A unique case of thrombophilia: the role of F9 gene duplication and increased factor IX activity in cerebral venous thrombosisTurkan Turkut Tan, Tahir Atık, Erhan Parıltay et al.|Journal of Thrombosis and Haemostasis|2023Cited by 8
From Clinical Observation to Genetic Confirmation: Somatic Mosaic Mutations in <i>RHOA</i> on Ectodermal Dysplasia With Multi‐System InvolvementEnise Avcı Durmuşalioğlu, Tahir Atık, Dilşah Çoğulu et al.|American Journal of Medical Genetics Part A|2024Cited by 0
A New Unc45a 5'utr Variant In Patients With Aagenaes SyndromeTurkan Turkut Tan, Tahir Atık, Zehra Burcu Yilmaz et al.|American Journal of Medical Genetics Part A|2025Cited by 0
Next generation sequencing in children with isolated congenital cataractGunay Amanova, Özgür Çoğulu, Esra Er et al.|European Journal of Ophthalmology|2025Cited by 0
Genotypic and Phenotypic Landscape of <scp>KBG</scp> Syndrome: A Study of 23 Turkish IndividualsEnise Avcı Durmuşalioğlu, Tahir Atık, Esra Işık et al.|American Journal of Medical Genetics Part A|2025Cited by 0