Bin Li

7PUBLICATIONS
7CO-AUTHORS
PharmacogenomicsCellular nervous systemNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Genetic immunology
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Publications (7)

|Jul 06, 2026
Perampanel in Chinese patients with Dravet syndrome: Efficacy and tolerability assessed via a multicenter, prospective, real-world observational study.

|Aug 15, 2025
Epilepsy in NHS actin remodeling regulator gene (NHS) and genotype-phenotype correlations.

Kai-Li Zhang, Jie Wang, Zhi-Hong Tang

|Jul 29, 2025
Missense variants in SLC9A6 cause partial epilepsy without neurodevelopmental delay.

Jun-Ping Jiao, Hong-Wei Zhang, Xi-Zhong Zhou

|Jan 22, 2025
RYR3 Variants Are Potentially Associated With Idiopathic (Non-Lesional) Partial Epilepsy/Susceptibility of Seizures, Toward Understanding the Gene-Disease Association by Genetic Dependent Nature.

Yang Tian, Yun-Qi Hou, Qiong-Xiang Zhai

|Jul 04, 2024
<i>IFIH1</i> variants are associated with generalised epilepsy preceded by febrile seizures.

Wang Song, Wen-Jun Bian, Hua Li

|Jun 24, 2024
Evaluating the Performance of <i>In Silico</i> Tools for <i>PRRT2</i> Missense Variants.

Hui Sun, Wang Song, Bin Li

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Frequent Collaborators

3 joint publications

Wei-Ping Liao

2 joint publications

Na He

1 joint publications

Yong-Jun Chen

1 joint publications

Wen-Jun Bian