Prof. Dr. HÜLYA KAYSERİLİ

HÜLYA KAYSERİLİ

Prof. Dr. HÜLYA KAYSERİLİ

Medical Genetics

Koç University Hospital

  • Head of the Department of Medical Genetics at Koç University Faculty of Medicine and responsible physician of the Genetic Diseases Diagnosis (Evaluation) Center at Koç University Hospital.
  • Received the title of Associate Professor in 2000 and Professor in 2009.
  • Between 1993 and 2007, worked abroad as a postdoctoral researcher and academic at various institutions (UCLA, Cedars-Sinai, LA-USA; Cardiff University, United Kingdom; Academisch Medisch Centrum & Free University of Amsterdam, the Netherlands).
  • Continues to serve as country representative in the European Union of Medical Specialists (UEMS) and in human genetics committees (ESHG-PPPC).
  • Has authored more than 200 international articles and more than 15 book chapters.
  • Experienced in the field of clinical genetics, particularly in molecular dysmorphology/syndromology, neurogenetics and prenatal genetics.
  • Together with the team, carries out studies aimed at determining the genetic etiopathogenesis of rare craniofacial dysmorphic syndromes and limb malformations.
  • Served as manager of the Turkey-Istanbul Group of the projects CRANIRARE and CRANIRARE2 (ERA-Net for research programs for rare diseases; multinational collaboration consortia; 2008-2016), which were funded under the European Union 7th Framework Programmes and whose main research topics were frontonasal dysplasias and Moebius syndrome.
  • Main clinical areas of interest:
  • Clinical genetics; rare syndromes and molecular dysmorphology,
  • Prenatal genetic diagnosis,
  • Skeletal dysplasias and dysostoses (limb anomalies),
  • Neuromuscular diseases.