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Personal profile

Education

  • 1998-2005 Ph.D., Graduate Institute of Clinical Medical Sciences, Chang Gung University
  • 1987-1994 M.D., School of Medicine, Taipei Medical University

Experience

  • 2019.08- Director, Division of Neurology, Taipei Medical University Hospital
  • 2017.10- Associate Professor, The Ph.D. Program for Neural Regenerative Medicine, Taipei Medical University

Research Interests

  • Neurology
  • genetic epidemiology
  • Neuroscience

Fingerprint Dive into the research topics where Tu-Hsueh Yeh is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 18 Similar Profiles

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Projects

醛脫氫酶對神經退化和認知功能影響之研究-醛代謝基因對神經退化疾病影響之研究

Yeh, T.

1/1/1912/1/19

Project: A - Government Institutiond - Ministry of Education

利用PLA2G6基因嵌入小鼠研究第十四型帕金森病分子病理機轉與治療(3/3)

Yeh, T.

8/1/1812/1/19

Project: A - Government Institutionb - Ministry of Science and Technology

新聘教師研究補助

Yeh, T.

1/1/1812/31/18

Project: B - Project of TMUg - Research Grants for Newly Hired Faculty

利用PLA2G6基因嵌入小鼠研究第十四型帕金森病分子病理機轉與治療(2/3)

Yeh, T.

8/1/177/31/18

Project: A - Government Institutionb - Ministry of Science and Technology

利用PLA2G6基因嵌入小鼠研究第十四型帕金森病分子病理機轉與治療(1/3)

Yeh, T.

8/1/167/31/17

Project: A - Government Institutionb - Ministry of Science and Technology

Research Output

  • 2463 Citations
  • 25 h-Index
  • 71 Article
  • 1 Letter

A novel missense mutation of the GTP cyclohydrolase 1 gene in a Taiwanese family with dopa-responsive dystonia: A case report

Yang, C. C., Wang, W. C., Yeh, T. H., Chen, T. H., Liu, Y. L., Lu, M. K., Lu, C. S. & Tsai, C. H., Feb 1 2018, In : Clinical Neurology and Neurosurgery. 165, p. 21-23 3 p.

Research output: Contribution to journalArticle

  • C9orf72 is essential for neurodevelopment and motility mediated by Cyclin G1

    Yeh, T. H., Liu, H. F., Li, Y. W., Lu, C. S., Shih, H. Y., Chiu, C. C., Lin, S. J., Huang, Y. C. & Cheng, Y. C., Jun 1 2018, In : Experimental Neurology. 304, p. 114-124 11 p.

    Research output: Contribution to journalArticle

  • 4 Citations (Scopus)

    Genetic diagnosis of neurofibromatosis type 1: Targeted next- generation sequencing with Multiple Ligation-Dependent Probe Amplification analysis

    Wu-Chou, Y. H., Hung, T. C., Lin, Y. T., Cheng, H. W., Lin, J. L., Lin, C. H., Yu, C. C., Chen, K. T., Yeh, T. H. & Chen, Y. R., Oct 5 2018, In : Journal of Biomedical Science. 25, 1, 72.

    Research output: Contribution to journalArticle

  • 1 Citation (Scopus)

    LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study

    International Parkinsonism Genetics Network, Jul 1 2018, In : The Lancet Neurology. 17, 7, p. 597-608 12 p.

    Research output: Contribution to journalArticle

  • 25 Citations (Scopus)

    PARK14 (D331Y) PLA2G6 Causes Early-Onset Degeneration of Substantia Nigra Dopaminergic Neurons by Inducing Mitochondrial Dysfunction, ER Stress, Mitophagy Impairment and Transcriptional Dysregulation in a Knockin Mouse Model

    Chiu, C. C., Lu, C. S., Weng, Y. H., Chen, Y. L., Huang, Y. Z., Chen, R. S., Cheng, Y. C., Huang, Y. C., Liu, Y. C., Lai, S. C., Lin, K. J., Lin, Y. W., Chen, Y. J., Chen, C. L., Yeh, T. H. & Wang, H. L., Jan 1 2018, (Accepted/In press) In : Molecular Neurobiology.

    Research output: Contribution to journalArticle

  • 5 Citations (Scopus)