Na He

7PUBLICATIONS

18CO-AUTHORS

PharmacogenomicsCellular nervous systemEpigenetics (incl. genome methylation and epigenomics)Gene mappingGenetic immunology

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Publications (7)

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|Jul 06, 2026

Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.

|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 <i>MACF1</i> 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

|Jul 04, 2024

<i>IFIH1</i> variants are associated with generalised epilepsy preceded by febrile seizures.

Wang Song, Wen-Jun Bian, Hua Li

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Frequent Collaborators

Weiping Liao

Xiao-Rong Liu

Sheng Luo

Yong-Hong Yi

Bin Li

Jie Wang

Wen-Jun Bian

Dong-Fang Zou

Xiao-Yu Liang

Xiang-Hong Meng

Frequent Collaborators

Weiping Liao

Xiao-Rong Liu

Sheng Luo

Yong-Hong Yi