Yue‐Sheng Long

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 · 206 citations

Life Sciences, Genetics, Molecular Genetics +17

CRISPR/Cas9 facilitates investigation of neural circuit disease using human iPSCs: mechanism of epilepsy caused by an SCN1A loss-of-function mutation

Jianche Liu, Caixia Gao, Wenli Chen et al. · Translational Psychiatry · 2016 · 98 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

Autapses enhance bursting and coincidence detection in neocortical pyramidal cells

Luping Yin, Rui Zheng, Ke Wei et al. · Nature Communications · 2018 · 95 citations · Full text

Life Sciences, Neurobiology, Neuroscience +17

A novel role of fragile X mental retardation protein in pre-mRNA alternative splicing through RNA-binding protein 14

Lintao Zhou, Shun-Hua Ye, Haixuan Yang et al. · Neuroscience · 2017 · 56 citations

Life Sciences, Molecular Biology, Molecular Genetics +15

Epigenetic Downregulation of Scn3a Expression by Valproate: a Possible Role in Its Anticonvulsant Activity

Na-Na Tan, Guo‐Wang Lin, Yonghong Chen et al. · Molecular Neurobiology · 2016 · 52 citations

Life Sciences, Neuroscience, Pharmacology +14