Yu Peng

De novo genic mutations among a Chinese autism spectrum disorder cohort

Tianyun Wang, Hui Guo, Bo Xiong et al. · Nature Communications · 2016 · 378 citations · Full text

Common genetic variants on 1p13.2 associate with risk of autism

Kun Xia, Hui Guo, Zhengmao Hu et al. · Molecular Psychiatry · 2013 · 106 citations

Syndromic Autism, Genetic Disorder, Genetics +7

Homozygous loss‐of‐function mutation of the <i><scp>LEPREL1</scp></i> gene causes severe non‐syndromic high myopia with early‐onset cataract

Hui Guo, Ping Tong, Yu Peng et al. · Clinical Genetics · 2013 · 59 citations · Full text

Ocular Disease, Genetics, Collagen Modification +16

Association analysis of CNTNAP2 polymorphisms with autism in the Chinese Han population

Xiaoping Li, Zhengmao Hu, Yiqun He et al. · Psychiatric Genetics · 2010 · 58 citations

Association of genetic variants of GRIN2B with autism

Yongcheng Pan, Jingjing Chen, Hui Guo et al. · Scientific Reports · 2015 · 56 citations · Full text