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Bernardi Francesco
Bernardi Francesco
Email verificata su unife.it
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Anno
Defining the role of common variation in the genomic and biological architecture of adult human height
AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ...
Nature genetics 46 (11), 1173-1186, 2014
20702014
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants
Heart Attack Risk in Puget Sound. Schwartz Stephen M 20 26 Siscovick David S ...
Nature genetics 41 (3), 334-341, 2009
12882009
Geographic distribution of the 20210 G to A prothrombin variant
FR Rosendaal, CJM Doggen, A Zivelin, VR Arruda, M Aiach, DS Siscovick, ...
Thrombosis and haemostasis 79 (04), 706-708, 1998
10001998
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
5372001
Mutations in GJB6 cause nonsyndromic autosomal dominant deafness at DFNA3 locus
A Grifa, CA Wagner, L D'Ambrosio, S Melchionda, F Bernardi, ...
Nature genetics 23 (1), 16-18, 1999
4961999
Protein C deficiency: a database of mutations, 1995 update
PH Reitsma, F Bernardi, RG Doig, S Gandrille, JS Greengard, H Ireland, ...
Thrombosis and haemostasis 73 (05), 876-889, 1995
4401995
Prospective evaluation of on-clopidogrel platelet reactivity over time in patients treated with percutaneous coronary intervention: relationship with gene polymorphisms and …
G Campo, G Parrinello, P Ferraresi, B Lunghi, M Tebaldi, M Miccoli, ...
Journal of the American College of Cardiology 57 (25), 2474-2483, 2011
4152011
Predictive value of D-dimer test for recurrent venous thromboembolism after anticoagulation withdrawal in subjects with a previous idiopathic event and in carriers of …
G Palareti, C Legnani, B Cosmi, L Valdré, B Lunghi, F Bernardi, ...
Circulation 108 (3), 313-318, 2003
3872003
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
3492000
A factor V genetic component differing from factor V R506Q contributes to the activated protein C resistance phenotype
F Bernardi, EM Faioni, E Castoldi, B Lunghi, G Castaman, E Sacchi, ...
Blood, The Journal of the American Society of Hematology 90 (4), 1552-1557, 1997
3251997
A randomized cross-over study on the effects of levonorgestrel-and desogestrel-containing oral contraceptives on the anticoagulant pathways
G Tans, J Curvers, S Middeldorp, MCLGD Thomassen, JCM Meijers, ...
Thrombosis and haemostasis 84 (07), 15-21, 2000
2822000
Clinical phenotypes and factor VII genotype in congenital factor VII deficiency
G Mariani, FH Herrmann, A Dolce, A Batorova, D Etro, F Peyvandi, K Wulff, ...
Thrombosis and haemostasis 93 (03), 481-487, 2005
2782005
Factor VII deficiency
G Mariani, F Bernardi
Seminars in thrombosis and hemostasis 35 (04), 400-406, 2009
2642009
Factor VII gene polymorphisms contribute about one third of the factor VII level variation in plasma
F Bernardi, G Marchetti, M Pinotti, P Arcieri, C Baroncini, M Papacchini, ...
Arteriosclerosis, thrombosis, and vascular biology 16 (1), 72-76, 1996
2511996
Resistance to activated protein C in nine thrombophilic families: interference in a protein S functional assay
EM Faioni, F Franchi, D Asti, E Sacchi, F Bernardi, PM Mannucci
Thrombosis and haemostasis 70 (12), 1067-1071, 1993
2371993
Rare coagulation disorders
F Peyvandi, PM Mannucci
Thrombosis and haemostasis 82 (10), 1207-1214, 1999
2331999
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
2312003
Detection of new polymorphic markers in the factor V gene: association with factor V levels in plasma
B Lunghi, L Iacoviello, D Gemmati, MG Dilasio, E Castoldi, M Pinotti, ...
Thrombosis and Haemostasis 75 (01), 045-048, 1996
2211996
The heterozygous 20210 G/A prothrombin genotype is associated with early venous thrombosis in inherited thrombophilias and is not increased in frequency in artery disease
P Ferraresi, G Marchetti, C Legnani, E Cavallari, E Castoldi, F Mascoli, ...
Arteriosclerosis, thrombosis, and vascular biology 17 (11), 2418-2422, 1997
2201997
Reevaluation of the incidence of thromboembolic complications in congenital factor XII deficiency
S Zeerleder, M Schloesser, M Redondo, WA Wuillemin, W Engel, ...
Thrombosis and haemostasis 82 (10), 1240-1246, 1999
1861999
Il sistema al momento non può eseguire l'operazione. Riprova più tardi.
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