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Gökhan Ozan Çetin

Observed names: Cetin, Gokhan Ozan, G. Ozan Cetin, G. Ozan ÇETİN, G. Ozan ÇEtin, G. Ozan Çetin, GO Cetin, Gokhan Ozan Cetin, Gökhan Ozan ÇETİN, Ozan G Cetin, Ozan Çetin, ÇETİN, GÖKHAN OZAN, ÇETİN, Gökhan Ozan
ORCID: 0000-0002-6100-7973
Observed ORCID: 0000-0002-6100-7973
OpenAlex ID: A5055709077
Cytogenetic studies in patients with reproductive failure
2003 · Füsun Düzcan, Münevver Atmaca, et al. · Acta Obstetricia Et Gynecologica Scandinavica · 51
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Diagnostic and Management Strategies of Bietti Crystalline Dystrophy: Current Perspectives
2023 · Ali Osman Saatci, Ferdane Ataş, et al. · Clinical ophthalmology · 24
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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
2022 · Munis Dundar, Umut Fahrioglu, et al. · Functional & Integrative Genomics · 20
Altered microRNA 5692b and microRNA let-7d expression levels in children and adolescents with attention deficit hyperactivity disorder
2019 · Sezai Ustun Aydin, Burge Kabukcu Basay, et al. · Journal of Psychiatric Research · 20
Familial influence on parkinsonism in a rural area of Turkey (Kızılcaboluk–Denizli): A community‐based case‐control study
2003 · Fusun Duzcan, Mehmet Zencir, et al. · Movement Disorders · 18
Progressive autosomal dominant optic atrophy and sensorineural hearing loss in a Turkish family
2002 · Serap Özden, Füsun Düzcan, et al. · Ophthalmic Genetics · 17
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
2021 · Vildan Caner, Gokhan Ozan Cetin, et al. · Cancer Biomarkers · 14
MYD88 Expression and L265P Mutation in Mature B-Cell Non-Hodgkin Lymphomas
2015 · Vildan Caner, Nilay Sen Turk, et al. · Genetic Testing and Molecular Biomarkers · 12
Downregulation of VANGL1 Inhibits Cellular Invasion Rather than Cell Motility in Hepatocellular Carcinoma Cells Without Stimulation
2015 · Gokhan Ozan Cetin, Asli Toylu, et al. · Genetic Testing and Molecular Biomarkers · 12
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
2011 · Esin Koç, Vildan Caner, et al. · Molecular Biology Reports · 10
Expression of ERCC1 and its clinicopathological correlations in non-small cell lung cancer
2011 · Emre Tepeli, Vildan Caner, et al. · Molecular Biology Reports · 10
Evaluation of the Patients with the Diagnosis of Pontocerebellar Hypoplasia: A Multicenter National Study
2024 · Dilek Cavusoglu, Gulten Ozturk, et al. · The Cerebellum · 9
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A novel nonsense mutation in CHST3 in a Turkish patient with spondyloepiphyseal dysplasia, Omani type
2019 · Burcu Albuz, Gökhan Ozan Çetin, et al. · Clinical Dysmorphology · 9
Vascular endothelial growth factor gene polymorphisms in age-related macular degeneration in a Turkish population.
2014 · Yunus Bulgu, Gokhan Ozan Cetin, et al. · Europe PMC (PubMed Central) · 9
Increased expression of pentraxin 3 in placental tissues from patients with unexplained recurrent pregnancy loss
2019 · S Zeybek, E Tepeli, et al. · Balkan Journal of Medical Genetics · 8
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The clinical phenotype of Koolen‐de Vries syndrome in Turkish patients and literature review
2023 · Gokcen Karamik, Beyhan Tuysuz, et al. · American Journal of Medical Genetics Part A · 7
Expression and Amplification of Topoisomerase-2α in Type 1 and Type 2 Papillary Renal Cell Carcinomas and Its Correlation with HER2/neu Amplification
2011 · Fusun Duzcan, Suleyman Ender Duzcan, et al. · Pathology & Oncology Research · 5
The mRNA expression of cytochrome P450 isoforms in human gastric tissue.
2010 · Pakize Canturk, Vildan Caner, et al. · PubMed · 5
Sex chromosome aneuploidy rates in the somatic cells of infertile men.
2006 · Fusun Duzcan, Zafer Aybek, et al. · PubMed · 5
Filippi syndrome: Three new families suggest that urinary system abnormalities may belong to clinical spectrum of the disease
2024 · Hasan Bas, Ceren Damla Durmaz, et al. · American Journal of Medical Genetics Part A · 3
Expanding the clinical and molecular features of trichorhino- phalangeal syndrome with a novel variant
2023 · Nuray Öztürk, Gökcen Karamık, et al. · The Turkish Journal of Pediatrics · 3
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Terminal 14q deletion with unbalanced t(Y;14)(q12;q32) translocation
2011 · Gülseren Bağcı, Gökhan Ozan Çetin, et al. · Clinical Dysmorphology · 3
Integrative and systematic genomic approaches to improve diagnosis in rare and undiagnosed diseases: results from the RareBoost project
2026 · Ayca Yigit, Mert Pekerbas, et al. · European Journal of Human Genetics · 2
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Early onset disease, anarthria, areflexia, and dystonia can be the distinctive features of SPG64 , a very rare form of hereditary spastic paraplegias
2022 · Akgün Ölmez, Gökhan Ozan Çetin, et al. · American Journal of Medical Genetics Part A · 2
Genotype and phenotype characteristics of X-linked retinoschisis: the first report of a Turkish population
2021 · Gokhan Ozan Cetin, Ebru Nevin Cetin, et al. · Ophthalmic Genetics · 2
Works count: 52
Citation count: 282
H-index: 10
I10-index: 11
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