Yi-Chung Lee (Y-C Lee)

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 42

Top Venues

Annals of clinical and translational neurology

Brain communications

EMBO molecular medicine

Science advances

Taipei Veterans General Hospital

National Yang-Ming University (PHD)

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

Affiliation History

Taipei Veterans General Hospital Jul 16 2018

Taiwan

Director :: Division of Peripheral Nerve System Disorders, Department of Neurology

National Yang-Ming University Aug 01 2016

Taiwan

Professor :: Department of Neurology

Education History

National Yang-Ming University

Taiwan

PHD :: Institute of Clinical Medicine

Publications

Yu-Jen Chang, Kai-Tai Lin, Orion Shih, Chi-Hua Yang, Ching-Yu Chuang, Ming-Han Fang, Wei-Bin Lai, Yi-Chung Lee, Hung-Chih Kuo, Shang-Cheng Hung, Chi-Kuang Yao, Yen-Ju Cheng, Yun-Ru Chen
Sulfated disaccharide protects membrane and DNA damages from arginine-rich dipeptide repeats in ALS. Science advances 10 (8) (2024)
Yu-Jen Chang, Kai-Tai Lin, Orion Shih, Chi-Hua Yang, Ching-Yu Chuang, Ming-Han Fang, Wei-Bin Lai, Yi-Chung Lee, Hung-Chih Kuo, Shang-Cheng Hung, Chi-Kuang Yao, Yen-Ju Cheng, Yun-Ru Chen
Sulfated disaccharide protects membrane and DNA damages from arginine-rich dipeptide repeats in ALS. Science advances 10 (8) (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)
Yu-Jen Chang, Kai-Tai Lin, Orion Shih, Chi-Hua Yang, Ching-Yu Chuang, Ming-Han Fang, Wei-Bin Lai, Yi-Chung Lee, Hung-Chih Kuo, Shang-Cheng Hung, Chi-Kuang Yao, Yen-Ju Cheng, Yun-Ru Chen
Sulfated disaccharide protects membrane and DNA damages from arginine-rich dipeptide repeats in ALS. Science advances 10 (8) (2024)
Cheng-Tsung Hsiao, Nai-Yi Liao, Yi-Chu Liao, Yi-Chung Lee
THAP11 CAG Repeat Expansion Is Rare or Absent in the Taiwanese Cohort with Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (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)
Danique Beijer, Maike F Dohrn, Adriana P Rebelo, Matt C Danzi, Bianca Rose Grosz, Melina Ellis, Kishore Raj Kumar, Steve Vucic, Horia Vais, Jillian S Weissenrieder, Olesia Lunko, Usha Paudel, Leah C Simpson, Jacquelyn Raposo, Mario Saporta, Yeisha Arcia, Isaac Xu, Shawna Feely, Christopher J Record, Julian Blake, Mary M Reilly, Steven Scherer, Marina Kennerson, Yi-Chung Lee, J Kevin Foskett, Michael Shy, Stephan Zuchner
A recurrent missense variant in ITPR3 causes demyelinating Charcot-Marie-Tooth with variable severity. Brain : a journal of neurology (2024)
Satoshi Saito, Satoshi Hosoki, Eriko Yamaguchi, Hiroyuki Ishiyama, Soichiro Abe, Takeshi Yoshimoto, Tomotaka Tanaka, Yorito Hattori, Yi Chu Liao, Yi-Chung Lee, Ikuko Mizuta, Toshiki Mizuno, Masafumi Ihara
Blended Phenotype of NOTCH3 and RNF213 Variants With Accelerated Large and Small Artery Crosstalk: A Case Report and Literature Review. Neurology. Genetics 10 (5) (2024)
Cheng-Tsung Hsiao, Nai-Yi Liao, Yi-Chu Liao, Yi-Chung Lee
THAP11 CAG Repeat Expansion Is Rare or Absent in the Taiwanese Cohort with Cerebellar Ataxia. Movement disorders : official journal of the Movement Disorder Society 39 (5) (2024)
Yu-Jen Chang, Kai-Tai Lin, Orion Shih, Chi-Hua Yang, Ching-Yu Chuang, Ming-Han Fang, Wei-Bin Lai, Yi-Chung Lee, Hung-Chih Kuo, Shang-Cheng Hung, Chi-Kuang Yao, Yen-Ju Cheng, Yun-Ru Chen
Sulfated disaccharide protects membrane and DNA damages from arginine-rich dipeptide repeats in ALS. Science advances 10 (8) (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)
Xiang Lin, Jun-Yi Jiang, Dao-Jun Hong, Kai-Jun Lin, Jin-Jing Li, Yi-Jun Chen, Yu-Sen Qiu, Zishuai Wang, Yi-Chu Liao, Kang Yang, Yan Shi, Meng-Wen Wang, Shao-Lun Hsu, Shunyan Hong, Yi-Heng Zeng, Xiao-Chun Chen, Ning Wang, Yi-Chung Lee, Wan-Jin Chen
Biallelic COQ4 Variants in Hereditary Spastic Paraplegia: Clinical and Molecular Characterization. Movement disorders : official journal of the Movement Disorder Society (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)
Hsu-Huai Chiu, Cheng-Tsung Hsaio, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee, Bing-Wen Soong
Clinical and Genetic Characterization of Autosomal Recessive Spinocerebellar Ataxia Type 16 (SCAR16) in Taiwan. Cerebellum (London, England) 19 (4) (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)
Y-N Huang, H-J Chuang, Hsueh-Wen Hsueh, H-C Huang, N-C Lee, Chi-Chao Chao, P-H Huang, Yi-Chung Lee, K-P Lin, C-C Yang, Sung-Tsang Hsieh
A case of GNE myopathy mimicking hereditary motor neuropathy. European journal of neurology 27 (11) (2021)
Pei-Chien Tsai, Kang-Yang Jih, Ting-Yi Shen, Yi-Hong Liu, Kon-Ping Lin, Yi-Chu Liao, Yi-Chung Lee
Genetic and Functional Analysis of Glycosyltransferase 8 Domain-Containing Protein 1 in Taiwanese Patients With Amyotrophic Lateral Sclerosis. Neurology. Genetics 7 (6) (2021)
Kang-Yang Jih, Pei-Chien Tsai, Yu-Shuen Tsai, Yi-Chu Liao, Yi-Chung Lee
Rapid progressive ALS in a patient with a DNAJC7 loss-of-function mutation. Neurology. Genetics 6 (5) (2020)
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)
Kang-Yang Jih, C-P Chung, Y-Y Chang, P-L Hung, B-W Soong, Y-C Liao, M-Y Lan, Yi-Chung Lee
Mutational analysis of CCM1, CCM2 and CCM3 in a Han Chinese cohort with multiple cerebral cavernous malformations in Taiwan. Clinical genetics 94 (3-4) (2018)
P-C Tsai, Y-S Tsai, B-W Soong, Y-H Huang, H-T Wu, Y-H Chen, K-P Lin, Y-C Liao, Yi-Chung Lee
A novel DNAJB6 mutation causes dominantly inherited distal-onset myopathy and compromises DNAJB6 function. Clinical genetics 92 (2) (2017)

Yi-Chung Lee.css-eqlu8i{font-size:small;padding-left:4px;} (Y-C Lee)

Publication Activity (10 Years)

Top Topics

Top Venues

Yi-Chung Lee (Y-C Lee)