She has experience in molecular dysmorphology/syndromology and neurogenetic and prenatal genetic in the field of the clinical genetic.
She and her team conduct studies to clarify the genetic ethiopathogenesis of rare craniofascial dysmoprhic syndromes and limb malformations.
She was the Manager of the Turkey – Istanbul Group of the CRANIRARE AND CRANIRARE2 (ERA-Net for research programs for rare diseases; multinational cooperation consortiums; 2008-2016) projects that are funded by the 7th Frame Programs of the European Union and principally investigate the Frontonasal Dysplasia and Moebius Syndrome.