Liwen Wu

Mutations in <i>PRRT2</i> result in paroxysmal dyskinesias with marked variability in clinical expression

Qing Liu, Zhan Qi, Xinhua Wan et al. · Journal of Medical Genetics · 2011 · 96 citations · Full text

Life Sciences, Genetics, Neurology +13

Novel West syndrome candidate genes in a Chinese cohort

Jing Peng, Ying Wang, Fang He et al. · CNS Neuroscience & Therapeutics · 2018 · 92 citations · Full text

Life Sciences, Genetics, Neurology +17

Notch Signaling Activation Promotes Seizure Activity in Temporal Lobe Epilepsy

Longze Sha, Xiaofeng Wu, Yuan Yao et al. · Molecular Neurobiology · 2013 · 51 citations · Full text

Medicine, Neurobiology, Neuroscience +12

Clinical and genetic analysis of six Chinese children with Poirier-Bienvenu neurodevelopmental syndrome caused by CSNK2B mutation

Sai Yang, Liwen Wu, Hongmei Liao et al. · Neurogenetics · 2021 · 17 citations

Medicine, Genetics, Pediatrics +17

Analysis copy number variation of Chinese children in early‐onset epileptic encephalopathies with unknown cause

Yan Ma, Chao Chen, Yibin Wang et al. · Clinical Genetics · 2016 · 15 citations

Life Sciences, Genetics, Molecular Genetics +17