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UMMET ABUR
UMMET ABUR
Tıbbi Genetik Yardımcı Doçent Doktor Ondokuz Mayıs Üniversitesi Tıp Fakültesi
Verified email at omu.edu.tr
Title
Cited by
Cited by
Year
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
442016
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
422019
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
362018
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
152021
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
92019
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
82020
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
52019
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
42018
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
42016
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
32021
Sitokalasin-B ile bloklanan hücrelerde yaşa bağlı mikronükleus oranları
YB Kutbay
Ondokuz Mayıs Üniversitesi, Tıp Fakultesi, 2001
32001
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
22023
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
22023
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
22022
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
12022
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
12017
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
Correction to: Clinical, cytogenomic, and molecular characterization of isodicentric Y‑chromosome and prediction of testicular sperm retrieval outcomes in azoospermic and …
U Abur, S Gunes, N Hekim, OS Akar, E Altundag, R Asci
Journal of Assisted Reproduction and Genetics 39 (11), 2685, 2022
2022
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