Wei-Ping Liao (Weiping Liao, W-P Liao)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 32

Top Venues

Journal of medical genetics

CNS neuroscience & therapeutics

Clinical genetics

Brain : a journal of neurology

This page only lists publications with an associated author ORCID identifier.

Publications

Cui-Xia Fan, Xiao-Rong Liu, Dao-Qi Mei, Bing-Mei Li, Wen-Bin Li, Huan-Cheng Xie, Jie Wang, Nan-Xiang Shen, Zi-Long Ye, Qiang-Long You, Ling-Ying Li, Xiao-Chong Qu, Li-Zhi Chen, Jin-Jie Liang, Ming-Rui Zhang, Na He, Jia Li, Jun-Ying Gao, Wei-Yi Deng, Wen-Zhe Liu, Wen-Ting Wang, Wei-Ping Liao, Qian Chen, Yi-Wu Shi
Heterozygous variants in USP25 cause genetic generalized epilepsy. Brain : a journal of neurology (2024)
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of medical genetics 61 (7) (2024)
Wang Song, Wen-Jun Bian, Hua Li, Qing-Hui Guo, Jie Wang, Bin Tang, Jia-Yuan Zhang, Wei Wei, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Na He
IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures. Journal of medical genetics 61 (9) (2024)
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of medical genetics 61 (7) (2024)
Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, null null
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics 105 (4) (2024)
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of medical genetics 61 (7) (2024)
Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, null null
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics (2024)
Wang Song, Wen-Jun Bian, Hua Li, Qing-Hui Guo, Jie Wang, Bin Tang, Jia-Yuan Zhang, Wei Wei, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Na He
IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures. Journal of medical genetics 61 (9) (2024)
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of medical genetics (2024)
Ming-Feng He, Li-Hong Liu, Sheng Luo, Juan Wang, Jia-Jun Guo, Peng-Yu Wang, Qiong-Xiang Zhai, Su-Li He, Dong-Fang Zou, Xiao-Rong Liu, Bing-Mei Li, Hai-Yan Ma, Jing-Da Qiao, Peng Zhou, Na He, Yong-Hong Yi, Wei-Ping Liao
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. Journal of medical genetics 61 (7) (2024)
Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, null null
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics 105 (4) (2024)
Wang Song, Wen-Jun Bian, Hua Li, Qing-Hui Guo, Jie Wang, Bin Tang, Jia-Yuan Zhang, Wei Wei, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Na He
IFIH1 variants are associated with generalised epilepsy preceded by febrile seizures. Journal of medical genetics (2024)
Yu-Jie Chen, Wen-Jie Wang, Dong-Fang Zou, Jun-Xia Luo, Pei-Yan Jin, Liang Jin, Xiao-Rong Liu, Wei-Ping Liao, Bin Li, Yong-Jun Chen, null null
CCDC88C variants are associated with focal epilepsy and genotype-phenotype correlation. Clinical genetics 105 (4) (2024)
Na He, Bao-Zhu Guan, Jie Wang, Han-Kui Liu, Yong Mao, Zhi-Gang Liu, Fei Yin, Jing Peng, Bo Xiao, Bei-Sha Tang, Dong Zhou, Guang Huang, Qi-Lin Dai, Ying Zeng, Hong Han, Qiong-Xiang Zhai, Bin Li, Bin Tang, Wen-Bin Li, Wang Song, Liu Liu, Yi-Wu Shi, Bing-Mei Li, Tao Su, Peng Zhou, Xiao-Rong Liu, Li-Wu Guo, Yong-Hong Yi, Wei-Ping Liao
HCFC1 variants in the proteolysis domain are associated with X-linked idiopathic partial epilepsy: Exploring the underlying mechanism. Clinical and translational medicine 13 (6) (2023)
Kerry A Mullan, Alison Anderson, Yi-Wu Shi, Jia-Hong Ding, Ching-Ching Ng, Zhibin Chen, Larry Baum, Stacey Cherny, Slave Petrovski, Pak C Sham, Kheng-Seang Lim, Wei-Ping Liao, Patrick Kwan
Potential role of regulatory DNA variants in modifying the risk of severe cutaneous reactions induced by aromatic anti-seizure medications. Epilepsia 63 (4) (2022)
Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin, Jie Wang, Sheng Luo, Liang-Di Gao, Xiao-Bin Chen, Xiao-Yu Liang, Zhi-Gang Liu, Na He, Yong-Hong Yi, Wei-Ping Liao, null null
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. CNS neuroscience & therapeutics 29 (2) (2022)
Tingting Ye, Jiwei Zhang, Jie Wang, Song Lan, Tao Zeng, Huaili Wang, Xuelian He, Bing-Mei Li, Weiwen Deng, Wei-Ping Liao, Xiao-Rong Liu
Variants in BSN gene associated with epilepsy with favourable outcome. Journal of medical genetics (2022)
Tingting Ye, Jiwei Zhang, Jie Wang, Song Lan, Tao Zeng, Huaili Wang, Xuelian He, Bing-Mei Li, Weiwen Deng, Wei-Ping Liao, Xiao-Rong Liu
Variants in BSN gene associated with epilepsy with favourable outcome. Journal of medical genetics (2022)
Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin, Jie Wang, Sheng Luo, Liang-Di Gao, Xiao-Bin Chen, Xiao-Yu Liang, Zhi-Gang Liu, Na He, Yong-Hong Yi, Wei-Ping Liao, null null
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. CNS neuroscience & therapeutics (2022)
Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin, Jie Wang, Sheng Luo, Liang-Di Gao, Xiao-Bin Chen, Xiao-Yu Liang, Zhi-Gang Liu, Na He, Yong-Hong Yi, Wei-Ping Liao, null null
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. CNS neuroscience & therapeutics 29 (2) (2022)
Zheng Chen, Sheng Luo, Zhi-Gang Liu, Yan-Chun Deng, Su-Li He, Xiao-Rong Liu, Yong-Hong Yi, Jie Wang, Liang-Di Gao, Bing-Mei Li, Zhi-Jun Wu, Zi-Long Ye, De-Hai Liang, Wen-Jun Bian, Wei-Ping Liao, null null
CELSR1 variants are associated with partial epilepsy of childhood. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 189 (7-8) (2022)
Jing-Da Qiao, Xin Li, Jia Li, Qing-Hui Guo, Xue-Qing Tang, Li-Zhi Chen, Tao Su, Yong-Hong Yi, Jie Wang, Wei-Ping Liao
Reply: UNC13B and focal epilepsy. Brain : a journal of neurology 145 (3) (2022)
Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin, Jie Wang, Sheng Luo, Liang-Di Gao, Xiao-Bin Chen, Xiao-Yu Liang, Zhi-Gang Liu, Na He, Yong-Hong Yi, Wei-Ping Liao, null null
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. CNS neuroscience & therapeutics 29 (2) (2022)
Mao-Qiang Tian, Xiao-Rong Liu, Si-Mei Lin, Jie Wang, Sheng Luo, Liang-Di Gao, Xiao-Bin Chen, Xiao-Yu Liang, Zhi-Gang Liu, Na He, Yong-Hong Yi, Wei-Ping Liao, null null
Variants in BRWD3 associated with X-linked partial epilepsy without intellectual disability. CNS neuroscience & therapeutics 29 (2) (2022)
Jia Li, Si-Mei Lin, Jing-Da Qiao, Xiao-Rong Liu, Jie Wang, Mi Jiang, Jing Zhang, Min Zhong, Xu-Qin Chen, Jing Zhu, Na He, Tao Su, Yi-Wu Shi, Yong-Hong Yi, Wei-Ping Liao, null null
CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures. CNS neuroscience & therapeutics 28 (3) (2021)
Xiao-Rong Liu, Ting-Ting Ye, Wen-Jun Zhang, Xuan Guo, Jie Wang, Shao-Ping Huang, Long-Shan Xie, Xing-Wang Song, Wei-Wen Deng, Bing-Mei Li, Na He, Qian-Yi Wu, Min-Zhi Zhuang, Meng Xu, Yi-Wu Shi, Tao Su, Yong-Hong Yi, Wei-Ping Liao, null null
CHD4 variants are associated with childhood idiopathic epilepsy with sinus arrhythmia. CNS neuroscience & therapeutics 27 (10) (2021)
Jie Wang, Jing-Da Qiao, Xiao-Rong Liu, De-Tian Liu, Yan-Hui Chen, Yi Wu, Yan Sun, Jing Yu, Rong-Na Ren, Zhen Mei, Yu-Xi Liu, Yi-Wu Shi, Mi Jiang, Si-Mei Lin, Na He, Bin Li, Wen-Jun Bian, Bing-Mei Li, Yong-Hong Yi, Tao Su, Han-Kui Liu, Wei-Yue Gu, Wei-Ping Liao
UNC13B variants associated with partial epilepsy with favourable outcome. Brain : a journal of neurology 144 (10) (2021)
Qiyu Zhu, Wei Ke, Quansheng He, Xiongfei Wang, Rui Zheng, Tianfu Li, Guoming Luan, Yue-Sheng Long, Wei-Ping Liao, Yousheng Shu
Laminar Distribution of Neurochemically-Identified Interneurons and Cellular Co-expression of Molecular Markers in Epileptic Human Cortex. Neuroscience bulletin 34 (6) (2018)
P Zhou, N He, J-W Zhang, Z-J Lin, J Wang, L-M Yan, H Meng, B Tang, B-M Li, X-R Liu, Y-W Shi, Q-X Zhai, Y-H Yi, Wei-Ping Liao
Novel mutations and phenotypes of epilepsy-associated genes in epileptic encephalopathies. Genes, brain, and behavior 17 (8) (2018)
Na He, Bing-Mei Li, Zhao-Xia Li, Jie Wang, Xiao-Rong Liu, Heng Meng, Bin Tang, Wen-Jun Bian, Yi-Wu Shi, Wei-Ping Liao
Few individuals with Lennox-Gastaut syndrome have autism spectrum disorder: a comparison with Dravet syndrome. Journal of neurodevelopmental disorders 10 (1) (2018)
Liwen Wu, Kazuichi Yagi, Zhen Hong, Wei-Ping Liao, Xuefeng Wang, Dong Zhou, Yushi Inoue, Yoko Ohtsuka, Mutsuo Sasagawa, Kiyohito Terada, Xinlu Du, Yoshihiro Muramoto, Tomonobu Sano
Adjunctive levetiracetam in the treatment of Chinese and Japanese adults with generalized tonic-clonic seizures: A double-blind, randomized, placebo-controlled trial. Epilepsia open 3 (4) (2018)
Jing-Yang Wang, Peng Zhou, Jie Wang, Bin Tang, Tao Su, Xiao-Rong Liu, Bing-Mei Li, Heng Meng, Yi-Wu Shi, Yong-Hong Yi, Na He, Wei-Ping Liao
ARHGEF9 mutations in epileptic encephalopathy/intellectual disability: toward understanding the mechanism underlying phenotypic variation. Neurogenetics 19 (1) (2017)

Wei-Ping Liao.css-eqlu8i{font-size:small;padding-left:4px;} (Weiping Liao, W-P Liao)

Publication Activity (10 Years)

Top Topics

Top Venues

Wei-Ping Liao (Weiping Liao, W-P Liao)