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TitleCited byYear
Genetic studies of body mass index yield new insights for obesity biology
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
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