Yi-Chu Liao (Yi Chu Liao)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 31

Top Venues

Annals of clinical and translational neurology

EMBO molecular medicine

Brain communications

Brain : a journal of neurology

National Yang Ming University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

National Yang Ming University

Taiwan

Professor :: School of Medicine

Taipei Veterans General Hospital

Taiwan

Dr. :: Department of Neurology

Publications

Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine 16 (5) (2024)
Cheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Pei-Chien Tsai
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of clinical and translational neurology 11 (7) (2024)
Cheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Pei-Chien Tsai
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of clinical and translational neurology 11 (7) (2024)
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine 16 (5) (2024)
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine (2024)
Kang-Yang Jih, Min-Yu Lan, Yi Hong Liu, Yu-Shuen Tsai, Po-Yu Lin, Kuan-Lin Lai, Yi-Chu Liao, Yi-Chung Lee
Nerve conduction features may serve as a diagnostic clue for neuronal intranuclear inclusion disease. Brain communications 6 (4) (2024)
Cheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Pei-Chien Tsai
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of clinical and translational neurology 11 (7) (2024)
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine 16 (5) (2024)
Cheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Pei-Chien Tsai
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of clinical and translational neurology 11 (7) (2024)
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine 16 (5) (2024)
Kang-Yang Jih, Min-Yu Lan, Yi Hong Liu, Yu-Shuen Tsai, Po-Yu Lin, Kuan-Lin Lai, Yi-Chu Liao, Yi-Chung Lee
Nerve conduction features may serve as a diagnostic clue for neuronal intranuclear inclusion disease. Brain communications 6 (4) (2024)
Cheng-Tsung Hsiao, Tzu-Yun Tsai, Ting-Yi Shen, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Pei-Chien Tsai
Characterization of a novel TFG variant causing autosomal recessive pure hereditary spastic paraplegia. Annals of clinical and translational neurology (2024)
Jui-Yu Yeh, Hua-Chuan Chao, Cheng-Li Hong, Yu-Chien Hung, Fei-Yang Tzou, Cheng-Tsung Hsiao, Jeng-Lin Li, Wen-Jie Chen, Cheng-Ta Chou, Yu-Shuen Tsai, Yi-Chu Liao, Yu-Chun Lin, Suewei Lin, Shu-Yi Huang, Marina Kennerson, Yi-Chung Lee, Chih-Chiang Chan
A missense mutation in human INSC causes peripheral neuropathy. EMBO molecular medicine 16 (5) (2024)
Ying-Tsen Chou, Shao-Lun Hsu, Yu-Shuen Tsai, Yi-Jiun Lu, Kai-Wei Yu, Hsiu-Mei Wu, Yi-Chu Liao, Yi-Chung Lee
Biallelic DDHD2 mutations in patients with adult-onset complex hereditary spastic paraplegia. Annals of clinical and translational neurology (2023)
Shao-Lun Hsu, Yi-Chu Liao, Chia-Hung Wu, Feng-Chi Chang, Yung-Lin Chen, Kuan-Lin Lai, Chih-Ping Chung, Shih-Pin Chen, Yi-Chung Lee
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Brain communications 6 (1) (2023)
Yi-Chu Liao, Cheng-Yu Wei, Fu-Pang Chang, Ying-Tsen Chou, Shao-Lun Hsu, Chih-Ping Chung, Takeshi Mizuguchi, Naomichi Matsumoto, Shaw-Fang Yet, Yi-Chung Lee
NOTCH2NLC GGC Repeat Expansion in Patients With Vascular Leukoencephalopathy. Stroke (2023)
Shih-Yu Fang, Ying-Tsen Chou, Kuo-Chou Hsu, Shao-Lun Hsu, Kai-Wei Yu, Yu-Shuen Tsai, Yi-Chu Liao, Pei-Chien Tsai, Yi-Chung Lee
Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Annals of clinical and translational neurology 10 (3) (2023)
Shih-Yu Fang, Ying-Tsen Chou, Kuo-Chou Hsu, Shao-Lun Hsu, Kai-Wei Yu, Yu-Shuen Tsai, Yi-Chu Liao, Pei-Chien Tsai, Yi-Chung Lee
Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Annals of clinical and translational neurology (2023)
Shao-Lun Hsu, Yi-Chu Liao, Chia-Hung Wu, Feng-Chi Chang, Yung-Lin Chen, Kuan-Lin Lai, Chih-Ping Chung, Shih-Pin Chen, Yi-Chung Lee
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Brain communications 6 (1) (2023)
Shao-Lun Hsu, Yi-Chu Liao, Chia-Hung Wu, Feng-Chi Chang, Yung-Lin Chen, Kuan-Lin Lai, Chih-Ping Chung, Shih-Pin Chen, Yi-Chung Lee
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Brain communications 6 (1) (2023)
Shih-Yu Fang, Ying-Tsen Chou, Kuo-Chou Hsu, Shao-Lun Hsu, Kai-Wei Yu, Yu-Shuen Tsai, Yi-Chu Liao, Pei-Chien Tsai, Yi-Chung Lee
Clinical and genetic characterization of NIPA1 mutations in a Taiwanese cohort with hereditary spastic paraplegia. Annals of clinical and translational neurology 10 (3) (2023)
Yu-Wen Cheng, Yi-Chu Liao, Chih-Hao Chen, Chih-Ping Chung, Cathy Shen-Jang Fann, Chien-Ching Chang, Yi-Chung Lee, Sung-Chun Tang
Contribution of the APOE Genotype to Cognitive Impairment in Individuals With NOTCH3 Cysteine-Altering Variants. Journal of the American Heart Association (2023)
Shao-Lun Hsu, Yi-Chu Liao, Chia-Hung Wu, Feng-Chi Chang, Yung-Lin Chen, Kuan-Lin Lai, Chih-Ping Chung, Shih-Pin Chen, Yi-Chung Lee
Impaired cerebral interstitial fluid dynamics in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy. Brain communications 6 (1) (2023)
Yi-Chung Lee, Yi-Chu Liao
Reply to: Adult-onset leukoencephalopathy caused by CSF1R mutations: Is all that glitters gold? Annals of clinical and translational neurology 9 (1) (2022)
Yi Hong Liu, Ying Tsen Chou, Fu Pang Chang, Wei Ju Lee, Yuh Cherng Guo, Cheng Ta Chou, Hui Chun Huang, Takeshi Mizuguchi, Chien Chen Chou, Hsiang Yu Yu, Kai Wei Yu, Hsiu Mei Wu, Pei Chien Tsai, Naomichi Matsumoto, Yi Chung Lee, Yi-Chu Liao
Neuronal intranuclear inclusion disease in patients with adult-onset non-vascular leukoencephalopathy. Brain : a journal of neurology 145 (9) (2022)
Pei-Chien Tsai, Jong-Ling Fuh, Chih-Chao Yang, Anna Chang, Li-Ming Lien, Pei-Ning Wang, Kuan-Lin Lai, Yu-Shuen Tsai, Yi-Chung Lee, Yi-Chu Liao
Clinical and genetic characterization of adult-onset leukoencephalopathy caused by CSF1R mutations. Annals of clinical and translational neurology 8 (11) (2021)
Yi-Chu Liao, Fu-Pang Chang, Han-Wei Huang, Ting-Bing Chen, Ying-Tsen Chou, Shao-Lun Hsu, Kangyang Jih, Yi-Hong Liu, Cheng-Tsung Hsiao, Hiromi Fukukda, Takeshi Mizuguchi, Kon-Ping Kp Lin, Chou-Ching K Lin, Naomichi Matsumoto, Marina Kennerson, Yi-Chung Lee
GGC Repeat Expansion of NOTCH2NLC in Taiwanese Patients With Inherited Neuropathies. Neurology (2021)
Cheng-Ta Chou, Bing-Wen Soong, Kon-Ping Lin, Yu-Shuen Tsai, Kang-Yang Jih, Yi-Chu Liao, Yi-Chung Lee
Clinical characteristics of Taiwanese patients with Hereditary spastic paraplegia type 5. Annals of clinical and translational neurology 7 (4) (2020)
Yu-Shuen Tsai, Kon-Ping Lin, Kang-Yang Jih, Pei-Chien Tsai, Yi-Chu Liao, Yi-Chung Lee
Hand-onset weakness is a common feature of ALS patients with a NEK1 loss-of-function variant. Annals of clinical and translational neurology 7 (6) (2020)
Yun-Hsin Hsu, Kon-Ping Lin, Yuh-Cherng Guo, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee
Mutation spectrum of Charcot-Marie-Tooth disease among the Han Chinese in Taiwan. Annals of clinical and translational neurology 6 (6) (2019)
Ying-Hao Chen, Yi-Chung Lee, Yu-Shuen Tsai, Yuh-Cherng Guo, Cheng-Tsung Hsiao, Pei-Chien Tsai, Jin-An Huang, Yi-Chu Liao, Bing-Wen Soong
Unmasking adrenoleukodystrophy in a cohort of cerebellar ataxia. PloS one 12 (5) (2017)

Yi-Chu Liao.css-eqlu8i{font-size:small;padding-left:4px;} (Yi Chu Liao)

Publication Activity (10 Years)

Top Topics

Top Venues

Yi-Chu Liao (Yi Chu Liao)