| Genes that affect brain structure and function identified by rare variant analyses of Mendelian neurologic disease E Karaca, T Harel, D Pehlivan, SN Jhangiani, T Gambin, ZC Akdemir, ... Neuron 88 (3), 499-513, 2015 | 293 | 2015 |
| High prevalence of multilocus pathogenic variation in neurodevelopmental disorders in the Turkish population T Mitani, S Isikay, A Gezdirici, EY Gulec, J Punetha, JM Fatih, I Herman, ... The American Journal of Human Genetics 108 (10), 1981-2005, 2021 | 45 | 2021 |
| Angiotensin-converting enzyme-1 gene insertion/deletion polymorphism may be associated with COVID-19 clinical severity: a prospective cohort study MDD Ozgur Gunal, Ozlem Sezer, Goksenin Unluguzel Ustun, Cagatay Erman Ozturk ... Annals of Saudi Medicine 41 (3), 141-146, 2021 | 37 | 2021 |
| Association between colchicine resistance and vitamin D in familial Mediterranean fever I Ozer, T Mete, O Turkeli Sezer, G Kolbasi Ozgen, GO Kucuk, C Kaya, ... Renal failure 37 (7), 1122-1125, 2015 | 21 | 2015 |
| Fibular aplasia, tibial campomelia, and oligosyndactyly: a further patient with a 2-year follow-up O Sezer, I Gebesoglu, B Yuan, E Karaca, E Gokce, S Gunes Clinical Dysmorphology 23 (4), 121-126, 2014 | 18 | 2014 |
| Assessment of vaginal and endometrial microbiota by real‐time PCR in women with unexplained infertility O Sezer, C Soyer Çalışkan, S Celik, SS Kilic, T Kuruoglu, ... Journal of Obstetrics and Gynaecology Research 48 (1), 129-139, 2022 | 15 | 2022 |
| 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 |
| The IL4-VNTR P1 allele, IL4-VNTR P2P2 genotype, and IL4-VNTR_IL6-174CG P2P1-GG genotype are associated with an increased risk of brucellosis O Gunal, S Yigit, AD Yalcın, B Celik, S Barut, O Demir, O Ates, F Duygu, ... Japanese journal of infectious diseases 70 (1), 61-64, 2017 | 10 | 2017 |
| Analysis of ACE2 and TMPRSS2 coding variants as a risk factor for SARS‐CoV‐2 from 946 whole‐exome sequencing data in the Turkish population N Duman, G Tuncel, A Bisgin, ST Bozdogan, SO Sag, S Gul, A Kiraz, ... Journal of medical virology 94 (11), 5225-5243, 2022 | 8 | 2022 |
| Interleukin-1Ra rs2234663 and Interleukin-4 rs79071878 polymorphisms in familial mediterranean fever AF Nursal, A Tekcan, SU Kaya, O Sezer, S Yigit Gene 582 (2), 173-177, 2016 | 8 | 2016 |
| MTHFR gene C677T and A1298C variants are associated with FMF risk in a Turkish cohort AF Nursal, S Kaya, O Sezer, N Karakus, S Yigit Journal of clinical laboratory analysis 32 (2), e22259, 2018 | 7 | 2018 |
| 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 |
| Derangements of vaginal and cervical canal microbiota determined with real-time PCR in women with recurrent miscarriages C Soyer Caliskan, N Yurtcu, S Celik, O Sezer, SS Kilic, A Cetin Journal of Obstetrics and Gynaecology 42 (6), 2105-2114, 2022 | 5 | 2022 |
| Possible effect of genetic background in thrombophilia genes on clinical severity of patients with coronavirus disease-2019: A prospective cohort study O Sezer, O Gunal, R Aci, A Keskin Baghdad Journal of Biochemistry and Applied Biological Sciences 3 (03), 183-199, 2022 | 4 | 2022 |
| Angiotensin converting enzyme gene insertion/deletion variant and familial Mediterranean fever-related amyloidosis AF Nursal, E Turkmen, SU Kaya, A Tekcan, O Sezer, SD Celik, S Yigit Iranian Society of Nephrology, 2018 | 4 | 2018 |
| Genetic Management Algorithm in High-Risk Fabry Disease Cases; Especially in Female Indexes With Mutations SC Ozlem Sezer Endocr Metab Immune Disord Drug Targets, 2020 | 3* | 2020 |
| Mozaik 45, X/46, X, der (X) karyotipi saptanan primer amenoreli bir olguda Trizomi Xq ve delesyon Xp fenotipi N Kara, G Ökten, Ş TURAL, S Artan, Ö Sezer, I Koçak Turkiye Klinikleri Journal of Medical Sciences 31 (3), 706-711, 2011 | 3 | 2011 |
| 0F PARTIAL TRIS0MY8AND PARTALM0N0S0MY9p G Okten, O Sezer, S Günes, S Küçüködük, G Ogur Genetic Counseling 20 (4), 341-347, 2009 | 3 | 2009 |
| Effect of vitamin D receptor gene BsmI polymorphism on hospitalization of SARS-CoV-2 positive patients R Aci, A Keskin, S Yigit, O Sezer, MT Kaya Nucleosides, Nucleotides & Nucleic Acids 43 (3), 264-275, 2024 | 2 | 2024 |
| Germ cell tumor showing partial trisomy 1 in a gonadectomized intersex child with monosomy X and double Y mosaicism G Ogur, FG Pnarl, A Dagdemir, S Artan, E Artürk, M Elli, ÖT Sezer, ... Journal of Pediatric Hematology/Oncology 28 (11), 750-754, 2006 | 2 | 2006 |
