| Issue Date | Title | Author(s) |
1 | 2019 | Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder | Aydin, S.U.; Kabukçu Başay, Bürge ; Çetin, Gökhan Ozan ; Güngör Aydın, Ayşegül ; Tepeli, E. |
2 | 2009 | A case of schizophrenia accompanying velocardiofacial syndrome | Şengül, Cem ; Efe, Muharrem ; Tepeli, Emre ; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Herken, Hasan |
3 | 2014 | Correlation of O6-Methylguanine DNA methyltransferase promoter methylation and clinicopathological parameters in bladder cancer | Çetin, Gökhan Ozan ; Caner, Vildan ; Türk, Nilay Şen ; Okur, V.; Can, O.; Eskicorapci, S.; Tuncay, L. |
4 | 2003 | Cytogenetic studies in patients with reproductive failure | Düzcan, Füsun ; Atmaca, Münevver; Çetin, Gökhan Ozan ; Bağcı, Hüseyin |
5 | 2012 | The determination of relationship between "excision repair cross-complementing group 1" (ERCC1) gene T19007C and C8092A single nucleotide polymorphisms and clinicopathological parameters in non-small cell lung cancer | Koç, Esin; Caner, Vildan ; Büyükpınarbaşılı, N.; Tepeli, Emre ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Bağcı, Gülseren |
6 | 2022 | Dominant Optik Atrofi | Çetin, Ebru Nevin ; Ün, Emine Şeker ; Çetin, G. Ozan |
7 | 2022 | Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64, a very rare form of hereditary spastic paraplegias | Olmez, Akgun; Cetin, Gokhan Ozan ; Karaer, Kadri |
8 | 2020 | Expression and DNA methylation profiles of EZH2-target genes in plasma exosomes and matched primary tumor tissues of the patients with diffuse large B-cell lymphoma | Barış, İkbal Cansu; Hacıoğlu, Sibel ; Türk, Nilay Şen ; Çetin, Gökhan Ozan ; Zencır, S.; Bağcı, Gülseren ; Caner, Vildan |
9 | 2012 | Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer | Tepeli, Emre ; Caner, Vildan ; Büyükpınarbaşılı, N.; Çetin, Gökhan Ozan ; Düzcan, Füsun ; Elmas, Levent ; Bağcı, Gülseren |
10 | 2003 | Familial influence on parkinsonism in a rural area of Turkey (Kizilcaboluk-Denizli): A community-based case-control study | Düzcan, Füsun ; Zencir, Mehmet ; Özdemir, Fatma; Çetin, Gökhan Ozan ; Bağcı, Hüseyin ; Heutink, P.; Bonifati, V. |
11 | 2010 | Familial translocation (2;18) ascertained through recurrent spontaneous abortions [Article] | Bağcı, Gülşen; Tepeli, Emre ; Düzcan, Füsun ; Çetin, G. Ozan ; Alataş, Erkan |
12 | 2024 | Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease | Bas, H.; Durmaz, C.D.; Tombak, M.C. ; Cetin, G.O. ; Karaer, K. |
13 | 2014 | GADD45? methylation is more common in benign prostatic hyperplasia than in prostate cancer | Can, O.; Caner, Vildan ; Türk, Nilay Şen ; Tuncay, Ömer Levent ; Eskicorapci, S.Y.; Tepeli, Emre ; Çetin, Ozan |
14 | 2022 | Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population | Cetin, Gokhan Ozan ; Cetin, Ebru Nevin ; Akyol, Tunahan ; Ilhan, Hatice Deniz; Pekel, Gokhan |
15 | 2021 | Herediter Retina Hastalıklarında Genetik Geçiş ve Mutasyonlar | Çetin G. Ozan ; Çetin, Ebru Nevin |
16 | 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. |
17 | 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 |
18 | 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 |
19 | 2024 | A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey | İmren, Işıl Göğem ; Ertürk, Sevilay ; Cetin, Gokhan Ozan ; Kaçar, Nida |
20 | 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. |