| Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ... The Lancet 380 (9841), 572-580, 2012 | 1942 | 2012 |
| Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ... Nature genetics 43 (4), 333-338, 2011 | 1750 | 2011 |
| Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants Myocardial Infarction Genetics Consortium Nature genetics 41 (3), 334, 2009 | 1121 | 2009 |
| Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis A Roetto, G Papanikolaou, M Politou, F Alberti, D Girelli, J Christakis, ... Nature genetics 33 (1), 21-22, 2003 | 1046 | 2003 |
| A common mutation in the 5, 10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status S Friso, SW Choi, D Girelli, JB Mason, GG Dolnikowski, PJ Bagley, ... Proceedings of the National Academy of Sciences 99 (8), 5606-5611, 2002 | 1035 | 2002 |
| Immunoassay for human serum hepcidin T Ganz, G Olbina, D Girelli, E Nemeth, M Westerman Blood, The Journal of the American Society of Hematology 112 (10), 4292-4297, 2008 | 804 | 2008 |
| Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction DF Gudbjartsson, US Bjornsdottir, E Halapi, A Helgadottir, P Sulem, ... Nature genetics 41 (3), 342-347, 2009 | 763 | 2009 |
| Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease TG and HDL Working Group of the Exome Sequencing Project, National Heart ... New England Journal of Medicine 371 (1), 22-31, 2014 | 565 | 2014 |
| Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction R Do, NO Stitziel, HH Won, AB Jørgensen, S Duga, PA Merlini, A Kiezun, ... Nature 518 (7537), 102-106, 2015 | 545 | 2015 |
| Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two … MP Reilly, M Li, J He, JF Ferguson, IM Stylianou, NN Mehta, MS Burnett, ... The Lancet 377 (9763), 383-392, 2011 | 472 | 2011 |
| Anti-oxidant status and lipid peroxidation in patients with essential hypertension C Russo, O Olivieri, D Girelli, G Faccini, ML Zenari, S Lombardi, ... Journal of hypertension 16 (9), 1267-1271, 1998 | 425 | 1998 |
| Mutation analysis of the HLA-H gene in Italian hemochromatosis patients. M Carella, L D'ambrosio, A Totaro, A Grifa, MA Valentino, A Piperno, ... American journal of human genetics 60 (4), 828, 1997 | 423 | 1997 |
| Polymorphisms in the factor VII gene and the risk of myocardial infarction in patients with coronary artery disease D Girelli, C Russo, P Ferraresi, O Olivieri, M Pinotti, S Friso, F Manzato, ... New England journal of medicine 343 (11), 774-780, 2000 | 329 | 2000 |
| FADS genotypes and desaturase activity estimated by the ratio of arachidonic acid to linoleic acid are associated with inflammation and coronary artery disease N Martinelli, D Girelli, G Malerba, P Guarini, T Illig, E Trabetti, M Sandri, ... The American journal of clinical nutrition 88 (4), 941-949, 2008 | 299 | 2008 |
| Distribution and medical impact of loss-of-function variants in the Finnish founder population ET Lim, P Würtz, AS Havulinna, P Palta, T Tukiainen, K Rehnström, ... PLoS Genet 10 (7), e1004494, 2014 | 297 | 2014 |
| Differential regulation of iron homeostasis during human macrophage polarized activation S Recalcati, M Locati, A Marini, P Santambrogio, F Zaninotto, M De Pizzol, ... European journal of immunology 40 (3), 824-835, 2010 | 295 | 2010 |
| Association of low-frequency and rare coding-sequence variants with blood lipids and coronary heart disease in 56,000 whites and blacks GM Peloso, PL Auer, JC Bis, A Voorman, AC Morrison, NO Stitziel, ... The American Journal of Human Genetics 94 (2), 223-232, 2014 | 286 | 2014 |
| Heterogeneity of hemochromatosis in Italy A Piperno, M Sampietro, A Pietrangelo, C Arosio, L Lupica, G Montosi, ... Gastroenterology 114 (5), 996-1002, 1998 | 275 | 1998 |
| Hepcidin in the diagnosis of iron disorders D Girelli, E Nemeth, DW Swinkels Blood 127 (23), 2809-2813, 2016 | 273 | 2016 |
| Methylenetetrahydrofolate Reductase C677T Mutation, Plasma Homocysteine, and Folate in Subjects From Northern Italy With or Without Angiographically … D Girelli, S Friso, E Trabetti, O Olivieri, C Russo, R Pessotto, G Faccini, ... Blood, The Journal of the American Society of Hematology 91 (11), 4158-4163, 1998 | 273 | 1998 |
Gaetano CairoProfessore di Patologia generale, Università di MilanoVerified email at unimi.it
