| Could familial Mediterranean fever gene mutations be related to PFAPA syndrome? MH Celiksoy, G Ogur, E Yaman, U Abur, S Fazla, R Sancak, A Yildiran Pediatric Allergy and Immunology 27 (1), 78-82, 2016 | 45 | 2016 |
| Chromosomal and Y‐chromosome microdeletion analysis in 1,300 infertile males and the fertility outcome of patients with AZFc microdeletions U Abur, S Gunes, R Ascı, E Altundag, OS Akar, B Ayas, ... Andrologia 51 (11), e13402, 2019 | 42 | 2019 |
| Which ischemic stroke subtype is associated with hyperhomocysteinemia? L Gungor, M Polat, MB Ozberk, B Avci, U Abur Journal of Stroke and Cerebrovascular Diseases 27 (7), 1921-1929, 2018 | 37 | 2018 |
| Semiquantitative promoter methylation of MLH1 and MSH2 genes and their impact on sperm DNA fragmentation and chromatin condensation in infertile men N Hekim, S Gunes, R Asci, R Henkel, U Abur Andrologia 53 (1), e13827, 2021 | 17 | 2021 |
| Tr-KIT/c-KIT ratio in renal cell carcinoma S Ergün, DU Altay, S Güneş, R Büyükalpelli, SC Karahan, L Tomak, ... Molecular Biology Reports 46 (5), 5287-5294, 2019 | 9 | 2019 |
| Multiscale analysis of SRY‐positive 46, XX testicular disorder of sex development: Presentation of nine cases OS Akar, S Gunes, U Abur, E Altundag, R Asci, OE Onat, T Ozcelik, ... Andrologia 52 (11), e13739, 2020 | 8 | 2020 |
| Genetic burden and outcome of cystic hygromas detected antenatally: results of 93 pregnancies from a single center in the northern region of Turkey HS Aymelek, G Oğur, M Tosun, Ü Abur, E Altundağ, H Çelik, E Kurtoğlu, ... Journal of medical ultrasound 27 (4), 181-186, 2019 | 5 | 2019 |
| Impact of fluorescent in situ hybridization aberrations and CLLU1 expression on the prognosis of chronic lymphocytic leukemia: presentation of 156 patients from Turkey Ü Abur, G Oğur, ÖS Akar, E Altundağ, HS Aymelek, D Özatlı, M Turgut Turkish Journal of Hematology 35 (1), 61, 2018 | 4 | 2018 |
| Vesicourethral reflux‐induced renal failure in a patient with ICF syndrome due to a novel DNMT3B mutation S Kutluğ, G Ogur, A Yilmaz, PE Thijssen, U Abur, A Yildiran American Journal of Medical Genetics Part A 170 (12), 3253-3257, 2016 | 4 | 2016 |
| Endocrine, sexual and reproductive functions in patients with Klinefelter syndrome compared to non‐obstructive azoospermic patients F Kocamanoglu, B Ayas, MS Bolat, U Abur, R Bolat, R Asci International Journal of Clinical Practice 75 (8), e14294, 2021 | 3 | 2021 |
| Sitokalasin-B ile bloklanan hücrelerde yaşa bağlı mikronükleus oranları YB Kutbay Ondokuz Mayıs Üniversitesi, Tıp Fakultesi, 2001 | 3 | 2001 |
| Genetic testing can change diagnosis and treatment in children with congenital hypothyroidism C Kara, J Mammadova, Ü Abur, C Gumuskaptan, Eİ Güllü, A Dağdemir, ... European Thyroid Journal 12 (3), 2023 | 2 | 2023 |
| The interrelationship between fyn and Mir-128/193a-5p/494 in imatinib resistance in prostate cancer S Ergün, O Akgün, NT Hekim, S Aslan, F Ari, S Güneş, Ü Abur Anti-Cancer Agents in Medicinal Chemistry (Formerly Current Medicinal …, 2023 | 2 | 2023 |
| Clinical, cytogenomic, and molecular characterization of isodicentric y-chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and severe … U Abur, S Gunes, N Hekim, OS Akar, E Altundag, R Asci Journal of Assisted Reproduction and Genetics 39 (12), 2799-2810, 2022 | 2 | 2022 |
| Evaluation of the promoter methylation status of hypoxia factor 3A and interleukin-6 genes and expression levels of mir-130b and mir-146b in childhood obesity E Tekcan, N Kara, HM Aydın, Ü Abur, M Abbaszadeh Revista da Associação Médica Brasileira 68, 1276-1281, 2022 | 1 | 2022 |
| Frequency and risk factors of neural tube defects in Samsun province A Sanrı, M Karayel, U Abur, E Altundag, O salih Akar, H Celik, M Tosun, ... Cumhuriyet Medical Journal 40 (4), 413-420, 2018 | 1 | 2018 |
| A Male Case of Aromatase Deficiency with a Novel CYP19A1 Mutation U Abur, A Atmaca, H Scott, L Gagliardi, E Altundağ, OS Akar, İK Bayrak, ... Journal of clinical research in pediatric endocrinology 9, 2-2, 2017 | 1 | 2017 |
| CGG Repeat Profile and Clinical Characteristics of Fragile X Full Mutant, Premutant and Gray Zone Patients. HU Kına, E Altundağ, A Yılmaz, U Abur Gazi Medical Journal 35, 2024 | | 2024 |
| Evaluation of Germline CHEK2 Variants and Challenges in Genetic Counseling. ÖS Akar, G Demirağ, AK Polat, İ Yalçın, M Kefeli, B Yılmaz, S Çalışkan, ... Gazi Medical Journal 35, 2024 | | 2024 |
| MVK, NLRP3, TNFRSF1A and MEFV gene mutation distributions in childhood autoinflammatory diseases: Experiences in North Anatolia E Altundağ, Ü Abur, ÖS Akar, A Yıldıran, MH Çeliksoy, AGA Paul, ... Journal of Experimental and Clinical Medicine 40 (4), 681-686, 2023 | | 2023 |
