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Laura Zagato

Researcher at Vita-Salute San Raffaele University

Publications -  74
Citations -  5769

Laura Zagato is an academic researcher from Vita-Salute San Raffaele University. The author has contributed to research in topics: Blood pressure & Medicine. The author has an hindex of 22, co-authored 60 publications receiving 5519 citations.

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Journal ArticleDOI

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Hana Lango Allen, +344 more
- 14 Oct 2010 - 
TL;DR: It is shown that hundreds of genetic variants, in at least 180 loci, influence adult height, a highly heritable and classic polygenic trait, and indicates that GWA studies can identify large numbers of loci that implicate biologically relevant genes and pathways.

Hundreds of variants clustered in genomic loci and biological pathways affect human height

Hana Lango Allen, +289 more
TL;DR: In this paper, the authors show that hundreds of genetic variants, in at least 180 loci, influence adult height, a highly heritable and classic polygenic trait, revealing patterns with important implications for genetic studies of common human diseases and traits.
Journal ArticleDOI

Polymorphisms of α-adducin and salt sensitivity in patients with essential hypertension

TL;DR: The findings of significant linkage of the α-adducin locus to essential hypertension and greater sensitivity to changes in sodium balance among patients with the mutant allele suggest that α- adducin is associated with a salt-sensitive form of essential hypertension.
Journal ArticleDOI

Genomewide Association Study Using a High-Density Single Nucleotide Polymorphism Array and Case-Control Design Identifies a Novel Essential Hypertension Susceptibility Locus in the Promoter Region of Endothelial NO Synthase

Erika Salvi, +58 more
- 01 Feb 2012 - 
TL;DR: Biological evidence links endothelial NO synthase with hypertension, because it is a critical mediator of cardiovascular homeostasis and blood pressure control via vascular tone regulation, and the hypothesis that there may be a causal genetic variation at this locus is supported.