Yan Chen

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

Bart Loeys, Junji Chen, Enid Neptune et al. · Nature Genetics · 2005 · 1.8K citations · Full text

Dentistry, Developmental Biology, Genetics +14

Single-Cell Exome Sequencing and Monoclonal Evolution of a JAK2-Negative Myeloproliferative Neoplasm

Yong Hou, Luting Song, Ping Zhu et al. · Cell · 2012 · 592 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

SCN8A mutations in Chinese patients with early onset epileptic encephalopathy and benign infantile seizures

Jiaping Wang, Hua Gao, Xinhua Bao et al. · BMC Medical Genetics · 2017 · 48 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17

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

Rett and Rett‐like syndrome: Expanding the genetic spectrum to <i>KIF1A</i> and <i>GRIN1</i> gene

Jiaping Wang, Qingping Zhang, Yan Chen et al. · Molecular Genetics & Genomic Medicine · 2019 · 41 citations · Full text

Life Sciences, Genetics, Molecular Genetics +11