Editorial: Sub-molecular mechanism of genetic epilepsy

por Liao, Wei-Ping, Chen, Qian, Jiang, Yu-Wu, Luo, Sheng, Liu, Xiao-Rong
Publicado 2022

Limbic Epileptogenesis in a Mouse Model of Fragile X Syndrome

por Qiu, Li-Feng, Lu, Ting-Jia, Hu, Xiao-Ling, Yi, Yong-Hong, Liao, Wei-Ping, Xiong, Zhi-Qi
Publicado 2009

Critical Role of E1623 Residue in S3-S4 Loop of Nav1.1 Channel and Correlation Between Nature of Substitution and Functional Alteration

por Su, Tao, Chen, Meng-Long, Liu, Li-Hong, Meng, Hen, Tang, Bin, Liu, Xiao-Rong, Liao, Wei-Ping
Publicado 2022

The association between oxcarbazepine-induced maculopapular eruption and HLA-B alleles in a Northern Han Chinese population

por Lv, Yu-Dan, Min, Fu-Li, Liao, Wei-Ping, He, Na, Zeng, Tao, Ma, Di-Hui, Shi, Yi-Wu
Publicado 2013

YWHAG Mutations Cause Childhood Myoclonic Epilepsy and Febrile Seizures: Molecular Sub-regional Effect and Mechanism

por Ye, Xing-Guang, Liu, Zhi-Gang, Wang, Jie, Dai, Jie-Min, Qiao, Pei-Xiu, Gao, Ping-Ming, Liao, Wei-Ping
Publicado 2021

Laminar Distribution of Neurochemically-Identified Interneurons and Cellular Co-expression of Molecular Markers in Epileptic Human Cortex

por Zhu, Qiyu, Ke, Wei, He, Quansheng, Wang, Xiongfei, Zheng, Rui, Li, Tianfu, Luan, Guoming, Long, Yue-Sheng, Liao, Wei-Ping, Shu, Yousheng
Publicado 2018

Neuroprotection of lamotrigine on hypoxic-ischemic brain damage in neonatal rats: Relations to administration time and doses

por Yi, Yong-Hong, Guo, Wen-Chao, Sun, Wei-Wen, Su, Tao, Lin, Han, Chen, Sheng-Qiang, Deng, Wen-Yi, Zhou, Wei, Liao, Wei-Ping
Publicado 2008

Variants in BSN gene associated with epilepsy with favourable outcome

por Ye, Tingting, Zhang, Jiwei, Wang, Jie, Lan, Song, Zeng, Tao, Wang, Huaili, He, Xuelian, Li, Bing-Mei, Deng, Weiwen, Liao, Wei-Ping, Liu, Xiao-Rong
Publicado 2023

Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome

por He, Na, Li, Bing-Mei, Li, Zhao-Xia, Wang, Jie, Liu, Xiao-Rong, Meng, Heng, Tang, Bin, Bian, Wen-Jun, Shi, Yi-Wu, Liao, Wei-Ping
Publicado 2018

Evaluating the pathogenic potential of genes with de novo variants in epileptic encephalopathies

por He, Na, Lin, Zhi-Jian, Wang, Jie, Wei, Feng, Meng, Heng, Liu, Xiao-Rong, Chen, Qian, Su, Tao, Shi, Yi-Wu, Yi, Yong-Hong, Liao, Wei-Ping
Publicado 2018

RYR2 Mutations Are Associated With Benign Epilepsy of Childhood With Centrotemporal Spikes With or Without Arrhythmia

por Ma, Mei-Gang, Liu, Xiao-Rong, Wu, Yuan, Wang, Jie, Li, Bing-Mei, Shi, Yi-Wu, Su, Tao, Li, Bin, Liu, De-Tian, Yi, Yong-Hong, Liao, Wei-Ping
Publicado 2021

Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation

por Wang, Jing-Yang, Wang, Jie, Lu, Xin-Guo, Song, Wang, Luo, Sheng, Zou, Dong-Fang, Hua, Li-Dong, Peng, Qian, Tian, Yang, Gao, Liang-Di, Liao, Wei-Ping, He, Na
Publicado 2022

Heterozygous PGM3 Variants Are Associated With Idiopathic Focal Epilepsy With Incomplete Penetrance

por Liu, Xiao-Rong, Bian, Wen-Jun, Wang, Jie, Ye, Ting-Ting, Li, Bing-Mei, Liu, De-Tian, Tang, Bin, Deng, Wei-Wen, Shi, Yi-Wu, Su, Tao, Yi, Yong-Hong, Liao, Wei-Ping
Publicado 2020

Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti‐seizure medications

por Mullan, Kerry A., Anderson, Alison, Shi, Yi‐Wu, Ding, Jia‐Hong, Ng, Ching‐Ching, Chen, Zhibin, Baum, Larry, Cherny, Stacey, Petrovski, Slave, Sham, Pak C., Lim, Kheng‐Seang, Liao, Wei‐Ping, Kwan, Patrick
Publicado 2022

Variants in BRWD3 associated with X‐linked partial epilepsy without intellectual disability

por Tian, Mao‐Qiang, Liu, Xiao‐Rong, Lin, Si‐Mei, Wang, Jie, Luo, Sheng, Gao, Liang‐Di, Chen, Xiao‐Bin, Liang, Xiao‐Yu, Liu, Zhi‐Gang, He, Na, Yi, Yong‐Hong, Liao, Wei‐Ping
Publicado 2022

GRIN2A Variants Associated With Idiopathic Generalized Epilepsies

por Liu, Xiao-Rong, Xu, Xing-Xing, Lin, Si-Mei, Fan, Cui-Ying, Ye, Ting-Ting, Tang, Bin, Shi, Yi-Wu, Su, Tao, Li, Bing-Mei, Yi, Yong-Hong, Luo, Jian-Hong, Liao, Wei-Ping
Publicado 2021

HLA-B(*)13:01 as a Risk Allele for Antiepileptic Drugs-Induced Cutaneous Adverse Reactions: Higher Risk for Cross-Reactivity?

por Min, Fu-Li, Mao, Bi-Jun, Zheng, Zhong-Zheng, He, Na, Fan, Cui-Xia, Cai, Rui-Yan, Wang, Juan, Ou, Yang-Mei, Qin, Bing, Liao, Wei-Ping, Yi, Yong-Hong, Li, Ze, Shi, Yi-Wu
Publicado 2019

Endoplasmic reticulum retention and degradation of a mutation in SLC6A1 associated with epilepsy and autism

por Wang, Jie, Poliquin, Sarah, Mermer, Felicia, Eissman, Jaclyn, Delpire, Eric, Wang, Juexin, Shen, Wangzhen, Cai, Kefu, Li, Bing-Mei, Li, Zong-Yan, Xu, Dong, Nwosu, Gerald, Flamm, Carson, Liao, Wei-Ping, Shi, Yi-Wu, Kang, Jing-Qiong
Publicado 2020

CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures

por Li, Jia, Lin, Si‐Mei, Qiao, Jing‐Da, Liu, Xiao‐Rong, Wang, Jie, Jiang, Mi, Zhang, Jing, Zhong, Min, Chen, Xu‐Qin, Zhu, Jing, He, Na, Su, Tao, Shi, Yi‐Wu, Yi, Yong‐Hong, Liao, Wei‐Ping
Publicado 2021

ATP6V0C Is Associated With Febrile Seizures and Epilepsy With Febrile Seizures Plus

por Tian, Yang, Zhai, Qiong-Xiang, Li, Xiao-Jing, Shi, Zhen, Cheng, Chuan-Fang, Fan, Cui-Xia, Tang, Bin, Zhang, Ying, He, Yun-Yan, Li, Wen-Bin, Luo, Sheng, Hou, Chi, Chen, Wen-Xiong, Liao, Wei-Ping, Wang, Jie
Publicado 2022