YUI TADA

Last Updated :2023/12/04

Affiliations, Positions
Hiroshima University Genome Editing Innovation Center, Assistant Professor (Special Appointment)
E-mail
tadayui27ehiroshima-u.ac.jp

Basic Information

Academic Degrees

  • Kyoto University

Educational Activity

Course in Charge

  1. 2023, Undergraduate Education, Intensive, Practice for medical research
  2. 2023, Graduate Education (Master's Program) , First Semester, Seminar
  3. 2023, Graduate Education (Master's Program) , Second Semester, Seminar
  4. 2023, Graduate Education (Master's Program) , First Semester, Research
  5. 2023, Graduate Education (Master's Program) , Second Semester, Research
  6. 2023, Graduate Education (Doctoral Program) , First Semester, Advanced Seminar
  7. 2023, Graduate Education (Doctoral Program) , Second Semester, Advanced Seminar
  8. 2023, Graduate Education (Doctoral Program) , First Semester, Advanced Research
  9. 2023, Graduate Education (Doctoral Program) , Second Semester, Advanced Research
  10. 2023, Graduate Education (Doctoral Program) , First Semester, Advanced Seminar on Molecular Epidemiology
  11. 2023, Graduate Education (Doctoral Program) , Second Semester, Advanced Seminar on Molecular Epidemiology
  12. 2023, Graduate Education (Doctoral Program) , First Semester, Advanced Research on Molecular Epidemiology
  13. 2023, Graduate Education (Doctoral Program) , Second Semester, Advanced Research on Molecular Epidemiology

Research Activities

Academic Papers

  1. C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8, JOURNAL OF THE NEUROLOGICAL SCIENCES, 402, 118-120, 2019
  2. Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia, JOURNAL OF HUMAN GENETICS, 65(4), 363-369, 2020
  3. Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report, BMC MEDICAL GENETICS, 21(1), 2020
  4. Optineurin regulates osteoblastogenesis through STAT1, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 525(4), 889-894, 2020
  5. Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia, NEUROLOGY-GENETICS, 6(1), 2020
  6. Aggressive periodontitis and NOD2 variants, JOURNAL OF HUMAN GENETICS, 65(10), 841-846, 2020
  7. The first Japanese case of primary familial brain calcification caused by an MYORG variant, JOURNAL OF HUMAN GENETICS, 65(10), 917-920, 2020
  8. ★, Comparison of two families with and without ataxia harboring novel variants in PRKCG, JOURNAL OF HUMAN GENETICS, 67(10), 595-599, 2022
  9. ★, Genetic screening for potassium channel mutations in Japanese autosomal dominant spinocerebellar ataxia, Journal of Human Genetics, 65, 363-369, 20200107
  10. Middle-age-onset cerebellar ataxia caused by a homozygous TWNK variant: a case report, BMC MEDICAL GENETICS, 21(1), 20200331
    Link to Paper Search Results by DOI
  11. Optineurin regulates osteoblastogenesis through STAT1, BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 525(4), 889-894, 20200514
    Link to Paper Search Results by DOI
  12. Biallelic mutation of HSD17B4 induces middle age-onset spinocerebellar ataxia, NEUROLOGY-GENETICS, 6(1), 202002
    Link to Paper Search Results by DOI
  13. Aggressive periodontitis and NOD2 variants, JOURNAL OF HUMAN GENETICS, 65(10), 841-846, 202010
    Link to Paper Search Results by DOI
  14. The first Japanese case of primary familial brain calcification caused by an MYORG variant, JOURNAL OF HUMAN GENETICS, 65(10), 917-920, 202010
    Link to Paper Search Results by DOI
  15. C-terminal mutations in SYNE1 are associated with motor neuron disease in patients with SCAR8, Journal of the Neurological Sciences, 402, 2019