Wenshu XiangWei

De novo mutations and rare variants occurring in NMDA receptors

Wenshu XiangWei, Yuwu Jiang, Hongjie Yuan · Current Opinion in Physiology · 2017 · 134 citations · Full text

Genetic Disorder, Genetics, Nmda Receptors +7

Heterogeneous clinical and functional features of GRIN2D-related developmental and epileptic encephalopathy

Wenshu XiangWei, Varun Kannan, Yuchen Xu et al. · Brain · 2019 · 87 citations · Full text

Receptor Surface Expression, Grin2d-related Developmental, Nmdar Subunits +25

Reanalysis of whole exome sequencing data in patients with epilepsy and intellectual disability/mental retardation

Jinliang Li, Kai Gao, Huifang Yan et al. · Gene · 2019 · 71 citations

Neuroimaging Biomarkers, Mendelian Disorder, Psychiatry +10

De novo<i>GRIN</i>variants in NMDA receptor M2 channel pore‐forming loop are associated with neurological diseases

Jia Li, Jin Zhang, Weiting Tang et al. · Human Mutation · 2019 · 66 citations · Full text

Nmdar Subunits, Synaptic Transmission, Neurotransmitter +23

Autophagy eliminates cytoplasmic β-catenin and NICD to promote the cardiac differentiation of P19CL6 cells

Zhuqing Jia, Jiaji Wang, Weiping Wang et al. · Cellular Signalling · 2014 · 63 citations · Full text

Cardiac Muscle, Cell Autophagy, Signal Transduction +13