M, Zastrow D, Zhao C, Allard P, Barseghyan H, Butte M, Dell'Angelica E, Dipple K, Dorrani N, Douine E, Eskin A, Fogel B, Lee H, Loo S, Martin M, Martínez-Agosto J, Nelson S, Palmer C, Papp J, Parker N, Signer R, Sinsheimer J, Vilain E, Wan J, Yoon A, Zheng A, Behnam B, Burke E, D'Souza P, Davids M, Draper D, Estwick T, Ferreira C, Godfrey R, Groden C, Johnston J, Lau C, Macnamara E, Maduro V, Markello T, Morimoto M, Murphy J, Nehrebecky M, Novacic D, Pusey B, Sharma P, CamiloToro, Wahl C, Yu G, Gropman A, Baker E, Adams D, Gahl W, Malicdan M, Tifft C, Wolfe L, Yang J, Postlethwait J, Westerfield M, Bican A, Brokamp E, Duncan L, Hamid R, Kozuira M, Newman J, Phillips J, Rives L, Robertson A, Shakachite L, Cogan J. Further evidence for the involvement of EFL1 in a Shwachman–Diamond-like syndrome and expansion of the phenotypic features. Molecular Case Studies 2018, 4: a003046. PMID: 29970384, PMCID: PMC6169826, DOI: 10.1101/mcs.a003046.
- Zhou H, Li C, Luo X, Wu L, Huang Y, Zhang L, Zou X, Xu X, Jiang YH, Yan W, Wang Y. Cross-Cultural Revision and Psychometric Properties of the Chinese Version of the Autism Spectrum Rating Scale (2–5 Years). Frontiers In Neurology 2018, 9: 460. PMID: 30013502, PMCID: PMC6036302, DOI: 10.3389/fneur.2018.00460.
- Shashi V, Schoch K, Spillmann R, Cope H, Tan Q, Walley N, Pena L, McConkie-Rosell A, Jiang YH, Stong N, Need AC, Goldstein DB, Network U, Adams D, Alejandro M, Allard P, Ashley E, Azamian M, Bacino C, Balasubramanyam A, Barseghyan H, Batzli G, Beggs A, Behnam B, Bellen H, Bernstein J, Bican A, Bick D, Birch C, Bonner D, Boone B, Bostwick B, Briere L, Brown D, Brush M, Burke E, Burrage L, Butte M, Chen S, Clark G, Coakley T, Cogan J, Cooper C, Cope H, Craigen W, D’Souza P, Davids M, Davidson J, Dayal J, Dell’Angelica E, Dhar S, Dipple K, Donnell-Fink L, Dorrani N, Dorset D, Douine E, Draper D, Dries A, Eckstein D, Emrick L, Eng C, Enns G, Eskin A, Esteves C, Estwick T, Fernandez L, Ferreira C, Fisher P, Fogel B, Friedman N, Gahl W, Glanton E, Godfrey R, Goldstein D, Gould S, Gourdine J, Groden C, Gropman A, Haendel M, Hamid R, Hanchard N, Handley L, Herzog M, Holm I, Hom J, Howerton E, Huang Y, Jacob H, Jain M, Jiang Y, Johnston J, Jones A, Koeller D, Kohane I, Kohler J, Krasnewich D, Krieg E, Krier J, Kyle J, Lalani S, Lau C, Lazar J, LeBlanc K, Lee B, Lee H, Levy S, Lewis R, Lincoln S, Loo S, Loscalzo J, Maas R, Macnamara E, MacRae C, Maduro V, Majcherska M, Malicdan M, Mamounas L, Manolio T, Markello T, Marom R, Martin M, Martínez-Agosto J, Marwaha S, May T, McConkie-Rosell A, McCormack C, McCray A, Merker J, Metz T, Might M, Moretti P, Morimoto M, Mulvihill J, Murphy J, Muzny D, Nehrebecky M, Nelson S, Newberry J, Newman J, Nicholas S, Novacic D, Orange J, Pallais J, Palmer C, Papp J, Parker N, Pena L, Phillips J, Posey J, Postlethwait J, Potocki L, Pusey B, Reuter C, Robertson A, Rodan L, Rosenfeld J, Sampson J, Samson S, Schoch K, Schroeder M, Scott D, Sharma P, Shashi V, Silverman E, Sinsheimer J, Smith K, Spillmann R, Stoler J, Stong N, Sullivan J, Sweetser D, Tan Q, Tifft C, Toro C, Tran A, Urv T, Valivullah Z, Vilain E, Vogel T, Waggott D, Wahl C, Walley N, Walsh C, Wan J, Wangler M, Ward P, Waters K, Webb-Robertson B, Westerfield M, Wheeler M, Wise A, Wolfe L, Worthey E, Yamamoto S, Yang Y, Yoon A, Yu G, Zastrow D, Zhao C, Zheng A. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative. Genetics In Medicine 2018, 21: 161-172. PMID: 29907797, PMCID: PMC6295275, DOI: 10.1038/s41436-018-0044-2.
- Cheng Y, Li Z, Manupipatpong S, Lin L, Li X, Xu T, Jiang YH, Shu Q, Wu H, Jin P. 5-Hydroxymethylcytosine alterations in the human postmortem brains of autism spectrum disorder. Human Molecular Genetics 2018, 27: 2955-2964. PMID: 29790956, PMCID: PMC6097011, DOI: 10.1093/hmg/ddy193.
- Zhang W, Kalulu M, Wang X, Xia X, Han X, Jiang Y. Reverse hydrophobic PDMS surface to hydrophilic by 1‐step hydrolysis reaction. Polymers For Advanced Technologies 2018, 29: 2103-2109. DOI: 10.1002/pat.4319.
- Bey AL, Wang X, Yan H, Kim N, Passman RL, Yang Y, Cao X, Towers AJ, Hulbert SW, Duffney LJ, Gaidis E, Rodriguiz RM, Wetsel WC, Yin HH, Jiang YH. Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors. Translational Psychiatry 2018, 8: 94. PMID: 29700290, PMCID: PMC5919902, DOI: 10.1038/s41398-018-0142-6.
- Duffney LJ, Valdez P, Tremblay MW, Cao X, Montgomery S, McConkie‐Rosell A, Jiang Y. Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review. American Journal Of Medical Genetics Part B Neuropsychiatric Genetics 2018, 177: 426-433. PMID: 29704315, PMCID: PMC5980735, DOI: 10.1002/ajmg.b.32631.
- Jiang Y, Wangler M, McGuire A, Lupski J, Posey J, Khayat M, Murdock D, Sanchez‐Pulido L, Ponting C, Xia F, Hunter J, Meng Q, Murugan M, Gibbs R. The phenotypic spectrum of Xia‐Gibbs syndrome. American Journal Of Medical Genetics Part A 2018, 176: 1315-1326. PMID: 29696776, PMCID: PMC6231716, DOI: 10.1002/ajmg.a.38699.
- Luo W, Zhang C, Jiang YH, Brouwer CR. Systematic reconstruction of autism biology from massive genetic mutation profiles. Science Advances 2018, 4: e1701799. PMID: 29651456, PMCID: PMC5895441, DOI: 10.1126/sciadv.1701799.
- Sibley A, Li Z, Jiang Y, Li Y, Chan C, Allen A, Owzar K. Facilitating the Calculation of the Efficient Score Using Symbolic Computing. The American Statistician 2018, 72: 199-205. PMID: 30122786, PMCID: PMC6092959, DOI: 10.1080/00031305.2017.1392361.
- Liu CX, Li CY, Hu CC, Wang Y, Lin J, Jiang YH, Li Q, Xu X. CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors. Molecular Autism 2018, 9: 23. PMID: 29619162, PMCID: PMC5879542, DOI: 10.1186/s13229-018-0204-x.
- Zhao H, Jiang Y, Zhang YQ. Modeling autism in non‐human primates: Opportunities and challenges. Autism Research 2018, 11: 686-694. PMID: 29573234, PMCID: PMC6188783, DOI: 10.1002/aur.1945.
- Wei J, Sun S, Lu Q, Gao P, Wang Y, Li X, Jiang Y. The formation of fibers via complementary base pairing of DNA-conjugated bovine serum albumin. Chinese Chemical Letters 2018, 29: 461-463. DOI: 10.1016/j.cclet.2017.09.055.
- Urrutia E, Chen H, Zhou Z, Zhang N, Jiang Y. Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny. Bioinformatics 2018, 34: 2126-2128. PMID: 29415173, PMCID: PMC6248831, DOI: 10.1093/bioinformatics/bty057.
- Xu L, Richman AR, Mitchell LC, Luo H, Jiang YH, Roy S, Floyd AE. Evaluating Web-based Educational Modules on Genetic Testing for Autism among Parents of Children with Autism. American Journal Of Health Behavior 2018, 42: 3-12. PMID: 29973306, DOI: 10.5993/AJHB.42.4.1.
- McConkie‐Rosell A, Hooper SR, Pena LDM, Schoch K, Spillmann RC, Jiang Y, Cope H, Network U, Palmer C, Shashi V. Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? Journal Of Genetic Counseling 2018, 27: 935-946. PMID: 29297108, PMCID: PMC6028305, DOI: 10.1007/s10897-017-0193-5.
- Abdelnour E, Gallentine W, McDonald M, Sachdev M, Jiang YH, Mikati MA. Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature. Seizure 2017, 55: 1-3. PMID: 29291456, DOI: 10.1016/j.seizure.2017.11.017.
- Wei J, Wang T, Li H, Lu Q, Jiang Y. Design and synthesis of organo-silica shell based dual-functional microencapsulated phase change material for thermal regulating systems. Chemical Papers 2017, 72: 1055-1064. DOI: 10.1007/s11696-017-0315-4.
- Garman B, Anastopoulos I, Krepler C, Brafford P, Sproesser K, Jiang Y, Wubbenhorst B, Amaravadi R, Bennett J, Beqiri M, Elder D, Flaherty K, Frederick D, Gangadhar T, Guarino M, Hoon D, Karakousis G, Liu Q, Mitra N, Petrelli N, Schuchter L, Shannan B, Shields C, Wargo J, Wenz B, Wilson M, Xiao M, Xu W, Xu X, Yin X, Zhang N, Davies M, Herlyn M, Nathanson K. Genetic and Genomic Characterization of 462 Melanoma Patient-Derived Xenografts, Tumor Biopsies, and Cell Lines. Cell Reports 2017, 21: 1936-1952. PMID: 29141224, PMCID: PMC5709812, DOI: 10.1016/j.celrep.2017.10.052.
- Chung L, Bey AL, Towers AJ, Cao X, Kim IH, Jiang YH. Lovastatin suppresses hyperexcitability and seizure in Angelman syndrome model. Neurobiology Of Disease 2017, 110: 12-19. PMID: 29097328, PMCID: PMC5903876, DOI: 10.1016/j.nbd.2017.10.016.
- Wu S, Gan G, Zhang Z, Sun J, Wang Q, Gao Z, Li M, Jin S, Huang J, Thomas U, Jiang YH, Li Y, Tian R, Zhang YQ. A Presynaptic Function of Shank Protein in Drosophila. Journal Of Neuroscience 2017, 37: 11592-11604. PMID: 29074576, PMCID: PMC6705749, DOI: 10.1523/jneurosci.0893-17.2017.
- Pappas A, Bey A, Wang X, Rossi M, Kim Y, Yan H, Porkka F, Duffney L, Phillips S, Cao X, Ding J, Rodriguiz R, Yin H, Weinberg R, Ji R, Wetsel W, Jiang Y. Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers. JCI Insight 2017, 2: e92052. PMID: 29046483, PMCID: PMC5846902, DOI: 10.1172/jci.insight.92052.
- Pena LDM, Jiang YH, Schoch K, Spillmann RC, Walley N, Stong N, Horn S, Sullivan JA, McConkie-Rosell A, Kansagra S, Smith EC, El-Dairi M, Bellet J, Keels MA, Jasien J, Kranz PG, Noel R, Nagaraj SK, Lark RK, Wechsler DSG, del Gaudio D, Leung ML, Hendon LG, Parker CC, Jones KL, Goldstein D, Shashi V, Members U, Alejandro M, Bacino C, Balasubramanyam A, Bostwick B, Burrage L, Chen S, Clark G, Craigen W, Dhar S, Emrick L, Graham B, Hanchard N, Jain M, Lalani S, Lee B, Lewis R, Azamian M, Moretti P, Nicholas S, Orange J, Posey J, Potocki L, Rosenfeld J, Samson S, Scott D, Tran A, Vogel T, Zhang J, Bellen H, Wangler M, Yamamoto S, Eng C, Muzny D, Ward P, Yang Y, Goldstein D, Stong N, Jiang Y, McConkie-Rosell A, Pena L, Schoch K, Shashi V, Spillmann R, Sullivan J, Walley N, Beggs A, Briere L, Cooper C, Donnell-Fink L, Krieg E, Krier J, Lincoln S, Loscalzo J, Maas R, MacRae C, Pallais J, Rodan L, Silverman E, Stoler J, Sweetser D, Walsh C, Esteves C, Holm I, Kohane I, Mazur P, McCray A, Might M, Ramoni R, Splinter K, Bick D, Birch C, Boone B, Brown D, Dorset D, Handley L, Jacob H, Jones A, Lazar J, Levy S, Newberry J, Schroeder M, Strong K, Worthey E, Dayal J, Eckstein D, Gould S, Howerton E, Krasnewich D, Mamounas L, Manolio T, Mulvihill J, Urv T, Wise A, Soldatos A, Brush M, Gourdine J, Haendel M, Koeller D, Kyle J, Metz T, Waters K, Webb-Robertson B, Ashley E, Bernstein J, Dries A, Fisher P, Kohler J, Waggott D, Wheeler M, Zornio P, Allard P, Barseghyan H, Dell'Angelica E, Dillon A, Dipple K, Dorrani N, Douine E, Eskin A, Fogel B, Herzog M, Lee H, Lipson A, Loo S, Martínez-Agosto J, Nelson S, Palmer C, Papp J, Parker N, Sinsheimer J, Vilain E, Zheng A, Adams C, Burke E, Chao K, Davids M, Draper D, Estwick T, Frisby T, Frost K, Gartner V, Godfrey R, Goheen M, Golas G, Gordon M, Groden C, Hackbarth M, Hardee I, Johnston J, Koehler A, Latham L, Latour Y, Lau C, Levy D, Liebendorfer A, Macnamara E, Maduro V, Markello T, McCarty A, Murphy J, Nehrebecky M, Novacic D, Pusey B, Sadozai S, Schaffer K, Sharma P, Thomas S, Tolman N, Toro C, Valivullah Z, Wahl C, Warburton M, Weech A, Yu G, Gropman A, Adams D, Gahl W, Malicdan M, Tifft C, Wolfe L, Lee P, Postlethwait J, Westerfield M, Bican A, Cogan J, Hamid R, Newman J, Phillips J, Robertson A. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases. Genetics In Medicine 2017, 20: 464-469. PMID: 28914269, PMCID: PMC5851806, DOI: 10.1038/gim.2017.128.
- Maxwell K, Wubbenhorst B, Wenz B, De Sloover D, Pluta J, Emery L, Barrett A, Kraya A, Anastopoulos I, Yu S, Jiang Y, Chen H, Zhang N, Hackman N, D’Andrea K, Daber R, Morrissette J, Mitra N, Feldman M, Domchek S, Nathanson K. BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers. Nature Communications 2017, 8: 319. PMID: 28831036, PMCID: PMC5567274, DOI: 10.1038/s41467-017-00388-9.
- Sachdev M, Gaínza-Lein M, Tchapyjnikov D, Jiang YH, Loddenkemper T, Mikati MA. Novel clinical manifestations in patients with KCNA2 mutations. Seizure 2017, 51: 74-76. PMID: 28806589, DOI: 10.1016/j.seizure.2017.07.018.
- Zhao H, Tu Z, Xu H, Yan S, Yan H, Zheng Y, Yang W, Zheng J, Li Z, Tian R, Lu Y, Guo X, Jiang YH, Li XJ, Zhang YQ. Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate. Cell Research 2017, 27: 1293-1297. PMID: 28741620, PMCID: PMC5630686, DOI: 10.1038/cr.2017.95.
- Tan Q, McConkie-Rosell A, Juusola J, Gustafson KE, Pizoli CE, Buckley AF, Jiang YH. The importance of managing the patient and not the gene: expanded phenotype of GLE1-associated arthrogryposis. Molecular Case Studies 2017, 3: a002063. PMID: 28729373, PMCID: PMC5701308, DOI: 10.1101/mcs.a002063.
- Zhao Z, Zhang D, Tai L, Jiang P, Jiang Y. A facile and low-cost preparation of durable amphiphobic coatings with fluoride–silica@poly(methacrylic acid) hybrid nanocomposites. Journal Of Coatings Technology And Research 2017, 14: 1369-1380. DOI: 10.1007/s11998-017-9940-7.
- Chen H, Jiang Y, Maxwell K, Nathanson K, Zhang N. Allele-specific copy number estimation by whole exome sequencing. The Annals Of Applied Statistics 2017, 11: 1169-1192. PMID: 28989557, PMCID: PMC5627665, DOI: 10.1214/17-aoas1043.
- Wang Y, Du X, Bin R, Yu S, Xia Z, Zheng G, Zhong J, Zhang Y, Jiang Y, Wang Y. Erratum: Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing. Scientific Reports 2017, 7: 46520. PMID: 28472029, PMCID: PMC5417344, DOI: 10.1038/srep46520.
- Jiang Y, Zhang N, Li M. SCALE: modeling allele-specific gene expression by single-cell RNA sequencing. Genome Biology 2017, 18: 74. PMID: 28446220, PMCID: PMC5407026, DOI: 10.1186/s13059-017-1200-8.
- Wei J, Li Y, Gao P, Lu Q, Wang Z, Zhou J, Jiang Y. Assembling gold nanoparticles into flower-like structures by complementary base pairing of DNA molecules with mediation by apoferritins. Chemical Communications 2017, 53: 4581-4584. PMID: 28387779, DOI: 10.1039/c6cc09858d.
- Spillmann RC, McConkie-Rosell A, Pena L, Jiang YH, Undiagnosed Diseases Network, Schoch K, Walley N, Sanders C, Sullivan J, Hooper SR, Shashi V. A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network. Orphanet Journal Of Rare Diseases 2017, 12: 71. PMID: 28416019, PMCID: PMC5392939, DOI: 10.1186/s13023-017-0623-3.
- Hulbert SW, Jiang YH. Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain. Neuroscience Bulletin 2017, 33: 205-218. PMID: 28271437, PMCID: PMC5360850, DOI: 10.1007/s12264-017-0112-7.
- Zhou H, Zhang L, Luo X, Wu L, Zou X, Xia K, Wang Y, Xu X, Ge X, Jiang YH, Fombonne E, Yan W, Wang Y. Modifying the Autism Spectrum Rating Scale (6–18 years) to a Chinese Context: An Exploratory Factor Analysis. Neuroscience Bulletin 2017, 33: 175-182. PMID: 28238114, PMCID: PMC5360853, DOI: 10.1007/s12264-017-0104-7.
- Zhou H, Zhang L, Zou X, Luo X, Xia K, Wu L, Wang Y, Xu X, Ge X, Jiang YH, Fombonne E, Yan W, Wang Y. Chinese Norms for the Autism Spectrum Rating Scale. Neuroscience Bulletin 2017, 33: 161-167. PMID: 28233147, PMCID: PMC5360852, DOI: 10.1007/s12264-017-0105-6.
- Zhao Z, Tai L, Zhang D, Jiang Y. Facile fabrication of siloxane @ poly (methylacrylic acid) core-shell microparticles with different functional groups. Journal Of Nanoparticle Research 2017, 19: 73. DOI: 10.1007/s11051-017-3777-y.
- Mulkey SB, Ben‐Zeev B, Nicolai J, Carroll JL, Grønborg S, Jiang Y, Joshi N, Kelly M, Koolen DA, Mikati MA, Park K, Pearl PL, Scheffer IE, Spillmann RC, Taglialatela M, Vieker S, Weckhuysen S, Cooper EC, Cilio MR. Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain‐of‐function variants R201C and R201H. Epilepsia 2017, 58: 436-445. PMID: 28139826, PMCID: PMC5339037, DOI: 10.1111/epi.13676.
- Wang X, Xu J, Wang Q, Xu A, Zhai Y, Luo J, Jiang Y, He N, Wang Z. Wet Chemical Synthesis of Silica Nanosheets via Ethyl Acetate‐Mediated Hydrolysis of Silica Precursors and Their Applications. Small 2017, 13 PMID: 28112861, DOI: 10.1002/smll.201603369.
- Wang Y, Du X, Bin R, Yu S, Xia Z, Zheng G, Zhong J, Zhang Y, Jiang YH, Wang Y. Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing. Scientific Reports 2017, 7: 40319. PMID: 28074849, PMCID: PMC5225856, DOI: 10.1038/srep40319.
- Wang T, Li H, Lu Q, Wu N, Jiang Y. Preparation and Characterization of Glauber's Salt Microcapsules for Thermal Energy Storage. Tenside Surfactants Detergents 2017, 54: 32-37. DOI: 10.3139/113.110477.
- Zhao Z, Tai L, Zhang D, Wang Z, Jiang Y. Preparation of poly (octadecyl methacrylate)/silica-(3-methacryloxypropyl trimethoxysilane)/silica multi-layer core-shell nanocomposite with thermostable hydrophobicity and good viscosity break property. Chemical Engineering Journal 2017, 307: 891-896. DOI: 10.1016/j.cej.2016.09.021.
- Kim Y, Lee HM, Xiong Y, Sciaky N, Hulbert SW, Cao X, Everitt JI, Jin J, Roth BL, Jiang YH. Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader–Willi syndrome. Nature Medicine 2016, 23: 213-222. PMID: 28024084, PMCID: PMC5589073, DOI: 10.1038/nm.4257.
- Zhao Z, Li H, Lu Q, Li Y, Jiang Y. Multifunctional sensors based on silicone hydrogel and their responses to solvents, pH and solution composition. Polymer International 2016, 66: 566-572. DOI: 10.1002/pi.5293.
- Jiang Y, Ji Y, Sibley A, Li Y, Allen A. Leveraging population information in family‐based rare variant association analyses of quantitative traits. Genetic Epidemiology 2016, 41: 98-107. PMID: 27917519, DOI: 10.1002/gepi.22022.
- Han Q, Kim YH, Wang X, Liu D, Zhang ZJ, Bey AL, Lay M, Chang W, Berta T, Zhang Y, Jiang YH, Ji RR. SHANK3 Deficiency Impairs Heat Hyperalgesia and TRPV1 Signaling in Primary Sensory Neurons. Neuron 2016, 92: 1279-1293. PMID: 27916453, PMCID: PMC5182147, DOI: 10.1016/j.neuron.2016.11.007.
- Zhang W, Xia W, Wang Q, Towers AJ, Chen J, Gao R, Zhang Y, Yen CA, Lee AY, Li Y, Zhou C, Liu K, Zhang J, Gu TP, Chen X, Chang Z, Leung D, Gao S, Jiang YH, Xie W. Isoform Switch of TET1 Regulates DNA Demethylation and Mouse Development. Molecular Cell 2016, 64: 1062-1073. PMID: 27916660, DOI: 10.1016/j.molcel.2016.10.030.
- Zhao Z, Xie H, Li Y, Jiang Y. A multi-responsive multicomponent hydrogel with micro-phase separation structure: Synthesis and special drug release. Journal Of Drug Delivery Science And Technology 2016, 35: 184-189. DOI: 10.1016/j.jddst.2016.06.016.
- Zhao Z, Zhang D, Meng Y, Tai L, Jiang Y. One-pot fabrication of fluoride-silica@silica raspberry-like nanoparticles for superhydrophobic coating. Ceramics International 2016, 42: 14601-14608. DOI: 10.1016/j.ceramint.2016.06.076.
- Jiang Y, Qiu Y, Minn A, Zhang N. Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing. Proceedings Of The National Academy Of Sciences Of The United States Of America 2016, 113: e5528-e5537. PMID: 27573852, PMCID: PMC5027458, DOI: 10.1073/pnas.1522203113.
- Mansour M, Haupt S, Chan AL, Godde N, Rizzitelli A, Loi S, Caramia F, Deb S, Takano EA, Bishton M, Johnstone C, Monahan B, Levav-Cohen Y, Jiang YH, Yap AS, Fox S, Bernard O, Anderson R, Haupt Y. The E3-ligase E6AP Represses Breast Cancer Metastasis via Regulation of ECT2-Rho Signaling. Cancer Research 2016, 76: 4236-4248. PMID: 27231202, DOI: 10.1158/0008-5472.can-15-1553.
- Wang T, Wu N, Li H, Lu Q, Jiang Y. Preparation and properties of a form‐stable phase‐change hydrogel for thermal energy storage. Journal Of Applied Polymer Science 2016, 133 DOI: 10.1002/app.43836.
- Wang X, Bey AL, Katz BM, Badea A, Kim N, David LK, Duffney LJ, Kumar S, Mague SD, Hulbert SW, Dutta N, Hayrapetyan V, Yu C, Gaidis E, Zhao S, Ding JD, Xu Q, Chung L, Rodriguiz RM, Wang F, Weinberg RJ, Wetsel WC, Dzirasa K, Yin H, Jiang YH. Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism. Nature Communications 2016, 7: 11459. PMID: 27161151, PMCID: PMC4866051, DOI: 10.1038/ncomms11459.
- Xu Q, Goldstein J, Wang P, Gadi IK, Labreche H, Rehder C, Wang WP, McConkie A, Xu X, Jiang YH. Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge. Pediatric Research 2016, 80: 371-381. PMID: 27119313, PMCID: PMC5382808, DOI: 10.1038/pr.2016.101.
- Lu Q, Li H, Li M, Yang Y, Fan C, Wu P, Jiang Y, Zhang Z. The influence of vulcanizer on the crystal transform of iPP during reactive extrusion process. Polymer Degradation And Stability 2016, 126: 125-133. DOI: 10.1016/j.polymdegradstab.2016.02.001.
- Rosell AM, Pena LD, Schoch K, Spillmann R, Sullivan J, Hooper SR, Jiang Y, Mathey‐Andrews N, Goldstein DB, Shashi V. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders. Journal Of Genetic Counseling 2016, 25: 1019-1031. PMID: 26868367, DOI: 10.1007/s10897-016-9933-1.
- Li Y, Zhu M, Li X, Li X, Jiang Y. A highly expandable and tough polyacrylamide – alginate microcapsule. RSC Advances 2016, 6: 44896-44901. DOI: 10.1039/c6ra05711j.
- Lu Q, Meng Y, Gao P, Wei J, Sun S, Zhou J, Wang Z, Jiang Y. A pH responsive micelle combined with Au nanoparticles for multi-stimuli release of both hydrophobic and hydrophilic drug. RSC Advances 2016, 6: 58654-58657. DOI: 10.1039/c6ra11159a.
- Hulbert SW, Jiang Y. Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links. Neuroscience 2015, 321: 3-23. PMID: 26733386, PMCID: PMC4803542, DOI: 10.1016/j.neuroscience.2015.12.040.
- Xie H, Zhao Z, An S, Jiang Y. The influence of the surface properties of silicon–fluorine hydrogel on protein adsorption. Colloids And Surfaces B Biointerfaces 2015, 136: 1113-1119. PMID: 26612726, DOI: 10.1016/j.colsurfb.2015.11.027.
- Mikati MA, Jiang YH, Carboni M, Shashi V, Petrovski S, Spillmann R, Milligan CJ, Li M, Grefe A, McConkie A, Berkovic S, Scheffer I, Mullen S, Bonner M, Petrou S, Goldstein D. Quinidine in the treatment of KCNT1‐positive epilepsies. Annals Of Neurology 2015, 78: 995-999. PMID: 26369628, PMCID: PMC4811613, DOI: 10.1002/ana.24520.
- Tanaka AJ, Cho MT, Retterer K, Jones JR, Nowak C, Douglas J, Jiang YH, McConkie-Rosell A, Schaefer GB, Kaylor J, Rahman OA, Telegrafi A, Friedman B, Douglas G, Monaghan KG, Chung WK. De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features. Molecular Case Studies 2015, 2: a000661. PMID: 27148580, PMCID: PMC4849844, DOI: 10.1101/mcs.a000661.
- Chung L, Wang X, Zhu L, Towers AJ, Cao X, Kim IH, Jiang YH. Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice. Brain Research 2015, 1629: 340-350. PMID: 26474913, PMCID: PMC4744651, DOI: 10.1016/j.brainres.2015.10.015.
- Zhu M, Lu Q, Ma K, Meng Y, Jiang Y. Preparation and properties of controllable amphiphilic P(NIPAM-co-LMA) gel for drug delivery. Journal Of Drug Delivery Science And Technology 2015, 29: 245-250. DOI: 10.1016/j.jddst.2015.08.007.
- Petrovski S, Shashi V, Petrou S, Schoch K, McSweeney KM, Dhindsa RS, Krueger B, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB. Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition. Molecular Case Studies 2015, 1: a000257. PMID: 27148561, PMCID: PMC4850896, DOI: 10.1101/mcs.a000257.
- Shashi V, Petrovski S, Schoch K, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB. Sustained therapeutic response to riboflavin in a child with a progressive neurological condition, diagnosed by whole-exome sequencing. Molecular Case Studies 2015, 1: a000265. PMID: 27148562, PMCID: PMC4850881, DOI: 10.1101/mcs.a000265.
- Zhou H, Zhang L, Wu L, Zou X, Luo X, Xia K, Wang Y, Xu X, Ge X, Sun C, Deng H, Fombonne E, Jiang YH, Yan W, Wang Y. Validity and reliability analysis of the Chinese parent version of the Autism Spectrum Rating Scale (6–18 years). Psychiatry Research 2015, 230: 255-261. PMID: 26384573, DOI: 10.1016/j.psychres.2015.09.003.
- Zhang Z, Gao P, Wang Z, Sun B, Jiang Y. DNA-caged gold nanoparticles for controlled release of doxorubicin triggered by a DNA enzyme and pH. Chemical Communications 2015, 51: 12996-12999. PMID: 26178750, DOI: 10.1039/c5cc05164a.
- Jiang Y, Han Y, Petrovski S, Owzar K, Goldstein D, Allen A. Incorporating Functional Information in Tests of Excess De Novo Mutational Load. American Journal Of Human Genetics 2015, 97: 272-283. PMID: 26235986, PMCID: PMC4573447, DOI: 10.1016/j.ajhg.2015.06.013.
- Meng Y, Wei J, Gao P, Jiang Y. Self-assembling amphiphilic poly(propargyl methacrylate) grafted DNA copolymers into multi-strand helices. Soft Matter 2015, 11: 5610-5613. PMID: 26096216, DOI: 10.1039/c5sm01325a.
- Zhao Z, An S, Xie H, Han X, Wang F, Jiang Y. The Relationship between the Hydrophilicity and Surface Chemical Composition Microphase Separation Structure of Multicomponent Silicone Hydrogels. The Journal Of Physical Chemistry B 2015, 119: 9780-9786. PMID: 26125331, DOI: 10.1021/acs.jpcb.5b04202.
- Williams C, Jiang Y, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S. Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy. Clinical Genetics 2015, 88: 597-599. PMID: 25823418, DOI: 10.1111/cge.12581.
- Wang Y, Wang P, Xu X, Goldstein J, McConkie A, Cheung S, Jiang Y. Genetics of Autism Spectrum Disorders: The Opportunity and Challenge in the Genetics Clinic. Contemporary Clinical Neuroscience 2015, 33-66. DOI: 10.1007/978-1-4939-2190-4_4.
- Shashi V, McConkie‐Rosell A, Schoch K, Kasturi V, Rehder C, Jiang YH, Goldstein DB, McDonald MT. Practical considerations in the clinical application of whole‐exome sequencing. Clinical Genetics 2015, 89: 173-181. PMID: 25678066, DOI: 10.1111/cge.12569.
- Williams JA, Hanna JM, Shah AA, Andersen ND, McDonald MT, Jiang YH, Wechsler SB, Zomorodi A, McCann RL, Hughes GC. Adult Surgical Experience With Loeys-Dietz Syndrome. The Annals Of Thoracic Surgery 2015, 99: 1275-1281. PMID: 25678502, DOI: 10.1016/j.athoracsur.2014.11.021.
- Jiang Y, McCarthy J, Allen A. Testing the Effect of Rare Compound‐Heterozygous and Recessive Mutations in Case–Parent Sequencing Studies. Genetic Epidemiology 2015, 39: 166-172. PMID: 25631493, DOI: 10.1002/gepi.21885.
- Jiang Y, Oldridge D, Diskin S, Zhang N. CODEX: a normalization and copy number variation detection method for whole exome sequencing. Nucleic Acids Research 2015, 43: e39-e39. PMID: 25618849, PMCID: PMC4381046, DOI: 10.1093/nar/gku1363.
- Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, Ben-Zeev B, Nissenkorn A, Anikster Y, Oz-Levi D, Dhindsa RS, Hitomi Y, Schoch K, Spillmann RC, Heimer G, Marek-Yagel D, Tzadok M, Han Y, Worley G, Goldstein J, Jiang YH, Lancet D, Pras E, Shashi V, McHale D, Need AC, Goldstein DB. Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genetics In Medicine 2015, 17: 774-781. PMID: 25590979, PMCID: PMC4791490, DOI: 10.1038/gim.2014.191.
- Zhu M, Li Y, Zhang Z, Jiang Y. Preparation and properties of stretchable and tough alginate/polyacrylamide hollow capsules. RSC Advances 2015, 5: 33262-33268. DOI: 10.1039/c5ra03465e.
- Zhao Z, Xie H, An S, Jiang Y. The Relationship between Oxygen Permeability and Phase Separation Morphology of the Multicomponent Silicone Hydrogels. The Journal Of Physical Chemistry B 2014, 118: 14640-14647. PMID: 25423615, DOI: 10.1021/jp507682k.
- Zhao Z, An S, Xie H, Jiang Y. Copolymerization and properties of multicomponent crosslinked hydrogels. Chinese Journal Of Polymer Science 2014, 33: 173-183. DOI: 10.1007/s10118-015-1565-7.
- Zhang Z, Meng Y, Zhu M, Wang Z, Jiang Y. Threading different metal nanomaterials on natural PhiX174 DNA to assemble a necklace. RSC Advances 2014, 4: 47268-47271. DOI: 10.1039/c4ra06722c.
- Hennessey JA, Boczek NJ, Jiang YH, Miller JD, Patrick W, Pfeiffer R, Sutphin BS, Tester DJ, Barajas-Martinez H, Ackerman MJ, Antzelevitch C, Kanter R, Pitt GS. A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis. PLOS ONE 2014, 9: e106982. PMID: 25184293, PMCID: PMC4153713, DOI: 10.1371/journal.pone.0106982.
- Bey AL, Jiang Y. Overview of Mouse Models of Autism Spectrum Disorders. Current Protocols In Pharmacology 2014, 66: 5.66.1-5.66.26. PMID: 25181011, PMCID: PMC4186887, DOI: 10.1002/0471141755.ph0566s66.
- Li Y, Meng Y, Zhang Z, Jiang Y. Detecting the Oligomeric State of Escherichia coli MutS from Its Geometric Architecture Observed by an Atomic Force Microscope at a Single Molecular Level. The Journal Of Physical Chemistry B 2014, 118: 9218-9224. PMID: 25029278, DOI: 10.1021/jp504644r.
- Jiang YH, Wang Y, Xiu X, Choy KW, Pursley AN, Cheung SW. Genetic diagnosis of autism spectrum disorders: The opportunity and challenge in the genomics era. Critical Reviews In Clinical Laboratory Sciences 2014, 51: 249-262. PMID: 24878448, PMCID: PMC5937018, DOI: 10.3109/10408363.2014.910747.
- Du X, An Y, Yu L, Liu R, Qin Y, Guo X, Sun D, Zhou S, Wu B, Jiang YH, Wang Y. A genomic copy number variant analysis implicates the MBD5 and HNRNPUgenes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion. BMC Medical Genomics 2014, 15: 62. PMID: 24885232, PMCID: PMC4061518, DOI: 10.1186/1471-2350-15-62.
- Jiang Y, Satten G, Han Y, Epstein M, Heinzen E, Goldstein D, Allen A. Utilizing Population Controls in Rare-Variant Case-Parent Association Tests. American Journal Of Human Genetics 2014, 94: 845-853. PMID: 24836453, PMCID: PMC4121482, DOI: 10.1016/j.ajhg.2014.04.014.
- Wang X, Xu Q, Bey AL, Lee Y, Jiang YH. Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice. Molecular Autism 2014, 5: 30. PMID: 25071925, PMCID: PMC4113141, DOI: 10.1186/2040-2392-5-30.
- Tian Y, Li Y, Wang Z, Jiang Y. Nuclease-responsive DNA–PEI hollow microcapsules for bio-stimuli controlled release. Journal Of Materials Chemistry B 2014, 2: 1667-1672. PMID: 32261395, DOI: 10.1039/c3tb21191f.
- Prasun P, Young S, Salomons G, Werneke A, Jiang Y, Struys E, Paige M, Avantaggiati M, McDonald M. Expanding the Clinical Spectrum of Mitochondrial Citrate Carrier (SLC25A1) Deficiency: Facial Dysmorphism in Siblings with Epileptic Encephalopathy and Combined D,L-2-Hydroxyglutaric Aciduria. JIMD Reports 2014, 19: 111-115. PMID: 25614306, PMCID: PMC4501236, DOI: 10.1007/8904_2014_378.
- Hayrapetyan V, Castro S, Sukharnikova T, Yu C, Cao X, Jiang YH, Yin HH. Region‐specific impairments in striatal synaptic transmission and impaired instrumental learning in a mouse model of Angelman syndrome. European Journal Of Neuroscience 2013, 39: 1018-1025. PMID: 24329862, PMCID: PMC5937017, DOI: 10.1111/ejn.12442.
- Zhu L, Wang X, Li XL, Towers A, Cao X, Wang P, Bowman R, Yang H, Goldstein J, Li YJ, Jiang YH. Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders. Human Molecular Genetics 2013, 23: 1563-1578. PMID: 24186872, PMCID: PMC3929093, DOI: 10.1093/hmg/ddt547.
- Wang X, Bey AL, Chang L, Krystal AD, Jiang Y. Therapeutic approaches for shankopathies. Developmental Neurobiology 2013, 74: 123-135. PMID: 23536326, PMCID: PMC3883807, DOI: 10.1002/dneu.22084.
- Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB. Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy. Neuron 2013, 80: 429-441. PMID: 24139043, PMCID: PMC3820368, DOI: 10.1016/j.neuron.2013.08.013.
- Shashi V, McConkie-Rosell A, Rosell B, Schoch K, Vellore K, McDonald M, Jiang YH, Xie P, Need A, Goldstein DB. The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders. Genetics In Medicine 2013, 16: 176-182. PMID: 23928913, DOI: 10.1038/gim.2013.99.
- Jiang YH, Yuen RK, Jin X, Wang M, Chen N, Wu X, Ju J, Mei J, Shi Y, He M, Wang G, Liang J, Wang Z, Cao D, Carter MT, Chrysler C, Drmic IE, Howe JL, Lau L, Marshall CR, Merico D, Nalpathamkalam T, Thiruvahindrapuram B, Thompson A, Uddin M, Walker S, Luo J, Anagnostou E, Zwaigenbaum L, Ring RH, Wang J, Lajonchere C, Wang J, Shih A, Szatmari P, Yang H, Dawson G, Li Y, Scherer SW. Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing. American Journal Of Human Genetics 2013, 93: 249-263. PMID: 23849776, PMCID: PMC3738824, DOI: 10.1016/j.ajhg.2013.06.012.
- Chan A, Grossman T, Zuckerman V, Di Giammartino D, Moshel O, Scheffner M, Monahan B, Pilling P, Jiang Y, Haupt S, Schueler-Furman O, Haupt Y. c‑Abl Phosphorylates E6AP and Regulates Its E3 Ubiquitin Ligase Activity. Biochemistry 2013, 52: 3119-3129. PMID: 23581475, DOI: 10.1021/bi301710c.
- Huang H, Philpot B, Jiang Y. Epigenetic Therapies in Neurological Diseases. Epigenetics And Human Health 2013, 167-193. DOI: 10.1007/978-3-642-36827-1_8.
- Jiang YH, Ehlers MD. Modeling Autism by SHANK Gene Mutations in Mice. Neuron 2013, 78: 8-27. PMID: 23583105, PMCID: PMC3659167, DOI: 10.1016/j.neuron.2013.03.016.
- Miao S, Chen R, Ye J, Tan G, Li S, Zhang J, Jiang Y, Xiong Z. The Angelman Syndrome Protein Ube3a Is Required for Polarized Dendrite Morphogenesis in Pyramidal Neurons. Journal Of Neuroscience 2013, 33: 327-333. PMID: 23283345, PMCID: PMC6618628, DOI: 10.1523/jneurosci.2509-12.2013.
- Wetsel W, Moy S, Jiang Y. Chapter 4.1 Mouse Behavioral Models for Autism Spectrum Disorders. 2013, 363-378. DOI: 10.1016/b978-0-12-391924-3.00026-0.
- Yin Y, Zhu W, Guo L, Yang R, Li X, Jiang Y. RGDC Functionalized Titanium Dioxide Nanoparticles Induce Less Damage to Plasmid DNA but Higher Cytotoxicity to HeLa Cells. The Journal Of Physical Chemistry B 2012, 117: 125-131. PMID: 23210915, DOI: 10.1021/jp3092804.
- Chung L, Bey AL, Jiang YH. Synaptic Plasticity in Mouse Models of Autism Spectrum Disorders. Korean Journal Of Physiology And Pharmacology 2012, 16: 369-378. PMID: 23269898, PMCID: PMC3526740, DOI: 10.4196/kjpp.2012.16.6.369.
- Wolyniec K, Levav-Cohen Y, Jiang Y, Haupt S, Haupt Y. The E6AP E3 ubiquitin ligase regulates the cellular response to oxidative stress. Oncogene 2012, 32: 3510-3519. PMID: 22986523, DOI: 10.1038/onc.2012.365.
- Bi C, Wu J, Jiang T, Liu Q, Cai W, Yu P, Cai T, Zhao M, Jiang Y, Sun ZS. Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility. Human Mutation 2012, 33: 1635-1638. PMID: 22865819, DOI: 10.1002/humu.22174.
- Wolyniec K, Shortt J, de Stanchina E, Levav-Cohen Y, Alsheich-Bartok O, Louria-Hayon I, Corneille V, Kumar B, Woods S, Opat S, Johnstone R, Scott C, Segal D, Pandolfi P, Fox S, Strasser A, Jiang Y, Lowe S, Haupt S, Haupt Y. E6AP ubiquitin ligase regulates PML-induced senescence in Myc-driven lymphomagenesis. Blood 2012, 120: 822-832. PMID: 22689861, PMCID: PMC3709628, DOI: 10.1182/blood-2011-10-387647.
- Jiang Y, Lai L, Zhou J. Single-bit failure analysis at a nanometer resolution by conductive atomic force microscopy. Microelectronics Reliability 2012, 52: 159-164. DOI: 10.1016/j.microrel.2011.08.008.
- Levav-Cohen Y, Wolyniec K, Alsheich-Bartok O, Chan A, Woods S, Jiang Y, Haupt S, Haupt Y. E6AP is required for replicative and oncogene-induced senescence in mouse embryo fibroblasts. Oncogene 2011, 31: 2199-2209. PMID: 21927031, DOI: 10.1038/onc.2011.402.
- Jiang Y, Marszalek P. Atomic force microscopy captures MutS tetramers initiating DNA mismatch repair. The EMBO Journal 2011, 30: 2881-2893. PMID: 21666597, PMCID: PMC3160242, DOI: 10.1038/emboj.2011.180.
- Wang X, McCoy PA, Rodriguiz RM, Pan Y, Je HS, Roberts AC, Kim CJ, Berrios J, Colvin JS, Bousquet-Moore D, Lorenzo I, Wu G, Weinberg RJ, Ehlers MD, Philpot BD, Beaudet AL, Wetsel WC, Jiang YH. Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3. Human Molecular Genetics 2011, 20: 3093-3108. PMID: 21558424, PMCID: PMC3131048, DOI: 10.1093/hmg/ddr212.
- Veerapandiyan A, Shashi V, Jiang Y, Gallentine W, Schoch K, Smith E. Pseudometabolic presentation of dystrophinopathy due to a missense mutation. Muscle & Nerve 2010, 42: 975-979. PMID: 21104870, PMCID: PMC5506871, DOI: 10.1002/mus.21823.
- Jiang Y, Rabbi M, Mieczkowski P, Marszalek P. Separating DNA with Different Topologies by Atomic Force Microscopy in Comparison with Gel Electrophoresis. The Journal Of Physical Chemistry B 2010, 114: 12162-12165. PMID: 20799746, PMCID: PMC2963572, DOI: 10.1021/jp105603k.
- Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL. Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3. PLOS ONE 2010, 5: e12278. PMID: 20808828, PMCID: PMC2924885, DOI: 10.1371/journal.pone.0012278.
- Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome. Neuroscience Letters 2009, 487: 129-133. PMID: 19563863, PMCID: PMC2888840, DOI: 10.1016/j.neulet.2009.06.079.
- Jiang Y, Fang P, Adesina AM, Furman P, Johnston JJ, Biesecker LG, Brown CW. Molecular characterization of co‐occurring Duchenne muscular dystrophy and X‐linked oculo‐facio‐cardio‐dental syndrome in a girl. American Journal Of Medical Genetics Part A 2009, 149A: 1249-1252. PMID: 19449433, PMCID: PMC2819399, DOI: 10.1002/ajmg.a.32863.
- Ke C, Loksztejn A, Jiang Y, Kim M, Humeniuk M, Rabbi M, Marszalek P. Detecting Solvent-Driven Transitions of poly(A) to Double-Stranded Conformations by Atomic Force Microscopy. Biophysical Journal 2009, 96: 2918-2925. PMID: 19348773, PMCID: PMC2711269, DOI: 10.1016/j.bpj.2008.12.3939.
- Louria-Hayon I, Alsheich-Bartok O, Levav-Cohen Y, Silberman I, Berger M, Grossman T, Matentzoglu K, Jiang Y, Muller S, Scheffner M, Haupt S, Haupt Y. E6AP promotes the degradation of the PML tumor suppressor. Cell Death & Differentiation 2009, 16: 1156-1166. PMID: 19325566, DOI: 10.1038/cdd.2009.31.
- Jiang Y, Rabbi M, Kim M, Ke C, Lee W, Clark R, Mieczkowski P, Marszalek P. UVA Generates Pyrimidine Dimers in DNA Directly. Biophysical Journal 2009, 96: 1151-1158. PMID: 19186150, PMCID: PMC2716568, DOI: 10.1016/j.bpj.2008.10.030.
- Jiang Y, Martinez JE, Ou Z, Cooper ML, Kang S, Pursley A, Cheung SW. De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently “balanced” paracentric inversion of 14(q21q23). American Journal Of Medical Genetics Part A 2008, 146A: 1986-1993. PMID: 18627051, DOI: 10.1002/ajmg.a.32408.
- Ke C, Jiang Y, Mieczkowski P, Muramoto G, Chute J, Marszalek P. Nanoscale Detection of Ionizing Radiation Damage to DNA by Atomic Force Microscopy. Small 2008, 4: 288-294. PMID: 18247386, DOI: 10.1002/smll.200700527.
- Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region. BMC Genomics 2008, 9: 50. PMID: 18226259, PMCID: PMC2268926, DOI: 10.1186/1471-2164-9-50.
- Jiang Y, Ke C, Mieczkowski P, Marszalek P. Detecting Ultraviolet Damage in Single DNA Molecules by Atomic Force Microscopy. Biophysical Journal 2007, 93: 1758-1767. PMID: 17483180, PMCID: PMC1948057, DOI: 10.1529/biophysj.107.108209.
- Wang Y, Chan C, Jiang Y, Li L, Ng K. AFM Studies of the Molecular Weight Dependence of Lamellar Growth Kinetics of Polymers near the Glass Transition Temperature. Macromolecules 2007, 40: 4002-4008. DOI: 10.1021/ma062717y.
- Organization process of the hierarchical structures in microbially synthesized polyhydroxyalkanoatesXu J, Guo B, Wu Q, Chen J, Chen G, Zhou J, Jiang Y, Li L. Organization process of the hierarchical structures in microbially synthesized polyhydroxyalkanoates. Current Applied Physics 2007, 7: e41-e44. DOI: 10.1016/j.cap.2006.11.012.
- Ke C, Jiang Y, Rivera M, Clark R, Marszalek P. Pulling Geometry-Induced Errors in Single Molecule Force Spectroscopy Measurements. Biophysical Journal 2007, 92: l76-l78. PMID: 17324999, PMCID: PMC1852342, DOI: 10.1529/biophysj.107.104901.
- van Woerden GM, Harris KD, Hojjati MR, Gustin RM, Qiu S, de Avila Freire R, Jiang YH, Elgersma Y, Weeber EJ. Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of αCaMKII inhibitory phosphorylation. Nature Neuroscience 2007, 10: 280-282. PMID: 17259980, DOI: 10.1038/nn1845.
- Lee G, Abdi K, Jiang Y, Michaely P, Bennett V, Marszalek P. Nanospring behaviour of ankyrin repeats. Nature 2006, 440: 246-249. PMID: 16415852, DOI: 10.1038/nature04437.
- Yu H, Liu R, Shen D, Jiang Y, Huang Y. Study on morphology and orientation of cellulose in the vascular bundle of wheat straw. Polymer 2005, 46: 5689-5694. DOI: 10.1016/j.polymer.2005.05.052.
- Chen W, Zhao Y, Jiang Y, Yan D, Han C. Light‐Scattering Study of the Aggregation of Syndiotactic Poly(methyl methacrylate) in Solution. ChemPhysChem 2004, 5: 1745-1749. PMID: 15580935, DOI: 10.1002/cphc.200400175.
- Duan Y, Jiang Y, Jiang S, Li L, Yan S, Schultz J. Depletion-Induced Nonbirefringent Banding in Thin Isotactic Polystyrene Thin Films. Macromolecules 2004, 37: 9283-9286. DOI: 10.1021/ma0483165.
- Jiang YH, Bressler J, Beaudet AL. EPIGENETICS AND HUMAN DISEASE. Annual Review Of Genomics And Human Genetics 2004, 5: 479-510. PMID: 15485357, DOI: 10.1146/annurev.genom.5.061903.180014.
- Jiang Y, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. American Journal Of Medical Genetics Part A 2004, 131A: 1-10. PMID: 15389703, DOI: 10.1002/ajmg.a.30297.
- Wang Y, Chan C, Ng K, Jiang Y, Li L. Real-Time Observation of Lamellar Branching Induced by an AFM Tip and the Stability of Induced Nuclei. Langmuir 2004, 20: 8220-8223. PMID: 15350095, DOI: 10.1021/la035293z.
- Jiang YH, Beaudet AL. Human disorders of ubiquitination and proteasomal degradation. Current Opinion In Pediatrics 2004, 16: 419-426. PMID: 15273504, DOI: 10.1097/01.mop.0000133634.79661.cd.
- Xu J, Guo B, Zhang Z, Zhou J, Jiang Y, Yan S, Li L, Wu Q, Chen G, Schultz J. Direct AFM Observation of Crystal Twisting and Organization in Banded Spherulites of Chiral Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate). Macromolecules 2004, 37: 4118-4123. DOI: 10.1021/ma0499122.
- Belmonte MK, Cook EH, Anderson GM, Rubenstein JL, Greenough WT, Beckel-Mitchener A, Courchesne E, Boulanger LM, Powell SB, Levitt PR, Perry EK, Jiang YH, DeLorey TM, Tierney E. Autism as a disorder of neural information processing: directions for research and targets for therapy. Molecular Psychiatry 2004, 9: 646-663. PMID: 15037868, DOI: 10.1038/sj.mp.4001499.
- Li-Mei Q, Yong J, Fen L, Liang-Zhong Z. XPS Investigation of the Spherulite Surface for Poly(ε-caprolactone)/poly(vinyl chloride). Acta Physico-Chimica Sinica 2004, 20: 47-49. DOI: 10.3866/pku.whxb20040110.
- Tsai T, Bressler J, Jiang Y, Beaudet AL. Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells. Genesis 2003, 37: 151-161. PMID: 14666508, DOI: 10.1002/gene.10237.
- Jiang Y, Jin X, Han C, Li L, Wang Y, Chan C. Melting Behaviors of Lamellar Crystals of Poly(bisphenol A-co-decane ether) Studied by in-Situ Atomic Force Microscopy. Langmuir 2003, 19: 8010-8018. DOI: 10.1021/la0343775.
- Jiang Y, Zhou J, Li L, Xu J, Guo B, Zhang Z, Wu Q, Chen G, Weng L, Cheung Z, Chan C. Surface Properties of Poly(3-hydroxybutyrate-co-3- hydroxyvalerate) Banded Spherulites Studied by Atomic Force Microscopy and Time-of-Flight Secondary Ion Mass Spectrometry. Langmuir 2003, 19: 7417-7422. DOI: 10.1021/la034865c.
- Lei Y, Chan C, Wang Y, Ng K, Jiang Y, Lin L. Growth process of homogeneously and heterogeneously nucleated spherulites as observed by atomic force microscopy. Polymer 2003, 44: 4673-4679. DOI: 10.1016/s0032-3861(03)00440-3.
- Jiang Y, Gu Q, Li L, Shen D, Jin X, Chan C. Conformational changes in the induction period of crystallization as measured by FT-IR. Polymer 2003, 44: 3509-3513. DOI: 10.1016/s0032-3861(03)00278-7.
- Jiang Y, Yan D, Gao X, Han C, Jin X, Li L, Wang Y, Chan C. Lamellar Branching of Poly(bisphenol A-co-decane) Spherulites at Different Temperatures Studied by High-Temperature AFM. Macromolecules 2003, 36: 3652-3655. DOI: 10.1021/ma0341061.
- Weeber EJ, Jiang YH, Elgersma Y, Varga AW, Carrasquillo Y, Brown SE, Christian JM, Mirnikjoo B, Silva A, Beaudet AL, Sweatt JD. Derangements of Hippocampal Calcium/Calmodulin-Dependent Protein Kinase II in a Mouse Model for Angelman Mental Retardation Syndrome. Journal Of Neuroscience 2003, 23: 2634-2644. PMID: 12684449, PMCID: PMC6742065, DOI: 10.1523/jneurosci.23-07-02634.2003.
- Luo Y, Jiang Y, Jin X, Li L, Chan C. Real‐time AFM study of lamellar growth of semi‐crystalline polymers. Macromolecular Symposia 2003, 192: 271-280. DOI: 10.1002/masy.200390037.
- Cooper B, Schneider S, Bohl J, Jiang Y, Beaudet A, Pol S. Requirement of e6ap and the features of human papillomavirus e6 necessary to support degradation of p53. Virology 2003, 306: 87-99. PMID: 12620801, DOI: 10.1016/s0042-6822(02)00012-0.
- Yong J, Yanhong L, Zefu F, Xiayu W, Jun X, Baohua G, Lin L. Observation of banded spherulites and lamellar structures by atomic force microscopy. Science China Chemistry 2003, 46: 152-159. DOI: 10.1360/03yb9022.
- Luo Y, Jiang Y, Jin X, Li L, Lei Y, Chan C. Recent progresses of polymer crystallization studied by AFM. Science Bulletin 2002, 47: 1761-1765. DOI: 10.1007/bf03183837.
- Jiang Y, Gu Q, Li L, Shen D, Jin X, Lei Y, Chan C. Structural changes during isothermal crystallization of a poly(bisphenol A-co-decane ether) polymer. Polymer 2002, 43: 5615-5621. DOI: 10.1016/s0032-3861(02)00441-x.
- Lei Y, Chan C, Li J, Ng K, Wang Y, Jiang Y, Li L. The Birth of an Embryo and Development of the Founding Lamella of Spherulites As Observed by Atomic Force Microscopy. Macromolecules 2002, 35: 6751-6753. DOI: 10.1021/ma0121619.
- Beaudet AL, Jiang YH. A Rheostat Model for a Rapid and Reversible Form of Imprinting-Dependent Evolution. American Journal Of Human Genetics 2002, 70: 1389-1397. PMID: 11992247, PMCID: PMC379123, DOI: 10.1086/340969.
- Smith CL, DeVera DG, Lamb DJ, Nawaz Z, Jiang YH, Beaudet AL, O’Malley B. Genetic Ablation of the Steroid Receptor Coactivator-Ubiquitin Ligase, E6-AP, Results in Tissue-Selective Steroid Hormone Resistance and Defects in Reproduction. Molecular And Cellular Biology 2002, 22: 525-535. PMID: 11756548, PMCID: PMC139730, DOI: 10.1128/mcb.22.2.525-535.2002.
- Jiang Y, Ding E, Li G. Study on transition characteristics of PEG/CDA solid–solid phase change materials. Polymer 2002, 43: 117-122. DOI: 10.1016/s0032-3861(01)00613-9.
- Ding E, Jiang Y, Li G. COMPARATIVE STUDIES OF THE STRUCTURES AND TRANSITION CHARACTERISTICS OF CELLULOSE DIACETATE MODIFIED WITH POLYETHYLENE GLYCOL PREPARED BY CHEMICAL BONDING AND PHYSICAL BLENDING METHODS*. Journal Of Macromolecular Science Part B 2001, 40: 1053-1068. DOI: 10.1081/mb-100107801.
- Cummings C, Reinstein E, Sun Y, Antalffy B, Jiang Y, Ciechanover A, Orr H, Beaudet A, Zoghbi H. Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice. Neuron 1999, 24: 879-892. PMID: 10624951, DOI: 10.1016/s0896-6273(00)81035-1.
- Tsai T, Jiang Y, Bressler J, Armstrong D, Beaudet A. Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing to Prader-Willi Syndrome. Human Molecular Genetics 1999, 8: 1357-1364. PMID: 10400982, DOI: 10.1093/hmg/8.8.1357.
- Jiang Y, Lev-Lehman E, Bressler J, Tsai T, Beaudet A. Genetics of Angelman Syndrome. American Journal Of Human Genetics 1999, 65: 1-6. PMID: 10364509, PMCID: PMC1378067, DOI: 10.1086/302473.
- Jiang Y, Armstrong D, Albrecht U, Atkins C, Noebels J, Eichele G, Sweatt J, Beaudet A. Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation. Neuron 1998, 21: 799-811. PMID: 9808466, DOI: 10.1016/s0896-6273(00)80596-6.
- Jiang Y, Tsai T, Bressler J, Beaudet A. Imprinting in Angelman and Prader-Willi syndromes. Current Opinion In Genetics & Development 1998, 8: 334-342. PMID: 9691003, DOI: 10.1016/s0959-437x(98)80091-9.
- Sutcliffe J, Jiang Y, Galjaard R, Matsuura T, Fang P, Kubota T, Christian S, Bressler J, Cattanach B, Ledbetter D, Beaudet A. The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region. Genome Research 1997, 7: 368-377. PMID: 9110176, PMCID: PMC139148, DOI: 10.1101/gr.7.4.368.
- Matsuura T, Sutcliffe J, Fang P, Galjaard R, Jiang Y, Benton C, Rommens J, Beaudet A. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nature Genetics 1997, 15: 74-77. PMID: 8988172, DOI: 10.1038/ng0197-74.
- Winchester Building25 York StreetNew Haven, CT 06511
- 1 Long Wharf DriveNew Haven, CT 06511
Biography
Yong-Hui Jiang, MD, PhD, chief of Medical Genetics, is trained in pediatrics and board certified in clinical genetics and medical biochemical genetics. He not only evaluates and treats rare and undiagnosed genetic diseases in infants through adults, but conducts basic and translational research.
“I joke with families that I am not just a specialist, but a super specialist because of my credentials and experience as a medical biochemical geneticist, one of two such physicians in the state, and we are both here at Yale,” says Dr. Jiang.
Adding lightness to what can be daunting medical appointments is one way Dr. Jiang connects with patients. Medical biochemical geneticists specialize in inherited metabolic conditions including inborn errors of metabolism. Inborn errors of metabolism (often diagnosed during standard screening at birth) are problems with how the body uses enzymes to digest proteins, fatty, and carbohydrates, which are important to the functions of all organs. Dr. Jiang also treats neurodevelopmental disorders such as Angelman’s, Prader-Willi, and Phelan-McDermid syndromes; and autism spectrum disorder.
“One of the challenges in my specialty is that the first job is to figure out what is going on. Sometimes, a family has been searching for a diagnosis for 10 years or more, and it is very rewarding to give them an answer,” Dr. Jiang says. “What motivates me, both in my clinical and research work, is developing treatments that will help them.”
Meanwhile, advances in clinical genetics continue at a rapid pace thanks to cutting-edge genetics testing technology at Yale and extensive experience on applying genome technology here, he notes. “The tools we have for reading your genome are now such better quality and lower cost,” he says. “There is a lot of hope of being able to evaluate and treat conditions to degrees that were not possible five years ago.”
Titles
- Professor of Genetics and Dorys McConnell Duberg Professor of Neuroscience; Chief of Medical Genetics
- Vice Chair, Dept. of Genetics, Genetics
- Chief of Medical Genetics, Genetics
Education & Training
- Medical Biochemical Genetics Training by Service PathwayBaylor College of Medicine (2008)
- Clinical Genetics and Genomics FellowBaylor College of Medicine (2007)
- Pediatric residentTexas Children's Hosital, Baylor College of Medicine (2005)
- PhDBaylor College of Medicine, Molecular and Human Genetics (1999)
- MDFormer Shanghai Medical Univeristy/Current Shanghai Medical College of Fudan University (1987)
Languages Spoken
- 官話 / 官话 (Chinese-Mandarin)
- English
Additional Information
- Yale Faculty Innovation Award: Yale University (2024)
- Yale Faculty Innovation Award : Yale University (2023)
- Cure Angelman Discovery Award 2022: Foundation for Angelman Syndrome Therapeutics (2022), (2023)
- No. 1 of top 10 autism research project: Autism Speaks (2020)
- NIH (2019 - Present): Standing Member
- Foundation for Angelman Syndrome Therapeuics (2014 - Present): Committee Member
- Hendry C, Zhou J, Jiang YH. Applying the FDA’s plausible mechanism guidance across the rare disease landscape. Nature Genetics 2026 DOI: 10.1038/s41588-026-02750-4.
- Sun J, Nie Z, Wu F, Lai F, Chen S, Wang Y, Jiang Y. Highly sensitive fluorescent lateral flow immunoassay based on core–shell PS@Dip@SiO2 microspheres for SARS-CoV-2 IgG detection. Microchimica Acta 2026, 193: 571. PMID: 42517932, DOI: 10.1007/s00604-026-08296-w.
- Zhang J, Wang Y, Ye X, Peng Y, Hou Y, Li Y, Jiang Y. One-Pot Synthesis of Soft, Shape-Stable and Conductive Phase Change Hydrogels. New Journal Of Chemistry 2026, 50: 11568-11576. DOI: 10.1039/d5nj04824a.
- Tong C, Li C, Jacq A, Nie X, Guy C, Suh J, Wong R, Merlin C, Menet J, Jiang Y. Single-cell Multiomic and Spatiotemporal Dissection of the Liver Circadian Clock. Genomics Proteomics & Bioinformatics 2026, qzag050. PMID: 42360761, DOI: 10.1093/gpbjnl/qzag050.
- Li Y, Zhang Y, Zhou Y, Zhou X, Liu H, Lu L, Chen J, Zhang J, Huang X, Yang X, Qian D, Jiang Y. Comparative study of three viscosity-enhancing strategies for chitosan-alginate composite hydrogels. The Journal Of Adhesion 2026, ahead-of-print: 1-19. DOI: 10.1080/00218464.2026.2691431.
- Yuan S, Shi Q, Zhao H, Guo K, Jiang Y, Zhang Y. Emerging gene-edited dog models for autism spectrum disorder. Genomic Psychiatry 2026, 1-7. DOI: 10.61373/gp026p.0036.
- Hou Y, Cao W, Peng Y, Huang J, Li Y, Jiang Y. Investigation of silicone hydrogel contact lenses functionalized with hollow silica nanoparticles for drug loading. New Journal Of Chemistry 2026, 50: 9823-9833. DOI: 10.1039/d6nj00915h.
- Nie Y, Zhao Z, Chen X, Wang F, Huang J, Jiang Y. Tunable Polymer-Brush Interfaces on Magnetic Beads Enable Enhanced Chemiluminescence Immunoassay. Langmuir 2026, 42: 17162-17174. PMID: 42234452, DOI: 10.1021/acs.langmuir.6c02340.
- Chen X, Nie Y, Zhao Z, Wang F, Huang J, Jiang Y. Tunable dendritic Fe3O4@mSiO2-Ni2+ core-shell magnetic nanospheres for selective enrichment of histidine-rich proteins. Talanta 2026, 307: 129774. PMID: 41962442, DOI: 10.1016/j.talanta.2026.129774.
- Qiao S, Wang S, Kim K, Jo S, Jiang Y. Inflammation increases the penetrance of behavioral impairment in Shank3 haploinsufficiency mice — can it explain the behavioral regression in Autism? Molecular Psychiatry 2026, 31: 4369-4385. PMID: 41882256, PMCID: PMC13364677, DOI: 10.1038/s41380-026-03534-2.
- Ashokkumar M, Ge R, Cooper-Volkheimer A, Margolis D, Li Q, Jiang Y, Murdoch D, Browne E. Single cell multiomic analysis of the impact of Delta-9-tetrahydrocannabinol on HIV infected CD4 T cells. Journal Of Cannabis Research 2026, 8: 52. PMID: 41782037, PMCID: PMC13069807, DOI: 10.1186/s42238-026-00412-0.
- Abdelhamed Z, Dykas D, DiAdamo A, Chai H, Ma D, Spencer-Mazon M, Jiang Y, Wen J, Bale A, Li P, Zhang H. Concomitant Chromosomal and Molecular Aberrations in Trisomy 8 Mosaicism and Associated Compound Phenotypes: Report of Three Cases and Review of Literature. Case Reports In Genetics 2026, 2026: 4494577. PMID: 41624216, PMCID: PMC12855162, DOI: 10.1155/crig/4494577.
- Knee K, Weeber E, Armstrong N, Stoub R, Copping N, Bailus B, Jiang Y, Berry-Kravis E, Berent A. Rodent Models and How They Define Potential Human Benefit: A Translational Review for Angelman Syndrome. 2026 DOI: 10.65856/ffkj4964.
- Wei L, Du X, Qiao Z, Yang B, Long S, Jiang Y, Wang Y, Wang H. Microstructural White Matter Alterations in Angelman Syndrome: A Fixel‐Based Analysis. Autism Research 2025, 19: e70160. PMID: 41437736, DOI: 10.1002/aur.70160.
- Chen X, Nie Y, Fan W, Zhao Z, Wang Z, Jiang Y. Yolk-shell magnetic hydrogel Fe3O4@P(DVB-co-MAA)@Ag composite microspheres for enhanced catalytic reduction of nitroaromatics. Colloids And Surfaces A Physicochemical And Engineering Aspects 2025, 727: 138336. DOI: 10.1016/j.colsurfa.2025.138336.
- Folkes O, Donahue M, Wang S, Negrón-Moreno P, Oo N, Qiao S, Wang X, Jiang Y. Deficiency of Shank3 in the nucleus accumbens reveals a loss of social-specific motivation. Communications Biology 2025, 8: 1569. PMID: 41238633, PMCID: PMC12618580, DOI: 10.1038/s42003-025-08942-8.
- Nie Z, Sun J, Wu F, Lai F, Yang X, Chen S, Wang Y, Jiang Y. Preparation of Fe3O4@PMAA-N protein magnetic beads for antibody detection of SARS-CoV-2 based on indirect ELISA smartphone visual strategy. Microchimica Acta 2025, 192: 785. PMID: 41175250, DOI: 10.1007/s00604-025-07646-4.
- Coulter A, Tong C, Ni Y, Jiang Y. distQTL: distribution quantitative trait loci identification by population-scale single-cell data. NAR Genomics And Bioinformatics 2025, 7: lqaf155. PMID: 41323105, PMCID: PMC12661327, DOI: 10.1093/nargab/lqaf155.
- Zhang Q, Yamanaka H, Li P, Li Y, Luo T, Xia M, Liu T, Liu X, Lu Q, Yang B, He F, Du K, Shu Y, Peng B, Jiang Y, Wang Y. Haploinsufficiency of brain‐specific kinase BRSK1 causes epilepsy and neurodevelopmental disorders. Epilepsia 2025, 66: 5033-5054. PMID: 41035394, PMCID: PMC12779330, DOI: 10.1111/epi.18621.
- Ye X, Peng Y, Hou Y, Huang J, Cao W, Jiang Y. pH‐Responsive Polyacrylic Acid Hydrogels Cross‐Linked with Functionalized Collagen Peptide for Controlled Drug Release. ChemistrySelect 2025, 10 DOI: 10.1002/slct.202503021.
- Wang S, Cheng Y, Lim J, Jang M, Forrest E, Kim Y, Donahue M, Jo S, Qiao S, Lee D, Hong J, Xiong Y, Jin J, Wang S, Jiang Y. Mechanism of EHMT2-mediated genomic imprinting associated with Prader-Willi syndrome. Nature Communications 2025, 16: 6125. PMID: 40610428, PMCID: PMC12229668, DOI: 10.1038/s41467-025-61156-8.
- Zhao H, Jiang Y, Zhang Y. Gene-Edited Canines as Emerging Models for Studies on Mental Disorders. National Science Review 2025, nwaf263. DOI: 10.1093/nsr/nwaf263.
- Gui L, Jiang Y, Wang J. Aggregating dependent signals with heavy-tailed combination tests. Biometrika 2025, 112: asaf038. PMID: 41169946, PMCID: PMC12570179, DOI: 10.1093/biomet/asaf038.
- Fan W, Zhao Z, Chen X, Nie Y, Wang Z, Jiang Y. Stable and Controllable Magnetic Functionalization of Polymer Microspheres via Covalent Layer-by-Layer Assembly. Langmuir 2025, 41: 14300-14310. PMID: 40445872, DOI: 10.1021/acs.langmuir.5c01372.
- Yuan S, Pang C, Wu L, Yi L, Guo K, Jiang Y, Zhang Y, Han S. Autism-like atypical face processing in Shank3 mutant dogs. Science Advances 2025, 11: eadu3793. PMID: 40173245, PMCID: PMC11963970, DOI: 10.1126/sciadv.adu3793.
- Lyu W, Li Y, Yao A, Tan Q, Zhang R, Zhao J, Guo K, Jiang Y, Tian R, Zhang Y. Oxytocin improves maternal licking behavior deficits in autism-associated Shank3 mutant dogs. Translational Psychiatry 2025, 15: 76. PMID: 40050270, PMCID: PMC11885833, DOI: 10.1038/s41398-025-03296-5.
- Kim Y, Kim M, Kim S, Lee R, Ujihara Y, Marquez-Wilkins E, Jiang Y, Yang E, Kim H, Lee C, Park C, Kim I. Endothelial SHANK3 regulates tight junctions in the neonatal mouse blood-brain barrier through β-Catenin signaling. Nature Communications 2025, 16: 1407. PMID: 39915488, PMCID: PMC11802743, DOI: 10.1038/s41467-025-56720-1.
- Zeng J, Xu Q, Nie Y, Han X, Jiang Y. Preparation and properties of silicone hydrogel contact lens based on PDMS-PU macromer. Colloid And Polymer Science 2025, 303: 793-804. DOI: 10.1007/s00396-025-05379-7.
- Weideman A, Wang R, Ibrahim J, Jiang Y. Canopy2: Tumor Phylogeny Inference by Bulk DNA and Single-Cell RNA Sequencing. Statistics In Biosciences 2025, 18: 68-110. PMID: 41694548, PMCID: PMC12904911, DOI: 10.1007/s12561-024-09466-1.
- Liao J, Yan W, Zhang Y, Berhane K, Chen W, Yang Z, Qiu C, Ge Y, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Zhang J, Huang G, Chen Z. Associations of preconception air pollution exposure with growth trajectory in young children: A prospective cohort study. Environmental Research 2024, 267: 120665. PMID: 39706320, PMCID: PMC11878012, DOI: 10.1016/j.envres.2024.120665.
- Chu X, Dou X, Yu J, Zhou J, Ma D, Miao M, Hu S, Sun K, Zhu S, Liu Q, Zhang X, Jiang Y, Wang Z. Synthesis of Polymers via Cancer Cell Metabolism-Mediated Controlled Radical Polymerization and Application in Engineering of Cell Surface. Biomacromolecules 2024, 26: 238-247. PMID: 39689279, DOI: 10.1021/acs.biomac.4c01020.
- Zhu S, Du D, Zhao Z, Chu X, Su D, Yu S, Tao T, Jiang Y, Wang Z. Fabrication of functional interface on magnetic beads via various amino acids and their application in chemiluminescent immunoassay as carrier. Colloids And Surfaces B Biointerfaces 2024, 245: 114364. PMID: 39527882, DOI: 10.1016/j.colsurfb.2024.114364.
- Shi Q, Wu L, Ren B, Guo K, Jiang Y, Zhang Y, Hu L. Impaired tactile processing in autism-associated Shank3 mutant dogs: neural mechanism and intervention. Science Bulletin 2024, 70: 483-487. PMID: 39294081, DOI: 10.1016/j.scib.2024.09.011.
- Liao J, Zhang Y, Yang Z, Chen W, Qiu C, Kiros B, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Zhang J, Yan W, Huang G, Chen Z. Association of Preconception Air Pollution Exposure with Growth Trajectory in Children. ISEE Conference Abstracts 2024, 2024 DOI: 10.1289/isee.2024.0146.
- Gao Y, Shonai D, Trn M, Zhao J, Soderblom E, Garcia-Moreno S, Gersbach C, Wetsel W, Dawson G, Velmeshev D, Jiang Y, Sloofman L, Buxbaum J, Soderling S. Proximity analysis of native proteomes reveals phenotypic modifiers in a mouse model of autism and related neurodevelopmental conditions. Nature Communications 2024, 15: 6801. PMID: 39122707, PMCID: PMC11316102, DOI: 10.1038/s41467-024-51037-x.
- Su D, Han J, Chen L, Zhu S, Jiang Y, Wang Z. Fabrication of dextran-grafted magnetic polymer microspheres with low nonspecific protein adsorption as carriers for chemiluminescence immunoassays. Colloids And Surfaces A Physicochemical And Engineering Aspects 2024, 694: 134115. DOI: 10.1016/j.colsurfa.2024.134115.
- Kose C, Lindsey-Boltz L, Sancar A, Jiang Y. Genome-wide analysis of transcription-coupled repair reveals novel transcription events in Caenorhabditis elegans. PLOS Genetics 2024, 20: e1011365. PMID: 39028758, PMCID: PMC11290646, DOI: 10.1371/journal.pgen.1011365.
- Xu Q, Zhao Z, Chen X, Fan W, Jiang Y. The Impact of Surface Modifier on Magnetic Nanoparticle Properties and Their Application in CD3+T Cell Separation. Langmuir 2024, 40: 15597-15609. PMID: 39024471, DOI: 10.1021/acs.langmuir.4c01332.
- Dalton G, Siecinski S, Nikolova V, Cofer G, Hornburg K, Qi Y, Johnson G, Jiang Y, Moy S, Gregory S. Transcriptome analysis identifies an ASD-Like phenotype in oligodendrocytes and microglia from C58/J amygdala that is dependent on sex and sociability. Behavioral And Brain Functions 2024, 20: 14. PMID: 38898502, PMCID: PMC11188533, DOI: 10.1186/s12993-024-00240-3.
- Lu X, Ni P, Suarez-Meade P, Ma Y, Forrest E, Wang G, Wang Y, Quiñones-Hinojosa A, Gerstein M, Jiang Y. Transcriptional determinism and stochasticity contribute to the complexity of autism-associated SHANK family genes. Cell Reports 2024, 43: 114376. PMID: 38900637, PMCID: PMC11328446, DOI: 10.1016/j.celrep.2024.114376.
- Nie Y, Xu Q, Wu D, Li J, Wang Z, Jiang Y, Lv Q, Jiang Y. Low-molecular-weight microspheres with soft-shell characteristics for remarkable signal enhancement in LOCI applications. Colloids And Surfaces A Physicochemical And Engineering Aspects 2024, 691: 133883. DOI: 10.1016/j.colsurfa.2024.133883.
- Wang S, Xiong Y, Jang M, Park K, Donahue M, Velez J, Jin J, Jiang Y. Newly developed oral bioavailable EHMT2 inhibitor as a potential epigenetic therapy for Prader-Willi syndrome. Molecular Therapy 2024, 32: 2662-2675. PMID: 38796700, PMCID: PMC11405540, DOI: 10.1016/j.ymthe.2024.05.034.
- Ashokkumar M, Mei W, Peterson J, Harigaya Y, Murdoch D, Margolis D, Kornfein C, Oesterling A, Guo Z, Rudin C, Jiang Y, Browne E. Integrated Single-cell Multiomic Analysis of HIV Latency Reversal Reveals Novel Regulators of Viral Reactivation. Genomics Proteomics & Bioinformatics 2024, 22: qzae003. PMID: 38902848, PMCID: PMC11189801, DOI: 10.1093/gpbjnl/qzae003.
- Su K, Ma Y, Zhou M, Liu Y, Li C, Jiang Y, Wu Q, Peng G, Wang Y, Fan S. De novo missense variants of UNC13A are implicated in epileptic encephalopathies and neurodevelopmental disorders. Genes & Diseases 2024, 12: 101315. PMID: 39634123, PMCID: PMC11615879, DOI: 10.1016/j.gendis.2024.101315.
- Lu X, Ng K, Pinto e Vairo F, Collins J, Cohn R, Riley K, Agre K, Gavrilova R, Klee E, Rosenfeld J, Jiang Y. Novel protein-truncating variants of a chromatin-modifying gene MSL2 in syndromic neurodevelopmental disorders. European Journal Of Human Genetics 2024, 32: 879-883. PMID: 38702431, PMCID: PMC11219747, DOI: 10.1038/s41431-024-01576-0.
- Li J, Zhang P, Xu Q, Nie Y, Shao S, Wang Z, Jiang Y. Preparation of dyed polymer microspheres by a physical–chemical dual-binding method and their application in lateral flow immunoassay. Analytical Methods 2024, 16: 2033-2043. PMID: 38497428, DOI: 10.1039/d3ay02279j.
- DiAdamo A, Chai H, Chong M, Wang G, Wen J, Jiang Y, Li P. Patterns of Cytogenomic Findings from a Case Series of Recurrent Pregnancy Loss Provide Insight into the Extent of Genetic Defects Causing Miscarriages. Global Medical Genetics 2024, 11: 123-131. PMID: 38560483, PMCID: PMC10980555, DOI: 10.1055/s-0044-1785227.
- Han J, Lv Q, Su D, Chen L, Zhu S, Liu Q, Jiang Y, Li X, Jiang Y, Wang Z. Polymer Microspheres Copolymerized with Deep Red Fluorescent Molecules as a Label for Lateral Flow Immunochromatography. Langmuir 2024, 40: 6971-6979. PMID: 38517386, DOI: 10.1021/acs.langmuir.3c04033.
- Lu X, Jiang Y. Intrathecal Injection of Newborn Mouse for Genome Editing and Drug Delivery. Journal Of Visualized Experiments 2024 PMID: 38526075, DOI: 10.3791/65761.
- Wu D, Xu Q, Nie Y, Jiang W, Wang Z, Jiang Y. Synergistic Fabrication of Magnetic Hypercrosslinked Porous P(VBC-DVB-AA)@Fe3O4 Microspheres for Removal of Cationic Dye. Journal Of Inorganic And Organometallic Polymers And Materials 2024, 34: 2746-2761. DOI: 10.1007/s10904-024-03009-3.
- Godse S, Brumer E, Kizilirmak T, Canapari C, Silva C, Morotti R, Jiang Y, Jeffries L, Chen L, Panacherry S. When lungs and weights tell different stories. Pediatric Pulmonology 2024, 59: 1047-1059. PMID: 38353400, DOI: 10.1002/ppul.26832.
- Xu Q, Nie Y, Wu D, Li J, Zeng J, Wang Z, Jiang Y. Anisotropic Magnetic Polymeric Particles with a Controllable Structure via Seeded Emulsion Polymerization. Langmuir 2024, 40: 3677-3690. PMID: 38343282, DOI: 10.1021/acs.langmuir.3c03379.
- Zhu F, Shi Q, Jiang Y, Zhang Y, Zhao H. Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs. Molecular Autism 2024, 15: 9. PMID: 38297387, PMCID: PMC10829216, DOI: 10.1186/s13229-024-00587-4.
- Yang Z, Liao J, Zhang Y, Lin Y, Ge Y, Chen W, Qiu C, Berhane K, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Chen Z, Huang G, Zhang J. Critical windows of greenness exposure during preconception and gestational periods in association with birthweight outcomes. Environmental Research Health 2023, 2: 015001. PMID: 38022394, PMCID: PMC10647935, DOI: 10.1088/2752-5309/ad0aa6.
- Nie Y, Man H, Shao S, Wang Y, Wang Z, Jiang Y. The influence of water on size of the monodisperse polystyrene microspheres prepared by dispersion polymerization. Journal Of Applied Polymer Science 2023, 141 DOI: 10.1002/app.54813.
- Liao J, Zhang Y, Yang Z, Qiu C, Chen W, Zhang J, Berhane K, Bai Z, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Huang G, Chen Z. Identifying critical windows of air pollution exposure during preconception and gestational period on birthweight: a prospective cohort study. Environmental Health 2023, 22: 71. PMID: 37858139, PMCID: PMC10585741, DOI: 10.1186/s12940-023-01022-6.
- Liao J, Zhang Y, Yang Z, Qiu C, Chen W, Zhang J, Berhane K, Han B, Xu J, Jiang Y, Gilliland F, Yan W, Huang G, Chen Z. Identifying Critical Windows of Air Pollution Exposure during Preconception and Gestational Period on Birthweight. ISEE Conference Abstracts 2023, 2023 DOI: 10.1289/isee.2023.fp-236.
- Tian R, Li Y, Zhao H, Lyu W, Zhao J, Wang X, Lu H, Xu H, Ren W, Tan Q, Shi Q, Wang G, Zhang Y, Lai L, Mi J, Jiang Y, Zhang Y. Modeling SHANK3-associated autism spectrum disorder in Beagle dogs via CRISPR/Cas9 gene editing. Molecular Psychiatry 2023, 28: 3739-3750. PMID: 37848710, DOI: 10.1038/s41380-023-02276-9.
- Wang S, Jiang Y. Novel epigenetic molecular therapies for imprinting disorders. Molecular Psychiatry 2023, 28: 3182-3193. PMID: 37626134, PMCID: PMC10618104, DOI: 10.1038/s41380-023-02208-7.
- Xu Q, Jiang W, Bu F, Wang Z, Jiang Y. Magnetic Dendritic Polymer Nanospheres for High-Performance Separation of Histidine-Rich Proteins. ACS Applied Materials & Interfaces 2023, 15: 30837-30848. PMID: 37332160, DOI: 10.1021/acsami.3c05475.
- Contestabile A, Casarotto G, Musardo S, Espinosa P, Maltese F, Jiang Y, Bellone C, Glangetas C. Shank3 deficits in the anteromedial bed nucleus of the stria terminalis trigger an anxiety phenotype in mice. European Journal Of Neuroscience 2023, 57: 1966-1979. PMID: 37165567, DOI: 10.1111/ejn.16043.
- Jiang W, Xu Q, Bu F, Wei Y, Wang Y, Wang Z, Jiang Y. Fabrication of Fe3O4@APF Magnetic Nanospheres with Tunable Core–Shell Structure: An Effective Carrier and Reducing Agent for Ag Nanoparticles. Journal Of Inorganic And Organometallic Polymers And Materials 2023, 33: 2562-2573. DOI: 10.1007/s10904-023-02704-x.
- Mann B, Zhang X, Bell N, Adefolaju A, Thang M, Dasari R, Kanchi K, Valdivia A, Yang Y, Buckley A, Lettry V, Quinsey C, Rauf Y, Kram D, Cassidy N, Vaziri C, Corcoran D, Rego S, Jiang Y, Graves L, Dunn D, Floyd S, Baldwin A, Hingtgen S, Satterlee A. A living ex vivo platform for functional, personalized brain cancer diagnosis. Cell Reports Medicine 2023, 4: 101042. PMID: 37192626, PMCID: PMC10313921, DOI: 10.1016/j.xcrm.2023.101042.
- Zhang J, Man H, Han X, Wang Z, Jiang Y. Facile preparation of magnetic P(MMA-co-GMA)@Fe3O4@PMAA microspheres using porous microsphere as templates for removal of methylene blue. Colloid And Polymer Science 2023, 301: 933-947. DOI: 10.1007/s00396-023-05099-w.
- Peng G, Zhou Q, Chai H, Wen J, Zhao H, Taylor H, Jiang Y, Li P. Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses. Molecular Genetics & Genomic Medicine 2023, 11: e2181. PMID: 37013615, PMCID: PMC10422064, DOI: 10.1002/mgg3.2181.
- Bu F, Xu Q, Jiang W, Wei Y, Wang Z, Jiang Y. Fabrication of magnetic Fe 3 O 4 @P(DVB- co -MAA) microspheres using hollow microspheres as templates for protein separation. New Journal Of Chemistry 2023, 47: 6176-6185. DOI: 10.1039/d3nj00069a.
- Li B, Zhao H, Tu Z, Yang W, Han R, Wang L, Luo X, Pan M, Chen X, Zhang J, Xu H, Guo X, Yan S, Yin P, Zhao Z, Liu J, Luo Y, Li Y, Yang Z, Zhang B, Tan Z, Xu H, Jiang T, Jiang Y, Li S, Zhang Y, Li X. CHD8 mutations increase gliogenesis to enlarge brain size in the nonhuman primate. Cell Discovery 2023, 9: 27. PMID: 36878905, PMCID: PMC9988832, DOI: 10.1038/s41421-023-00525-3.
- Hu W, Nie Y, Wang Y, Gao P, Jiang Y. Synthesis of inorganic/organic raspberry-like composite particles for superhydrophobic and superlipophilic coatings. Colloids And Surfaces A Physicochemical And Engineering Aspects 2023, 660: 130843. DOI: 10.1016/j.colsurfa.2022.130843.
- Li Y, Huang C, Duan A, Li M, Zhang X, Lu L, Yu L, Yu L, Liu P, Chen K, Jiang Y. A temperature-sensitive DNA-PNIPAAm hydrogel prepared by base pairing. Colloid And Polymer Science 2023, 301: 383-388. DOI: 10.1007/s00396-023-05071-8.
- Xing X, lv Q, Sun C, Song J, Chen Z, Jiang Y, Wang Y, Jiang Y, Wang Z. One-step preparation of PEG segment-functionalized polystyrene microspheres and their application as latex in LOCI. New Journal Of Chemistry 2023, 47: 3970-3977. DOI: 10.1039/d2nj05630e.
- Guan P, Lee J, Wang L, Lin K, Mei W, Chen L, Jiang Y. Destin2: Integrative and cross-modality analysis of single-cell chromatin accessibility data. Frontiers In Genetics 2023, 14: 1089936. PMID: 36873935, PMCID: PMC9981783, DOI: 10.3389/fgene.2023.1089936.
- Du X, Wei L, Yang B, Long S, Wang J, Sun A, Jiang Y, Qiao Z, Wang H, Wang Y. Cortical and subcortical morphological alteration in Angelman syndrome. Journal Of Neurodevelopmental Disorders 2023, 15: 7. PMID: 36788499, PMCID: PMC9930225, DOI: 10.1186/s11689-022-09469-3.
- Chen Z, Yu J, Sun K, Song J, Chen L, Jiang Y, Wang Z. Rational design of a turn-on near-infrared fluorescence probe for the highly sensitive and selective monitoring of carboxylesterase 2 in living systems. Analyst 2023, 148: 876-887. PMID: 36661088, DOI: 10.1039/d2an01874h.
- Zhang L, Bang S, He Q, Matsuda M, Luo X, Jiang Y, Ji R. SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis. Frontiers In Immunology 2023, 14: 1124356. PMID: 36845137, PMCID: PMC9944123, DOI: 10.3389/fimmu.2023.1124356.
- Agarwal A, Zhao F, Jiang Y, Chen L. TIVAN-indel: a computational framework for annotating and predicting non-coding regulatory small insertions and deletions. Bioinformatics 2023, 39: btad060. PMID: 36707993, PMCID: PMC9900211, DOI: 10.1093/bioinformatics/btad060.
- Preparation and characterization of a form-stable phase change hydrogel for heat-protective clothingWang Y, Zhang J, Han X, Jiang Y. Preparation and characterization of a form-stable phase change hydrogel for heat-protective clothing. New Journal Of Chemistry 2023, 47: 1818-1824. DOI: 10.1039/d2nj05096j.
- Dai H, Zhu W, Yuan B, Walley N, Schoch K, Jiang Y, Phillips J, Jones M, Liu P, Murdock D, Burrage L, Lee B, Rosenfeld J, Xiao R, Network U. A recurrent single‐exon deletion in TBCK might be under‐recognized in patients with infantile hypotonia and psychomotor delay. Human Mutation 2022, 43: 1816-1823. PMID: 36317458, PMCID: PMC9772143, DOI: 10.1002/humu.24497.
- Yang X, Zhang P, Xing X, lv Q, Jiang Y, Jiang Y, Wang Z. Improving the fluorescence intensity of lanthanide-doped microspheres via incorporation of lauryl methacrylate: Synthesis and their application in C-reactive protein detection. Colloids And Surfaces A Physicochemical And Engineering Aspects 2022, 653: 130065. DOI: 10.1016/j.colsurfa.2022.130065.
- Thaler R, Khani F, Sturmlechner I, Dehghani SS, Denbeigh JM, Zhou X, Pichurin O, Dudakovic A, Jerez SS, Zhong J, Lee JH, Natarajan R, Kalajzic I, Jiang YH, Deyle DR, Paschalis EP, Misof BM, Ordog T, van Wijnen AJ. Vitamin C epigenetically controls osteogenesis and bone mineralization. Nature Communications 2022, 13: 5883. PMID: 36202795, PMCID: PMC9537512, DOI: 10.1038/s41467-022-32915-8.
- Wei Y, Chen L, Jiang Y. Self-healing polyacrylamide (PAAm) gels at room temperature based on complementary guanine and cytosine base pairs. Soft Matter 2022, 18: 7394-7401. PMID: 36125115, DOI: 10.1039/d2sm00933a.
- Wei Y, Du Q, Wang Y, Gao P, Wang Z, Jiang Y. Two-dimensional cellulose acetate membrane-supported mesoporous silica nanosheets for efficient nanosize-based molecules separation. Journal Of Molecular Liquids 2022, 363: 119827. DOI: 10.1016/j.molliq.2022.119827.
- Jiang Y, Harigaya Y, Zhang Z, Zhang H, Zang C, Zhang N. Nonparametric single-cell multiomic characterization of trio relationships between transcription factors, target genes, and cis-regulatory regions. Cell Systems 2022, 13: 737-751.e4. PMID: 36055233, PMCID: PMC9509445, DOI: 10.1016/j.cels.2022.08.004.
- Gao P, Wei Y, Xu Q, Jiang Y. A cysteine-induced one-pot synthesis of Au nanoparticle chains with tuneable NIR absorption and application in photothermal-chemo cancer therapy. New Journal Of Chemistry 2022, 46: 16359-16369. DOI: 10.1039/d2nj02339c.
- Al‐Ali S, Jeffries L, Faustino EVS, Ji W, Mis E, Konstantino M, Zerillo C, Jiang Y, Spencer‐Manzon M, Bale A, Zhang H, McGlynn J, McGrath JM, Tremblay T, Brodsky NN, Lucas CL, Pierce R, Deniz E, Khokha MK, Lakhani SA. A retrospective cohort analysis of the Yale pediatric genomics discovery program. American Journal Of Medical Genetics Part A 2022, 188: 2869-2878. PMID: 35899841, PMCID: PMC9474639, DOI: 10.1002/ajmg.a.62918.
- Wei L, Du X, Yang Z, Ding M, Yang B, Wang J, Long S, Qiao Z, Jiang Y, Wang Y, Wang H. Disrupted Topological Organization of White Matter Network in Angelman Syndrome. Journal Of Magnetic Resonance Imaging 2022, 57: 1212-1221. PMID: 35856797, DOI: 10.1002/jmri.28360.
- Man H, Nie Y, Shao S, Wang Y, Wang Z, Jiang Y. Fabrication of Fe 3 O 4 @poly(methyl methacrylate- co -glycidyl methacrylate) microspheres via miniemulsion polymerization using porous microspheres as templates for removal of cationic dyes. New Journal Of Chemistry 2022, 46: 13442-13453. DOI: 10.1039/d2nj01440h.
- Wang R, Jiang Y. Copy Number Variation Detection by Single-Cell DNA Sequencing with SCOPE. Methods In Molecular Biology 2022, 2493: 279-288. PMID: 35751822, DOI: 10.1007/978-1-0716-2293-3_18.
- Hong H, Zhao Z, Huang X, Guo C, Zhao H, Wang GD, Zhang YP, Zhao JP, Shi J, Wu QF, Jiang YH, Wang Y, Li LM, Du Z, Zhang YQ, Xiong Y. Comparative Proteome and Cis-Regulatory Element Analysis Reveals Specific Molecular Pathways Conserved in Dog and Human Brains. Molecular & Cellular Proteomics 2022, 21: 100261. PMID: 35738554, PMCID: PMC9304787, DOI: 10.1016/j.mcpro.2022.100261.
- Wang R, Lin D, Jiang Y. EPIC: Inferring relevant cell types for complex traits by integrating genome-wide association studies and single-cell RNA sequencing. PLOS Genetics 2022, 18: e1010251. PMID: 35709291, PMCID: PMC9242467, DOI: 10.1371/journal.pgen.1010251.
- Yang-Li D, Fei-Hong L, Hui-Wen Z, Ming-Sheng M, Xiao-Ping L, Li L, Yi W, Qing Z, Yong-Hui J, Chao-Chun Z. Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China. Orphanet Journal Of Rare Diseases 2022, 17: 221. PMID: 35698200, PMCID: PMC9195308, DOI: 10.1186/s13023-022-02302-z.
- Kim S, Kim YE, Song I, Ujihara Y, Kim N, Jiang YH, Yin HH, Lee TH, Kim IH. Neural circuit pathology driven by Shank3 mutation disrupts social behaviors. Cell Reports 2022, 39: 110906. PMID: 35675770, PMCID: PMC9210496, DOI: 10.1016/j.celrep.2022.110906.
- Xu Q, Gao P, Wang Y, Jiang W, Wang Z, Jiang Y, Jiao Z. Using supercritical carbon dioxide to synthesize polymer nanospheres with an open hole on the surface and the application of spatially structured PS/P(DVB-co-MAA)@Fe3O4/TA@Ag nanocomposites. The Journal Of Supercritical Fluids 2022, 184: 105561. DOI: 10.1016/j.supflu.2022.105561.
- Wang S, Jiang Y. Epigenetic Epidemiology of Autism and Other Neurodevelopmental Disorders. 2022, 405-426. DOI: 10.1007/978-3-030-94475-9_17.
- Barish S, Senturk M, Schoch K, Minogue AL, Lopergolo D, Fallerini C, Harland J, Seemann JH, Stong N, Kranz PG, Kansagra S, Mikati MA, Jasien J, El-Dairi M, Galluzzi P, Acosta M, Adam M, Adams D, Agrawal P, Alejandro M, Alvey J, Amendola L, Andrews A, Ashley E, Azamian M, Bacino C, Bademci G, Baker E, Balasubramanyam A, Baldridge D, Bale J, Bamshad M, Barbouth D, Bayrak-Toydemir P, Beck A, Beggs A, Behrens E, Bejerano G, Bennet J, Berg-Rood B, Bernstein J, Berry G, Bican A, Bivona S, Blue E, Bohnsack J, Bonnenmann C, Bonner D, Botto L, Boyd B, Briere L, Brokamp E, Brown G, Burke E, Burrage L, Butte M, Byers P, Byrd W, Carey J, Carrasquillo O, Chang T, Chanprasert S, Chao H, Clark G, Coakley T, Cobban L, Cogan J, Coggins M, Cole F, Colley H, Cooper C, Cope H, Craigen W, Crouse A, Cunningham M, D'Souza P, Dai H, Dasari S, Davids M, Dayal J, Deardorff M, Dell'Angelica E, Dhar S, Dipple K, Doherty D, Dorrani N, Douine E, Draper D, Duncan L, Earl D, Eckstein D, Emrick L, Eng C, Esteves C, Estwick T, Falk M, Fernandez L, Ferreira C, Fieg E, Findley L, Fisher P, Fogel B, Forghani I, Fresard L, GahlIan-Glass W, Godfrey R, Golden-Grant K, Goldman A, Goldstein D, Grajewski A, Groden C, Gropman A, Gutierrez I, Hahn S, Hamid R, Hanchard N, Hassey K, Hayes N, High F, Hing A, Hisama F, Holm I, Hom J, Horike-Pyne M, Huang A, Huang Y, Isasi R, Jamal F, Jarvik G, Jarvik J, Jayadev S, Johnston J, Karaviti L, Kelley E, Kennedy J, Kiley D, Kohane I, Kohler J, Krakow D, Krasnewich D, Kravets E, Korrick S, Koziura M, Krier J, Lalani S, Lam B, Lam C, Lanpher B, Lanza I, Lau C, LeBlanc K, Lee B, Lee H, Levitt R, Lewis R, Lincoln S, Liu P, Liu X, Longo N, Loo S, Loscalzo J, Maas R, Macnamara E, MacRae C, Maduro V, Majcherska M, Mak B, Malicdan M, Mamounas L, Manolio T, Mao R, Maravilla K, Markello T, Marom R, Marth G, Martin B, Martin M, Martínez-Agosto J, Marwaha S, McCauley J, McConkie-Rosell A, McCormack C, McCray A, McGee E, Mefford H, Merritt J, Might M, Mirzaa G, Morava E, Moretti P, Morimoto M, Mulvihill J, Murdock D, Nakano-Okuno M, Nath A, Nelson S, Newman J, Nicholas S, Nickerson D, Nieves-Rodriguez S, Novacic D, Oglesbee D, Orengo J, Pace L, Pak S, Pallais J, Palmer C, Papp J, Parker N, Phillips III J, Posey J, Potocki L, Pusey B, Quinlan A, Raskind W, Raja A, Rao D, Renteria G, Reuter C, Rives L, Robertson A, Rodan L, Rosenfeld J, Rosenwasser N, Ruzhnikov M, Sacco R, Sampson J, Samson S, Saporta M, Scott C, Schaechter J, Schedl T, Schoch K, Scott D, Sharma P, Shashi V, Shin J, Signer R, Sillari C, Silverman E, Sinsheimer J, Sisco K, Smith E, Smith K, Solem E, Solnica-Krezel L, Spillmann R, Stoler J, StongJ N, Sullivan E, Sullivan K, Sun A, Sutton S, Sweetser D, Sybert V, Tabor H, Tamburro C, K-GTan Q, Tekin M, Telischi F, Thorson W, Tifft C, Toro C, Tran A, Tucker B, Urv T, Vanderver A, Velinder M, Viskochil D, Vogel T, Wahl C, Wallace S, Walley N, Walsh C, Walker M, Wambach J, Wan J, Wang L, Wangler M, Ward P, Wegner D, Wener M, Wenger T, Perry K, Westerfield M, Wheeler M, Whitlock J, Wolfe L, Woods J, Yamamoto S, Yang J, Yu G, Zastrow D, Zhao C, Zuchner S, Ariani F, Renieri A, Mari F, Wangler M, Arur S, Jiang Y, Yamamoto S, Shashi V, Bellen H. The microRNA processor DROSHA is a candidate gene for a severe progressive neurological disorder. Human Molecular Genetics 2022, 31: 2934-2950. PMID: 35405010, PMCID: PMC9433733, DOI: 10.1093/hmg/ddac085.
- Shao S, Man H, Nie Y, Wang Y, Xu Q, Wang Z, Jiang Y. Preparation of fluorescence-encoded microbeads with large encoding capacities and application of suspension array technology. New Journal Of Chemistry 2022, 46: 6986-6994. DOI: 10.1039/d2nj00628f.
- Mague SD, Talbot A, Blount C, Walder-Christensen KK, Duffney LJ, Adamson E, Bey AL, Ndubuizu N, Thomas GE, Hughes DN, Grossman Y, Hultman R, Sinha S, Fink AM, Gallagher NM, Fisher RL, Jiang YH, Carlson DE, Dzirasa K. Brain-wide electrical dynamics encode individual appetitive social behavior. Neuron 2022, 110: 1728-1741.e7. PMID: 35294900, PMCID: PMC9126093, DOI: 10.1016/j.neuron.2022.02.016.
- Wen J, Chai H, Grommisch B, DiAdamo A, Dykas D, Ma D, Popa A, Zhao C, Spencer‐Manzon M, Jiang Y, McGrath J, Li P, Bale A, Zhang H. Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients. American Journal Of Medical Genetics Part A 2022, 188: 1728-1738. PMID: 35199448, DOI: 10.1002/ajmg.a.62693.
- Dong M, He Y, Jiang Y, Zou F. Joint Gene Network Construction by Single-Cell RNA Sequencing Data. Biometrics 2022, 79: 915-925. PMID: 35184277, PMCID: PMC10548400, DOI: 10.1111/biom.13645.
- Tzanoulinou S, Musardo S, Contestabile A, Bariselli S, Casarotto G, Magrinelli E, Jiang YH, Jabaudon D, Bellone C. Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism. Molecular Psychiatry 2022, 27: 2080-2094. PMID: 35022531, PMCID: PMC9126815, DOI: 10.1038/s41380-021-01427-0.
- Isidor B, Ebstein F, Hurst A, Vincent M, Bader I, Rudy NL, Cogne B, Mayr J, Brehm A, Bupp C, Warren K, Bacino CA, Gerard A, Ranells JD, Metcalfe KA, van Bever Y, Jiang YH, Mendelssohn BA, Cope H, Rosenfeld JA, Blackburn PR, Goodenberger ML, Kearney HM, Kennedy J, Scurr I, Szczaluba K, Ploski R, de Saint Martin A, Alembik Y, Piton A, Bruel AL, Thauvin-Robinet C, Strong A, Diderich KEM, Bourgeois D, Dahan K, Vignard V, Bonneau D, Colin E, Barth M, Camby C, Baujat G, Briceño I, Gómez A, Deb W, Conrad S, Besnard T, Bézieau S, Krüger E, Küry S, Stankiewicz P. Stankiewicz-Isidor syndrome: expanding the clinical and molecular phenotype. Genetics In Medicine : Official Journal Of The American College Of Medical Genetics 2022, 24: 179-191. PMID: 34906456, DOI: 10.1016/j.gim.2021.09.005.
- Gao P, Sun S, Wang Y, Wei Y, Jiang Y. Biodegradable T2-phage-like Janus nanoparticles for actively-targeted and chemo-photothermal synergistic therapy. Chemical Engineering Journal 2022, 428: 131284. DOI: 10.1016/j.cej.2021.131284.
- Wang Y, Wei Y, Xu Q, Shao S, Man H, Nie Y, Wang Z, Jiang Y. Fabrication of Yolk–Shell Fe3O4@NiSiO3/Ni Microspheres for Efficient Purification of Histidine-Rich Proteins. Langmuir 2021, 37: 14167-14176. PMID: 34839664, DOI: 10.1021/acs.langmuir.1c02433.
- Tremblay MW, Green MV, Goldstein BM, Aldridge AI, Rosenfeld JA, Streff H, Tan WD, Craigen W, Bekheirnia N, Al Tala S, West AE, Jiang YH. Mutations of the histone linker H1–4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human Molecular Genetics 2021, 31: 1430-1442. PMID: 34788807, PMCID: PMC9271223, DOI: 10.1093/hmg/ddab321.
- Werner KM, Cox AJ, Qian E, Jain P, Ji W, Tikhonova I, Castaldi C, Bilguvar K, Knight J, Ferdinandusse S, Fawaz R, Jiang Y, Gallagher PG, Bizzarro M, Gruen JR, Bale A, Zhang H. D‐bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American Journal Of Medical Genetics Part A 2021, 188: 357-363. PMID: 34623748, PMCID: PMC8678290, DOI: 10.1002/ajmg.a.62520.
- Liu Z, Ruter D, Quigley K, Tanke N, Jiang Y, Bautch V. Single-Cell RNA Sequencing Reveals Endothelial Cell Transcriptome Heterogeneity Under Homeostatic Laminar Flow. Arteriosclerosis Thrombosis And Vascular Biology 2021, 41: 2575-2584. PMID: 34433297, PMCID: PMC8454496, DOI: 10.1161/atvbaha.121.316797.
- Khayat M, Hu J, Jiang Y, Li H, Chander V, Dawood M, Hansen A, Li S, Friedman J, Cross L, Bijlsma E, Ruivenkamp C, Sansbury F, Innis J, O’Shea J, Meng Q, Rosenfeld J, McWalter K, Wangler M, Lupski J, Posey J, Murdock D, Gibbs R. AHDC1 missense mutations in Xia-Gibbs syndrome. Human Genetics And Genomics Advances 2021, 2: 100049. PMID: 34950897, PMCID: PMC8694554, DOI: 10.1016/j.xhgg.2021.100049.
- Zhang L, Qian Y, Li J, Zhou X, Xu H, Yan J, Xiang J, Yuan X, Sun B, Sisodia SS, Jiang YH, Cao X, Jing N, Lin A. BAD-mediated neuronal apoptosis and neuroinflammation contribute to Alzheimer's disease pathology. IScience 2021, 24: 102942. PMID: 34430820, PMCID: PMC8369003, DOI: 10.1016/j.isci.2021.102942.
- Zhao C, Chai H, Zhou Q, Wen J, Reddy U, Kastury R, Jiang Y, Mak W, Bale A, Zhang H, Li P. Exome Sequencing Analysis on Products of Conception: A Cohort Study to Evaluate Clinical Utility and Genetic Etiology for Pregnancy Loss. Obstetrical & Gynecological Survey 2021, 76: 468-469. DOI: 10.1097/01.ogx.0000791680.43228.b1.
- Xu Q, Wang Y, Gao P, Jiang Y. Preparation of “pomegranate”-like QD/SiO 2 /poly(St- co -MAA) fluorescent nanobeads in two steps to improve stability and biocompatibility. New Journal Of Chemistry 2021, 45: 10618-10625. DOI: 10.1039/d1nj00526j.
- Moss T, May M, Flanagan-Steet H, Caylor R, Jiang YH, McDonald M, Friez M, McConkie-Rosell A, Steet R. Severe multisystem pathology, metabolic acidosis, mitochondrial dysfunction, and early death associated with an X-linked AIFM1 variant. Molecular Case Studies 2021, 7: a006081. PMID: 34117073, PMCID: PMC8208043, DOI: 10.1101/mcs.a006081.
- Zhao C, Xie X, Ji W, Qi M, Zhou Q, Li M, Li P, Jiang Y, Zhang H. A review of consensus statements, practice resources, standards and guidelines for clinical applications of next-generation sequencing technologies in the United States. 中华医学遗传学杂志 2021, 38: 513-520. PMID: 34096016, DOI: 10.3760/cma.j.cn511374-20200924-00691.
- Moyon S, Frawley R, Marechal D, Huang D, Marshall-Phelps KLH, Kegel L, Bøstrand SMK, Sadowski B, Jiang YH, Lyons DA, Möbius W, Casaccia P. TET1-mediated DNA hydroxymethylation regulates adult remyelination in mice. Nature Communications 2021, 12: 3359. PMID: 34099715, PMCID: PMC8185117, DOI: 10.1038/s41467-021-23735-3.
- Wei Y, An S, Sun S, Jiang Y. Photo-polymerized and thermal-polymerized silicon hydrogels with different surface microstructure and wettability. Colloids And Surfaces A Physicochemical And Engineering Aspects 2021, 618: 126284. DOI: 10.1016/j.colsurfa.2021.126284.
- Wang Y, Jiang Y, Yao B, Huang K, Liu Y, Wang Y, Qin X, Saykin A, Chen L. WEVar: a novel statistical learning framework for predicting noncoding regulatory variants. Briefings In Bioinformatics 2021, 22: bbab189. PMID: 34021560, PMCID: PMC8574971, DOI: 10.1093/bib/bbab189.
- Ma Y, Zhou H, Li C, Zou X, Luo X, Wu L, Li T, Chen X, Mao M, Huang Y, Li E, An Y, Zhang L, Wang T, Xu X, Yan W, Jiang Y, Wang Y. Differential Metabolites in Chinese Autistic Children: A Multi-Center Study Based on Urinary 1H-NMR Metabolomics Analysis. Frontiers In Psychiatry 2021, 12: 624767. PMID: 34045978, PMCID: PMC8144639, DOI: 10.3389/fpsyt.2021.624767.
- Yan W, Siegert RJ, Zhou H, Zou X, Wu L, Luo X, Li T, Huang Y, Guan H, Chen X, Mao M, Xia K, Zhang L, Li E, Li C, Zhang X, Zhou Y, Shih A, Fombonne E, Zheng Y, Han J, Sun Z, Jiang YH, Wang Y. Psychometric properties of the Chinese Parent Version of the Autism Spectrum Rating Scale: Rasch analysis. Autism 2021, 25: 1872-1884. PMID: 33845648, PMCID: PMC8548063, DOI: 10.1177/13623613211004054.
- Wang Y, Wei Y, Gao P, Sun S, Du Q, Wang Z, Jiang Y. Preparation of Fe3O4@PMAA@Ni Microspheres towards the Efficient and Selective Enrichment of Histidine-Rich Proteins. ACS Applied Materials & Interfaces 2021, 13: 11166-11176. PMID: 33635047, DOI: 10.1021/acsami.0c19734.
- Li Y, Sun S, Gao P, Zhang M, Fan C, Lu Q, Li C, Chen C, Lin B, Jiang Y. A tough chitosan-alginate porous hydrogel prepared by simple foaming method. Journal Of Solid State Chemistry 2021, 294: 121797. DOI: 10.1016/j.jssc.2020.121797.
- Jiang Y, Li W, Lindsey-Boltz L, Yang Y, Li Y, Sancar A. Super hotspots and super coldspots in the repair of UV-induced DNA damage in the human genome. Journal Of Biological Chemistry 2021, 296: 100581. PMID: 33771559, PMCID: PMC8081918, DOI: 10.1016/j.jbc.2021.100581.
- Liu C, Li D, Yang H, Li H, Xu Q, Zhou B, Hu C, Li C, Wang Y, Qiao Z, Jiang YH, Xu X. Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling. Progress In Neurobiology 2020, 200: 101985. PMID: 33388374, PMCID: PMC8572121, DOI: 10.1016/j.pneurobio.2020.101985.
- Wang T, Wang J, Ma Y, Zhou H, Ding D, Li C, Du X, Jiang YH, Wang Y, Long S, Li S, Lu G, Chen W, Zhou Y, Zhou S, Wang Y. High genetic burden in 163 Chinese children with status epilepticus. Seizure 2020, 84: 40-46. PMID: 33278787, DOI: 10.1016/j.seizure.2020.10.032.
- Du Q, Zhang C, Sun S, Wang Y, Liu H, Wei Y, Jiang Y. Magnetically Superamphiphobic Nanoparticles for Magnetic Response Surface Preparation. Langmuir 2020, 36: 14318-14323. PMID: 33205988, DOI: 10.1021/acs.langmuir.0c02582.
- Zhao C, Chai H, Zhou Q, Wen J, Reddy UM, Kastury R, Jiang Y, Mak W, Bale AE, Zhang H, Li P. Exome sequencing analysis on products of conception: a cohort study to evaluate clinical utility and genetic etiology for pregnancy loss. Genetics In Medicine 2020, 23: 435-442. PMID: 33100332, DOI: 10.1038/s41436-020-01008-6.
- Wang Y, Gao P, Wei Y, Jin Y, Sun S, Wang Z, Jiang Y. Silver nanoparticles decorated magnetic polymer composites (Fe3O4@PS@Ag) as highly efficient reusable catalyst for the degradation of 4-nitrophenol and organic dyes. Journal Of Environmental Management 2020, 278: 111473. PMID: 33120097, DOI: 10.1016/j.jenvman.2020.111473.
- Sun S, Xiao Q, Ye C, Jiang Y. Biomacromolecular fluorescent nanoparticles co-assembled by bovine serum albumin and DNA segments for living cell imaging. Colloids And Surfaces A Physicochemical And Engineering Aspects 2020, 603: 125255. DOI: 10.1016/j.colsurfa.2020.125255.
- Zhou H, Lin Y, Zhao W, Teng Y, Cui Y, Wang T, Li C, Jiang YH, Zhang JJ, Wang Y. The role of Hipk2-p53 pathways in arsenic-induced autistic behaviors: A translational study from rats to humans. Environmental Pollution 2020, 267: 115568. PMID: 33254717, DOI: 10.1016/j.envpol.2020.115568.
- Kishnani S, Riley K, Mikati M, Jiang Y. Phenotypic Variability of an Inherited Pathogenic Variant in CIC Gene: A New Case Report in Two-Generation Family and Literature Review. Journal Of Pediatric Neurology 2020, 19: 193-201. DOI: 10.1055/s-0040-1714070.
- Hulbert SW, Wang X, Gbadegesin SO, Xu Q, Xu X, Jiang Y. A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination. Autism Research 2020, 13: 1685-1697. PMID: 32815320, PMCID: PMC7780289, DOI: 10.1002/aur.2353.
- Mei W, Jiang Z, Chen Y, Chen L, Sancar A, Jiang Y. Genome-wide circadian rhythm detection methods: systematic evaluations and practical guidelines. Briefings In Bioinformatics 2020, 22: bbaa135. PMID: 32672832, PMCID: PMC8138819, DOI: 10.1093/bib/bbaa135.
- Zhou H, Xu X, Yan W, Zou X, Wu L, Luo X, Li T, Huang Y, Guan H, Chen X, Mao M, Xia K, Zhang L, Li E, Ge X, Zhang L, Li C, Zhang X, Zhou Y, Ding D, Shih A, Fombonne E, Zheng Y, Han J, Sun Z, Jiang YH, Wang Y. Prevalence of Autism Spectrum Disorder in China: A Nationwide Multi-center Population-based Study Among Children Aged 6 to 12 Years. Neuroscience Bulletin 2020, 36: 961-971. PMID: 32607739, PMCID: PMC7475160, DOI: 10.1007/s12264-020-00530-6.
- Wang Y, Bhattacharya T, Jiang Y, Qin X, Wang Y, Liu Y, Saykin A, Chen L. A novel deep learning method for predictive modeling of microbiome data. Briefings In Bioinformatics 2020, 22: bbaa073. PMID: 32406914, PMCID: PMC13017428, DOI: 10.1093/bib/bbaa073.
- Xiao Q, Sun S, Cheraga N, Wu K, Jiang Y, Huang N. Highly sensitive hair springs to measure the contraction force of engineered cardiac tissues. Materials Horizons 2020, 7: 1327-1330. DOI: 10.1039/c9mh01712g.
- Schoch K, Tan Q, Stong N, Deak KL, McConkie-Rosell A, McDonald MT, Network U, Goldstein D, Jiang Y, Shashi V. Alternative transcripts in variant interpretation: the potential for missed diagnoses and misdiagnoses. Genetics In Medicine 2020, 22: 1269-1275. PMID: 32366967, PMCID: PMC7335342, DOI: 10.1038/s41436-020-0781-x.
- Wang R, Lin D, Jiang Y. SCOPE: A Normalization and Copy-Number Estimation Method for Single-Cell DNA Sequencing. Cell Systems 2020, 10: 445-452.e6. PMID: 32437686, PMCID: PMC7250054, DOI: 10.1016/j.cels.2020.03.005.
- Wang Y, Shi L, Jin Y, Sun S, Gao P, Wei Y, Wang Z, Jiang Y. Surface-initiated polymerization for the preparation of magnetic polymer composites. Polymer Chemistry 2020, 11: 1797-1805. DOI: 10.1039/c9py01744e.
- Bey AL, Gorman MP, Gallentine W, Kohlenberg TM, Frankovich J, Jiang YH, Van Haren K. Subacute Neuropsychiatric Syndrome in Girls With SHANK3 Mutations Responds to Immunomodulation. PEDIATRICS 2020, 145: e20191490. PMID: 32015180, PMCID: PMC7802010, DOI: 10.1542/peds.2019-1490.
- Zhang C, Li Y, Sun S, Kalulu M, Wang Y, Zhou X, Wang X, Du Q, Jiang Y. Novel magnetic and flame-retardant superhydrophobic sponge for solar-assisted high-viscosity oil/water separation. Progress In Organic Coatings 2020, 139: 105369. DOI: 10.1016/j.porgcoat.2019.105369.
- Dong M, Thennavan A, Urrutia E, Li Y, Perou C, Zou F, Jiang Y. SCDC: bulk gene expression deconvolution by multiple single-cell RNA sequencing references. Briefings In Bioinformatics 2020, 22: 416-427. PMID: 31925417, PMCID: PMC7820884, DOI: 10.1093/bib/bbz166.
- An P, Gu D, Gao Z, Fan F, Jiang Y, Sun B. Hypoxia-augmented and photothermally-enhanced ferroptotic therapy with high specificity and efficiency. Journal Of Materials Chemistry B 2020, 8: 78-87. PMID: 31769461, DOI: 10.1039/c9tb02268f.
- Sun S, Xiao Q, Wei J, Wei Y, Wang Y, Gao P, Jiang Y. Bioinspired DNA self-assembly for targeted cancer cell imaging and drug delivery. Colloids And Surfaces A Physicochemical And Engineering Aspects 2020, 585: 124182. DOI: 10.1016/j.colsurfa.2019.124182.
- Sun A, Yuan Q, Fukuda M, Yu W, Yan H, Lim G, Nai M, D'Agostino G, Tran H, Itahana Y, Wang D, Lokman H, Itahana K, Lim S, Tang J, Chang Y, Zhang M, Cook S, Rackham O, Lim C, Tan E, Ng H, Lim K, Jiang Y, Je H. Potassium channel dysfunction in human neuronal models of Angelman syndrome. Science 2019, 366: 1486-1492. PMID: 31857479, PMCID: PMC7735558, DOI: 10.1126/science.aav5386.
- Sun S, Cheraga N, Jiang H, Xiao Q, Gao P, Wang Y, Wei Y, Wang X, Jiang Y. Bioinspired DNA nanocockleburs for targeted delivery of doxorubicin. Colloids And Surfaces B Biointerfaces 2019, 186: 110733. PMID: 31864113, DOI: 10.1016/j.colsurfb.2019.110733.
- Zhou X, Sun S, Zhang C, Wang X, Li Y, Jiang Y. Facile fabrication of durable superamphiphobic PET fabrics. Journal Of Coatings Technology And Research 2019, 17: 711-718. DOI: 10.1007/s11998-019-00289-0.
- Wang Y, Sun S, Shi L, Gao P, Wei Y, Zhang C, Jiang Y. Synthesis of Fe3O4@SiO2-PHEMA via redox of H2O2 and Fe2+ for efficient removal of Cu2+ from aqueous solution. Journal Of Molecular Liquids 2019, 296: 111865. DOI: 10.1016/j.molliq.2019.111865.
- Huh R, Yang Y, Jiang Y, Shen Y, Li Y. SAME-clustering: Single-cell Aggregated Clustering via Mixture Model Ensemble. Nucleic Acids Research 2019, 48: 86-95. PMID: 31777938, PMCID: PMC6943136, DOI: 10.1093/nar/gkz959.
- Zhao H, Wang Q, Yan T, Zhang Y, Xu H, Yu H, Tu Z, Guo X, Jiang Y, Li X, Zhou H, Zhang Y. Maternal valproic acid exposure leads to neurogenesis defects and autism-like behaviors in non-human primates. Translational Psychiatry 2019, 9: 267. PMID: 31636273, PMCID: PMC6803711, DOI: 10.1038/s41398-019-0608-1.
- McConkie‐Rosell A, Schoch K, Sullivan J, Cope H, Spillmann R, Palmer C, Pena L, Jiang Y, Daniels N, Walley N, Tan K, Network U, Hooper S, Shashi V. The genome empowerment scale: An assessment of parental empowerment in families with undiagnosed disease. Clinical Genetics 2019, 96: 521-531. PMID: 31448412, PMCID: PMC6983919, DOI: 10.1111/cge.13635.
- Wang X, Zhang C, Sun S, Kalulu M, Chen L, Zhou X, Jiang Y. Durable superhydrophobic coating based on inorganic/organic double-network polysiloxane and functionalized nanoparticles. Colloids And Surfaces A Physicochemical And Engineering Aspects 2019, 578: 123550. DOI: 10.1016/j.colsurfa.2019.06.016.
- Chen L, Peng H, Wei Y, Wang X, Jin Y, Liu H, Jiang Y. Self‐Healing Properties of PDMS Elastomers via Guanine and Cytosine Base Pairs. Macromolecular Chemistry And Physics 2019, 220 DOI: 10.1002/macp.201900280.
- Yang R, Walder-Christensen KK, Lalani S, Yan H, García-Prieto ID, Álvarez S, Fernández-Jaén A, Speltz L, Jiang YH, Bennett V. Neurodevelopmental mutation of giant ankyrin-G disrupts a core mechanism for axon initial segment assembly. Proceedings Of The National Academy Of Sciences Of The United States Of America 2019, 116: 19717-19726. PMID: 31451636, PMCID: PMC6765234, DOI: 10.1073/pnas.1909989116.
- Holt RJ, Young RM, Crespo B, Ceroni F, Curry CJ, Bellacchio E, Bax DA, Ciolfi A, Simon M, Fagerberg CR, van Binsbergen E, De Luca A, Memo L, Dobyns WB, Mohammed AA, Clokie SJH, Seco C, Jiang YH, Sørensen KP, Andersen H, Sullivan J, Powis Z, Chassevent A, Smith-Hicks C, Petrovski S, Antoniadi T, Shashi V, Gelb BD, Wilson SW, Gerrelli D, Tartaglia M, Chassaing N, Calvas P, Ragge NK. De Novo Missense Variants in FBXW11 Cause Diverse Developmental Phenotypes Including Brain, Eye, and Digit Anomalies. American Journal Of Human Genetics 2019, 105: 640-657. PMID: 31402090, PMCID: PMC6731360, DOI: 10.1016/j.ajhg.2019.07.005.
- Wang SE, Jiang YH. Potential of Epigenetic Therapy for Prader-Willi Syndrome. Trends In Pharmacological Sciences 2019, 40: 605-608. PMID: 31353046, DOI: 10.1016/j.tips.2019.07.002.
- Yang R, Walder-Christensen KK, Kim N, Wu D, Lorenzo DN, Badea A, Jiang YH, Yin HH, Wetsel WC, Bennett V. ANK2 autism mutation targeting giant ankyrin-B promotes axon branching and ectopic connectivity. Proceedings Of The National Academy Of Sciences Of The United States Of America 2019, 116: 15262-15271. PMID: 31285321, PMCID: PMC6660793, DOI: 10.1073/pnas.1904348116.
- Mansour M, Haupt S, Chan A, Godde N, Rizzitelli A, Loi S, Caramia F, Deb S, Takano E, Bishton M, Johnstone C, Monahan B, Levav-Cohen Y, Jiang Y, Yap A, Fox S, Bernard O, Anderson R, Haupt Y. Retraction: The E3-ligase E6AP Represses Breast Cancer Metastasis via Regulation of ECT2-Rho Signaling. Cancer Research 2019, 79: 3008-3008. PMID: 31160311, DOI: 10.1158/0008-5472.can-19-1133.
- Environmentally safe, durable and transparent superhydrophobic coating prepared by one-step sprayingZhang C, Kalulu M, Sun S, Jiang P, Zhou X, Wei Y, Jiang Y. Environmentally safe, durable and transparent superhydrophobic coating prepared by one-step spraying. Colloids And Surfaces A Physicochemical And Engineering Aspects 2019, 570: 147-155. DOI: 10.1016/j.colsurfa.2019.03.015.
- Li Z, Lin J, Sibley A, Truong T, Chua K, Jiang Y, McCarthy J, Kroetz D, Allen A, Owzar K. Efficient estimation of grouped survival models. BMC Bioinformatics 2019, 20: 269. PMID: 31138120, PMCID: PMC6540566, DOI: 10.1186/s12859-019-2899-x.
- Cheng K, Zhang Y, Li Y, Gao Z, Chen F, Sun K, An P, Sun C, Jiang Y, Sun B. A novel pH-responsive hollow mesoporous silica nanoparticle (HMSN) system encapsulating doxorubicin (DOX) and glucose oxidase (GOX) for potential cancer treatment. Journal Of Materials Chemistry B 2019, 7: 3291-3302. DOI: 10.1039/c8tb03198c.
- Abdelnour E, Gallentine W, McDonald M, Sachdev M, Jiang YH, Mikati MA. Corrigendum to “Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature” [Seizure 55 (February) (2018) 1–3]. Seizure 2019, 69: 305. PMID: 31072785, DOI: 10.1016/j.seizure.2019.04.014.
- Kalulu M, Oderinde O, Wei Y, Zhang C, Hussain I, Han X, Jiang Y. Robust solvent‐free fabrication and characterization of (polydimethylsiloxane‐co‐2‐hydroxyethylmethacrylate)/poly (ethylene glycol) methacrylate (PDMS‐HEMA)/PEGMA hydrogels. Polymers For Advanced Technologies 2019, 30: 1922-1932. DOI: 10.1002/pat.4623.
- Kim Y, Wang SE, Jiang YH. Epigenetic therapy of Prader–Willi syndrome. Translational Research 2019, 208: 105-118. PMID: 30904443, PMCID: PMC6527448, DOI: 10.1016/j.trsl.2019.02.012.
- Urrutia E, Chen L, Zhou H, Jiang Y. Destin: toolkit for single-cell analysis of chromatin accessibility. Bioinformatics 2019, 35: 3818-3820. PMID: 30821321, PMCID: PMC6761983, DOI: 10.1093/bioinformatics/btz141.
- Li W, Liu W, Kakoki A, Wang R, Adebali O, Jiang Y, Sancar A. Nucleotide excision repair capacity increases during differentiation of human embryonic carcinoma cells into neurons and muscle cells. Journal Of Biological Chemistry 2019, 294: 5914-5922. PMID: 30808711, PMCID: PMC6463700, DOI: 10.1074/jbc.ra119.007861.
- Dong M, Jiang Y. Single-Cell Allele-Specific Gene Expression Analysis. Methods In Molecular Biology 2019, 1935: 155-174. PMID: 30758826, DOI: 10.1007/978-1-4939-9057-3_11.
- Xia X, Wang X, Zhang W, Han X, Chen P, Jiang Y. Improving the wettability and antiprotein adsorption property of PDMS by swelling–deswelling approach. Journal Of Coatings Technology And Research 2019, 16: 353-361. DOI: 10.1007/s11998-018-0070-7.
- Tremblay MW, Jiang YH. DNA Methylation and Susceptibility to Autism Spectrum Disorder. Annual Review Of Medicine 2019, 70: 151-166. PMID: 30691368, PMCID: PMC6597259, DOI: 10.1146/annurev-med-120417-091431.
- Yimit A, Adebali O, Sancar A, Jiang Y. Differential damage and repair of DNA-adducts induced by anti-cancer drug cisplatin across mouse organs. Nature Communications 2019, 10: 309. PMID: 30659176, PMCID: PMC6338751, DOI: 10.1038/s41467-019-08290-2.
- Jiang YH, Huang T. The history and current status of medical genetics and genomics system in the United States. 中华医学遗传学杂志 2019, 36: 1-6. PMID: 30722085, DOI: 10.3760/cma.j.issn.1003-9406.2019.01.001.
- Murdock D, Jiang Y, Wangler M, Khayat M, Sabo A, Juusola J, McWalter K, Schatz K, Gunay-Aygun M, Gibbs R. Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition. Molecular Case Studies 2019, 5: a003608. PMID: 30622101, PMCID: PMC6549549, DOI: 10.1101/mcs.a003608.
- Machol K, Rousseau J, Ehresmann S, Garcia T, Nguyen TTM, Spillmann RC, Sullivan JA, Shashi V, Jiang YH, Stong N, Fiala E, Willing M, Pfundt R, Kleefstra T, Cho MT, McLaughlin H, Rosello Piera M, Orellana C, Martínez F, Caro-Llopis A, Monfort S, Roscioli T, Nixon CY, Buckley MF, Turner A, Jones WD, van Hasselt PM, Hofstede FC, van Gassen KLI, Brooks AS, van Slegtenhorst MA, Lachlan K, Sebastian J, Madan-Khetarpal S, Sonal D, Sakkubai N, Thevenon J, Faivre L, Maurel A, Petrovski S, Krantz ID, Tarpinian JM, Rosenfeld JA, Lee BH, Campeau PM. Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay. American Journal Of Human Genetics 2019, 104: 164-178. PMID: 30580808, PMCID: PMC6323608, DOI: 10.1016/j.ajhg.2018.11.007.
- Xu Q, Liu YY, Wang X, Tan GH, Li HP, Hulbert SW, Li CY, Hu CC, Xiong ZQ, Xu X, Jiang YH. Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons. Molecular Autism 2018, 9: 65. PMID: 30574290, PMCID: PMC6299922, DOI: 10.1186/s13229-018-0244-2.
- Towers AJ, Tremblay MW, Chung L, Li XL, Bey AL, Zhang W, Cao X, Wang X, Wang P, Duffney LJ, Siecinski SK, Xu S, Kim Y, Kong X, Gregory S, Xie W, Jiang YH. Epigenetic dysregulation of Oxtr in Tet1-deficient mice has implications for neuropsychiatric disorders. JCI Insight 2018, 3: e120592. PMID: 30518695, PMCID: PMC6328031, DOI: 10.1172/jci.insight.120592.
- Sun S, Xiao Q, Zhou X, Wei Y, Shi L, Jiang Y. A bio-based environment-friendly membrane with facile preparation process for oil-water separation. Colloids And Surfaces A Physicochemical And Engineering Aspects 2018, 559: 18-22. DOI: 10.1016/j.colsurfa.2018.09.038.
- Jiang Y, Wang R, Urrutia E, Anastopoulos I, Nathanson K, Zhang N. CODEX2: full-spectrum copy number variation detection by high-throughput DNA sequencing. Genome Biology 2018, 19: 202. PMID: 30477554, PMCID: PMC6260772, DOI: 10.1186/s13059-018-1578-y.
- Yang Y, Hu J, Selby C, Li W, Yimit A, Jiang Y, Sancar A. Single-nucleotide resolution analysis of nucleotide excision repair of ribosomal DNA in humans and mice. Journal Of Biological Chemistry 2018, 294: 210-217. PMID: 30413533, PMCID: PMC6322885, DOI: 10.1074/jbc.ra118.006121.
- Xu Q, Li CY, Wang Y, Li HP, Wu BB, Jiang YH, Xu X. Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature. BMC Medical Genomics 2018, 11: 92. PMID: 30352594, PMCID: PMC6199733, DOI: 10.1186/s12920-018-0421-3.
- Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencingWu J, Yu P, Jin X, Xu X, Li J, Li Z, Wang M, Wang T, Wu X, Jiang Y, Cai W, Mei J, Min Q, Xu Q, Zhou B, Guo H, Wang P, Zhou W, Hu Z, Li Y, Cai T, Wang Y, Xia K, Jiang YH, Sun ZS. Genomic landscapes of Chinese sporadic autism spectrum disorders revealed by whole-genome sequencing. Journal Of Genetics And Genomics 2018, 45: 527-538. PMID: 30392784, DOI: 10.1016/j.jgg.2018.09.002.
- Tu Z, Zhao H, Li B, Yan S, Wang L, Tang Y, Li Z, Bai D, Li C, Lin Y, Li Y, Liu J, Xu H, Guo X, Jiang YH, Zhang YQ, Li XJ. CRISPR/Cas9-mediated disruption of SHANK3 in monkey leads to drug-treatable autism-like symptoms. Human Molecular Genetics 2018, 28: 561-571. PMID: 30329048, PMCID: PMC6489410, DOI: 10.1093/hmg/ddy367.
- Hulbert SW, Bey AL, Jiang Y. Environmental enrichment has minimal effects on behavior in the Shank3 complete knockout model of autism spectrum disorder. Brain And Behavior 2018, 8: e01107. PMID: 30317697, PMCID: PMC6236244, DOI: 10.1002/brb3.1107.
- Chung C, Ha S, Kang H, Lee J, Um SM, Yan H, Yoo YE, Yoo T, Jung H, Lee D, Lee E, Lee S, Kim J, Kim R, Kwon Y, Kim W, Kim H, Duffney L, Kim D, Mah W, Won H, Mo S, Kim JY, Lim CS, Kaang BK, Boeckers TM, Chung Y, Kim H, Jiang YH, Kim E. Early Correction of N-Methyl-D-Aspartate Receptor Function Improves Autistic-like Social Behaviors in Adult Shank2 −/− Mice. Biological Psychiatry 2018, 85: 534-543. PMID: 30466882, PMCID: PMC6420362, DOI: 10.1016/j.biopsych.2018.09.025.
- Sun S, Xiao Q, Wang Y, Jiang Y. Roles of alcohol desolvating agents on the size control of bovine serum albumin nanoparticles in drug delivery system. Journal Of Drug Delivery Science And Technology 2018, 47: 193-199. DOI: 10.1016/j.jddst.2018.07.018.
- Walley NM, Pena LDM, Hooper SR, Cope H, Jiang YH, McConkie-Rosell A, Sanders C, Schoch K, Spillmann RC, Strong K, McCray AT, Mazur P, Esteves C, LeBlanc K, Undiagnosed Diseases Network, Wise AL, Shashi V. Characteristics of undiagnosed diseases network applicants: implications for referring providers. BMC Health Services Research 2018, 18: 652. PMID: 30134969, PMCID: PMC6106923, DOI: 10.1186/s12913-018-3458-2.
- Wang Y, Zeng C, Li J, Zhou Z, Ju X, Xia S, Li Y, Liu A, Teng H, Zhang K, Shi L, Bi C, Xie W, He X, Jia Z, Jiang Y, Cai T, Wu J, Xia K, Sun Z. PAK2 Haploinsufficiency Results in Synaptic Cytoskeleton Impairment and Autism-Related Behavior. Cell Reports 2018, 24: 2029-2041. PMID: 30134165, DOI: 10.1016/j.celrep.2018.07.061.
- Jiang P, Li Y, Zhang C, Zhou X, Jiang Y. Fabrication of a superamphiphobic coating by a simple and flexible method. Particuology 2018, 39: 33-39. DOI: 10.1016/j.partic.2017.09.004.
- Kalulu M, Zhang W, Xia X, Oderinde O, Jiang Y. Hydrophilic surface modification of polydimetylsiloxane‐co‐2‐hydroxyethylmethacrylate (PDMS‐HEMA) by Silwet L‐77 (heptamethyltrisiloxane) surface treatment. Polymers For Advanced Technologies 2018, 29: 2601-2611. DOI: 10.1002/pat.4373.
- Tan Q, Cope H, Spillmann RC, Stong N, Jiang YH, McDonald MT, Rothman JA, Butler MW, Frush DP, Lachman RS, Lee B, Bacino CA, Bonner MJ, McCall CM, Pendse AA, Walley N, Network U, Shashi V, Pena L, Alejandro M, Azamian M, Bacino C, Balasubramanyam A, Bostwick B, Burrage L, Chen S, Clark G, Craigen W, Dhar S, Emrick L, Goldman A, Hanchard N, Jamal F, Karaviti L, Lalani S, Lee B, Lewis R, Marom R, Moretti P, Murdock D, Nicholas S, Orange J, Orengo J, Posey J, Potocki L, Rosenfeld J, Samson S, Scott D, Tran A, Vogel T, Bellen H, Wangler M, Yamamoto S, Eng C, Muzny D, Ward P, Yang Y, Goldstein D, Stong N, Cope H, Jiang Y, McConkie-Rosell A, Pena L, Schoch K, Shashi V, Spillmann R, Sullivan J, Tan Q, Walley N, Aaron A, Beggs A, Berry G, Briere L, Cooper C, Donnell-Fink L, Fieg E, High F, Korrick S, Krier J, Lincoln S, Loscalzo J, Maas R, MacRae C, Pallais J, Rodan L, Silverman E, Stoler J, Sweetser D, Walker M, Walsh C, Esteves C, Glanton E, Holm I, Kohane I, McCray A, Might M, LeBlanc K, Bick D, Birch C, Boone B, Brown D, Dorset D, Jones A, Lazar J, Levy S, May T, Newberry J, Worthey E, Batzli G, Colley H, Dayal J, Eckstein D, Gould S, Howerton E, Krasnewich D, Mamounas L, Manolio T, Mulvihill J, Urv T, Wise A, Brush M, Gourdine J, Haendel M, Koeller D, Kyle J, Metz T, Waters K, Webb-Robertson B, Ashley E, Bernstein J, Bonner D, Coakley T, Davidson J, Dries A, Enns G, Fernandez L, Fisher P, Friedman N, Hom J, Huang Y, Kohler J, Majcherska M, Marwaha S, McCormack C, Merker J, Reuter C, Sampson J, Smith K, Waggott D, Wheeler M, Zastrow D, Zhao C, Allard P, Barseghyan H, Butte M, Dell'Angelica E, Dipple K, Dorrani N, Douine E, Eskin A, Fogel B, Lee H, Loo S, Martin M, Martínez-Agosto J, Nelson S, Palmer C, Papp J, Parker N, Signer R, Sinsheimer J, Vilain E, Wan J, Yoon A, Zheng A, Behnam B, Burke E, D'Souza P, Davids M, Draper D, Estwick T, Ferreira C, Godfrey R, Groden C, Johnston J, Lau C, Macnamara E, Maduro V, Markello T, Morimoto M, Murphy J, Nehrebecky M, Novacic D, Pusey B, Sharma P, CamiloToro, Wahl C, Yu G, Gropman A, Baker E, Adams D, Gahl W, Malicdan M, Tifft C, Wolfe L, Yang J, Postlethwait J, Westerfield M, Bican A, Brokamp E, Duncan L, Hamid R, Kozuira M, Newman J, Phillips J, Rives L, Robertson A, Shakachite L, Cogan J. Further evidence for the involvement of EFL1 in a Shwachman–Diamond-like syndrome and expansion of the phenotypic features. Molecular Case Studies 2018, 4: a003046. PMID: 29970384, PMCID: PMC6169826, DOI: 10.1101/mcs.a003046.
- Zhou H, Li C, Luo X, Wu L, Huang Y, Zhang L, Zou X, Xu X, Jiang YH, Yan W, Wang Y. Cross-Cultural Revision and Psychometric Properties of the Chinese Version of the Autism Spectrum Rating Scale (2–5 Years). Frontiers In Neurology 2018, 9: 460. PMID: 30013502, PMCID: PMC6036302, DOI: 10.3389/fneur.2018.00460.
- Shashi V, Schoch K, Spillmann R, Cope H, Tan Q, Walley N, Pena L, McConkie-Rosell A, Jiang YH, Stong N, Need AC, Goldstein DB, Network U, Adams D, Alejandro M, Allard P, Ashley E, Azamian M, Bacino C, Balasubramanyam A, Barseghyan H, Batzli G, Beggs A, Behnam B, Bellen H, Bernstein J, Bican A, Bick D, Birch C, Bonner D, Boone B, Bostwick B, Briere L, Brown D, Brush M, Burke E, Burrage L, Butte M, Chen S, Clark G, Coakley T, Cogan J, Cooper C, Cope H, Craigen W, D’Souza P, Davids M, Davidson J, Dayal J, Dell’Angelica E, Dhar S, Dipple K, Donnell-Fink L, Dorrani N, Dorset D, Douine E, Draper D, Dries A, Eckstein D, Emrick L, Eng C, Enns G, Eskin A, Esteves C, Estwick T, Fernandez L, Ferreira C, Fisher P, Fogel B, Friedman N, Gahl W, Glanton E, Godfrey R, Goldstein D, Gould S, Gourdine J, Groden C, Gropman A, Haendel M, Hamid R, Hanchard N, Handley L, Herzog M, Holm I, Hom J, Howerton E, Huang Y, Jacob H, Jain M, Jiang Y, Johnston J, Jones A, Koeller D, Kohane I, Kohler J, Krasnewich D, Krieg E, Krier J, Kyle J, Lalani S, Lau C, Lazar J, LeBlanc K, Lee B, Lee H, Levy S, Lewis R, Lincoln S, Loo S, Loscalzo J, Maas R, Macnamara E, MacRae C, Maduro V, Majcherska M, Malicdan M, Mamounas L, Manolio T, Markello T, Marom R, Martin M, Martínez-Agosto J, Marwaha S, May T, McConkie-Rosell A, McCormack C, McCray A, Merker J, Metz T, Might M, Moretti P, Morimoto M, Mulvihill J, Murphy J, Muzny D, Nehrebecky M, Nelson S, Newberry J, Newman J, Nicholas S, Novacic D, Orange J, Pallais J, Palmer C, Papp J, Parker N, Pena L, Phillips J, Posey J, Postlethwait J, Potocki L, Pusey B, Reuter C, Robertson A, Rodan L, Rosenfeld J, Sampson J, Samson S, Schoch K, Schroeder M, Scott D, Sharma P, Shashi V, Silverman E, Sinsheimer J, Smith K, Spillmann R, Stoler J, Stong N, Sullivan J, Sweetser D, Tan Q, Tifft C, Toro C, Tran A, Urv T, Valivullah Z, Vilain E, Vogel T, Waggott D, Wahl C, Walley N, Walsh C, Wan J, Wangler M, Ward P, Waters K, Webb-Robertson B, Westerfield M, Wheeler M, Wise A, Wolfe L, Worthey E, Yamamoto S, Yang Y, Yoon A, Yu G, Zastrow D, Zhao C, Zheng A. A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative. Genetics In Medicine 2018, 21: 161-172. PMID: 29907797, PMCID: PMC6295275, DOI: 10.1038/s41436-018-0044-2.
- Cheng Y, Li Z, Manupipatpong S, Lin L, Li X, Xu T, Jiang YH, Shu Q, Wu H, Jin P. 5-Hydroxymethylcytosine alterations in the human postmortem brains of autism spectrum disorder. Human Molecular Genetics 2018, 27: 2955-2964. PMID: 29790956, PMCID: PMC6097011, DOI: 10.1093/hmg/ddy193.
- Zhang W, Kalulu M, Wang X, Xia X, Han X, Jiang Y. Reverse hydrophobic PDMS surface to hydrophilic by 1‐step hydrolysis reaction. Polymers For Advanced Technologies 2018, 29: 2103-2109. DOI: 10.1002/pat.4319.
- Bey AL, Wang X, Yan H, Kim N, Passman RL, Yang Y, Cao X, Towers AJ, Hulbert SW, Duffney LJ, Gaidis E, Rodriguiz RM, Wetsel WC, Yin HH, Jiang YH. Brain region-specific disruption of Shank3 in mice reveals a dissociation for cortical and striatal circuits in autism-related behaviors. Translational Psychiatry 2018, 8: 94. PMID: 29700290, PMCID: PMC5919902, DOI: 10.1038/s41398-018-0142-6.
- Duffney LJ, Valdez P, Tremblay MW, Cao X, Montgomery S, McConkie‐Rosell A, Jiang Y. Epigenetics and autism spectrum disorder: A report of an autism case with mutation in H1 linker histone HIST1H1E and literature review. American Journal Of Medical Genetics Part B Neuropsychiatric Genetics 2018, 177: 426-433. PMID: 29704315, PMCID: PMC5980735, DOI: 10.1002/ajmg.b.32631.
- Jiang Y, Wangler M, McGuire A, Lupski J, Posey J, Khayat M, Murdock D, Sanchez‐Pulido L, Ponting C, Xia F, Hunter J, Meng Q, Murugan M, Gibbs R. The phenotypic spectrum of Xia‐Gibbs syndrome. American Journal Of Medical Genetics Part A 2018, 176: 1315-1326. PMID: 29696776, PMCID: PMC6231716, DOI: 10.1002/ajmg.a.38699.
- Luo W, Zhang C, Jiang YH, Brouwer CR. Systematic reconstruction of autism biology from massive genetic mutation profiles. Science Advances 2018, 4: e1701799. PMID: 29651456, PMCID: PMC5895441, DOI: 10.1126/sciadv.1701799.
- Sibley A, Li Z, Jiang Y, Li Y, Chan C, Allen A, Owzar K. Facilitating the Calculation of the Efficient Score Using Symbolic Computing. The American Statistician 2018, 72: 199-205. PMID: 30122786, PMCID: PMC6092959, DOI: 10.1080/00031305.2017.1392361.
- Liu CX, Li CY, Hu CC, Wang Y, Lin J, Jiang YH, Li Q, Xu X. CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors. Molecular Autism 2018, 9: 23. PMID: 29619162, PMCID: PMC5879542, DOI: 10.1186/s13229-018-0204-x.
- Zhao H, Jiang Y, Zhang YQ. Modeling autism in non‐human primates: Opportunities and challenges. Autism Research 2018, 11: 686-694. PMID: 29573234, PMCID: PMC6188783, DOI: 10.1002/aur.1945.
- Wei J, Sun S, Lu Q, Gao P, Wang Y, Li X, Jiang Y. The formation of fibers via complementary base pairing of DNA-conjugated bovine serum albumin. Chinese Chemical Letters 2018, 29: 461-463. DOI: 10.1016/j.cclet.2017.09.055.
- Urrutia E, Chen H, Zhou Z, Zhang N, Jiang Y. Integrative pipeline for profiling DNA copy number and inferring tumor phylogeny. Bioinformatics 2018, 34: 2126-2128. PMID: 29415173, PMCID: PMC6248831, DOI: 10.1093/bioinformatics/bty057.
- Xu L, Richman AR, Mitchell LC, Luo H, Jiang YH, Roy S, Floyd AE. Evaluating Web-based Educational Modules on Genetic Testing for Autism among Parents of Children with Autism. American Journal Of Health Behavior 2018, 42: 3-12. PMID: 29973306, DOI: 10.5993/AJHB.42.4.1.
- McConkie‐Rosell A, Hooper SR, Pena LDM, Schoch K, Spillmann RC, Jiang Y, Cope H, Network U, Palmer C, Shashi V. Psychosocial Profiles of Parents of Children with Undiagnosed Diseases: Managing Well or Just Managing? Journal Of Genetic Counseling 2018, 27: 935-946. PMID: 29297108, PMCID: PMC6028305, DOI: 10.1007/s10897-017-0193-5.
- Abdelnour E, Gallentine W, McDonald M, Sachdev M, Jiang YH, Mikati MA. Does age affect response to quinidine in patients with KCNT1 mutations? Report of three new cases and review of the literature. Seizure 2017, 55: 1-3. PMID: 29291456, DOI: 10.1016/j.seizure.2017.11.017.
- Wei J, Wang T, Li H, Lu Q, Jiang Y. Design and synthesis of organo-silica shell based dual-functional microencapsulated phase change material for thermal regulating systems. Chemical Papers 2017, 72: 1055-1064. DOI: 10.1007/s11696-017-0315-4.
- Garman B, Anastopoulos I, Krepler C, Brafford P, Sproesser K, Jiang Y, Wubbenhorst B, Amaravadi R, Bennett J, Beqiri M, Elder D, Flaherty K, Frederick D, Gangadhar T, Guarino M, Hoon D, Karakousis G, Liu Q, Mitra N, Petrelli N, Schuchter L, Shannan B, Shields C, Wargo J, Wenz B, Wilson M, Xiao M, Xu W, Xu X, Yin X, Zhang N, Davies M, Herlyn M, Nathanson K. Genetic and Genomic Characterization of 462 Melanoma Patient-Derived Xenografts, Tumor Biopsies, and Cell Lines. Cell Reports 2017, 21: 1936-1952. PMID: 29141224, PMCID: PMC5709812, DOI: 10.1016/j.celrep.2017.10.052.
- Chung L, Bey AL, Towers AJ, Cao X, Kim IH, Jiang YH. Lovastatin suppresses hyperexcitability and seizure in Angelman syndrome model. Neurobiology Of Disease 2017, 110: 12-19. PMID: 29097328, PMCID: PMC5903876, DOI: 10.1016/j.nbd.2017.10.016.
- Wu S, Gan G, Zhang Z, Sun J, Wang Q, Gao Z, Li M, Jin S, Huang J, Thomas U, Jiang YH, Li Y, Tian R, Zhang YQ. A Presynaptic Function of Shank Protein in Drosophila. Journal Of Neuroscience 2017, 37: 11592-11604. PMID: 29074576, PMCID: PMC6705749, DOI: 10.1523/jneurosci.0893-17.2017.
- Pappas A, Bey A, Wang X, Rossi M, Kim Y, Yan H, Porkka F, Duffney L, Phillips S, Cao X, Ding J, Rodriguiz R, Yin H, Weinberg R, Ji R, Wetsel W, Jiang Y. Deficiency of Shank2 causes mania-like behavior that responds to mood stabilizers. JCI Insight 2017, 2: e92052. PMID: 29046483, PMCID: PMC5846902, DOI: 10.1172/jci.insight.92052.
- Pena LDM, Jiang YH, Schoch K, Spillmann RC, Walley N, Stong N, Horn S, Sullivan JA, McConkie-Rosell A, Kansagra S, Smith EC, El-Dairi M, Bellet J, Keels MA, Jasien J, Kranz PG, Noel R, Nagaraj SK, Lark RK, Wechsler DSG, del Gaudio D, Leung ML, Hendon LG, Parker CC, Jones KL, Goldstein D, Shashi V, Members U, Alejandro M, Bacino C, Balasubramanyam A, Bostwick B, Burrage L, Chen S, Clark G, Craigen W, Dhar S, Emrick L, Graham B, Hanchard N, Jain M, Lalani S, Lee B, Lewis R, Azamian M, Moretti P, Nicholas S, Orange J, Posey J, Potocki L, Rosenfeld J, Samson S, Scott D, Tran A, Vogel T, Zhang J, Bellen H, Wangler M, Yamamoto S, Eng C, Muzny D, Ward P, Yang Y, Goldstein D, Stong N, Jiang Y, McConkie-Rosell A, Pena L, Schoch K, Shashi V, Spillmann R, Sullivan J, Walley N, Beggs A, Briere L, Cooper C, Donnell-Fink L, Krieg E, Krier J, Lincoln S, Loscalzo J, Maas R, MacRae C, Pallais J, Rodan L, Silverman E, Stoler J, Sweetser D, Walsh C, Esteves C, Holm I, Kohane I, Mazur P, McCray A, Might M, Ramoni R, Splinter K, Bick D, Birch C, Boone B, Brown D, Dorset D, Handley L, Jacob H, Jones A, Lazar J, Levy S, Newberry J, Schroeder M, Strong K, Worthey E, Dayal J, Eckstein D, Gould S, Howerton E, Krasnewich D, Mamounas L, Manolio T, Mulvihill J, Urv T, Wise A, Soldatos A, Brush M, Gourdine J, Haendel M, Koeller D, Kyle J, Metz T, Waters K, Webb-Robertson B, Ashley E, Bernstein J, Dries A, Fisher P, Kohler J, Waggott D, Wheeler M, Zornio P, Allard P, Barseghyan H, Dell'Angelica E, Dillon A, Dipple K, Dorrani N, Douine E, Eskin A, Fogel B, Herzog M, Lee H, Lipson A, Loo S, Martínez-Agosto J, Nelson S, Palmer C, Papp J, Parker N, Sinsheimer J, Vilain E, Zheng A, Adams C, Burke E, Chao K, Davids M, Draper D, Estwick T, Frisby T, Frost K, Gartner V, Godfrey R, Goheen M, Golas G, Gordon M, Groden C, Hackbarth M, Hardee I, Johnston J, Koehler A, Latham L, Latour Y, Lau C, Levy D, Liebendorfer A, Macnamara E, Maduro V, Markello T, McCarty A, Murphy J, Nehrebecky M, Novacic D, Pusey B, Sadozai S, Schaffer K, Sharma P, Thomas S, Tolman N, Toro C, Valivullah Z, Wahl C, Warburton M, Weech A, Yu G, Gropman A, Adams D, Gahl W, Malicdan M, Tifft C, Wolfe L, Lee P, Postlethwait J, Westerfield M, Bican A, Cogan J, Hamid R, Newman J, Phillips J, Robertson A. Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases. Genetics In Medicine 2017, 20: 464-469. PMID: 28914269, PMCID: PMC5851806, DOI: 10.1038/gim.2017.128.
- Maxwell K, Wubbenhorst B, Wenz B, De Sloover D, Pluta J, Emery L, Barrett A, Kraya A, Anastopoulos I, Yu S, Jiang Y, Chen H, Zhang N, Hackman N, D’Andrea K, Daber R, Morrissette J, Mitra N, Feldman M, Domchek S, Nathanson K. BRCA locus-specific loss of heterozygosity in germline BRCA1 and BRCA2 carriers. Nature Communications 2017, 8: 319. PMID: 28831036, PMCID: PMC5567274, DOI: 10.1038/s41467-017-00388-9.
- Sachdev M, Gaínza-Lein M, Tchapyjnikov D, Jiang YH, Loddenkemper T, Mikati MA. Novel clinical manifestations in patients with KCNA2 mutations. Seizure 2017, 51: 74-76. PMID: 28806589, DOI: 10.1016/j.seizure.2017.07.018.
- Zhao H, Tu Z, Xu H, Yan S, Yan H, Zheng Y, Yang W, Zheng J, Li Z, Tian R, Lu Y, Guo X, Jiang YH, Li XJ, Zhang YQ. Altered neurogenesis and disrupted expression of synaptic proteins in prefrontal cortex of SHANK3-deficient non-human primate. Cell Research 2017, 27: 1293-1297. PMID: 28741620, PMCID: PMC5630686, DOI: 10.1038/cr.2017.95.
- Tan Q, McConkie-Rosell A, Juusola J, Gustafson KE, Pizoli CE, Buckley AF, Jiang YH. The importance of managing the patient and not the gene: expanded phenotype of GLE1-associated arthrogryposis. Molecular Case Studies 2017, 3: a002063. PMID: 28729373, PMCID: PMC5701308, DOI: 10.1101/mcs.a002063.
- Zhao Z, Zhang D, Tai L, Jiang P, Jiang Y. A facile and low-cost preparation of durable amphiphobic coatings with fluoride–silica@poly(methacrylic acid) hybrid nanocomposites. Journal Of Coatings Technology And Research 2017, 14: 1369-1380. DOI: 10.1007/s11998-017-9940-7.
- Chen H, Jiang Y, Maxwell K, Nathanson K, Zhang N. Allele-specific copy number estimation by whole exome sequencing. The Annals Of Applied Statistics 2017, 11: 1169-1192. PMID: 28989557, PMCID: PMC5627665, DOI: 10.1214/17-aoas1043.
- Wang Y, Du X, Bin R, Yu S, Xia Z, Zheng G, Zhong J, Zhang Y, Jiang Y, Wang Y. Erratum: Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing. Scientific Reports 2017, 7: 46520. PMID: 28472029, PMCID: PMC5417344, DOI: 10.1038/srep46520.
- Jiang Y, Zhang N, Li M. SCALE: modeling allele-specific gene expression by single-cell RNA sequencing. Genome Biology 2017, 18: 74. PMID: 28446220, PMCID: PMC5407026, DOI: 10.1186/s13059-017-1200-8.
- Wei J, Li Y, Gao P, Lu Q, Wang Z, Zhou J, Jiang Y. Assembling gold nanoparticles into flower-like structures by complementary base pairing of DNA molecules with mediation by apoferritins. Chemical Communications 2017, 53: 4581-4584. PMID: 28387779, DOI: 10.1039/c6cc09858d.
- Spillmann RC, McConkie-Rosell A, Pena L, Jiang YH, Undiagnosed Diseases Network, Schoch K, Walley N, Sanders C, Sullivan J, Hooper SR, Shashi V. A window into living with an undiagnosed disease: illness narratives from the Undiagnosed Diseases Network. Orphanet Journal Of Rare Diseases 2017, 12: 71. PMID: 28416019, PMCID: PMC5392939, DOI: 10.1186/s13023-017-0623-3.
- Hulbert SW, Jiang YH. Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain. Neuroscience Bulletin 2017, 33: 205-218. PMID: 28271437, PMCID: PMC5360850, DOI: 10.1007/s12264-017-0112-7.
- Zhou H, Zhang L, Luo X, Wu L, Zou X, Xia K, Wang Y, Xu X, Ge X, Jiang YH, Fombonne E, Yan W, Wang Y. Modifying the Autism Spectrum Rating Scale (6–18 years) to a Chinese Context: An Exploratory Factor Analysis. Neuroscience Bulletin 2017, 33: 175-182. PMID: 28238114, PMCID: PMC5360853, DOI: 10.1007/s12264-017-0104-7.
- Zhou H, Zhang L, Zou X, Luo X, Xia K, Wu L, Wang Y, Xu X, Ge X, Jiang YH, Fombonne E, Yan W, Wang Y. Chinese Norms for the Autism Spectrum Rating Scale. Neuroscience Bulletin 2017, 33: 161-167. PMID: 28233147, PMCID: PMC5360852, DOI: 10.1007/s12264-017-0105-6.
- Zhao Z, Tai L, Zhang D, Jiang Y. Facile fabrication of siloxane @ poly (methylacrylic acid) core-shell microparticles with different functional groups. Journal Of Nanoparticle Research 2017, 19: 73. DOI: 10.1007/s11051-017-3777-y.
- Mulkey SB, Ben‐Zeev B, Nicolai J, Carroll JL, Grønborg S, Jiang Y, Joshi N, Kelly M, Koolen DA, Mikati MA, Park K, Pearl PL, Scheffer IE, Spillmann RC, Taglialatela M, Vieker S, Weckhuysen S, Cooper EC, Cilio MR. Neonatal nonepileptic myoclonus is a prominent clinical feature of KCNQ2 gain‐of‐function variants R201C and R201H. Epilepsia 2017, 58: 436-445. PMID: 28139826, PMCID: PMC5339037, DOI: 10.1111/epi.13676.
- Wang X, Xu J, Wang Q, Xu A, Zhai Y, Luo J, Jiang Y, He N, Wang Z. Wet Chemical Synthesis of Silica Nanosheets via Ethyl Acetate‐Mediated Hydrolysis of Silica Precursors and Their Applications. Small 2017, 13 PMID: 28112861, DOI: 10.1002/smll.201603369.
- Wang Y, Du X, Bin R, Yu S, Xia Z, Zheng G, Zhong J, Zhang Y, Jiang YH, Wang Y. Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing. Scientific Reports 2017, 7: 40319. PMID: 28074849, PMCID: PMC5225856, DOI: 10.1038/srep40319.
- Wang T, Li H, Lu Q, Wu N, Jiang Y. Preparation and Characterization of Glauber's Salt Microcapsules for Thermal Energy Storage. Tenside Surfactants Detergents 2017, 54: 32-37. DOI: 10.3139/113.110477.
- Zhao Z, Tai L, Zhang D, Wang Z, Jiang Y. Preparation of poly (octadecyl methacrylate)/silica-(3-methacryloxypropyl trimethoxysilane)/silica multi-layer core-shell nanocomposite with thermostable hydrophobicity and good viscosity break property. Chemical Engineering Journal 2017, 307: 891-896. DOI: 10.1016/j.cej.2016.09.021.
- Kim Y, Lee HM, Xiong Y, Sciaky N, Hulbert SW, Cao X, Everitt JI, Jin J, Roth BL, Jiang YH. Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader–Willi syndrome. Nature Medicine 2016, 23: 213-222. PMID: 28024084, PMCID: PMC5589073, DOI: 10.1038/nm.4257.
- Zhao Z, Li H, Lu Q, Li Y, Jiang Y. Multifunctional sensors based on silicone hydrogel and their responses to solvents, pH and solution composition. Polymer International 2016, 66: 566-572. DOI: 10.1002/pi.5293.
- Jiang Y, Ji Y, Sibley A, Li Y, Allen A. Leveraging population information in family‐based rare variant association analyses of quantitative traits. Genetic Epidemiology 2016, 41: 98-107. PMID: 27917519, DOI: 10.1002/gepi.22022.
- Han Q, Kim YH, Wang X, Liu D, Zhang ZJ, Bey AL, Lay M, Chang W, Berta T, Zhang Y, Jiang YH, Ji RR. SHANK3 Deficiency Impairs Heat Hyperalgesia and TRPV1 Signaling in Primary Sensory Neurons. Neuron 2016, 92: 1279-1293. PMID: 27916453, PMCID: PMC5182147, DOI: 10.1016/j.neuron.2016.11.007.
- Zhang W, Xia W, Wang Q, Towers AJ, Chen J, Gao R, Zhang Y, Yen CA, Lee AY, Li Y, Zhou C, Liu K, Zhang J, Gu TP, Chen X, Chang Z, Leung D, Gao S, Jiang YH, Xie W. Isoform Switch of TET1 Regulates DNA Demethylation and Mouse Development. Molecular Cell 2016, 64: 1062-1073. PMID: 27916660, DOI: 10.1016/j.molcel.2016.10.030.
- Zhao Z, Xie H, Li Y, Jiang Y. A multi-responsive multicomponent hydrogel with micro-phase separation structure: Synthesis and special drug release. Journal Of Drug Delivery Science And Technology 2016, 35: 184-189. DOI: 10.1016/j.jddst.2016.06.016.
- Zhao Z, Zhang D, Meng Y, Tai L, Jiang Y. One-pot fabrication of fluoride-silica@silica raspberry-like nanoparticles for superhydrophobic coating. Ceramics International 2016, 42: 14601-14608. DOI: 10.1016/j.ceramint.2016.06.076.
- Jiang Y, Qiu Y, Minn A, Zhang N. Assessing intratumor heterogeneity and tracking longitudinal and spatial clonal evolutionary history by next-generation sequencing. Proceedings Of The National Academy Of Sciences Of The United States Of America 2016, 113: e5528-e5537. PMID: 27573852, PMCID: PMC5027458, DOI: 10.1073/pnas.1522203113.
- Mansour M, Haupt S, Chan AL, Godde N, Rizzitelli A, Loi S, Caramia F, Deb S, Takano EA, Bishton M, Johnstone C, Monahan B, Levav-Cohen Y, Jiang YH, Yap AS, Fox S, Bernard O, Anderson R, Haupt Y. The E3-ligase E6AP Represses Breast Cancer Metastasis via Regulation of ECT2-Rho Signaling. Cancer Research 2016, 76: 4236-4248. PMID: 27231202, DOI: 10.1158/0008-5472.can-15-1553.
- Wang T, Wu N, Li H, Lu Q, Jiang Y. Preparation and properties of a form‐stable phase‐change hydrogel for thermal energy storage. Journal Of Applied Polymer Science 2016, 133 DOI: 10.1002/app.43836.
- Wang X, Bey AL, Katz BM, Badea A, Kim N, David LK, Duffney LJ, Kumar S, Mague SD, Hulbert SW, Dutta N, Hayrapetyan V, Yu C, Gaidis E, Zhao S, Ding JD, Xu Q, Chung L, Rodriguiz RM, Wang F, Weinberg RJ, Wetsel WC, Dzirasa K, Yin H, Jiang YH. Altered mGluR5-Homer scaffolds and corticostriatal connectivity in a Shank3 complete knockout model of autism. Nature Communications 2016, 7: 11459. PMID: 27161151, PMCID: PMC4866051, DOI: 10.1038/ncomms11459.
- Xu Q, Goldstein J, Wang P, Gadi IK, Labreche H, Rehder C, Wang WP, McConkie A, Xu X, Jiang YH. Chromosomal microarray analysis in clinical evaluation of neurodevelopmental disorders-reporting a novel deletion of SETDB1 and illustration of counseling challenge. Pediatric Research 2016, 80: 371-381. PMID: 27119313, PMCID: PMC5382808, DOI: 10.1038/pr.2016.101.
- Lu Q, Li H, Li M, Yang Y, Fan C, Wu P, Jiang Y, Zhang Z. The influence of vulcanizer on the crystal transform of iPP during reactive extrusion process. Polymer Degradation And Stability 2016, 126: 125-133. DOI: 10.1016/j.polymdegradstab.2016.02.001.
- Rosell AM, Pena LD, Schoch K, Spillmann R, Sullivan J, Hooper SR, Jiang Y, Mathey‐Andrews N, Goldstein DB, Shashi V. Not the End of the Odyssey: Parental Perceptions of Whole Exome Sequencing (WES) in Pediatric Undiagnosed Disorders. Journal Of Genetic Counseling 2016, 25: 1019-1031. PMID: 26868367, DOI: 10.1007/s10897-016-9933-1.
- Li Y, Zhu M, Li X, Li X, Jiang Y. A highly expandable and tough polyacrylamide – alginate microcapsule. RSC Advances 2016, 6: 44896-44901. DOI: 10.1039/c6ra05711j.
- Lu Q, Meng Y, Gao P, Wei J, Sun S, Zhou J, Wang Z, Jiang Y. A pH responsive micelle combined with Au nanoparticles for multi-stimuli release of both hydrophobic and hydrophilic drug. RSC Advances 2016, 6: 58654-58657. DOI: 10.1039/c6ra11159a.
- Hulbert SW, Jiang Y. Monogenic mouse models of autism spectrum disorders: Common mechanisms and missing links. Neuroscience 2015, 321: 3-23. PMID: 26733386, PMCID: PMC4803542, DOI: 10.1016/j.neuroscience.2015.12.040.
- Xie H, Zhao Z, An S, Jiang Y. The influence of the surface properties of silicon–fluorine hydrogel on protein adsorption. Colloids And Surfaces B Biointerfaces 2015, 136: 1113-1119. PMID: 26612726, DOI: 10.1016/j.colsurfb.2015.11.027.
- Mikati MA, Jiang YH, Carboni M, Shashi V, Petrovski S, Spillmann R, Milligan CJ, Li M, Grefe A, McConkie A, Berkovic S, Scheffer I, Mullen S, Bonner M, Petrou S, Goldstein D. Quinidine in the treatment of KCNT1‐positive epilepsies. Annals Of Neurology 2015, 78: 995-999. PMID: 26369628, PMCID: PMC4811613, DOI: 10.1002/ana.24520.
- Tanaka AJ, Cho MT, Retterer K, Jones JR, Nowak C, Douglas J, Jiang YH, McConkie-Rosell A, Schaefer GB, Kaylor J, Rahman OA, Telegrafi A, Friedman B, Douglas G, Monaghan KG, Chung WK. De novo pathogenic variants in CHAMP1 are associated with global developmental delay, intellectual disability, and dysmorphic facial features. Molecular Case Studies 2015, 2: a000661. PMID: 27148580, PMCID: PMC4849844, DOI: 10.1101/mcs.a000661.
- Chung L, Wang X, Zhu L, Towers AJ, Cao X, Kim IH, Jiang YH. Parental origin impairment of synaptic functions and behaviors in cytoplasmic FMRP interacting protein 1 (Cyfip1) deficient mice. Brain Research 2015, 1629: 340-350. PMID: 26474913, PMCID: PMC4744651, DOI: 10.1016/j.brainres.2015.10.015.
- Zhu M, Lu Q, Ma K, Meng Y, Jiang Y. Preparation and properties of controllable amphiphilic P(NIPAM-co-LMA) gel for drug delivery. Journal Of Drug Delivery Science And Technology 2015, 29: 245-250. DOI: 10.1016/j.jddst.2015.08.007.
- Petrovski S, Shashi V, Petrou S, Schoch K, McSweeney KM, Dhindsa RS, Krueger B, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB. Exome sequencing results in successful riboflavin treatment of a rapidly progressive neurological condition. Molecular Case Studies 2015, 1: a000257. PMID: 27148561, PMCID: PMC4850896, DOI: 10.1101/mcs.a000257.
- Shashi V, Petrovski S, Schoch K, Crimian R, Case LE, Khalid R, El-Dairi MA, Jiang YH, Mikati MA, Goldstein DB. Sustained therapeutic response to riboflavin in a child with a progressive neurological condition, diagnosed by whole-exome sequencing. Molecular Case Studies 2015, 1: a000265. PMID: 27148562, PMCID: PMC4850881, DOI: 10.1101/mcs.a000265.
- Zhou H, Zhang L, Wu L, Zou X, Luo X, Xia K, Wang Y, Xu X, Ge X, Sun C, Deng H, Fombonne E, Jiang YH, Yan W, Wang Y. Validity and reliability analysis of the Chinese parent version of the Autism Spectrum Rating Scale (6–18 years). Psychiatry Research 2015, 230: 255-261. PMID: 26384573, DOI: 10.1016/j.psychres.2015.09.003.
- Zhang Z, Gao P, Wang Z, Sun B, Jiang Y. DNA-caged gold nanoparticles for controlled release of doxorubicin triggered by a DNA enzyme and pH. Chemical Communications 2015, 51: 12996-12999. PMID: 26178750, DOI: 10.1039/c5cc05164a.
- Jiang Y, Han Y, Petrovski S, Owzar K, Goldstein D, Allen A. Incorporating Functional Information in Tests of Excess De Novo Mutational Load. American Journal Of Human Genetics 2015, 97: 272-283. PMID: 26235986, PMCID: PMC4573447, DOI: 10.1016/j.ajhg.2015.06.013.
- Meng Y, Wei J, Gao P, Jiang Y. Self-assembling amphiphilic poly(propargyl methacrylate) grafted DNA copolymers into multi-strand helices. Soft Matter 2015, 11: 5610-5613. PMID: 26096216, DOI: 10.1039/c5sm01325a.
- Zhao Z, An S, Xie H, Han X, Wang F, Jiang Y. The Relationship between the Hydrophilicity and Surface Chemical Composition Microphase Separation Structure of Multicomponent Silicone Hydrogels. The Journal Of Physical Chemistry B 2015, 119: 9780-9786. PMID: 26125331, DOI: 10.1021/acs.jpcb.5b04202.
- Williams C, Jiang Y, Shashi V, Crimian R, Schoch K, Harper A, McHale D, Goldstein D, Petrovski S. Additional evidence that PGAP1 loss of function causes autosomal recessive global developmental delay and encephalopathy. Clinical Genetics 2015, 88: 597-599. PMID: 25823418, DOI: 10.1111/cge.12581.
- Wang Y, Wang P, Xu X, Goldstein J, McConkie A, Cheung S, Jiang Y. Genetics of Autism Spectrum Disorders: The Opportunity and Challenge in the Genetics Clinic. Contemporary Clinical Neuroscience 2015, 33-66. DOI: 10.1007/978-1-4939-2190-4_4.
- Shashi V, McConkie‐Rosell A, Schoch K, Kasturi V, Rehder C, Jiang YH, Goldstein DB, McDonald MT. Practical considerations in the clinical application of whole‐exome sequencing. Clinical Genetics 2015, 89: 173-181. PMID: 25678066, DOI: 10.1111/cge.12569.
- Williams JA, Hanna JM, Shah AA, Andersen ND, McDonald MT, Jiang YH, Wechsler SB, Zomorodi A, McCann RL, Hughes GC. Adult Surgical Experience With Loeys-Dietz Syndrome. The Annals Of Thoracic Surgery 2015, 99: 1275-1281. PMID: 25678502, DOI: 10.1016/j.athoracsur.2014.11.021.
- Jiang Y, McCarthy J, Allen A. Testing the Effect of Rare Compound‐Heterozygous and Recessive Mutations in Case–Parent Sequencing Studies. Genetic Epidemiology 2015, 39: 166-172. PMID: 25631493, DOI: 10.1002/gepi.21885.
- Jiang Y, Oldridge D, Diskin S, Zhang N. CODEX: a normalization and copy number variation detection method for whole exome sequencing. Nucleic Acids Research 2015, 43: e39-e39. PMID: 25618849, PMCID: PMC4381046, DOI: 10.1093/nar/gku1363.
- Zhu X, Petrovski S, Xie P, Ruzzo EK, Lu YF, McSweeney KM, Ben-Zeev B, Nissenkorn A, Anikster Y, Oz-Levi D, Dhindsa RS, Hitomi Y, Schoch K, Spillmann RC, Heimer G, Marek-Yagel D, Tzadok M, Han Y, Worley G, Goldstein J, Jiang YH, Lancet D, Pras E, Shashi V, McHale D, Need AC, Goldstein DB. Whole-exome sequencing in undiagnosed genetic diseases: interpreting 119 trios. Genetics In Medicine 2015, 17: 774-781. PMID: 25590979, PMCID: PMC4791490, DOI: 10.1038/gim.2014.191.
- Zhu M, Li Y, Zhang Z, Jiang Y. Preparation and properties of stretchable and tough alginate/polyacrylamide hollow capsules. RSC Advances 2015, 5: 33262-33268. DOI: 10.1039/c5ra03465e.
- Zhao Z, Xie H, An S, Jiang Y. The Relationship between Oxygen Permeability and Phase Separation Morphology of the Multicomponent Silicone Hydrogels. The Journal Of Physical Chemistry B 2014, 118: 14640-14647. PMID: 25423615, DOI: 10.1021/jp507682k.
- Zhao Z, An S, Xie H, Jiang Y. Copolymerization and properties of multicomponent crosslinked hydrogels. Chinese Journal Of Polymer Science 2014, 33: 173-183. DOI: 10.1007/s10118-015-1565-7.
- Zhang Z, Meng Y, Zhu M, Wang Z, Jiang Y. Threading different metal nanomaterials on natural PhiX174 DNA to assemble a necklace. RSC Advances 2014, 4: 47268-47271. DOI: 10.1039/c4ra06722c.
- Hennessey JA, Boczek NJ, Jiang YH, Miller JD, Patrick W, Pfeiffer R, Sutphin BS, Tester DJ, Barajas-Martinez H, Ackerman MJ, Antzelevitch C, Kanter R, Pitt GS. A CACNA1C Variant Associated with Reduced Voltage-Dependent Inactivation, Increased CaV1.2 Channel Window Current, and Arrhythmogenesis. PLOS ONE 2014, 9: e106982. PMID: 25184293, PMCID: PMC4153713, DOI: 10.1371/journal.pone.0106982.
- Bey AL, Jiang Y. Overview of Mouse Models of Autism Spectrum Disorders. Current Protocols In Pharmacology 2014, 66: 5.66.1-5.66.26. PMID: 25181011, PMCID: PMC4186887, DOI: 10.1002/0471141755.ph0566s66.
- Li Y, Meng Y, Zhang Z, Jiang Y. Detecting the Oligomeric State of Escherichia coli MutS from Its Geometric Architecture Observed by an Atomic Force Microscope at a Single Molecular Level. The Journal Of Physical Chemistry B 2014, 118: 9218-9224. PMID: 25029278, DOI: 10.1021/jp504644r.
- Jiang YH, Wang Y, Xiu X, Choy KW, Pursley AN, Cheung SW. Genetic diagnosis of autism spectrum disorders: The opportunity and challenge in the genomics era. Critical Reviews In Clinical Laboratory Sciences 2014, 51: 249-262. PMID: 24878448, PMCID: PMC5937018, DOI: 10.3109/10408363.2014.910747.
- Du X, An Y, Yu L, Liu R, Qin Y, Guo X, Sun D, Zhou S, Wu B, Jiang YH, Wang Y. A genomic copy number variant analysis implicates the MBD5 and HNRNPUgenes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion. BMC Medical Genomics 2014, 15: 62. PMID: 24885232, PMCID: PMC4061518, DOI: 10.1186/1471-2350-15-62.
- Jiang Y, Satten G, Han Y, Epstein M, Heinzen E, Goldstein D, Allen A. Utilizing Population Controls in Rare-Variant Case-Parent Association Tests. American Journal Of Human Genetics 2014, 94: 845-853. PMID: 24836453, PMCID: PMC4121482, DOI: 10.1016/j.ajhg.2014.04.014.
- Wang X, Xu Q, Bey AL, Lee Y, Jiang YH. Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice. Molecular Autism 2014, 5: 30. PMID: 25071925, PMCID: PMC4113141, DOI: 10.1186/2040-2392-5-30.
- Tian Y, Li Y, Wang Z, Jiang Y. Nuclease-responsive DNA–PEI hollow microcapsules for bio-stimuli controlled release. Journal Of Materials Chemistry B 2014, 2: 1667-1672. PMID: 32261395, DOI: 10.1039/c3tb21191f.
- Prasun P, Young S, Salomons G, Werneke A, Jiang Y, Struys E, Paige M, Avantaggiati M, McDonald M. Expanding the Clinical Spectrum of Mitochondrial Citrate Carrier (SLC25A1) Deficiency: Facial Dysmorphism in Siblings with Epileptic Encephalopathy and Combined D,L-2-Hydroxyglutaric Aciduria. JIMD Reports 2014, 19: 111-115. PMID: 25614306, PMCID: PMC4501236, DOI: 10.1007/8904_2014_378.
- Hayrapetyan V, Castro S, Sukharnikova T, Yu C, Cao X, Jiang YH, Yin HH. Region‐specific impairments in striatal synaptic transmission and impaired instrumental learning in a mouse model of Angelman syndrome. European Journal Of Neuroscience 2013, 39: 1018-1025. PMID: 24329862, PMCID: PMC5937017, DOI: 10.1111/ejn.12442.
- Zhu L, Wang X, Li XL, Towers A, Cao X, Wang P, Bowman R, Yang H, Goldstein J, Li YJ, Jiang YH. Epigenetic dysregulation of SHANK3 in brain tissues from individuals with autism spectrum disorders. Human Molecular Genetics 2013, 23: 1563-1578. PMID: 24186872, PMCID: PMC3929093, DOI: 10.1093/hmg/ddt547.
- Wang X, Bey AL, Chang L, Krystal AD, Jiang Y. Therapeutic approaches for shankopathies. Developmental Neurobiology 2013, 74: 123-135. PMID: 23536326, PMCID: PMC3883807, DOI: 10.1002/dneu.22084.
- Ruzzo EK, Capo-Chichi JM, Ben-Zeev B, Chitayat D, Mao H, Pappas AL, Hitomi Y, Lu YF, Yao X, Hamdan FF, Pelak K, Reznik-Wolf H, Bar-Joseph I, Oz-Levi D, Lev D, Lerman-Sagie T, Leshinsky-Silver E, Anikster Y, Ben-Asher E, Olender T, Colleaux L, Décarie JC, Blaser S, Banwell B, Joshi RB, He XP, Patry L, Silver RJ, Dobrzeniecka S, Islam MS, Hasnat A, Samuels ME, Aryal DK, Rodriguiz RM, Jiang YH, Wetsel WC, McNamara JO, Rouleau GA, Silver DL, Lancet D, Pras E, Mitchell GA, Michaud JL, Goldstein DB. Deficiency of Asparagine Synthetase Causes Congenital Microcephaly and a Progressive Form of Encephalopathy. Neuron 2013, 80: 429-441. PMID: 24139043, PMCID: PMC3820368, DOI: 10.1016/j.neuron.2013.08.013.
- Shashi V, McConkie-Rosell A, Rosell B, Schoch K, Vellore K, McDonald M, Jiang YH, Xie P, Need A, Goldstein DB. The utility of the traditional medical genetics diagnostic evaluation in the context of next-generation sequencing for undiagnosed genetic disorders. Genetics In Medicine 2013, 16: 176-182. PMID: 23928913, DOI: 10.1038/gim.2013.99.
- Jiang YH, Yuen RK, Jin X, Wang M, Chen N, Wu X, Ju J, Mei J, Shi Y, He M, Wang G, Liang J, Wang Z, Cao D, Carter MT, Chrysler C, Drmic IE, Howe JL, Lau L, Marshall CR, Merico D, Nalpathamkalam T, Thiruvahindrapuram B, Thompson A, Uddin M, Walker S, Luo J, Anagnostou E, Zwaigenbaum L, Ring RH, Wang J, Lajonchere C, Wang J, Shih A, Szatmari P, Yang H, Dawson G, Li Y, Scherer SW. Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing. American Journal Of Human Genetics 2013, 93: 249-263. PMID: 23849776, PMCID: PMC3738824, DOI: 10.1016/j.ajhg.2013.06.012.
- Chan A, Grossman T, Zuckerman V, Di Giammartino D, Moshel O, Scheffner M, Monahan B, Pilling P, Jiang Y, Haupt S, Schueler-Furman O, Haupt Y. c‑Abl Phosphorylates E6AP and Regulates Its E3 Ubiquitin Ligase Activity. Biochemistry 2013, 52: 3119-3129. PMID: 23581475, DOI: 10.1021/bi301710c.
- Huang H, Philpot B, Jiang Y. Epigenetic Therapies in Neurological Diseases. Epigenetics And Human Health 2013, 167-193. DOI: 10.1007/978-3-642-36827-1_8.
- Jiang YH, Ehlers MD. Modeling Autism by SHANK Gene Mutations in Mice. Neuron 2013, 78: 8-27. PMID: 23583105, PMCID: PMC3659167, DOI: 10.1016/j.neuron.2013.03.016.
- Miao S, Chen R, Ye J, Tan G, Li S, Zhang J, Jiang Y, Xiong Z. The Angelman Syndrome Protein Ube3a Is Required for Polarized Dendrite Morphogenesis in Pyramidal Neurons. Journal Of Neuroscience 2013, 33: 327-333. PMID: 23283345, PMCID: PMC6618628, DOI: 10.1523/jneurosci.2509-12.2013.
- Wetsel W, Moy S, Jiang Y. Chapter 4.1 Mouse Behavioral Models for Autism Spectrum Disorders. 2013, 363-378. DOI: 10.1016/b978-0-12-391924-3.00026-0.
- Yin Y, Zhu W, Guo L, Yang R, Li X, Jiang Y. RGDC Functionalized Titanium Dioxide Nanoparticles Induce Less Damage to Plasmid DNA but Higher Cytotoxicity to HeLa Cells. The Journal Of Physical Chemistry B 2012, 117: 125-131. PMID: 23210915, DOI: 10.1021/jp3092804.
- Chung L, Bey AL, Jiang YH. Synaptic Plasticity in Mouse Models of Autism Spectrum Disorders. Korean Journal Of Physiology And Pharmacology 2012, 16: 369-378. PMID: 23269898, PMCID: PMC3526740, DOI: 10.4196/kjpp.2012.16.6.369.
- Wolyniec K, Levav-Cohen Y, Jiang Y, Haupt S, Haupt Y. The E6AP E3 ubiquitin ligase regulates the cellular response to oxidative stress. Oncogene 2012, 32: 3510-3519. PMID: 22986523, DOI: 10.1038/onc.2012.365.
- Bi C, Wu J, Jiang T, Liu Q, Cai W, Yu P, Cai T, Zhao M, Jiang Y, Sun ZS. Mutations of ANK3 identified by exome sequencing are associated with autism susceptibility. Human Mutation 2012, 33: 1635-1638. PMID: 22865819, DOI: 10.1002/humu.22174.
- Wolyniec K, Shortt J, de Stanchina E, Levav-Cohen Y, Alsheich-Bartok O, Louria-Hayon I, Corneille V, Kumar B, Woods S, Opat S, Johnstone R, Scott C, Segal D, Pandolfi P, Fox S, Strasser A, Jiang Y, Lowe S, Haupt S, Haupt Y. E6AP ubiquitin ligase regulates PML-induced senescence in Myc-driven lymphomagenesis. Blood 2012, 120: 822-832. PMID: 22689861, PMCID: PMC3709628, DOI: 10.1182/blood-2011-10-387647.
- Jiang Y, Lai L, Zhou J. Single-bit failure analysis at a nanometer resolution by conductive atomic force microscopy. Microelectronics Reliability 2012, 52: 159-164. DOI: 10.1016/j.microrel.2011.08.008.
- Levav-Cohen Y, Wolyniec K, Alsheich-Bartok O, Chan A, Woods S, Jiang Y, Haupt S, Haupt Y. E6AP is required for replicative and oncogene-induced senescence in mouse embryo fibroblasts. Oncogene 2011, 31: 2199-2209. PMID: 21927031, DOI: 10.1038/onc.2011.402.
- Jiang Y, Marszalek P. Atomic force microscopy captures MutS tetramers initiating DNA mismatch repair. The EMBO Journal 2011, 30: 2881-2893. PMID: 21666597, PMCID: PMC3160242, DOI: 10.1038/emboj.2011.180.
- Wang X, McCoy PA, Rodriguiz RM, Pan Y, Je HS, Roberts AC, Kim CJ, Berrios J, Colvin JS, Bousquet-Moore D, Lorenzo I, Wu G, Weinberg RJ, Ehlers MD, Philpot BD, Beaudet AL, Wetsel WC, Jiang YH. Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3. Human Molecular Genetics 2011, 20: 3093-3108. PMID: 21558424, PMCID: PMC3131048, DOI: 10.1093/hmg/ddr212.
- Veerapandiyan A, Shashi V, Jiang Y, Gallentine W, Schoch K, Smith E. Pseudometabolic presentation of dystrophinopathy due to a missense mutation. Muscle & Nerve 2010, 42: 975-979. PMID: 21104870, PMCID: PMC5506871, DOI: 10.1002/mus.21823.
- Jiang Y, Rabbi M, Mieczkowski P, Marszalek P. Separating DNA with Different Topologies by Atomic Force Microscopy in Comparison with Gel Electrophoresis. The Journal Of Physical Chemistry B 2010, 114: 12162-12165. PMID: 20799746, PMCID: PMC2963572, DOI: 10.1021/jp105603k.
- Jiang YH, Pan Y, Zhu L, Landa L, Yoo J, Spencer C, Lorenzo I, Brilliant M, Noebels J, Beaudet AL. Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3. PLOS ONE 2010, 5: e12278. PMID: 20808828, PMCID: PMC2924885, DOI: 10.1371/journal.pone.0012278.
- Su H, Fan W, Coskun PE, Vesa J, Gold JA, Jiang YH, Potluri P, Procaccio V, Acab A, Weiss JH, Wallace DC, Kimonis VE. Mitochondrial dysfunction in CA1 hippocampal neurons of the UBE3A deficient mouse model for Angelman syndrome. Neuroscience Letters 2009, 487: 129-133. PMID: 19563863, PMCID: PMC2888840, DOI: 10.1016/j.neulet.2009.06.079.
- Jiang Y, Fang P, Adesina AM, Furman P, Johnston JJ, Biesecker LG, Brown CW. Molecular characterization of co‐occurring Duchenne muscular dystrophy and X‐linked oculo‐facio‐cardio‐dental syndrome in a girl. American Journal Of Medical Genetics Part A 2009, 149A: 1249-1252. PMID: 19449433, PMCID: PMC2819399, DOI: 10.1002/ajmg.a.32863.
- Ke C, Loksztejn A, Jiang Y, Kim M, Humeniuk M, Rabbi M, Marszalek P. Detecting Solvent-Driven Transitions of poly(A) to Double-Stranded Conformations by Atomic Force Microscopy. Biophysical Journal 2009, 96: 2918-2925. PMID: 19348773, PMCID: PMC2711269, DOI: 10.1016/j.bpj.2008.12.3939.
- Louria-Hayon I, Alsheich-Bartok O, Levav-Cohen Y, Silberman I, Berger M, Grossman T, Matentzoglu K, Jiang Y, Muller S, Scheffner M, Haupt S, Haupt Y. E6AP promotes the degradation of the PML tumor suppressor. Cell Death & Differentiation 2009, 16: 1156-1166. PMID: 19325566, DOI: 10.1038/cdd.2009.31.
- Jiang Y, Rabbi M, Kim M, Ke C, Lee W, Clark R, Mieczkowski P, Marszalek P. UVA Generates Pyrimidine Dimers in DNA Directly. Biophysical Journal 2009, 96: 1151-1158. PMID: 19186150, PMCID: PMC2716568, DOI: 10.1016/j.bpj.2008.10.030.
- Jiang Y, Martinez JE, Ou Z, Cooper ML, Kang S, Pursley A, Cheung SW. De novo and complex imbalanced chromosomal rearrangements revealed by array CGH in a patient with an abnormal phenotype and apparently “balanced” paracentric inversion of 14(q21q23). American Journal Of Medical Genetics Part A 2008, 146A: 1986-1993. PMID: 18627051, DOI: 10.1002/ajmg.a.32408.
- Ke C, Jiang Y, Mieczkowski P, Muramoto G, Chute J, Marszalek P. Nanoscale Detection of Ionizing Radiation Damage to DNA by Atomic Force Microscopy. Small 2008, 4: 288-294. PMID: 18247386, DOI: 10.1002/smll.200700527.
- Jiang YH, Wauki K, Liu Q, Bressler J, Pan Y, Kashork CD, Shaffer LG, Beaudet AL. Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region. BMC Genomics 2008, 9: 50. PMID: 18226259, PMCID: PMC2268926, DOI: 10.1186/1471-2164-9-50.
- Jiang Y, Ke C, Mieczkowski P, Marszalek P. Detecting Ultraviolet Damage in Single DNA Molecules by Atomic Force Microscopy. Biophysical Journal 2007, 93: 1758-1767. PMID: 17483180, PMCID: PMC1948057, DOI: 10.1529/biophysj.107.108209.
- Wang Y, Chan C, Jiang Y, Li L, Ng K. AFM Studies of the Molecular Weight Dependence of Lamellar Growth Kinetics of Polymers near the Glass Transition Temperature. Macromolecules 2007, 40: 4002-4008. DOI: 10.1021/ma062717y.
- Organization process of the hierarchical structures in microbially synthesized polyhydroxyalkanoatesXu J, Guo B, Wu Q, Chen J, Chen G, Zhou J, Jiang Y, Li L. Organization process of the hierarchical structures in microbially synthesized polyhydroxyalkanoates. Current Applied Physics 2007, 7: e41-e44. DOI: 10.1016/j.cap.2006.11.012.
- Ke C, Jiang Y, Rivera M, Clark R, Marszalek P. Pulling Geometry-Induced Errors in Single Molecule Force Spectroscopy Measurements. Biophysical Journal 2007, 92: l76-l78. PMID: 17324999, PMCID: PMC1852342, DOI: 10.1529/biophysj.107.104901.
- van Woerden GM, Harris KD, Hojjati MR, Gustin RM, Qiu S, de Avila Freire R, Jiang YH, Elgersma Y, Weeber EJ. Rescue of neurological deficits in a mouse model for Angelman syndrome by reduction of αCaMKII inhibitory phosphorylation. Nature Neuroscience 2007, 10: 280-282. PMID: 17259980, DOI: 10.1038/nn1845.
- Lee G, Abdi K, Jiang Y, Michaely P, Bennett V, Marszalek P. Nanospring behaviour of ankyrin repeats. Nature 2006, 440: 246-249. PMID: 16415852, DOI: 10.1038/nature04437.
- Yu H, Liu R, Shen D, Jiang Y, Huang Y. Study on morphology and orientation of cellulose in the vascular bundle of wheat straw. Polymer 2005, 46: 5689-5694. DOI: 10.1016/j.polymer.2005.05.052.
- Chen W, Zhao Y, Jiang Y, Yan D, Han C. Light‐Scattering Study of the Aggregation of Syndiotactic Poly(methyl methacrylate) in Solution. ChemPhysChem 2004, 5: 1745-1749. PMID: 15580935, DOI: 10.1002/cphc.200400175.
- Duan Y, Jiang Y, Jiang S, Li L, Yan S, Schultz J. Depletion-Induced Nonbirefringent Banding in Thin Isotactic Polystyrene Thin Films. Macromolecules 2004, 37: 9283-9286. DOI: 10.1021/ma0483165.
- Jiang YH, Bressler J, Beaudet AL. EPIGENETICS AND HUMAN DISEASE. Annual Review Of Genomics And Human Genetics 2004, 5: 479-510. PMID: 15485357, DOI: 10.1146/annurev.genom.5.061903.180014.
- Jiang Y, Sahoo T, Michaelis RC, Bercovich D, Bressler J, Kashork CD, Liu Q, Shaffer LG, Schroer RJ, Stockton DW, Spielman RS, Stevenson RE, Beaudet AL. A mixed epigenetic/genetic model for oligogenic inheritance of autism with a limited role for UBE3A. American Journal Of Medical Genetics Part A 2004, 131A: 1-10. PMID: 15389703, DOI: 10.1002/ajmg.a.30297.
- Wang Y, Chan C, Ng K, Jiang Y, Li L. Real-Time Observation of Lamellar Branching Induced by an AFM Tip and the Stability of Induced Nuclei. Langmuir 2004, 20: 8220-8223. PMID: 15350095, DOI: 10.1021/la035293z.
- Jiang YH, Beaudet AL. Human disorders of ubiquitination and proteasomal degradation. Current Opinion In Pediatrics 2004, 16: 419-426. PMID: 15273504, DOI: 10.1097/01.mop.0000133634.79661.cd.
- Xu J, Guo B, Zhang Z, Zhou J, Jiang Y, Yan S, Li L, Wu Q, Chen G, Schultz J. Direct AFM Observation of Crystal Twisting and Organization in Banded Spherulites of Chiral Poly(3-hydroxybutyrate-co-3-hydroxyhexanoate). Macromolecules 2004, 37: 4118-4123. DOI: 10.1021/ma0499122.
- Belmonte MK, Cook EH, Anderson GM, Rubenstein JL, Greenough WT, Beckel-Mitchener A, Courchesne E, Boulanger LM, Powell SB, Levitt PR, Perry EK, Jiang YH, DeLorey TM, Tierney E. Autism as a disorder of neural information processing: directions for research and targets for therapy. Molecular Psychiatry 2004, 9: 646-663. PMID: 15037868, DOI: 10.1038/sj.mp.4001499.
- Li-Mei Q, Yong J, Fen L, Liang-Zhong Z. XPS Investigation of the Spherulite Surface for Poly(ε-caprolactone)/poly(vinyl chloride). Acta Physico-Chimica Sinica 2004, 20: 47-49. DOI: 10.3866/pku.whxb20040110.
- Tsai T, Bressler J, Jiang Y, Beaudet AL. Disruption of the genomic imprint in trans with homologous recombination at Snrpn in ES cells. Genesis 2003, 37: 151-161. PMID: 14666508, DOI: 10.1002/gene.10237.
- Jiang Y, Jin X, Han C, Li L, Wang Y, Chan C. Melting Behaviors of Lamellar Crystals of Poly(bisphenol A-co-decane ether) Studied by in-Situ Atomic Force Microscopy. Langmuir 2003, 19: 8010-8018. DOI: 10.1021/la0343775.
- Jiang Y, Zhou J, Li L, Xu J, Guo B, Zhang Z, Wu Q, Chen G, Weng L, Cheung Z, Chan C. Surface Properties of Poly(3-hydroxybutyrate-co-3- hydroxyvalerate) Banded Spherulites Studied by Atomic Force Microscopy and Time-of-Flight Secondary Ion Mass Spectrometry. Langmuir 2003, 19: 7417-7422. DOI: 10.1021/la034865c.
- Lei Y, Chan C, Wang Y, Ng K, Jiang Y, Lin L. Growth process of homogeneously and heterogeneously nucleated spherulites as observed by atomic force microscopy. Polymer 2003, 44: 4673-4679. DOI: 10.1016/s0032-3861(03)00440-3.
- Jiang Y, Gu Q, Li L, Shen D, Jin X, Chan C. Conformational changes in the induction period of crystallization as measured by FT-IR. Polymer 2003, 44: 3509-3513. DOI: 10.1016/s0032-3861(03)00278-7.
- Jiang Y, Yan D, Gao X, Han C, Jin X, Li L, Wang Y, Chan C. Lamellar Branching of Poly(bisphenol A-co-decane) Spherulites at Different Temperatures Studied by High-Temperature AFM. Macromolecules 2003, 36: 3652-3655. DOI: 10.1021/ma0341061.
- Weeber EJ, Jiang YH, Elgersma Y, Varga AW, Carrasquillo Y, Brown SE, Christian JM, Mirnikjoo B, Silva A, Beaudet AL, Sweatt JD. Derangements of Hippocampal Calcium/Calmodulin-Dependent Protein Kinase II in a Mouse Model for Angelman Mental Retardation Syndrome. Journal Of Neuroscience 2003, 23: 2634-2644. PMID: 12684449, PMCID: PMC6742065, DOI: 10.1523/jneurosci.23-07-02634.2003.
- Luo Y, Jiang Y, Jin X, Li L, Chan C. Real‐time AFM study of lamellar growth of semi‐crystalline polymers. Macromolecular Symposia 2003, 192: 271-280. DOI: 10.1002/masy.200390037.
- Cooper B, Schneider S, Bohl J, Jiang Y, Beaudet A, Pol S. Requirement of e6ap and the features of human papillomavirus e6 necessary to support degradation of p53. Virology 2003, 306: 87-99. PMID: 12620801, DOI: 10.1016/s0042-6822(02)00012-0.
- Yong J, Yanhong L, Zefu F, Xiayu W, Jun X, Baohua G, Lin L. Observation of banded spherulites and lamellar structures by atomic force microscopy. Science China Chemistry 2003, 46: 152-159. DOI: 10.1360/03yb9022.
- Luo Y, Jiang Y, Jin X, Li L, Lei Y, Chan C. Recent progresses of polymer crystallization studied by AFM. Science Bulletin 2002, 47: 1761-1765. DOI: 10.1007/bf03183837.
- Jiang Y, Gu Q, Li L, Shen D, Jin X, Lei Y, Chan C. Structural changes during isothermal crystallization of a poly(bisphenol A-co-decane ether) polymer. Polymer 2002, 43: 5615-5621. DOI: 10.1016/s0032-3861(02)00441-x.
- Lei Y, Chan C, Li J, Ng K, Wang Y, Jiang Y, Li L. The Birth of an Embryo and Development of the Founding Lamella of Spherulites As Observed by Atomic Force Microscopy. Macromolecules 2002, 35: 6751-6753. DOI: 10.1021/ma0121619.
- Beaudet AL, Jiang YH. A Rheostat Model for a Rapid and Reversible Form of Imprinting-Dependent Evolution. American Journal Of Human Genetics 2002, 70: 1389-1397. PMID: 11992247, PMCID: PMC379123, DOI: 10.1086/340969.
- Smith CL, DeVera DG, Lamb DJ, Nawaz Z, Jiang YH, Beaudet AL, O’Malley B. Genetic Ablation of the Steroid Receptor Coactivator-Ubiquitin Ligase, E6-AP, Results in Tissue-Selective Steroid Hormone Resistance and Defects in Reproduction. Molecular And Cellular Biology 2002, 22: 525-535. PMID: 11756548, PMCID: PMC139730, DOI: 10.1128/mcb.22.2.525-535.2002.
- Jiang Y, Ding E, Li G. Study on transition characteristics of PEG/CDA solid–solid phase change materials. Polymer 2002, 43: 117-122. DOI: 10.1016/s0032-3861(01)00613-9.
- Ding E, Jiang Y, Li G. COMPARATIVE STUDIES OF THE STRUCTURES AND TRANSITION CHARACTERISTICS OF CELLULOSE DIACETATE MODIFIED WITH POLYETHYLENE GLYCOL PREPARED BY CHEMICAL BONDING AND PHYSICAL BLENDING METHODS*. Journal Of Macromolecular Science Part B 2001, 40: 1053-1068. DOI: 10.1081/mb-100107801.
- Cummings C, Reinstein E, Sun Y, Antalffy B, Jiang Y, Ciechanover A, Orr H, Beaudet A, Zoghbi H. Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice. Neuron 1999, 24: 879-892. PMID: 10624951, DOI: 10.1016/s0896-6273(00)81035-1.
- Tsai T, Jiang Y, Bressler J, Armstrong D, Beaudet A. Paternal Deletion from Snrpn to Ube3a in the Mouse Causes Hypotonia, Growth Retardation and Partial Lethality and Provides Evidence for a Gene Contributing to Prader-Willi Syndrome. Human Molecular Genetics 1999, 8: 1357-1364. PMID: 10400982, DOI: 10.1093/hmg/8.8.1357.
- Jiang Y, Lev-Lehman E, Bressler J, Tsai T, Beaudet A. Genetics of Angelman Syndrome. American Journal Of Human Genetics 1999, 65: 1-6. PMID: 10364509, PMCID: PMC1378067, DOI: 10.1086/302473.
- Jiang Y, Armstrong D, Albrecht U, Atkins C, Noebels J, Eichele G, Sweatt J, Beaudet A. Mutation of the Angelman Ubiquitin Ligase in Mice Causes Increased Cytoplasmic p53 and Deficits of Contextual Learning and Long-Term Potentiation. Neuron 1998, 21: 799-811. PMID: 9808466, DOI: 10.1016/s0896-6273(00)80596-6.
- Jiang Y, Tsai T, Bressler J, Beaudet A. Imprinting in Angelman and Prader-Willi syndromes. Current Opinion In Genetics & Development 1998, 8: 334-342. PMID: 9691003, DOI: 10.1016/s0959-437x(98)80091-9.
- Sutcliffe J, Jiang Y, Galjaard R, Matsuura T, Fang P, Kubota T, Christian S, Bressler J, Cattanach B, Ledbetter D, Beaudet A. The E6–AP Ubiquitin–Protein Ligase (UBE3A) Gene Is Localized within a Narrowed Angelman Syndrome Critical Region. Genome Research 1997, 7: 368-377. PMID: 9110176, PMCID: PMC139148, DOI: 10.1101/gr.7.4.368.
- Matsuura T, Sutcliffe J, Fang P, Galjaard R, Jiang Y, Benton C, Rommens J, Beaudet A. De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome. Nature Genetics 1997, 15: 74-77. PMID: 8988172, DOI: 10.1038/ng0197-74.
- Winchester Building25 York StreetNew Haven, CT 06511
- 1 Long Wharf DriveNew Haven, CT 06511
- Winchester Building25 York StreetNew Haven, CT 06511
- 1 Long Wharf DriveNew Haven, CT 06511