A unique case of thrombophilia: the role of F9 gene duplication and increased factor IX activity in cerebral venous thrombosisTurkan Turkut Tan, Tahir Atık, Esra Işık et al.|Journal of Thrombosis and Haemostasis|2023Cited by 8
Molecular insights into genodermatoses: Genetic findings from 43 patientsArzu Deniz Sama, Tahir Atık, Esra Işık et al.|Archives of Dermatological Research|2025Cited by 1
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
From Clinical Observation to Genetic Confirmation: Somatic Mosaic Mutations in <i>RHOA</i> on Ectodermal Dysplasia With Multi‐System InvolvementEnise Avcı Durmuşalioğlu, Tahir Atık, Esra Işık et al.|American Journal of Medical Genetics Part A|2024Cited by 0
Next generation sequencing in children with isolated congenital cataractGunay Amanova, Özgür Çoğulu, Mahmut Çöker et al.|European Journal of Ophthalmology|2025Cited by 0