Taiwan Society of Gene Therapy_Supervisor

SupervisorYu-Yuan Ke

Professional license
  • Taiwan License to practice Medicine
  • Diplomate, Taiwan Pediatric association of Pediatrics
  • Diplomate, The society of Medical Genetics in Medical Genetics
  • Diplomate, The society of Endocrinology/Metabolism in specialist
  • Taiwanese Association of Diabetes Educators
Educational qualifications
  • Master. Chang Jung Christian University, Tainan, Taiwan
  • M.D. Kaohsiung Medical University, Kaohsiung, Taiwan
Experience
  1. Attending, Division of Genetics, Metabolism, Pediatric Endocrinology. Department of Pediatrics, Taichung Veterans General Hospital
  2. Deputy head, Department of Genomic Medicine, Center for Medical Genetics, Changhua Christian Hospital
  3. Attending, Division of Genetics, Endocrinology and Metabolism, Department of Pediatrics, Changhua Christian Hospital
  4. Division of Medical Genetics, Research Fellowship, Kaohsiung Medical University, Chung-Ho memorial Hospital, Department of Pediatrics, Molecular Human Genetics, Medical Resident, Kaohsiung, Taiwan
  5. Division of Medical Genetics, Metabolism, and Endocrionlolgy, Department of Pediatric, Taipei Veterans General Hospital, Research Fellowship, Taipei, Taiwan
  6. Department of Pediatrics, Kaohsiung Medical University, Chung-Ho memorial Hospital, Resident , Kaohsiung, Taiwan
Areas of expertise
  1. Genetics, Metabolism and Pediatric Endocrinology.
Professional writings
  • Professional writings
  • Li MH, Chen IC, Yang HW, Yen HC, Huang YC, Hsu CC, Chen YM, Ke YY. The characterization and comorbidities of heterozygous Bardet-Biedl syndrome carriers. Int J Med Sci. 2024 Feb 25;21(5):784-794.
  • Su PH, Yu JS, Wu YZ, Tsai YS, Lo FS, Lin JL, Chao MC, Hsu CC, Ke YY, Chiu PC, Chen JC, Huang YH, Lin SP, Chou YY, Ting WH, Wang SY, Chiu CF, Huang YC, Hsiao HP, Lin CH, Wang CH, Bau DT, Lin CY. Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 Patients. In Vivo. 2024 Jan-Feb;38(1):341-350.
  • Yen HC, Chen IC, Lin GC, Ke YY, Lin MC, Chen YM, Hsu CC. Sex-specific genetic variants associated with adult-onset inguinal hernia in a Taiwanese population. Int J Med Sci. 2023 Mar 27;20(5):607-615.
  • Kuan-Jung Chen, Hsin-Ru Wu, Mei-Chyn Chao, Tung-Ming Chang, Jien-Wen Chien , Ming Chen, Gwo-Chin Ma, Yu-Yuan Ke. Genotype and phenotype studies of Lowe syndrome in three families in Taiwan. Pediatrics and Neonatology 62(2021)327-328
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