Yongxin Wen

Rett syndrome-causing mutations compromise MeCP2-mediated liquid–liquid phase separation of chromatin

Liang Wang, Mingli Hu, Mei-Qing Zuo et al. · Cell Research · 2020 · 156 citations · Full text

Life Sciences, Genetics, Molecular Biology +12

Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome

Jiaping Wang, Yongxin Wen, Qingping Zhang et al. · Seizure · 2019 · 42 citations

Life Sciences, Genetics, Molecular Genetics +17

Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort

Qingping Zhang, Xiaoxu Yang, Jiaping Wang et al. · Genetics in Medicine · 2018 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

Novel MEF2C point mutations in Chinese patients with Rett (−like) syndrome or non-syndromic intellectual disability: insights into genotype-phenotype correlation

Jiaping Wang, Qingping Zhang, Yan Chen et al. · BMC Medical Genetics · 2018 · 31 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

The genetic and clinical characteristics of aromatic L-amino acid decarboxylase deficiency in mainland China

Yongxin Wen, Jiaping Wang, Qingping Zhang et al. · Journal of Human Genetics · 2020 · 26 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14