| A polymorphism in the VKORC1 gene is associated with an interindividual variability in the dose-anticoagulant effect of warfarin G D'Andrea, RL D'Ambrosio, P Di Perna, M Chetta, R Santacroce, ... Blood 105 (2), 645-649, 2005 | 845 | 2005 |
| Risk factors and clinical presentation of portal vein thrombosis in patients with liver cirrhosis L Amitrano, MA Guardascione, V Brancaccio, M Margaglione, F Manguso, ... Journal of hepatology 40 (5), 736-741, 2004 | 543 | 2004 |
| Combined effect of factor V Leiden and prothrombin 20210A on the risk of venous thromboembolism J Emmerich, FR Rosendaal, M Cattaneo, M Margaglione, V De Stefano, ... Thrombosis and haemostasis 86 (09), 809-816, 2001 | 419 | 2001 |
| Factor V Leiden is associated with repeated and recurrent unexplained fetal losses E Grandone, M Margaglione, D Colaizzo, M d'Addedda, G Cappucci, ... Thrombosis and haemostasis 77 (05), 0822-0824, 1997 | 332 | 1997 |
| Prothrombotic genetic risk factors in young survivors of myocardial infarction D Ardissino, PM Mannucci, PA Merlini, F Duca, R Fetiveau, L Tagliabue, ... Blood 94 (1), 46-51, 1999 | 300 | 1999 |
| Genetic modulation of oral anticoagulation with warfarin M Margaglione, D Colaizzo, G D’Andrea, V Brancaccio, A Ciampa, ... Thrombosis and haemostasis 84 (11), 775-778, 2000 | 297 | 2000 |
| Factor V Leiden, C> T MTHFR polymorphism and genetic susceptibility to preeclampsia E Grandone, M Margaglione, D Colaizzo, G Cappucci, D Paladini, ... Thrombosis and haemostasis 77 (06), 1052-1054, 1997 | 288 | 1997 |
| Inherited coagulation disorders in cirrhotic patients with portal vein thrombosis L Amitrano, V Brancaccio, MA Guardascione, M Margaglione, ... Hepatology 31 (2), 345-348, 2000 | 277 | 2000 |
| Increased risk for venous thrombosis in carriers of the prothrombin G→ A20210 gene variant M Margaglione, V Brancaccio, N Giuliani, G D'Andrea, G Cappucci, ... Annals of Internal Medicine 129 (2), 89-93, 1998 | 275 | 1998 |
| F8 gene mutation type and inhibitor development in patients with severe hemophilia A: systematic review and meta-analysis SC Gouw, HM van den Berg, J Oldenburg, J Astermark, PG de Groot, ... Blood 119 (12), 2922-2934, 2012 | 243 | 2012 |
| Prognostic factors in noncirrhotic patients with splanchnic vein thromboses L Amitrano, MA Guardascione, M Scaglione, L Pezzullo, N Sangiuliano, ... The American journal of gastroenterology 102 (11), 2464, 2007 | 235 | 2007 |
| Genetic susceptibility to pregnancy-related venous thromboembolism: roles of factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations E Grandone, M Margaglione, D Colaizzo, G D’Andrea, G Cappucci, ... American journal of obstetrics and gynecology 179 (5), 1324-1328, 1998 | 234 | 1998 |
| Abnormally high thromboxane biosynthesis in homozygous homocystinuria. Evidence for platelet involvement and probucol-sensitive mechanism. G Di Minno, G Davi, M Margaglione, F Cirillo, E Grandone, G Ciabattoni, ... The Journal of clinical investigation 92 (3), 1400-1406, 1993 | 206 | 1993 |
| Plasma thrombin-activatable fibrinolysis inhibitor antigen concentration and genotype in relation to myocardial infarction in the north and south of Europe I Juhan-Vague, PE Morange, H Aubert, M Henry, MF Aillaud, MC Alessi, ... Arteriosclerosis, thrombosis, and vascular biology 22 (5), 867-873, 2002 | 199 | 2002 |
| No evidence of association between prothrombotic gene polymorphisms and the development of acute myocardial infarction at a young age Atherosclerosis, Thrombosis, and Vascular Biology Italian Study Group Circulation 107 (8), 1117-1122, 2003 | 188 | 2003 |
| Insight into the nature of the CRP–coronary event association using Mendelian randomization JP Casas, T Shah, J Cooper, E Hawe, AD McMahon, D Gaffney, ... International journal of epidemiology 35 (4), 922-931, 2006 | 184 | 2006 |
| The PAI-1 gene locus 4G/5G polymorphism is associated with a family history of coronary artery disease M Margaglione, G Cappucci, D Colaizzo, N Giuliani, G Vecchione, ... Arteriosclerosis, thrombosis, and vascular biology 18 (2), 152-156, 1998 | 183 | 1998 |
| The JAK2 V617F mutation frequently occurs in patients with portal and mesenteric venous thrombosis D Colaizzo, L Amitrano, GL Tiscia, G Scenna, E Grandone, ... Journal of Thrombosis and Haemostasis 5 (1), 55-61, 2007 | 180 | 2007 |
| Low-grade inflammation may play a role in the etiology of the metabolic syndrome in patients with coronary heart disease: the HIFMECH study JS Yudkin, I Juhan-Vague, E Hawe, SE Humphries, G Di Minno, ... Metabolism 53 (7), 852-857, 2004 | 178 | 2004 |
| PAI-1 plasma levels in a general population without clinical evidence of atherosclerosis: relation to environmental and genetic determinants M Margaglione, G Cappucci, M d’Addedda, D Colaizzo, N Giuliani, ... Arteriosclerosis, thrombosis, and vascular biology 18 (4), 562-567, 1998 | 175 | 1998 |
