Sheng Wang

Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of “ <i>de novo</i> ” <i>SCN1A</i> Mutations in Children with Dravet Syndrome

Xiaojing Xu, Xiaoxu Yang, Qixi Wu et al. · Human Mutation · 2015 · 134 citations · Full text

Scn1a Mutations, Dravet Syndrome, Allelic Variant +15

De Novo Sequence and Copy Number Variants Are Strongly Associated with Tourette Disorder and Implicate Cell Polarity in Pathogenesis

Sheng Wang, Jeffrey D. Mandell, Yogesh Kumar et al. · Cell Reports · 2018 · 129 citations · Full text

Postzygotic single‐nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations

Yanmei Dou, Xiaoxu Yang, Ziyi Li et al. · Human Mutation · 2017 · 78 citations · Full text

Postzygotic Single‐nucleotide Mosaicisms, Autism Spectrum Disorders, Medicine +15

Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort

Xiaoxu Yang, Aijie Liu, Xiaojing Xu et al. · Scientific Reports · 2017 · 66 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +20

Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals

August Yue Huang, Xiaojing Xu, Adam Yongxin Ye et al. · Cell Research · 2014 · 59 citations · Full text