Xiaoling Yang

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

The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures

Rosemary Burgess, Shuyu Wang, Amy McTague et al. · Annals of Neurology · 2019 · 130 citations · Full text

Association between the <i>FOXP2</i> gene and autistic disorder in Chinese population

Xiaohong Gong, Meixiang Jia, Yan Ruan et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 2004 · 83 citations

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