Molecular insights into genodermatoses: Genetic findings from 43 patientsArzu Deniz Sama, Tahir Atık, Enise Avcı Durmuşalioğlu et al.|Archives of Dermatological Research|2025Cited by 1
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
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
Genotypic and Phenotypic Landscape of <scp>KBG</scp> Syndrome: A Study of 23 Turkish IndividualsEnise Avcı Durmuşalioğlu, Tahir Atık, Pelin Özlem Şimşek‐Kiper et al.|American Journal of Medical Genetics Part A|2025Cited by 0
Strengthening the candidacy of the <i>ITSN1</i> gene: a novel <i>de novo</i> variant in a patient with autism spectrum disorderTurkan Turkut Tan, Esra Işık, Zehra Burcu Yilmaz et al.|International Journal of Developmental Disabilities|2025Cited by 0