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International Journal of Molecular Sciences|August 7, 2021
Rare Gain-of-Function KCND3 Variant Associated with Cerebellar Ataxia, Parkinsonism, Cognitive Dysfunction, and Brain Iron AccumulationCheng-Tsung Hsiao, Thomas F Tropea, Ssu-Ju Fu, et al.
Cells|May 30, 2020
CUL4-DDB1-CRBN E3 Ubiquitin Ligase Regulates Proteostasis of ClC-2 Chloride Channels: Implication for Aldosteronism and LeukodystrophySsu-Ju Fu, Meng-Chun Hu, Yi-Jheng Peng, et al.
Annals of Clinical and Translational Neurology|July 25, 2025
NOTCH2NLC Repeat Expansions in Parkinsonian Disorders: Clinical and Neuroimaging CharacteristicsHan-Lin Chiang, Kang-Yang Jih, Cheng-Tsung Hsiao, et al.
Annals of Clinical and Translational Neurology|December 3, 2024
Investigating ITM2B-associated ataxia in a Taiwanese cerebellar ataxia cohortShih-Yu Fang, Cheng-Tsung Hsiao, Kang-Yang Jih, et al.
Multiple Sclerosis and Related Disorders|October 17, 2024
Preceding hepatitis B virus infection is highly prevalent in patients with neuromyelitis optica spectrum disorder in TaiwanWen-Yu Ou Yang, Yu-Shuen Tsai, Yi-Hong Liu, et al.
Neurobiology of Aging|January 26, 2016
Mutational analysis of TBK1 in Taiwanese patients with amyotrophic lateral sclerosisPei-Chien Tsai, Yi-Chien Liu, Kon-Ping Lin, et al.
Plos One|May 9, 2017
Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxiaYing-Hao Chen, Yi-Chung Lee, Yu-Shuen Tsai, et al.
International Journal of Molecular Sciences|June 2, 2021
Novel KCND3 Variant Underlying Nonprogressive Congenital Ataxia or SCA19/22 Disrupt KV4.3 Protein Expression and K+ Currents with Variable Effects on Channel PropertiesGinevra Zanni, Cheng-Tsung Hsiao, Ssu-Ju Fu, et al.
Plos One|January 28, 2016
Clinical and Molecular Characterization of BSCL2 Mutations in a Taiwanese Cohort with Hereditary NeuropathyCheng-Tsung Hsiao, Pei-Chien Tsai, Chou-Ching Lin, et al.
Plos Genetics|December 3, 2025
A fly model of SCA36 reveals combinatorial neurotoxicity of hexanucleotide and dipeptide repeatsCheng-Tsung Hsiao, Ssu-Ju Fu, Ting-Ni Guo, et al.
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