| 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 | 10 | 2022 |
| Propranolol decreases DRD3 and SLC1A2 gene expression in patients with essential tremor N Kandemir, M Gultekin, M Kara, A Bayram, N Tascioglu, M Mirza, ... Universa Medicina 39 (2), 105-112, 2020 | 2 | 2020 |
| Evaluation of Utilizing the Distinct Genes as Predictive Biomarkers in Late-Onset Alzheimer's Disease S Kenanoglu, N Kandemir, H Akalin, N Gokce, MF Gol, M Gultekin, ... Global Medical Genetics 9 (02), 110-117, 2022 | | 2022 |
| Hla-A* 32 Is Associated With Severity Of Covid-19 Patients N KANDEMİR, A BN, C ŞAKAR, H SAAT, A KAPUAĞASI, I ŞENCAN | | 2022 |
| evaluation of mutation distribution in MODY patients NK Hanife Saat, Hande Kulak Abay, Merve Ulak | | 2022 |
| Propranolol significantly reduced DNA polymerase β expression in patients with essential tremor N Kandemir, S Kenanoglu, M Gultekin, N Gokce, H Akalin, N Taşçıoğlu, ... Universa Medicina 40 (3), 207-215, 2021 | | 2021 |
| Assessment Of Patogenic Mutations In Different Cases With Hereditary Ovarian And Endometrial Cancer NK Hanife Saat, Filiz Dişçi | | 2021 |
| A case of cockayne syndrome: a novel homozygous missense variant N Kandemir, NK Karaduman, SB Arslan, K Baysal, M Dündar Journal of Biotechnology 305, S88, 2019 | | 2019 |
| Investigation of the effect of propranolol treatment on HTRA2, DRD3, SLC1A2 genes expression in the patients with essential tremor of the hands N Kandemir, R Bayramov, M Gultekin, M Dundar Journal of Biotechnology 305, S28, 2019 | | 2019 |
| A novel nonsense variant in COL1A1 gene in a family with clinical symptoms of osteogenesis imperfecta N Kandemir, U Kazimli, ÖA Dirican, M Dündar Journal of Biotechnology 305, S88, 2019 | | 2019 |
| Investigation of the Effects of Propranolol on DRD3, SLC1A2 and HTRA2 Gene Expression in Patients with Essential Tremor M Gultekin, N Kandemir, M Mirza, M Kara, N Tascioglu, M Dundar MOVEMENT DISORDERS 34, S576-S576, 2019 | | 2019 |
| Atypical case of Angelman syndrome in infant with 45, X, der (15) t (y; 15)(q12; q10) karyotype. U Kazimli, MC Gunes, OA Dirican, N Kandemir, ME Dogan, C Saatci, ... Erciyes Medical Journal 41 (S1), 53-54, 2019 | | 2019 |
