臨床服務：

1. 脊髓肌肉萎縮症診斷治療、家族性澱粉樣多發性神經病變診斷治療
2. 慢性發炎性脫髓鞘多發神經炎臨床試驗、重肌無力症臨床試驗
3. 周邊神經肌肉疾病（家族性周邊神經病變、慢性神經痛、肌肉病變、肌強直症、重肌無力症）；神經退化性疾病（小腦萎縮症、甘迺迪氏症、漸凍症、亨丁頓氏舞蹈症、帕金森氏症、顫抖症、腦白質病變）；家族性腦中風；神經電生理檢查；神經基因學之分子診斷...等。

研究方向：

       神經元核內包涵體病、核苷酸重複序列疾病、小腦萎縮症、家族性周邊神經病變、家族性腦中風

1. 神經基因學之臨床與分子研究
2. 果蠅基因學與分子生物學研究
3. 細胞電生理與離子通道蛋白相關疾病之研究

得獎紀錄：

論文發表：

1. CT Hsiao, NY Liao, YC Liao, YC Lee*. THAP11 CAG Repeat Expansion is rare or absent in the Taiwanese cohort with Cerebellar Ataxia. Accepted for publication in Mov Disord. 2024.
2. NY Liao, KL Lai, YC Liao, CT Hsiao*, YC Lee*. Identification of m.3243A>G mitochondrial DNA mutation in patients with cerebellar ataxia. J Formos Med Assoc . 2023 Oct;122(10):1028-1034.
3. CT Hsiao, SJ Fu, YT Liu, YH Lu, CY Zhong, CY Tang, BW Soong , CJ Jeng*. 2019 Nor. Novel SCA19/22-associated KCND3 mutations disrupt human K_V4.3 protein biosynthesis and channel gating. Human mutation. 2088-2107.
4. YC Liao^#, CT Hsiao^#, JL Fuh, CM Chern, WJ Lee, YC Guo, SJ Wang, IH Lee, YT Liu, YF Wang, FC Chang, MH Chang, BW Soong, YC Lee*. 2015 Aug. Characterization of CADASIL among the Han Chinese in Taiwan: Distinct Genotypic and Phenotypic Profiles. PLoS One. e0136501.
5. CT Hsiao, PC Tsai, YC Liao, YC Lee, BW Soong*. 2014 Dec. C9ORF72 repeat expansion is not a significant cause of late onset cerebellar ataxia syndrome. J Neurol Sci. 322-4.