Weiping Liao

29PUBLICATIONS
38CO-AUTHORS
Cellular nervous systemNaturopathyEpigenetics (incl. genome methylation and epigenomics)Gene mappingDevelopmental genetics (incl. sex determination)
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Publications (29)

|Aug 06, 2026
CACNA1C variants associated with focal epilepsy and their correlations with arrhythmias and developmental disorders.

|Mar 27, 2026
A phase 3, randomized clinical trial of soticlestat as adjunctive therapy for Lennox-Gastaut syndrome.

Renzo Guerrini, Eric D Marsh, Wei-Ping Liao

|Oct 27, 2025
De novo SRCAP variants cause developmental and epileptic encephalopathy and the phenotypic spectrum.

Xiao-Yu Liang, Xiang-Hong Meng, Wu-Chen Wu

|Jul 09, 2025
Variants in CSMD2 and CSMD3, genes involved in synaptogenesis, are associated with epilepsies.

Xiang Li, Lin Wang, Xiao-Yu Liang

|May 11, 2025
Identification of MACF1 as a causative gene of generalised epilepsy.

Xiao-Yun Lei, Meng-Wen Zhang, Hui Sun

|Apr 11, 2025
Characteristic spatial and frequency distribution of mutations in SCN1A.

Mengwen Zhang, Jing Guo, Bin Li

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Frequent Collaborators

6 joint publications

Xiao-Rong Liu

6 joint publications

Na He

5 joint publications

Sheng Luo

3 joint publications

Yong-Hong Yi