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Nature Communications|August 4, 2019
Galectin-3 is required for the microglia-mediated brain inflammation in a model of Huntington's diseaseJian Jing Siew, Hui-Mei Chen, Huan-Yuan Chen, et al.Journal of the Neurological Sciences|November 20, 2022
Scale for Ocular motor Disorders in Ataxia (SODA)Aasef G Shaikh, Ji-Soo Kim, Caroline Froment, et al.Orphanet Journal of Rare Diseases|October 28, 2019
Neutral lipid storage disease with myopathy in China: a large multicentric cohort studyWei Zhang, Bing Wen, Jun Lu, et al.The Journal of Clinical Investigation|March 16, 2011
Dysregulated brain creatine kinase is associated with hearing impairment in mouse models of Huntington diseaseYow-Sien Lin, Chiung-Mei Chen, Bing-wen Soong, et al.Oncotarget|May 14, 2016
PRRT2 mutations lead to neuronal dysfunction and neurodevelopmental defectsYo-Tsen Liu, Fang-Shin Nian, Wan-Ju Chou, et al.Human Molecular Genetics|January 11, 2007
Dysregulation of C/EBPalpha by mutant Huntingtin causes the urea cycle deficiency in Huntington's diseaseMing-Chang Chiang, Hui-Mei Chen, Yi-Hsin Lee, et al.American Journal of Human Genetics|February 26, 2013
Exome sequencing identifies GNB4 mutations as a cause of dominant intermediate Charcot-Marie-Tooth diseaseBing-Wen Soong, Yen-Hua Huang, Pei-Chien Tsai, et al.Movement Disorders : Official Journal of the Movement Disorder Society|December 24, 2021
A PIAS1 Protective Variant S510G Delays polyQ Disease Onset by Modifying Protein HomeostasisYan Hua Lee, Yu-Shuen Tsai, Che-Chang Chang, et al.Parkinsonism & Related Disorders|May 20, 2021
Clinical and genetic characterization of hereditary spastic paraplegia type 3A in TaiwanShao-Lun Hsu, Hsueh-Wen Hsueh, Shih-Ying Chen, et al.Clinica Chimica Acta; International Journal of Clinical Chemistry|October 4, 2012
FGF21 in ataxia patients with spinocerebellar atrophy and mitochondrial diseaseShih-Li Su, Wen-Fu Wang, Shey-Lin Wu, et al.Pageof 44