| 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 | 23 | 2016 |
| 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 | 14 | 2015 |
| Association and prognostic significance of the functional− 1562C/T polymorphism in the promoter region of MMP-9 in Turkish patients with gastric cancer N Avcı, M Ture, A Deligonul, E Cubukcu, OF Olmez, S Sahinturk, A Topak, ... Pathology & Oncology Research 21, 1243-1247, 2015 | 12 | 2015 |
| Associations analysis of GSTM1, T1 and P1 Ile105Val polymorphisms with carpal tunnel syndrome P Eroğlu, E Erkol İnal, ŞÖ Sağ, Ö Görükmez, A Topak, T Yakut Clinical rheumatology 35, 1245-1251, 2016 | 11 | 2016 |
| 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 | 10 | 2021 |
| Spectrum of EGFR gene mutations and ALK rearrangements in lung cancer patients in Turkey SO Sag, O Gorukmez, M Ture, O Gorukmez, A Deligonul, S Sahinturk, ... Springerplus 5, 1-6, 2016 | 10 | 2016 |
| AFERTILE PATIENT WITH 45/4700 (M0SAICISM S Sahinturk, SO Sag, M Ture, O Gorukmez, A Topak, T Yakut, T Gulten Genetic Counseling 26 (1), 29-34, 2015 | 10 | 2015 |
| Association of GSTM1, GSTT1, GSTP1-ILE105VAL and ACE I/D polymorphisms with ankylosing spondylitis EE Inal, O Görükmez, S Eroğlu, Ö Görükmez, Ö Solak, A Topak, T Yakut Rheumatology international 36, 17-23, 2016 | 7 | 2016 |
| Recurrent c. 776T> C mutation in CHST3 with four other novel mutations and a literature review MB Duz, A Topak Clinical dysmorphology 29 (4), 167-172, 2020 | 6 | 2020 |
| A novel mutation in the FRAS1 gene in a patient with Fraser syndrome SO Sag, O Gorukmez, M Ture, S Sahinturk, A Topak, T Gulten, D Schanze, ... Genetic Counseling 26 (1), 21, 2015 | 6 | 2015 |
| Expanding the clinical spectrum of mitochondrial 3‐hydroxy‐3‐methylglutaryl‐CoA synthase deficiency with Turkish cases harboring novel HMGCS2 gene … M Kılıç, S Dorum, A Topak, MU Yazıcı, FS Ezgu, T Coskun American Journal of Medical Genetics Part A 182 (7), 1608-1614, 2020 | 5 | 2020 |
| Association of the ACE I/D Gene Polymorphisms with JAK2V617F-Positive Polycythemia Vera and Essential Thrombocythemia O Gorukmez, ŞO Sag, Ö Gorukmez, M Ture, A Topak, S Sahinturk, ... Genetic Testing and Molecular Biomarkers 19 (6), 303-308, 2015 | 4 | 2015 |
| Clinical features of pediatric renal glucosuria cases due to SLC5A2 gene variants S Dorum, H Erdoğan, AY Köksoy, A Topak, Ö Görükmez Pediatrics International 64 (1), e14948, 2022 | 3 | 2022 |
| Recently defined epileptic encephalopathy related to WWOX gene mutation: six patients and new mutations C Havali, A Ekici, S Dorum, Ö Görükmez, A Topak Neurological Research 43 (9), 744-750, 2021 | 3 | 2021 |
| A novel mutation in Npr2 gene in a patient with acromesomelic dysplasia, Maroteaux type SO Sag, O Gorukmez, A Topak, M Ture, S Sahinturk, T Gulten, T Yakut Genetic Counseling 26 (2), 219, 2015 | 3 | 2015 |
| NOTCH3 Variants in patients with suspected CADASIL O Gorukmez, O Gorukmez, A Topak, M Seferoglu, AO Sivaci, A Ali, ... Annals of Indian Academy of Neurology, 2023 | 2 | 2023 |
| A case with isochromosome 18p and 2q13 deletion including the BUB1 gene A Ayaz, A Topak, S Yalcintepe, T Celik, K Yararbas, M Eser, OO Yuregir Clinical Dysmorphology 27 (3), 101-104, 2018 | 1 | 2018 |
| Molecular diagnostic results of a nephropathy gene panel in patients with suspected hereditary kidney disease A Topak Laboratory Medicine 55 (1), 13-19, 2024 | | 2024 |
| ATP7B Gene Variant Profile İdentified by NGS in Wilson’s Disease O Gorukmez, T Özgür, O Gorukmez, A Topak Fetal and Pediatric Pathology 42 (6), 891-900, 2023 | | 2023 |
| Next-generation sequencing panel test results in pediatric patients with progressive familial intrahepatic cholestasis: a single-center experience A Topak The European Research Journal, 1-6, 2023 | | 2023 |
