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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.

  • 6 Similar Profiles
Parkinson Disease Medicine & Life Sciences
Mutation Medicine & Life Sciences
Transgenic Mice Medicine & Life Sciences
Machado-Joseph Disease Medicine & Life Sciences
Dopaminergic Neurons Medicine & Life Sciences
Neuroglia Medicine & Life Sciences
Neurofibromatosis 1 Medicine & Life Sciences
Neurons Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 2016 2019

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 1997 2018

  • 2379 Citations
  • 24 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

GTP Cyclohydrolase
Missense Mutation
Dystonia
Genes
Leg
4 Citations (Scopus)

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

Cyclin G1
Embryonic Structures
GTP Phosphohydrolases
Zebrafish
Apoptosis
1 Citation (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

Neurofibromatosis 1
Ligation
Amplification
Genes
Screening
20 Citations (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

Lewy Body Disease
Parkinson Disease
Genome
Dementia
Genes
3 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

Mitochondrial Degradation
Dopaminergic Neurons
Substantia Nigra
Mutation
Parkinson Disease