| Common Familial Mediterranean Fever gene mutations in a Turkish cohort M Dundar, EF Emirogullari, A Kiraz, S Taheri, M Baskol Molecular biology reports 38, 5065-5069, 2011 | 81 | 2011 |
| TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis H Cangul, Z Aycan, H Saglam, JR Forman, S Cetinkaya, O Tarim, E Bober, ... Journal of Pediatric Endocrinology and Metabolism 25 (5-6), 419-426, 2012 | 30 | 2012 |
| The role of TNF-α and PAI-1 gene polymorphisms in familial Mediterranean fever M Dundar, A Kiraz, B Balta, EF Emirogullari, G Zararsiz, A Yurci, D Aslan, ... Modern rheumatology 23, 140-145, 2013 | 18 | 2013 |
| Micronucleus testing as a cancer detector: endometrial hyperplasia to carcinoma A Kiraz, G Açmaz, G Uysal, D Unal, H Dönmez-Altuntas Archives of gynecology and obstetrics 293, 1065-1071, 2016 | 17 | 2016 |
| A molecular analysis of familial Mediterranean fever disease in a cohort of Turkish patients M Dundar, A Kiraz, EF Emirogullari, Ç Saatci, S Taheri, M Baskol, S Polat, ... Annals of Saudi medicine 32 (4), 343-348, 2012 | 17 | 2012 |
| A comprehensive molecular analysis and genotype–phenotype correlation in patients with familial mediterranean fever B Balta, M Erdogan, A Kiraz, T Akalın, F Baştug, A Bayram Molecular Biology Reports 47, 1835-1843, 2020 | 16 | 2020 |
| Unbalanced 3; 22 translocation with 22q11 and 3p deletion syndrome M Dundar, A Kiraz, S Tasdemir, H Akalin, S Kurtoglu, F Hafo, N Cine, ... American Journal of Medical Genetics Part A 152 (11), 2791-2795, 2010 | 15 | 2010 |
| Wiedemann–Rautenstrauch syndrome: Report of a variant case A Kiraz, S Ozen, F Tubas, Y Usta, O Aldemir, Y Alanay American Journal of Medical Genetics Part A 158 (6), 1434-1436, 2012 | 12 | 2012 |
| Retrospective analysis of 2295 cases with invasive prenatal diagnosis Ç Saatçi, Y Özkul, Ş Taşdemir, A Kiraz, İ Müderris, N Taşçıoğlu, ... Perinatal Journal 15 (3), 120-126-120-126, 2007 | 11 | 2007 |
| 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 |
| Investigation of the relationship between inherited thrombophilia and novel coronavirus pneumonia A Kiraz, S Guzeldag, E Eren, M Goksu, A Bayram Future Virology 16 (5), 341-345, 2021 | 10 | 2021 |
| Netherton syndrome previously misdiagnosed as hyper IgE syndrome caused by a probable mutation in SPINK5 C K Özyurt, M Atasoy, R Ertaş, Y Ulaş, MR Akkuş, A Kiraz, HC Hennies The Turkish Journal of Pediatrics 61 (4), 604-607, 2019 | 9 | 2019 |
| Asymmetric crying face in a newborn with isotretinoin embryopathy D Sarici, MA Akin, S Kurtoglu, K Uzum, A Kiraz Pediatric Dermatology 30 (6), e289-e290, 2013 | 9 | 2013 |
| 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 |
| Cytogenetic damage of radiotherapy in long-term head and neck cancer survivors D Unal, A Kiraz, D Avci, A Tasdemir, TD Unal, S Cagli, C Eroglu, I Yuce, ... International Journal of Radiation Biology 92 (7), 364-370, 2016 | 8 | 2016 |
| İnvazif prenatal tanı yöntemleri uygulanan 2295 olgunun retrospektif analizi Ç Saatçi, Y Özkul, Ş Taşdemir, A Kiraz, İ Müderris, N Taşcıoğlu, ... Perinatoloji Dergisi 15 (3), 120-126, 2007 | 8 | 2007 |
| Does thiol–disulphide balance show oxidative stress in different MEFV mutations? B Balta, M Erdogan, M Alisik, A Kiraz, T Akalin, F Bastug, O Erel Rheumatology International 38, 97-104, 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 |
| The genetic analysis of cystic fibrosis patients with seven novel mutations in the CFTR gene in the central Anatolian region of Turkey M Erdoğan, M Köse, S Pekcan, M Hangül, B Balta, A Kiraz, GA Gönen, ... Balkan medical journal 38 (6), 357, 2021 | 6 | 2021 |
| A rare cause of neonatal hemolytic anemia: glutathione synthetase deficiency PS Ustkoyuncu, FT Mutlu, A Kiraz, ZT Balkis, S Yel Journal of Pediatric Hematology/Oncology 40 (1), e45-e49, 2018 | 6 | 2018 |
