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Sara Lupoli

Researcher at University of Milan

Publications -  37
Citations -  4634

Sara Lupoli is an academic researcher from University of Milan. The author has contributed to research in topics: Genome-wide association study & Population. The author has an hindex of 19, co-authored 35 publications receiving 4203 citations. Previous affiliations of Sara Lupoli include Vita-Salute San Raffaele University.

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Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

Stephen Sawcer, +265 more
- 10 Aug 2011 - 
TL;DR: In this article, a collaborative GWAS involving 9,772 cases of European descent collected by 23 research groups working in 15 different countries, they have replicated almost all of the previously suggested associations and identified at least a further 29 novel susceptibility loci.
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Genome-wide meta-analyses identify three loci associated with primary biliary cirrhosis

Xiangdong Liu, +75 more
- 01 Aug 2010 - 
TL;DR: A genome-wide association screen for primary biliary cirrhosis risk alleles was performed in an Italian cohort, and a combined meta-analysis using a Canadian dataset identified newly associated loci at SPIB.
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Genome-wide meta-analysis of 241,258 adults accounting for smoking behaviour identifies novel loci for obesity traits

Anne E. Justice, +370 more
TL;DR: The results suggest that tobacco smoking may alter the genetic susceptibility to overall adiposity and body fat distribution, and highlight the importance of accounting for environment in genetic analyses.
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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.