| The effects of Ankaferd Blood Stopper on transcription factors in HUVEC and the erythrocyte protein profile. E Yılmaz, Ş Güleç, D Torun, İC Haznedaroğlu, N Akar Turkish Journal of Hematology, 2011 | 53 | 2011 |
| Novel mutations of integrin αIIb and β3 genes in Turkish children with Glanzmann’s thrombasthenia H Tokgoz, D Torun Ozkan, U Caliskan, N Akar Platelets 26 (8), 779-782, 2015 | 11 | 2015 |
| Association of methylenetetrahydrofolate reductase C677T and cystathionine β-synthase polymorphisms in cardiovascular disease in the algerian population B Houcher, Z Houcher, A Touabti, S Begag, D Torun, Y Eğin, N Akar, ... Genetic Testing and Molecular Biomarkers 14 (6), 775-780, 2010 | 7 | 2010 |
| Two new mutations at ERGIC-53 gene in a Turkish family D Torun, E Yılmaz, A Atay, E Kürekçi, N Akar Clinical and Applied Thrombosis/Hemostasis 17 (3), 248-250, 2011 | 4 | 2011 |
| Pathogenic Ala303Val mutation in the PROS1 gene is associated with the pathogenesis of deep vein thrombosis. DFA Bali, T Eroğlu, DT Özkan | 3 | 2022 |
| Identification of novel TUBB1 variants in patients with macrothrombocytopenia ZO Çalişkaner, AA Waheed, MT Öztürk, Y Oymak, UH Tazebay, MN AKAR, ... Turkish Journal of Medical Sciences 51 (2), 490-500, 2021 | 3 | 2021 |
| Analysis of Protein C Inhibitor/ SERPINA5 D Torun Özkan, N Akar Turkish Journal of Clinics and Laboratory 11 (1), 75-79, 2020 | 3 | 2020 |
| Hemoglobin Lansing (Alpha)[HBA2 CD87 (HIS> GLU)(C> A)] in a Turkish Individual Resulting from Another Nucleotide Substitution/Bir Türk Bireyde Baska Bir Nükleotid Substitusyonu … N Akar, D Torun, A Öztürk Turkish Journal of Haematology 31 (3), 317, 2014 | 3 | 2014 |
| Role of ZIP14 (SLC39A14) gene histidine rich regions in neural tube defects D Torun, E Yılmaz, E Akar, N Akar Egyptian Journal of Medical Human Genetics 12 (2), 135-137, 2011 | 3 | 2011 |
| Molecular profiling of TAM tyrosine kinase receptors and ligands in endometrial carcinoma: An in silico-study DF Akin, D Özkan Taiwanese Journal of Obstetrics and Gynecology 62 (2), 311-324, 2023 | 2 | 2023 |
| Genetic analysis of afibrinogenemia and hypofibrinogenemia: novel mutations in the FGB gene in the Turkish population DT Özkan, N Sarper, N Akar Acta Haematologica 143 (6), 529-532, 2020 | 2 | 2020 |
| A novel protein C inhibitor gene mutation in pediatric stroke patients after bone marrow transplantation D Torun, G Deda, M Ertem, Z Uysal, E Yılmaz, N Akar Molecular biology reports 40, 5465-5468, 2013 | 2 | 2013 |
| Identification of circadian-related gene mutation and expression patterns in skin cancer DF AKIN, D Özkan Sağlık Profesyonelleri Araştırma Dergisi 4 (3), 140-152, 2022 | 1 | 2022 |
| A novel 110-bp insertion in a patient with homocysteinuria D Torun, T İleri, K Gündüz, N Akar Turk J Hematol 28, 354-6, 2011 | 1 | 2011 |
| Angiotensinogen (AGT) gene screening and nutrigenetic approaches in patients diagnosed with hypertension S Becer, D ÖZKAN Turkish Journal of Clinics and Laboratory 13 (3), 316-321, 2022 | | 2022 |
| Beta-lactam antibiotic-induced thrombocytopenia: MYH9 & TUBB1 genes NA Didem Özkan, Yasemin Ardıçoğlu Akışın, Dilara Fatma Akın Balı Ann Clin Anal Med 13 (9), 973-977, 2022 | | 2022 |
| Case Report: A novel MYH9 mutation in a beta thalassemia major patient with thrombocytopenia DT Özkan, N Akar Egyptian Journal of Medical Human Genetics 19 (3), 271–272-271–272, 2018 | | 2018 |
| Screening of EPCR gene mutations in children with acute lymphoblastic leukemia DFA Balı, DT Özkan, E Kürekçi, N Akar The Egyptian Journal of Haematology 43 (3), 149-150, 2018 | | 2018 |
| Screening of single nucleotide polymorphism in CD95 (APO-1/FAS) promoter region (G-1377A) in children with acute leukemia DF Akın, DT Özkan, E Kürekçi, N Akar The Egyptian Journal of Haematology 43 (2), 45-48, 2018 | | 2018 |
| Investigation of SLC30A4 and SLC39A14 Zinc Transporter Gene’s Mutations in the Pathogenesis of Neural Tube Defects in Setif, Algeria R Bourouba, D Torun, N Akar Annual Research & Review in Biology 24 (6), 1-7, 2018 | | 2018 |
