| Neurologic involvement in atypical hemolytic uremic syndrome and successful treatment with eculizumab K Gulleroglu, K Fidan, VS Hancer, U Bayrakci, E Baskin, O Soylemezoglu Pediatric Nephrology 28, 827-830, 2013 | 75 | 2013 |
| The association between factor XIII Val34Leu polymorphism and early myocardial infarction VS Hancer, R Diz-Kucukkaya, AK Bilge, B Ozben, A Oncul, G Ergen, ... Circulation Journal 70 (3), 239-242, 2006 | 67 | 2006 |
| Eculizumab therapy in a child with hemolytic uremic syndrome and CFI mutation FS Caycı, N Cakar, VS Hancer, N Uncu, B Acar, G Gur Pediatric Nephrology 27, 2327-2331, 2012 | 43 | 2012 |
| Polymorphisms of the angiotensin-converting enzyme and angiotensinogen gene in patients with atrial fibrillation NP Topal, B Ozben, VS Hancer, AM Tanrikulu, R Diz-Kucukkaya, AS Fak, ... Journal of the Renin-Angiotensin-Aldosterone System 12 (4), 549-556, 2011 | 42 | 2011 |
| Pretransplant genetic susceptibility: clinical relevance in transplant-associated thrombotic microangiopathy E Gavriilaki, T Touloumenidou, I Sakellari, I Batsis, D Mallouri, ... Thrombosis and haemostasis 120 (04), 638-646, 2020 | 40 | 2020 |
| MPL W515L/K mutations in chronic myeloproliferative neoplasms TS Akpınar, VS Hançer, M Nalçacı, R Diz-Küçükkaya | 37 | 2013 |
| The clinical significance of JAK2V617F mutation for Philadelphia-negative chronic myeloproliferative neoplasms in patients with splanchnic vein thrombosis I Yonal, B Pinarbası, F Hindilerden, VS Hancer, M Nalcaci, S Kaymakoglu, ... Journal of thrombosis and thrombolysis 34, 388-396, 2012 | 31 | 2012 |
| Dual effects of testosterone in Behcet's disease: implications for a role in disease pathogenesis S Yavuz, T Akdeniz, V Hancer, M Bicakcigil, M Can, G Yanikkaya-Demirel Genes & Immunity 17 (6), 335-341, 2016 | 30 | 2016 |
| Activation-induced cytidine deaminase mRNA levels in chronic lymphocytic leukemia VS Hancer, M Kose, R Diz-Kucukkaya, AS Yavuz, M Aktan Leukemia & lymphoma 52 (1), 79-84, 2011 | 30 | 2011 |
| Coronary artery ectasia is associated with the c. 894G> T (Glu298Asp) polymorphism of the endothelial nitric oxide synthase gene AA Yalcin, IF Akturk, O Celik, M Erturk, VS Hancer, B Yalcin, N Isiksacan, ... The Tohoku Journal of Experimental Medicine 232 (2), 137-144, 2014 | 28 | 2014 |
| The prevalence and clinical significance of inherited thrombophilic risk factors in patients with antiphospholipid syndrome R Diz-Kucukkaya, VS Hancer, B Artim-Esen, Y Pekcelen, M Inanc Journal of thrombosis and thrombolysis 29, 303-309, 2010 | 28 | 2010 |
| The impact of platelet membrane glycoprotein Ib alpha and Ia/IIa polymorphisms on the risk of thrombosis in the antiphospholipid syndrome I Yonal, F Hindilerden, VS Hancer, B Artim-Esen, A Daglar, B Akadam, ... Thrombosis research 129 (4), 486-491, 2012 | 25 | 2012 |
| Glycoprotein Ib-alpha Kozak polymorphism in ischemic stroke FI Esen, VS Hancer, RD Küçükkaya, N Yeşilot, O Coban, S Bahar, ... Neurological Research 34 (1), 68-71, 2012 | 24 | 2012 |
| Factor XIII Val34Leu polymorphism does not contribute to the prevention of thrombotic complications in patients with antiphospholipid syndrome R Diz-Kucukkaya, VS Hancer, M Inanc, M Nalcaci, Y Pekcelen Lupus 13 (1), 32-35, 2004 | 22 | 2004 |
| Overexpression of Fc mu receptor (FCMR, TOSO) gene in chronic lymphocytic leukemia patients VS Hancer, R Diz-Kucukkaya, M Aktan Medical oncology 29, 1068-1072, 2012 | 19 | 2012 |
| The association of P-selectin glycoprotein ligand-1 VNTR polymorphisms with coronary stent restenosis B Ozben, R Diz-Kucukkaya, AK Bilge, VS Hancer, A Oncul Journal of thrombosis and thrombolysis 23, 181-187, 2007 | 17 | 2007 |
| Comparison of KRAS Mutation Tests in Colorectal Cancer Patients VS Hancer, M Buyukdogan, I Türkmen, N Bassullu, T Altug, ... Genetic Testing and Molecular Biomarkers 15 (11), 831-834, 2011 | 14 | 2011 |
| Impact of genetic polymorphisms on platelet function and aspirin resistance B Pamukcu, H Oflaz, I Onur, V Hancer, S Yavuz, Y Nisanci Blood coagulation & fibrinolysis 21 (1), 53-56, 2010 | 13 | 2010 |
| Prevalence of human papilloma virus types in Turkish and Albanian women VS Hancer, M Buyukdogan, I Bylykbashi, B Oksuz, M Acar Journal of cytology 35 (4), 252-254, 2018 | 12 | 2018 |
| A novel ATP6V0A2 mutation causing recessive cutis laxa with unusual manifestations of bleeding diathesis and defective wound healing İ Karacan, RD Küçükkaya, FN Karakuş, S Solakoğlu, A Tolun, VS Hançer, ... Turkish Journal of Hematology 36 (1), 29, 2019 | 11 | 2019 |
