| Evaluation of the JAK2-V617F gene mutation in Turkish patients with essential thrombocythemia and polycythemia vera M Karkucak, T Yakut, V Ozkocaman, F Ozkalemkas, R Ali, M Bayram, ... Molecular biology reports 39, 8663-8667, 2012 | 28 | 2012 |
| Glutathione S-transferase T1, M1 and P1 genetic polymorphisms and susceptibility to colorectal cancer in Turkey O Gorukmez, T Yakut, O Gorukmez, A Topak, S Sahinturk, O Kanat Asian Pacific Journal of Cancer Prevention 17 (8), 3855-3859, 2016 | 26 | 2016 |
| Lack of association of ACE gene I/D polymorphism with obstructive sleep apnea syndrome in Turkish patients T Yakut, M Karkucak, A Ursavaş, T Gülten, B Burgazlıoğlu, O Görükmez, ... Funpec-Editora, 2010 | 26 | 2010 |
| Distribution of KRAS and BRAF mutations in metastatic colorectal cancers in Turkish Patients O Gorukmez, T Yakut, O Gorukmez, M Karkucak, O Kanat Asian Pacific Journal of Cancer Prevention 17 (3), 1175-1179, 2016 | 18 | 2016 |
| The role of genetic mutations in intrahepatic cholestasis of pregnancy GA Aydın, G Özgen, O Görükmez Taiwanese Journal of Obstetrics and Gynecology 59 (5), 706-710, 2020 | 17 | 2020 |
| Novel MECR mutation in childhood-onset dystonia, optic atrophy, and basal ganglia signal abnormalities O Gorukmez, O Gorukmez, C Havalı Neuropediatrics 50 (05), 336-337, 2019 | 16 | 2019 |
| The influence of polymorphisms of interleukin-17A and-17F genes on susceptibility and activity of rheumatoid arthritis E Erkol İnal, O Görükmez, Ü Dündar, Ö Görükmez, M Yener, ... Genetic testing and molecular biomarkers 19 (8), 461-464, 2015 | 15 | 2015 |
| MMP2 gene-735 C/T and MMP9 gene-1562 C/T polymorphisms in JAK2V617F positive myeloproliferative disorders SO Sag, O Gorukmez, M Ture, O Gorukmez, A Topak, S Sahinturk, ... Asian Pacific Journal of Cancer Prevention 16 (2), 443-449, 2015 | 15 | 2015 |
| Newly defined peroxisomal disease with novel ACBD5 mutation O Gorukmez, C Havalı, O Gorukmez, S Dorum Journal of Pediatric Endocrinology and Metabolism 35 (1), 11-18, 2022 | 14 | 2022 |
| Patients with cerebrotendinous xanthomatosis diagnosed with diverse multisystem involvement PT Kısa, GK Yildirim, BO Hismi, S Dorum, OY Kusbeci, A Topak, F Baydan, ... Metabolic brain disease 36 (6), 1201-1211, 2021 | 14 | 2021 |
| A Very Rare Congenital Dyserythropoietic Anemia Variant—Type IV in a Patient With a Novel Mutation in the KLF1 Gene: A Case Report and Review of the Literature T Belgemen-Ozer, O Gorukmez Journal of Pediatric Hematology/Oncology 42 (6), e536-e540, 2020 | 14 | 2020 |
| Effect of cycline D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinoma S Cander, E Ertürk, M Karkucak, ÖÖ Gül, O Görükmez, T Yakut, OK Ünal, ... Gene 509 (1), 158-163, 2012 | 12 | 2012 |
| The relationship between CRP gene polymorphism (rs2794521, rs3091244), ASDAS-CRP and ASDAS-ESR in ankylosing spondylitis M Kasapoğlu Aksoy, L Altan, O Görükmez, A Güner, K Ayar Modern Rheumatology 30 (4), 715-720, 2020 | 11 | 2020 |
| Delayed puberty and gonadal failure in patients with HAX1 mutation S Cekic, H Saglam, O Gorukmez, T Yakut, O Tarim, SS Kilic Journal of Clinical Immunology 37, 524-528, 2017 | 11 | 2017 |
| Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with familial Mediterranean fever MF Öksuz, M Karkucak, O Görukmez, G Ocakoğlu, A Yıldız, M Ture, ... Revista Brasileira de Reumatologia 57 (6), 501-506, 2017 | 11 | 2017 |
| A fertile patient with 45X/47XXX mosaicism S Sahinturk, SO Sag, M Ture, O Gorukmez, A Topak, T Yakut, T Gulten Genetic Counseling 26 (1), 29, 2015 | 10 | 2015 |
| Two patients with glutaric aciduria type 3: a novel mutation and brain magnetic resonance imaging findings S Dorum, C Havalı, Ö Görükmez, O Görükmez The Turkish Journal of Pediatrics 62 (4), 657-662, 2020 | 9 | 2020 |
| Qualitative and Quantitative Evaluation of the BCR-ABL Fusion Gene in Chronic Myelogenous Leukemia by Flourescence In Situ Hybridization and Molecular … S Ozemri Sag, T Yakut, O Gorukmez, O Gorukmez, M Ture, M Karkucak, ... Genetic testing and molecular biomarkers 19 (10), 584-588, 2015 | 9 | 2015 |
| A Novel Nonsense FMN2 Mutation in Nonsyndromic Autosomal Recessive Intellectual Disability Syndrome O Gorukmez, O Gorukmez, A Ekici Fetal and Pediatric Pathology 40 (6), 702-706, 2021 | 8 | 2021 |
| An investigation of the gene Val158Met polymorphism in patients admitted to the emergency department because of synthetic cannabinoid use Y Nennicioglu, H Kaya, S Eraybar, S Atmaca, O Gorukmez, E Armagan Balkan Journal of Medical Genetics 23 (1), 63-68, 2020 | 8 | 2020 |
