| Issue Date | Title | Author(s) |
| 2022 | A 7-Year Girl With Renal Medullary Hyperechogenicity and Hypertension: Questions | Girisgen, Ilknur ; Yuksel, Selcuk ; Ufuk, Furkan ; Durak, Taner ; Becerir, Tulay |
| 2022 | A 7-year-old girl with renal medullary hyperechogenicity and hypertension: Answers | Girisgen, Ilknur ; Yuksel, Selcuk ; Ufuk, Furkan ; Durak, Taner ; Becerir, Tulay |
| 2024 | A case report of Hennekam syndrome with a mutation in the CCBE1 gene | Durak, T. ; Karaer, D. ; Karaer, K. |
| 2024 | Coffin-Lowry Syndrome: Two Novel Variants in RPS6KA3 Gene | Karaer, Derya ; Durak, Taner ; Karaer, Kadri̇ |
| 2021 | Comparative Analysis of Mefv Mutations in Patients With Familial Mediterranean Fever by Real Time Polymerase Chain Reaction and Next Generation Sequencing-Single Center Experience | Tokgün, O. ; Türel, S.; Tokgün, P.E.; Durak, T. ; Karagenç, N. ; Demiray, A. ; Akça, H. |
| 2023 | The effects of MYC on exosomes derived from cancer cells in the context of breast cancer | Çelikkaya, Busra; Durak, Taner ; Farooqi, Ammad Ahmad; Inci, Kubilay; Tokgün, Pervin Elvan; Tokgün, Onur |
| 2022 | The Impact Of Hereditary Thrombophilias In Recurrent Pregnancy Loss | Karagür, E.R.; Alay, M.T.; Demiray, A. ; Karagenç, N. ; Tokgün, O. ; Durak, T. ; Akca, Hakan |
| 2024 | Metachronous or synchronous presentation of acute myeloid leukemia and lung cancer: A single-center experience | Koluman, Basak Ünver ; Gökçen Demiray, Atike ; Akgün Çaglıyan, Gülsüm ; Kabukcu Hacıoğlu, Sibel ; Güler, Nil ; Durak, Taner ; Arman Karakaya, Yeliz ; Bir, Ferda |
| 2024 | Mikroarray testi için yönlendirilen hastaların analiz sonuçları ve klinik özelliklerinin literatür eşliğinde tartışılması | Aracı, Duygu Gamze |
| 2024 | Noonan syndrome: molecular and clinical findings in individuals with PTPN11 pathogenic variants | Karaer, Derya ; Durak, Taner ; Karaer, Kadri |
