Projects per year
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.
- 7 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
- 5 Finished
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
1/1/19 → 12/1/19
Project: A - Government Institution › d - 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)
8/1/18 → 12/1/19
Project: A - Government Institution › b - 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(2/3)
8/1/17 → 7/31/18
Project: A - Government Institution › b - 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)
8/1/16 → 7/31/17
Project: A - Government Institution › b - Ministry of Science and Technology
Research Output 1997 2018
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 journal › Article
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 journal › Article
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 journal › Article
Neurofibromatosis 1
Ligation
Amplification
Genes
Screening
23
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 journal › Article
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 journal › Article
Mitochondrial Degradation
Dopaminergic Neurons
Substantia Nigra
Mutation
Parkinson Disease