-
A Whole-Exome Sequencing Study of Tourette Disorder in a Chinese Population. DNA Cell Biol. 2020 Jan; 39(1):63-68.
Zhao X, Wang S, Hao J, Zhu P, Zhang X, Wu M. PMID: 31855460.
View in:
PubMed Mentions:
1 Fields:
Translation:
Humans
-
Targeted resequencing of 358 candidate genes for autism spectrum disorder in a Chinese cohort reveals diagnostic potential and genotype-phenotype correlations. Hum Mutat. 2019 06; 40(6):801-815.
Zhou WZ, Zhang J, Li Z, Lin X, Li J, Wang S, Yang C, Wu Q, Ye AY, Wang M, Wang D, Pu TZ, Wu YY, Wei L. PMID: 30763456.
View in:
PubMed Mentions:
6 Fields:
Translation:
Humans
-
ATP1A3 mosaicism in families with alternating hemiplegia of childhood. Clin Genet. 2019 07; 96(1):43-52.
Yang X, Yang X, Chen J, Li S, Zeng Q, Huang AY, Ye AY, Yu Z, Wang S, Jiang Y, Wu X, Wu Q, Wei L, Zhang Y. PMID: 30891744.
View in:
PubMed Mentions:
1 Fields:
Translation:
Humans
-
De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis. Cell Rep. 2018 09 25; 24(13):3441-3454.e12.
Wang S, Mandell JD, Kumar Y, Sun N, Morris MT, Arbelaez J, Nasello C, Dong S, Duhn C, Zhao X, Yang Z, Padmanabhuni SS, Yu D, King RA, Dietrich A, Khalifa N, Dahl N, Huang AY, Neale BM, Coppola G, Mathews CA, Scharf JM, Tourette International Collaborative Genetics Study (TIC Genetics) , Tourette Syndrome Genetics Southern and Eastern Europe Initiative (TSGENESEE) , Tourette Association of America International Consortium for Genetics (TAAICG) , Fernandez TV, Buxbaum JD, De Rubeis S, Grice DE, Xing J, Heiman GA, Tischfield JA, Paschou P, Willsey AJ, State MW. PMID: 30257206.
View in:
PubMed Mentions:
16 Fields:
Translation:
Humans
-
The Psychiatric Cell Map Initiative: A Convergent Systems Biological Approach to Illuminating Key Molecular Pathways in Neuropsychiatric Disorders. Cell. 2018 07 26; 174(3):505-520.
Willsey AJ, Morris MT, Wang S, Willsey HR, Sun N, Teerikorpi N, Baum TB, Cagney G, Bender KJ, Desai TA, Srivastava D, Davis GW, Doudna J, Chang E, Sohal V, Lowenstein DH, Li H, Agard D, Keiser MJ, Shoichet B, von Zastrow M, Mucke L, Finkbeiner S, Gan L, Sestan N, Ward ME, Huttenhain R, Nowakowski TJ, Bellen HJ, Frank LM, Khokha MK, Lifton RP, Kampmann M, Ideker T, State MW, Krogan NJ. PMID: 30053424.
View in:
PubMed Mentions:
33 Fields:
Translation:
Humans
-
A model for postzygotic mosaicisms quantifies the allele fraction drift, mutation rate, and contribution to de novo mutations. Genome Res. 2018 07; 28(7):943-951.
Ye AY, Dou Y, Yang X, Wang S, Huang AY, Wei L. PMID: 29875290.
View in:
PubMed Mentions:
4 Fields:
Translation:
Humans
-
Distinctive types of postzygotic single-nucleotide mosaicisms in healthy individuals revealed by genome-wide profiling of multiple organs. PLoS Genet. 2018 05; 14(5):e1007395.
Huang AY, Yang X, Wang S, Zheng X, Wu Q, Ye AY, Wei L. PMID: 29763432.
View in:
PubMed Mentions:
10 Fields:
Translation:
HumansCells
-
Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort. Sci Rep. 2017 Nov 15; 7(1):15677.
Yang X, Liu A, Xu X, Yang X, Zeng Q, Ye AY, Yu Z, Wang S, Huang AY, Wu X, Wu Q, Wei L, Zhang Y. PMID: 29142202.
View in:
PubMed Mentions:
14 Fields:
Translation:
HumansCells
-
Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations. Hum Mutat. 2017 08; 38(8):1002-1013.
Dou Y, Yang X, Li Z, Wang S, Zhang Z, Ye AY, Yan L, Yang C, Wu Q, Li J, Zhao B, Huang AY, Wei L. PMID: 28503910.
View in:
PubMed Mentions:
20 Fields:
Translation:
Humans
-
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome. Hum Mutat. 2015 Sep; 36(9):861-72.
Xu X, Yang X, Wu Q, Liu A, Yang X, Ye AY, Huang AY, Li J, Wang M, Yu Z, Wang S, Zhang Z, Wu X, Wei L, Zhang Y. PMID: 26096185.
View in:
PubMed Mentions:
31 Fields:
Translation:
Humans
-
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals. Cell Res. 2014 Nov; 24(11):1311-27.
Huang AY, Xu X, Ye AY, Wu Q, Yan L, Zhao B, Yang X, He Y, Wang S, Zhang Z, Gu B, Zhao HQ, Wang M, Gao H, Gao G, Zhang Z, Yang X, Wu X, Zhang Y, Wei L. PMID: 25312340.
View in:
PubMed Mentions:
31 Fields:
Translation:
HumansCells