| Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci T Aung, M Ozaki, MC Lee, U Schlötzer-Schrehardt, G Thorleifsson, ... Nature genetics 49 (7), 993-1004, 2017 | 136 | 2017 |
| A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome T Aung, M Ozaki, T Mizoguchi, RR Allingham, Z Li, A Haripriya, S Nakano, ... Nature genetics 47 (4), 387-392, 2015 | 117 | 2015 |
| Investigation of key miRNAs and target genes in bladder cancer using miRNA profiling and bioinformatic tools KM Canturk, M Ozdemir, C Can, S Öner, R Emre, H Aslan, O Cilingir, ... Molecular biology reports 41, 8127-8135, 2014 | 57 | 2014 |
| 2-Chloro-1, 4-naphthoquinone derivative of quercetin as an inhibitor of aldose reductase and anti-inflammatory agent I Milackova, MS Prnova, M Majekova, R Sotnikova, M Stasko, ... Journal of Enzyme Inhibition and Medicinal Chemistry 30 (1), 107-113, 2015 | 53 | 2015 |
| Prevalence of nonclassic congenital adrenal hyperplasia in Turkish children presenting with premature pubarche, hirsutism, or oligomenorrhoea C Binay, E Simsek, O Cilingir, Z Yuksel, O Kutlay, S Artan International Journal of Endocrinology 2014, 2014 | 34 | 2014 |
| Exploring the relationship between the severity of oligozoospermia and the frequencies of sperm chromosome aneuploidies B Durak Aras, I Aras, C Can, C Toprak, E Dikoglu, G Bademci, M Ozdemir, ... Andrologia 44 (6), 416-422, 2012 | 27 | 2012 |
| Relation of glutathione S-transferase genotypes (GSTM1 and GSTT1) to laryngeal squamous cell carcinoma risk H Acar, K Ozturk, MH Muslumanoglu, MS Yildirim, T Cora, O Cilingir, ... Cancer Genetics and Cytogenetics 169 (2), 89-93, 2006 | 27 | 2006 |
| Biosorption of chromium(VI), nickel(II) and Remazol Blue by Rhodotorula muciloginosa biomass NO San, G Dönmez Water Science and Technology 65 (3), 471-477, 2012 | 21 | 2012 |
| Study on potential role of apolipoprotein E in recurrent pregnancy loss E Korkmazer, E Ustunyurt, B Tekin, O Cilingir Experimental and therapeutic medicine 5 (5), 1408-1410, 2013 | 20 | 2013 |
| A novel mutation in the ARS (component B) gene encoding SLURP‐1 in a Turkish family with mal de Meleda MH Muslumanoglu, N Saracoglu, O Cilingir, T Basmaci, S Urer, I Sabuncu, ... British Journal of Dermatology 155 (2), 467-469, 2006 | 17 | 2006 |
| Association of rare CYP39A1 variants with exfoliation syndrome involving the anterior chamber of the eye Z Li, Z Wang, MC Lee, M Zenkel, E Peh, M Ozaki, F Topouzis, S Nakano, ... Jama 325 (8), 753-764, 2021 | 16 | 2021 |
| Which prognostic marker is responsible for the clinical heterogeneity in CLL with 13q deletion? B Durak Aras, S Isik, H Uskudar Teke, A Aslan, F Yavasoglu, Z Gulbas, ... Molecular cytogenetics 14, 1-7, 2021 | 14 | 2021 |
| The impact of klotho gene polymorphisms on urinary tract stone disease A Gürel, İ Üre, HE Temel, O Çilingir, S Uslu, MF Celayir, S Aslan, ... World journal of urology 34, 1045-1050, 2016 | 13 | 2016 |
| Conventional and molecular cytogenetic analyses in Turkish patients with multiple myeloma B Durak Aras, OM Akay, G Sungar, G Bademci, V Aslan, J Caferler, ... | 13 | 2011 |
| Clinical, histochemical, and molecular study of three Turkish siblings diagnosed with H syndrome, and literature review E Simsek, T Simsek, M Eren, E Yilmaz, D Arik, O Cilingir, S Ceylaner, ... Hormone Research in Paediatrics 91 (5), 346-355, 2019 | 12 | 2019 |
| Three single nucleotide polymorphisms of LOXL1’in a Turkish population with pseudoexfoliation syndrome and pseudoexfoliation glaucoma Y Yaz, N Yıldırım, YA Yaz, O Çilingir, Z Yüksel, F Mutlu Turkish Journal of Ophthalmology 48 (5), 215, 2018 | 12 | 2018 |
| Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium M Dundar, U Fahrioglu, SH Yildiz, B Bakir-Gungor, SG Temel, H Akin, ... Functional & integrative genomics 22 (3), 291-315, 2022 | 10 | 2022 |
| Fenilketonüri hastalığında prenatal-postnatal tanıda VNTR bağlantısı ve direkt mutasyon analizleri birlikteliğinin avantajları MH Müslümanoğlu, N Çine, M Özdemir, O Çilingir, N Başaran, B Durak, ... Kocatepe Tıp Dergisi 5 (1), 2004 | 10 | 2004 |
| The relationship of retinopathy of prematurity with brain-derivated neurotrophic factor, vascular endotelial growth factor-A, endothelial PAD domain protein 1 and nitric oxide … S Ilguy, O Cilingir, MD Bilgec, O Ozalp, E Erzurumluoglu Gokalp, S Arslan, ... Ophthalmic Genetics 42 (6), 725-731, 2021 | 9 | 2021 |
| Genetic variants associated with atrial fibrillation and long-term recurrence after catheter ablation for atrial fibrillation in Turkish patients T Ulus, M Dural, P Meşe, F Yetmiş, KU Mert, B Görenek, O Çilingir, ... Anatolian journal of cardiology 25 (2), 129, 2021 | 9 | 2021 |
Sevilhan ArtanTıp Fakültesi Profesoru, Eskisehir Osmangazi UniversitesiVerified email at ogu.edu.tr
