|Genetic studies of body mass index yield new insights for obesity biology|
KBMIGC Locke AE
Nature 518 (7538), 197-206, 2015
|MTHFR 677C→ T polymorphism and risk of coronary heart disease: a meta-analysis|
M Klerk, P Verhoef, R Clarke, HJ Blom, FJ Kok, EG Schouten
Jama 288 (16), 2023-2031, 2002
|Genome-wide association of early-onset myocardial infarction with common single nucleotide polymorphisms, common copy number variants, and rare copy number variants|
Myocardial Infarction Genetics Consortium
Nature genetics 41 (3), 334, 2009
|Defining the role of common variations in the genoma and biological architecture of adult human height|
R Wood, Andrew, T Esko, J Yang, S Vedantam, H Pers, Tune, ...
Nature Genetics 46 (11), 1173-1186, 2014
|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
|Association of apolipoprotein E genotypes with lipid levels and coronary risk|
AM Bennet, E Di Angelantonio, Z Ye, F Wensley, A Dahlin, A Ahlbom, ...
Jama 298 (11), 1300-1311, 2007
|A survey of adverse events in 11 241 patients with chronic viral hepatitis treated with alfa interferon|
G Fattovich, G Giustina, S Favarato, A Ruol
Journal of hepatology 24 (1), 38-47, 1996
|Hemolytic anemia induced by ribavirin therapy in patients with chronic hepatitis C virus infection: role of membrane oxidative damage|
L De Franceschi, G Fattovich, F Turrini, K Ayi, C Brugnara, F Manzato, ...
Hepatology 31 (4), 997-1004, 2000
|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
|Identification of a novel antibody associated with autoimmune pancreatitis|
L Frulloni, C Lunardi, R Simone, M Dolcino, C Scattolini, M Falconi, ...
New England Journal of Medicine 361 (22), 2135-2142, 2009
|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
|Systemic sclerosis immunoglobulin G autoantibodies bind the human cytomegalovirus late protein UL94 and induce apoptosis in human endothelial cells|
C Lunardi, C Bason, R Navone, E Millo, G Damonte, R Corrocher, ...
Nature medicine 6 (10), 1183, 2000
|Long‐term outcome of hepatitis B e antigen–positive patients with compensated cirrhosis treated with interferon alfa|
G Fattovich, G Giustina, G Realdi, R Corrocher, SW Schalm
Hepatology 26 (5), 1338-1342, 1997
|Methylenetetrahydrofolate reductase C677T mutation, plasma homocysteine, and folate in subjects from northern Italy with or without angiographically documented severe coronary …|
D Girelli, S Friso, E Trabetti, O Olivieri, C Russo, R Pessotto, G Faccini, ...
Blood 91 (11), 4158-4163, 1998
|Effectiveness of interferon alfa on incidence of hepatocellular carcinoma and decompensation in cirrhosis type C|
G Fattovich, G Giustina, F Degos, G Diodati, F Tremolada, F Nevens, ...
Journal of hepatology 27 (1), 201-205, 1997
|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
|In celiac disease, a subset of autoantibodies against transglutaminase binds toll-like receptor 4 and induces activation of monocytes|
G Zanoni, R Navone, C Lunardi, G Tridente, C Bason, S Sivori, R Beri, ...
PLoS medicine 3 (9), e358, 2006
|Delayed clearance of serum HBsAg in compensated cirrhosis B: relation to interferon alpha therapy and disease prognosis|
G Fattovich, G Giustina, J Sanchez-Tapias, C Quero, A Mas, PG Olivotto, ...
The American journal of gastroenterology 93 (6), 896, 1998
|Molecular basis for the recently described hereditary hyperferritinemia-cataract syndrome: a mutation in the iron-responsive element of ferritin L-subunit gene (the" Verona …|
D Girelli, R Corrocher, L Bisceglia, O Olivieri, L De Franceschi, L Zelante, ...
Blood 86 (11), 4050-4053, 1995
|SNPs of the FADS Gene Cluster are Associated with Polyunsaturated Fatty Acids in a Cohort of Patients with Cardiovascular Disease|
G Malerba, L Schaeffer, L Xumerle, N Klopp, E Trabetti, M Biscuola, ...
Lipids 43 (4), 289-299, 2008