| The IL-1RN and IL-4 gene polymorphisms are potential genetic markers of susceptibility to bladder cancer: a case–control study ST Bozdoğan, B Erol, A Dursun, G Bozdoğan, I Dönmez, NA Mungan, ... World journal of urology 33, 389-395, 2015 | 18 | 2015 |
| The prevalence of gap junction protein beta 2 (GJB2) mutations in non syndromic sensorineural hearing loss in cukurova region. ST Bozdoğan, G Kuran, ÖÖ Yüregir, H Aslan, S Haytoğlu, A Ayaz, ... Journal of International Advanced Otology 11 (2), 2015 | 15 | 2015 |
| Late-onset Leigh syndrome due to NDUFV1 mutation in a 10-year-old boy initially presenting with ataxia F Incecik, OM Herguner, S Besen, ST Bozdoğan, NO Mungan Journal of Pediatric Neurosciences 13 (2), 205-207, 2018 | 13 | 2018 |
| Clinical, radiological, and genetic variation in pontocerebellar hypoplasia disorder and our clinical experience S Bilge, GG Mert, Ö Hergüner, D Özcanyüz, ST Bozdoğan, Ö Kaya, ... Italian Journal of Pediatrics 48 (1), 169, 2022 | 10 | 2022 |
| Shprintzen-Goldberg Syndrome: Case Report/Shprintzen-Goldberg Sendromu: Olgu Sunumu S Yalcintepe, OO Yuregir, ST Bozdogan, H Aslan Meandros Medical and Dental Journal 19 (2), 175-178, 2018 | 7 | 2018 |
| Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene OH Kılınç, D Giray, A Bişgin, ST Bozdoğan, D Karpuz Turk Kardiyol Dern Ars 45 (5), 450-453, 2017 | 7 | 2017 |
| Contribution of genotypes in Prothrombin and Factor V Leiden to COVID‐19 and disease severity in patients at high risk for hereditary thrombophilia A Kiraz, O Sezer, A Alemdar, S Canbek, N Duman, A Bisgin, T Cora, ... Journal of medical virology 95 (2), e28457, 2023 | 6 | 2023 |
| IL-1RN VNTR, IL-2 (-330), and IL-4 VNTR gene polymorphisms in patients with chronic rhinosinusitis with sinonasal polyposis G Kuran, H Aslan, S Haytoğlu, ÖÖ Yüreğir, ST Bozdoğan Turkish Journal of medical sciences 49 (5), 1411-1417, 2019 | 6 | 2019 |
| A novel mutation of ROBO3 in horizontal gaze palsy with progressive scoliosis ST Bozdoğan, E Dinç, AA Sarı, A Özgür, A Bişgin Ophthalmic Genetics 38 (3), 284-285, 2017 | 6 | 2017 |
| A novel intronic mutation reduces HAX1 level and is associated with severe congenital neutropenia S Goktas, ZB Azizoglu, D Petersheim, M Erdogan, HE Gungor, A Bisgin, ... Journal of pediatric hematology/oncology 44 (1), e62-e67, 2022 | 4 | 2022 |
| Vandetanib in a child affected by neurofibromatosis type 1 and medullary thyroid carcinoma with both NF1 and homozygous RET proto-oncogen germ-line mutations BD Gündoğan, F Sağcan, ST Bozdoğan, Y Balcı, FT Daloğlu, EÇ Çıtak Journal of clinical research in pediatric endocrinology 13 (3), 342, 2021 | 4 | 2021 |
| Spectrum of FAR1 (fatty acyl-CoA reductase 1) variants and related neurological conditions A Westenberger, A Ruiz-Herrera, S Bozdoğan, A Bisgin, M Almuqbil, ... Movement disorders: official journal of the Movement Disorder Society 38 (3 …, 2023 | 2 | 2023 |
| Epilepsi ve anlıksal yetiyitimi olan hastalarda moleküler karyotiplemenin klinik yararı A Bişgin, ST Bozdoğan Cukurova Medical Journal 43 (Ek 1), 44-48, 2018 | 2 | 2018 |
| Bialelic Pathogenic (c.830G>A(p.R277Q)) Variant Disrupting the GNE Gene Function and Causes Nonaka myopathy Phenotype M Doğan, E Akbulut, A Gezdirici, R Eroz, ST Bozdoğan Cytology and Genetics 57 (4), 347-355, 2023 | 1 | 2023 |
| Clinical findings and mutational spectrum of neurofibromatosis type 1 patients in a single center of south part of Turkey. YS Ayhan, C Müjde, A Bişgin, EÇ Çitak Turkish Journal of Medical Sciences, 2021 | 1 | 2021 |
| The importance of genetic diagnosis for inherited metabolic Diseases: distribution and experience of Cukurova University Faculty of Medicine Balcali Hospital ST Bozdoğan, HNÖ Mungan, B İbrahim, HM Yaşar, S Büyükkurt, A Bişgin Acıbadem Üniversitesi Sağlık Bilimleri Dergisi 12 (1), 29-32, 2020 | 1 | 2020 |
| Varikoseli olan hastalarda Y kromozomu mikrodelesyonu-infertilite ilişkisi S Bozdoğan, A Dursun, Ç Yeşilli, İ Seçkiner, F Çabuk, K Altan, ... SDÜ Tıp Fakültesi Dergisi 14 (1), 15-19, 2006 | 1 | 2006 |
| Early diagnostic clues of mucolipidosis type II: Significance of radiological findings E Burgac, İ Kaplan, B Köseci, E Kara, D Kor, FD Bulut, A Atmış, F Pişkin, ... American Journal of Medical Genetics Part A, 2024 | | 2024 |
| Evaluation of Genetic Heterogeneity in Joubert Syndrome Case Series. N Shirinova, MB Bereketoğlu, Ö Sönmezler, Ç Rencüzoğulları, ... Gazi Medical Journal 35, 2024 | | 2024 |
| Muscular Dystrophies and Genetic Counseling. ST Bozdoğan Gazi Medical Journal 35, 2024 | | 2024 |
