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Epilepsia Open|February 18, 2025
Self-limited familial focal epilepsy caused by ANK2 variants: A potentially under-recognized conditionPo-Hsi Lin, Chen-Jui Ho, Chih-Hsiang Lin, et al.
Cells|August 16, 2020
Ischemic Stroke Risk Associated with Mitochondrial Haplogroup F in the Asian PopulationMeng-Han Tsai, Chung-Wen Kuo, Tsu-Kung Lin, et al.
Neurocritical Care|March 21, 2019
Perampanel Treatment for Refractory Status Epilepticus in a Neurological Intensive Care UnitChen-Jui Ho, Chih-Hsiang Lin, Yan-Ting Lu, et al.
Neurology International|December 24, 2025
Rare Variants of Immune-Related Genes Increase Susceptibility to Autoimmune Encephalitis: An Association StudyChih-Hsiang Lin, Shiau-Ching Chen, Chen-Jui Ho, et al.
Brain and Behavior|February 7, 2023
S100A6 participates in initiation of autoimmune encephalitis and is under epigenetic controlChih-Hsiang Lin, Sung-Chou Li, Ming-Hong Lin, et al.
Frontiers in Neurology|April 1, 2022
Impaired Color Recognition in <i>HCN1</i> Epilepsy: A Single Case ReportChaseley E Mckenzie, Chen-Jui Ho, Ian C Forster, et al.
Frontiers in Genetics|December 19, 2019
S100A6 Promotes B Lymphocyte Penetration Through the Blood-Brain Barrier in Autoimmune EncephalitisMeng-Han Tsai, Chih-Hsiang Lin, Kuo-Wang Tsai, et al.
Cells|August 14, 2020
Circulating MicroRNAs from Serum Exosomes May Serve as a Putative Biomarker in the Diagnosis and Treatment of Patients with Focal Cortical DysplasiaShang-Der Chen, Hsiu-Yung Pan, Jyun-Bin Huang, et al.
Biomedical Journal|June 6, 2022
The clinical and imaging features of FLNA positive and negative periventricular nodular heterotopiaYan-Ting Lu, Chung-Yao Hsu, Yo-Tsen Liu, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypesSiwei Chen, Bassel W Abou-Khalil, Zaid Afawi, et al.
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