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Plos One|September 13, 2011
Identification of single- and multiple-class specific signature genes from gene expression profiles by group marker indexYu-Shuen Tsai, Kripamoy Aguan, Nikhil R Pal, et al.BMC Bioinformatics|October 10, 2008
Discovery of dominant and dormant genes from expression data using a novel generalization of SNR for multi-class problemsYu-Shuen Tsai, Chin-Teng Lin, George C Tseng, et al.Cerebellum (London, England)|May 6, 2020
Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in TaiwanHsu-Huai Chiu, Cheng-Tsung Hsaio, Yu-Shuen Tsai, et al.STAR Protocols|August 31, 2022
Generating transcriptional regulatory networks from time-ordered stem cell differentiation RNA sequencing dataYu-Shuen Tsai, Yao-Ming Chang, Yang-Mooi Lim, et al.Journal of the Neurological Sciences|August 1, 2021
Expanding the phenotype of AFG3L2 mutations: Late-onset autosomal recessive spinocerebellar ataxiaHan-Lin Chiang, Jong-Ling Fuh, Yu-Shuen Tsai, et al.Annals of Clinical and Translational Neurology|May 29, 2020
Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variantYu-Shuen Tsai, Kon-Ping Lin, Kang-Yang Jih, et al.Annals of Clinical and Translational Neurology|June 19, 2019
Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in TaiwanYun-Hsin Hsu, Kon-Ping Lin, Yuh-Cherng Guo, et al.Scientific Reports|May 14, 2017
Airway Microbial Diversity is Inversely Associated with Mite-Sensitized Rhinitis and Asthma in Early ChildhoodChih-Yung Chiu, Yi-Ling Chan, Yu-Shuen Tsai, et al.Annals of Clinical and Translational Neurology|March 24, 2020
Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5Cheng-Ta Chou, Bing-Wen Soong, Kon-Ping Lin, et al.Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 27, 2021
Investigating ZFYVE26 mutations in a Taiwanese cohort with hereditary spastic paraplegiaShao-Lun Hsu, Yi-Jiun Lu, Yu-Shuen Tsai, et al.Pageof 4