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Pier Mannuccio Mannucci

Researcher at Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

Publications -  817
Citations -  52759

Pier Mannuccio Mannucci is an academic researcher from Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico. The author has contributed to research in topics: Von Willebrand factor & Von Willebrand disease. The author has an hindex of 110, co-authored 777 publications receiving 48578 citations. Previous affiliations of Pier Mannuccio Mannucci include Harvard University & University of Milan.

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Plasma HDL cholesterol and risk of myocardial infarction: A mendelian randomisation study

Benjamin F. Voight, +140 more
TL;DR: In this paper, a Mendelian randomisation analysis was performed to compare the effect of HDL cholesterol, LDL cholesterol, and genetic score on risk of myocardial infarction.
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Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease

Heribert Schunkert, +166 more
- 01 Apr 2011 - 
TL;DR: This paper performed a meta-analysis of 14 genome-wide association studies of coronary artery disease (CAD) comprising 22,233 individuals with CAD (cases) and 64,762 controls of European descent followed by genotyping of top association signals in 56,682 additional individuals.

Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study

Benjamin F. Voight, +125 more
TL;DR: Mendelian randomisation analyses challenge the concept that raising of plasma HDL cholesterol will uniformly translate into reductions in risk of myocardial infarction.
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Genome-wide meta-analyses identify multiple loci associated with smoking behavior

Helena Furberg, +123 more
- 01 May 2010 - 
TL;DR: A meta-analyses of several smoking phenotypes within cohorts of the Tobacco and Genetics Consortium found the strongest association was a synonymous 15q25 SNP in the nicotinic receptor gene CHRNA3, and three loci associated with number of cigarettes smoked per day were identified.
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Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.

Sekar Kathiresan, +118 more
- 08 Feb 2009 - 
TL;DR: SNPs at nine loci were reproducibly associated with myocardial infarction, but tests of common and rare CNVs failed to identify additional associations with my Cardiovascular Infarction risk.