| Analysis of genetics and risk factors of Alzheimer’s Disease MP Ates, Y Karaman, S Guntekin, MA Ergun Neuroscience 325, 124-131, 2016 | 50 | 2016 |
| Thiopurine methyltransferase polymorphisms and mercaptopurine tolerance in Turkish children with acute lymphoblastic leukemia M Albayrak, U Konyssova, Z Kaya, T Gursel, S Guntekin, EF Percin, ... Cancer chemotherapy and pharmacology 68, 1155-1159, 2011 | 32 | 2011 |
| CFH Y402H and VEGF polymorphisms and anti-VEGF treatment response in exudative age-related macular degeneration B Kepez Yildiz, S Ozdek, MA Ergun, S Ergun, F Yaylacioglu Tuncay, ... Ophthalmic Research 56 (3), 132-138, 2016 | 30 | 2016 |
| Okul öncesi öğretmenliği bölümüne devam eden öğrencilerin yaşam boyu öğrenme eğilimleri S Ergün, S Cömert Özata International Journal of Human Sciences 13 (1), 1851-1861, 2016 | 28 | 2016 |
| Synthesis of novel indole-isoxazole hybrids and evaluation of their cytotoxic activities on hepatocellular carcinoma cell lines M Hawash, DC Kahraman, SG Ergun, R Cetin-Atalay, SN Baytas BMC chemistry 15, 1-14, 2021 | 27 | 2021 |
| Pharmacophore modeling and virtual screening studies to identify novel selective SIRT2 inhibitors G Eren, A Bruno, S Guntekin-Ergun, R Cetin-Atalay, F Ozgencil, Y Ozkan, ... Journal of Molecular Graphics and Modelling 89, 60-73, 2019 | 24 | 2019 |
| Influence of folate-related gene polymorphisms on high-dose methotrexate-related toxicity and prognosis in Turkish children with acute lymphoblastic leukemia B Yazıcıoğlu, Z Kaya, SG Ergun, F Perçin, Ü Koçak, İ Yenicesu, T Gürsel Turkish Journal of Hematology 34 (2), 143, 2017 | 24 | 2017 |
| Design and synthesis of novel substituted indole-acrylamide derivatives and evaluation of their anti-cancer activity as potential tubulin-targeting agents M Hawash, DC Kahraman, A Olgac, SG Ergun, E Hamel, R Cetin-Atalay, ... Journal of Molecular Structure 1254, 132345, 2022 | 22 | 2022 |
| Genetic analysis of CHST6 and TGFBI in Turkish patients with corneal dystrophies: Five novel variations in CHST6 FY Tuncay, GK Kurekci, SG Ergun, OT Pasaoglu, RF Akata, PR Dincer Molecular Vision 22, 1267, 2016 | 21 | 2016 |
| Twenty-four genes are upregulated in patients with hypospadias R Karabulut, Z Turkyilmaz, K Sonmez, G Kumas, SG Ergun, MA Ergun, ... Balkan Journal of Medical Genetics 16 (2), 39-43, 2013 | 19 | 2013 |
| Novel indole-pyrazole hybrids as potential tubulin-targeting agents; Synthesis, antiproliferative evaluation, and molecular modeling studies M Hawash, SG Ergun, DC Kahraman, A Olgac, E Hamel, R Cetin-Atalay, ... Journal of Molecular Structure 1285, 135477, 2023 | 14 | 2023 |
| 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 | 12 | 2022 |
| The evaluation of long-term effects of ionizing radiation through measurement of current sister chromatid exchange (SCE) rates in radiology technologists, compared with … E Tug, G Kayhan, D Kan, S Guntekin, MA Ergun Mutation Research/Genetic Toxicology and Environmental Mutagenesis 757 (1 …, 2013 | 12 | 2013 |
| Evaluation of GenoFlow Thrombophilia Array Test Kit in Its Detection of Mutations in Factor V Leiden (G1691A), Prothrombin G20210A, MTHFR C677T and … E Aytekin, SG Ergun, MA Ergun, FE Percin Genetic testing and molecular biomarkers 18 (11), 717-721, 2014 | 11 | 2014 |
| The correlation of attention deficit hyperactivity disorder with DRD4 gene polymorphism in Turkey E Guney, E Iseri, SG Ergun, EF Percin, MA Ergun, O Yalcin, S Sener International Journal of Human Genetics 13 (3), 145-152, 2013 | 11 | 2013 |
| Identification of Three Novel FBN1 Mutations and Their Phenotypic Relationship of Marfan Syndrome G Kayhan, MA Ergun, SG Ergun, S Kula, FE Percin Genetic Testing and Molecular Biomarkers 22 (8), 474-480, 2018 | 10 | 2018 |
| Association of polymorphisms in APOE and LOXL1 with pseudoexfoliation syndrome and pseudoexfoliation glaucoma in a Turkish population F Yaylacioğlu Tuncay, Z Aktaş, MA Ergün, SG Ergün, M Hasanreisoğlu, ... Ophthalmic Genetics 38 (1), 95-97, 2017 | 10 | 2017 |
| EGF-SNX3-EGFR axis drives tumor progression and metastasis in triple-negative breast cancers E Cicek, A Circir, M Oyken, O Akbulut Caliskan, DN Dioken, ... Oncogene 41 (2), 220-232, 2022 | 9 | 2022 |
| Single-nucleotide polymorphisms in IL23R-IL12RB2 (rs1495965) are highly prevalent in patients with Behcet’s uveitis and vary between populations M Kramer, M Hasanreisoglu, S Weiss, D Kumova, M Schaap-Fogler, ... Ocular Immunology and Inflammation, 2019 | 9 | 2019 |
| LRP5-linked osteoporosis-pseudoglioma syndrome mimicking isolated microphthalmia SG Ergun, GG Akay, MA Ergun, EF Perçin European Journal of Medical Genetics 60 (3), 200-204, 2017 | 8 | 2017 |
Mehmet Ali ErgunProfessor of Medical Genetics在 gazi.edu.tr 的电子邮件经过验证
