Wei‐Ping Liao

The<i>SCN1A</i>Mutation Database: Updating Information and Analysis of the Relationships among Genotype, Functional Alteration, and Phenotype

Heng Meng, Haiqing Xu, Lu Yu et al. · Human Mutation · 2015 · 197 citations

Dysfunction of cortical GABAergic neurons leads to sensory hyper-reactivity in a Shank3 mouse model of ASD

Qian Chen, Christopher A Deister, Baolin Guo et al. · Nature Neuroscience · 2020 · 191 citations · Full text

Shank3 Mouse Model, Neurophysiology, Neuroanatomy +10

Modeling Dravet syndrome using induced pluripotent stem cells (iPSCs) and directly converted neurons

Jiao Jiao, Yuanyuan Yang, Yi‐Wu Shi et al. · Human Molecular Genetics · 2013 · 145 citations · Full text

Cellular Neurobiology, Social Sciences, Regenerative Medicine +23

Autism in Dravet syndrome: Prevalence, features, and relationship to the clinical characteristics of epilepsy and mental retardation

Bing-Mei Li, Xiao‐Rong Liu, Yong‐Hong Yi et al. · Epilepsy & Behavior · 2011 · 113 citations

Neurodevelopmental Disorders, Dravet Syndrome, Developmental Disability +10

Long-read sequencing identified intronic repeat expansions in <i>SAMD12</i> from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Sheng Zeng, Xuejing Wang, Zhengmao Hu et al. · Journal of Medical Genetics · 2018 · 103 citations