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 · 197 citations

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 · 96 citations · Full text

Neurogenomics, Synaptic Transmission, Neural Circuit Disease +25

Autapses enhance bursting and coincidence detection in neocortical pyramidal cells

Luping Yin, Rui Zheng, Ke Wei et al. · Nature Communications · 2018 · 94 citations · Full text

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

Rna Processing, Natural Sciences, Genetics +13

Partial epilepsy with antecedent febrile seizures and seizure aggravation by antiepileptic drugs: Associated with loss of function of Na_v1.1

Wei‐Ping Liao, Yi‐Wu Shi, Yue‐Sheng Long et al. · Epilepsia · 2010 · 51 citations