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American Journal of Public Health|May 18, 2018
Determinants of Mental Disorders in Syrian Refugees in Turkey Versus Internally Displaced Persons in SyriaSidika Tekeli-Yesil, Esra Isik, Yesim Unal, et al.
American Journal of Medical Genetics. Part A|April 14, 2017
A further family of Stromme syndrome carrying CENPF mutationFerda Ozkinay, Tahir Atik, Esra Isik, et al.
European Journal of Medical Genetics|September 13, 2022
LSM1 is the new candidate gene for neurodevelopmental disorderGizem Kok Kilic, Esra Isik, Omer Alpay, et al.
American Journal of Medical Genetics. Part A|November 20, 2024
From Clinical Observation to Genetic Confirmation: Somatic Mosaic Mutations in RHOA on Ectodermal Dysplasia With Multi-System InvolvementEnise Avci Durmusalioglu, Yusuf Can Dogan, Turkan Turkut Tan, et al.
BMC Medical Genomics|October 1, 2024
Diagnostic yield of exome sequencing-based copy number variation analysis in Mendelian disorders: a clinical applicationTahir Atik, Enise Avci Durmusalioglu, Esra Isik, et al.
Annals of Human Genetics|March 13, 2020
Clinical and molecular aspects of PTEN mutations in 10 pediatric patientsEsra Isik, Ozguc Semih Simsir, Asli Ece Solmaz, et al.
Molecular Syndromology|December 7, 2023
Dual Diagnosis of Trichohepatoenteric Syndrome and Lipoid Proteinosis in a Turkish ChildHatice Ceren Eser, Durdugul Ayyildiz Emecen, Ezgi Topyildiz, et al.
Clinical Child Psychology and Psychiatry|June 6, 2022
Evaluation of social cognition, autistic traits, and dysmorphology in comorbid specific learning disorder and attention-deficit/hyperactivity disorderNazli Burcu Ozbaran, Senay Celenay Ozyasar, Nurhak Dogan, et al.
American Journal of Medical Genetics. Part A|December 1, 2020
A rare cause of syndromic short stature: 3M syndrome in three familiesEsra Isik, Duygu Arican, Tahir Atik, et al.
Archives of Dermatological Research|March 2, 2025
Molecular insights into genodermatoses: Genetic findings from 43 patientsArzu Deniz Sama, Enise Avci Durmusalioglu, Esra Isik, et al.
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