| An Mll–AF9 fusion gene made by homologous recombination causes acute leukemia in chimeric mice: a method to create fusion oncogenes J Corral, I Lavenir, H Impey, AJ Warren, A Forster, TA Larson, S Bell, ... Cell 85 (6), 853-861, 1996 | 620 | 1996 |
| Prothrombotic genetic risk factors in young survivors of myocardial infarction D Ardissino, PM Mannucci, PA Merlini, F Duca, R Fetiveau, L Tagliabue, ... Blood, The Journal of the American Society of Hematology 94 (1), 46-51, 1999 | 343 | 1999 |
| Polymorphisms of Platelet Membrane Glycoprotein Ib Associated With Arterial Thrombotic Disease R Gonzalez-Conejero, ML Lozano, J Rivera, J Corral, JA Iniesta, ... Blood, The Journal of the American Society of Hematology 92 (8), 2771-2776, 1998 | 289 | 1998 |
| The Mll–AF9 gene fusion in mice controls myeloproliferation and specifies acute myeloid leukaemogenesis CL Dobson, AJ Warren, R Pannell, A Forster, I Lavenir, J Corral, ... The EMBO journal, 1999 | 237 | 1999 |
| Biological assessment of aspirin efficacy on healthy individuals: heterogeneous response or aspirin failure? R Gonzalez-Conejero, J Rivera, J Corral, C Acuna, JA Guerrero, ... Stroke 36 (2), 276-280, 2005 | 233 | 2005 |
| Genome-wide association study identifies a sequence variant within the DAB2IP gene conferring susceptibility to abdominal aortic aneurysm S Gretarsdottir, AF Baas, G Thorleifsson, H Holm, M Den Heijer, ... Nature genetics 42 (8), 692-697, 2010 | 231 | 2010 |
| Apolipoprotein (a) genetic sequence variants associated with systemic atherosclerosis and coronary atherosclerotic burden but not with venous thromboembolism A Helgadottir, S Gretarsdottir, G Thorleifsson, H Holm, RS Patel, ... Journal of the American College of Cardiology 60 (8), 722-729, 2012 | 218 | 2012 |
| Acute leukemias of different lineages have similar MLL gene fusions encoding related chimeric proteins resulting from chromosomal translocation. J Corral, A Forster, S Thompson, F Lampert, Y Kaneko, R Slater, ... Proceedings of the National Academy of Sciences 90 (18), 8538-8542, 1993 | 195 | 1993 |
| The FXIII Val34Leu polymorphism in venous and arterial thromboembolism J Corral, R González-Conejero, JA Iniesta, J Rivera, C Martínez, ... Haematologica 85 (3), 293-297, 2000 | 153 | 2000 |
| Antithrombin Cambridge II (A384S): an underestimated genetic risk factor for venous thrombosis J Corral, D Hernandez-Espinosa, JM Soria, R Gonzalez-Conejero, ... Blood 109 (10), 4258-4263, 2007 | 139 | 2007 |
| The venous thrombosis risk factor 20210 A allele of the prothrombin gene is not a major risk factor for arterial thrombotic disease J Corral, R Gonzalez‐Conejero, ML Lozano, J Rivera, I Heras, V Vicente British journal of haematology 99 (2), 304-307, 1997 | 137 | 1997 |
| Contribution of factor VII genotype to activated FVII levels: differences in genotype frequencies between northern and southern European populations F Bernardi, P Arcieri, RM Bertina, F Chiarotti, J Corral, M Pinotti, H Prydz, ... Arteriosclerosis, thrombosis, and vascular biology 17 (11), 2548-2553, 1997 | 135 | 1997 |
| Role of the 807 C/T polymorphism of the α2 gene in platelet GP Ia collagen receptor expression and function J Corral, R Gonzalez-Conejero, J Rivera, F Ortuno, P Aparicio, V Vicente Thrombosis and haemostasis 81 (06), 951-956, 1999 | 123 | 1999 |
| Identification of miRNAs as potential modulators of tissue factor expression in patients with systemic lupus erythematosus and antiphospholipid syndrome R Teruel, C Perez‐Sanchez, J Corral, MT Herranz, V Perez‐Andreu, ... Journal of Thrombosis and Haemostasis 9 (10), 1985-1992, 2011 | 121 | 2011 |
| Polymorphisms of clotting factors modify the risk for primary intracranial hemorrhage J Corral, JA Iniesta, R González-Conejero, M Villalón, V Vicente Blood, The Journal of the American Society of Hematology 97 (10), 2979-2982, 2001 | 119 | 2001 |
| Pharmacogenetic relevance of CYP4F2 V433M polymorphism on acenocoumarol therapy V Perez-Andreu, V Roldán, AI Antón, N Garcia-Barbera, J Corral, ... Blood, The Journal of the American Society of Hematology 113 (20), 4977-4979, 2009 | 117 | 2009 |
| International clinical guidelines for the management of phosphomannomutase 2‐congenital disorders of glycosylation: diagnosis, treatment and follow up R Altassan, R Péanne, J Jaeken, R Barone, M Bidet, D Borgel, S Brasil, ... Journal of inherited metabolic disease 42 (1), 5-28, 2019 | 108 | 2019 |
| The genetics of antithrombin J Corral, ME de la Morena-Barrio, V Vicente Thrombosis research 169, 23-29, 2018 | 105 | 2018 |
| Thyroglobulin gene point mutation associated with non-endemic simple goitre J Corral, C Martin, R Perez, I Sánchez, R González-Sarmiento, MT Mories, ... The Lancet 341 (8843), 462-464, 1993 | 104 | 1993 |
| The prothrombin gene variant 20210A in venous and arterial thromboembolism V Vicente, R González-Conejero, J Rivera, J Corral Haematologica 84 (4), 356-362, 1999 | 93 | 1999 |
Vicente Vicente GarciaProfesor Universidad de MurciaVerified email at carm.es
