| Issue Date | Title | Author(s) |
| 21 | 2015 | HIF1A as a major vascular endothelial growth factor regulator: Do its polymorphisms have an association with age-related macular degeneration? | Okur, Volkan.; Çetin, Ozan ; Çetin, Ebru ; Tepeli, E.; Bulgu, Y.; Yildirim, C. |
| 2 | 2019 | Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss | Zeybek, S.; Tepeli, E.; Çetin, Gökhan Ozan ; Caner, Vildan ; Şenol, Hande ; Yildirim, B.; Bağcı, Gülseren |
| 3 | 2023 | Interleukin-23 receptor gene polymorphisms in osteoporosis | Ulutaş, Firdevs ; Çetin, Gökhan Ozan ; Çobankara, Veli |
| 4 | 2021 | Kliniğimizde invaziv prenatal tanı yöntemi olarak amniyosentez uygulanan olguların retrospektif değerlendirilmesi | Gök, Soner ; Gök, Berfin Can; Çetin, Gökhan Ozan |
| 5 | 2021 | The miRNA content of circulating exosomes in DLBCL patients and in vitro influence of DLBCL-derived exosomes on miRNA expression of healthy B-cells from peripheral blood | Caner, Vildan ; Cetin, Gokhan Ozan ; Hacioglu, Sibel ; Baris, Ikbal Cansu ; Tepeli, Emre ; Turk, Nilay Sen ; Bagci, Gulseren ; Yararbas, Kanay; Cagliyan, Gulsum |
| 6 | 2016 | Mutational status of EZH2 and CD79B hot spots in mature B-cell non-Hodgkin's lymphomas: Novel CD79B variations have been revealed | Çetin Gökhan Ozan ; Barış, İkbal Cansu; Caner, Vildan ; Sarıkepe, Bilge; Şen Türk, Nilay ; Tepeli, Emre ; Hacıoglu, Sibel |
| 7 | 2024 | A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey | İmren, Işıl Göğem ; Ertürk, Sevilay ; Cetin, Gokhan Ozan ; Kaçar, Nida |
| 8 | 2020 | A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type | Albuz, B.; Çetin, Gökhan Ozan ; Özhan, Bayram ; Sarikepe, B.; Anlaş, Ö.; Öztürk, M.; Zeybek, S. |
| 9 | 2015 | Possible role of GADD45? methylation in diffuse large B-cell Lymphoma: Does it affect the progression and tissue involvement? | Barış, İkbal Cansu ; Caner, Vildan ; Türk, Nilay Şen ; Sarı, Hakan İsmail ; Hacıoğlu, Sibel ; Doğu, Mehmet Hilmi ; Çetin, Ozan |
| 10 | 2023 | The relation of vitamin D receptor gene polymorphisms with risk of obesity, metabolic syndrome, hepatostetosis in Turkish children | Ağladıoğlu, Kadir; Özhan, Bayram ; Bilgihan, Elif ; Çetin, Ozan |
| 11 | 2022 | The Relationship Between Methylation of the Glucocorticoid Receptor Gene (NR3C1) and Childhood Trauma and Alexithymia | Çetin, Ş. ; Sözeri-Varma, G. ; Çetin, G.O. ; Türel, S.; Uğurlu, T.T. ; Özdel, O. |
| 12 | 2021 | The Relationship Between Methylation of the Glucocorticoid Receptor Gene (NR3C1) and Childhood Trauma and Alexithymia | Cetin, Sahabettin; Sozeri-Varma, Gulfizar ; Cetin, Gokhan Ozan ; Turel, Samet; Ugurlu, Tugce Toker ; Ozdel, Osman |
| 13 | 2006 | Sex chromosome aneuploidy rates in the somatic cells of infertile men | Düzcan, Füsun.; Aybek, Zafer. ; Tepeli, E.; Caner, Vildan. ; Çetin, Gökhan Ozan. ; Aybek, Hülya. ; Bağcı, Hüseyin. |
| 14 | 2012 | Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation | Bagcı, Gülseren; Çetin, Gökhan Ozan ; Semerci, Nur; Toruner, G. A.; Cinbiş, Mine |
| 15 | 2024 | Transient neonatal diabetes mellitus: a case report | Demir, G.S.; Yıldırımçakar, D. ; Öcal, M. ; Özdemir, Ö.M.A. ; Altıncık, S.A. ; Çetin, G.O. ; Ergin, H. |
| 16 | 2012 | Translocation Y;21 in an infertile male patient having 45, X karyotype: Case report | Semerci, Cavidan Nur; Eser, Metin ; Tufan, Lale Satıroğlu; Kalkan, Tarkan ; Çetin, Gökhan Ozan ; Öztürk, O.; Bagcı, Gülseren |
| 17 | 2014 | Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population | Bulgu, Y; Çetin, Gökhan Ozan ; Caner, Vildan ; Çetin, Ebru Nevin ; Yaylali, V; Yildirim, C |
| 18 | 2020 | Williams-Beuren Sendromlu Çocukların Klinik ve Ekokardiyografik Değerlendirilmesi | Gürses, Dolunay ; Kayakıran, Eda Didem ; Albuz, Burcu ; Çetin, G. Ozan |
| 19 | 2017 | Yaş Tip (Neovasküler) Yaşa Bağlı Makula Dejenerasyonunda Risk Faktörleri ve Genetik | Çetin, Ebru Nevin ; Çetin, Gökhan Ozan |
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