
DirectorChia-Chi Hsu
Professional license
- Pediatric specialist
- Neonatologist
- Pediatric Pulmonologist
- Pediatric Medical Genetics and Metabolism Specialist
- Pediatric endocrinologist
- Pediatric Intensive Care Physician
- Adolescent Medicine Specialist
- Pediatric Ultrasound Specialist
- Diabetes Shared Care Network Medical Staff
Educational qualifications
- Graduated from the Department of Medicine, Kaohsiung Medical University
- Director of the Department of Pediatric Genetics, Metabolism and Endocrinology, Taichung Veterans General Hospital
- Director of the Genetic Counseling Center at Taichung Veterans General Hospital
- Attending Physician, Children's Medical Center, Taichung Veterans General Hospital
- Research Physician, Department of Genetics and Metabolism, National Taiwan University Hospital
- Research Physician, Department of Genetics and Metabolism, Mackay Memorial Hospital
- Chief Physician, Children's Medical Center, Taichung Veterans General Hospital
- Resident Physician, Children's Medical Center, Taichung Veterans General Hospital
- Medical Genetics (Congenital Genetics, Genetic Counseling)
- Department of Pediatric Endocrinology and Metabolism (endocrine and metabolic diseases, thyroid and diabetes diseases, growth and development assessment of children and adolescents (early or slow development), adolescent medicine and health care)
- Neonatology (premature infant diseases, care, health education and consultation)
- Li MH, Chen IC, Yang HW, Yen HC, Ke YY, Chen YM, Hsu CC. Association of methylenetetrahydrofolate reductase rs1801133 polymorphism with osteoporosis and fracture risk in Taiwan. Int J Med Sci. 2024; 21(12):2261-2271 (SCI)
- 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; 21(5):784-794 (SCI)
- 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; 20(5):607-615 (SCI)
- Lee HF, Hsu CC, Chi CS, Tsai CR. Genotype-phenotype dissociation in two Taiwanese children with molybdenum cofactor deficiency caused by MOCS2 mutation. Neuropediatrics. 2022; 53(3):200-203 (SCI)
- Lin HY, Chuang CK, Ke YY, Hsu CC, Chiu PC, Niu DM, Tsai FJ, Hwu WL, Lin JL, Lin SP. Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVA. Pediatr Neonatol. 2019; 60(3):342-3 (SCI)