| Founder von Willebrand factor haplotype associated with type 1 von Willebrand disease LA O'Brien, PD James, M Othman, E Berber, C Cameron, CRP Notley, ... Blood 102 (2), 549-557, 2003 | 122 | 2003 |
| An assessment of the pathogenic significance of the R924Q von Willebrand factor substitution E Berber, PD James, C Hough, D Lillicrap Journal of Thrombosis and Haemostasis 7 (10), 1672-1679, 2009 | 46 | 2009 |
| Influence of a GT repeat element on shear stress responsiveness of the VWF gene promoter C Hough, CL Cameron, CRP Notley, C Brown, L O’brien, AM Keightley, ... Journal of Thrombosis and Haemostasis 6 (7), 1183-1190, 2008 | 42 | 2008 |
| Cell type–specific regulation of von Willebrand factor expression by the E4BP4 transcriptional repressor C Hough, CD Cuthbert, C Notley, C Brown, C Hegadorn, E Berber, ... Blood 105 (4), 1531-1539, 2005 | 34 | 2005 |
| The molecular genetics of von Willebrand disease E Berber Turkish Journal of Haematology 29 (4), 313, 2012 | 29 | 2012 |
| Molecular characterization of FXI deficiency E Berber Clinical and Applied Thrombosis/Hemostasis 17 (1), 27-32, 2011 | 24 | 2011 |
| DNA microarray analysis for the detection of mutations in hemophilia A E Berber, J Leggo, C Brown, N Gallo, H Feilotter, D Lillicrap Journal of Thrombosis and Haemostasis 4 (8), 1756-1762, 2006 | 24 | 2006 |
| Genetic background of von Willebrand disease: history, current state, and future perspectives J Zolkova, J Sokol, T Simurda, L Vadelova, Z Snahnicanova, D Loderer, ... Seminars in thrombosis and hemostasis 46 (04), 484-500, 2020 | 23 | 2020 |
| Von Willebrand disease and Weibel-Palade bodies JW Wang, J Eikenboom Hämostaseologie 30 (03), 150-155, 2010 | 19 | 2010 |
| Characterization of the genetic basis of FXI deficiency in two Turkish patients E Berber, V Rimoldi, S Usluer, S Aksu, Y Pekcelen, SH Cağlayan, S Duga Haemophilia 16 (3), 564-566, 2010 | 14 | 2010 |
| Sequencing of the factor 8(F8) coding regions in 10 Turkish hemophilia A patients reveals three novel pathological mutations, and one rediagnosis of von … E Berber, ID Fidanci, C Un, O EL‐MAARRI, G Aktuglu, A Gurgey, T Celkan, ... Haemophilia 12 (4), 398-400, 2006 | 12 | 2006 |
| Molecular genetic analysis of the F11 gene in 14 Turkish patients with factor XI deficiency: identification of novel and recurrent mutations and their inheritance within families S Colakoglu, T Bayhan, B Tavil, EY Keskin, V Cakir, F Gümrük, M Çetin, ... Blood Transfusion 16 (1), 105, 2018 | 9 | 2018 |
| Exploring the role of miRNAs in the diagnosis of MODY3 OF BALTACI, Ş Çolakoğlu, GG Amuran, N Aydin, M SARĞIN, ... Turkish Journal of Medical Sciences 48 (3), 620-626, 2018 | 8 | 2018 |
| Whole exome sequencing reveals novel candidate gene variants for MODY ÖY Çapan, N Aydın, T Yılmaz, E Berber Clinica Chimica Acta 510, 97-104, 2020 | 7 | 2020 |
| A common VWF exon 28 haplotype in the Turkish population E Berber, F Pehlevan, M Akin, OY Capan, K Kavakli, SH Çaglayan Clinical and Applied Thrombosis/Hemostasis 19 (5), 550-556, 2013 | 7 | 2013 |
| Gene therapy in haemophilia: literature review and regional perspectives for Turkey KAZB 19. Kavaklı K, Antmen B, Okan V, Şahin F, Aytaç S, Balkan C, Berber E ... Therapeutic Advances in Hematology 13, 1-17, 2022 | 5* | 2022 |
| Functional characterisation of the type 1 von Willebrand disease candidate VWF gene variants: p. M771I, p. L881R and p. P1413L E Berber, M Ozbil, C Brown, Z Baslar, SH Caglayan, D Lillicrap Blood Transfusion 15 (6), 548, 2017 | 5 | 2017 |
| Spontaneous thrombosis in a patient with factor XI deficiency homozygous for the p. Cys398Tyr mutation SÇ Kılıç, FD İçağasıoğlu, AS Güven, E Berber Blood Transfusion 12 (3), 446, 2014 | 5 | 2014 |
| R506Q (FV Leiden) and R485K mutations in the factor V gene: incidence in deep venous thrombosis and hemophilia A patients E Berber, K Kavaklı, N Akar, E Berber, SH Çağlayan | 5 | 2003 |
| Higher expression of the novel gene upregulated gene 4 in two acute lymphoblastic leukemia patients with poor prednisolone response Y Oymak, Y Dodurga, A Turedi, Y Yaman, G Ozek, O Carti, BT Gunes, ... Acta Haematologica 128 (2), 73-76, 2012 | 3 | 2012 |
