Author Information
Beyhan Tüysüz is affiliated with the Department of Pediatric Genetics at Istanbul University-Cerrahpaşa, Cerrahpaşa Medical Faculty in Istanbul, Turkey. Beyhan Tüysüz has made significant contributions to the field of genetics, particularly in pediatric genetics, through extensive research and publication efforts.
Research Contributions
Beyhan Tüysüz has authored numerous papers focusing on various genetic disorders and syndromes. Notable works include studies on osteogenesis imperfecta type XX, syndromic congenital anomalies of the kidney and urinary tract, Beckwith-Wiedemann spectrum, RASopathies, neurofibromatosis type 1, Smith-McCort Dysplasia 2, Prader-Willi Syndrome, 3M syndrome, and metabolic disorders related to intrauterine growth restriction. These contributions have provided valuable insights into the genetic and epigenetic mechanisms underlying these conditions, along with their clinical manifestations and long-term follow-up findings.
Aliases
Beyhan Tüysüz is also known by the names B Tüysüz, B. Tüysüz, and B. Tüysüz. Publication and Citation Metrics
| Metric |
Value |
| Citation Count |
3065 |
| h-index |
23 |
| Paper Count |
127 |
