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Sökning: WFRF:(Volpato V)

  • Resultat 1-7 av 7
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  • Ferreira, Mjv, et al. (författare)
  • Poster Session 3 : Tuesday 5 May 2015, 08
  • 2015
  • Ingår i: European Heart Journal Cardiovascular Imaging. - : Oxford University Press (OUP). - 2047-2404 .- 2047-2412. ; 16 Suppl 1
  • Tidskriftsartikel (refereegranskat)
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  • Cornwall, L. A., et al. (författare)
  • Authentication and authorization mechanisms for multi-domain grid environments
  • 2004
  • Ingår i: Journal of Grid Computing. - : Springer Science and Business Media LLC. - 1570-7873 .- 1572-9184. ; 2:4, s. 301-311
  • Tidskriftsartikel (refereegranskat)abstract
    • This article discusses the authentication and the authorization aspects of security in grid environments spanning multiple administrative domains. Achievements in these areas are presented using the EU DataGrid project as an example implementation. It also gives an outlook on future directions of development.
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  • Emmert, David B., et al. (författare)
  • Genetic and Metabolic Determinants of Atrial Fibrillation in a General Population Sample : The CHRIS Study
  • 2021
  • Ingår i: Biomolecules. - : MDPI. - 2218-273X. ; 11:11
  • Tidskriftsartikel (refereegranskat)abstract
    • Atrial fibrillation (AF) is a supraventricular arrhythmia deriving from uncoordinated electrical activation with considerable associated morbidity and mortality. To expand the limited understanding of AF biological mechanisms, we performed two screenings, investigating the genetic and metabolic determinants of AF in the Cooperative Health Research in South Tyrol study. We found 110 AF cases out of 10,509 general population individuals. A genome-wide association scan (GWAS) identified two novel loci (p-value < 5 x 10(-8)) around SNPs rs745582874, next to gene PBX1, and rs768476991, within gene PCCA, with genotype calling confirmed by Sanger sequencing. Risk alleles at both SNPs were enriched in a family detected through familial aggregation analysis of the phenotype, and both rare alleles co-segregated with AF. The metabolic screening of 175 metabolites, in a subset of individuals, revealed a 41% lower concentration of lysophosphatidylcholine lysoPC a C20:3 in AF cases compared to controls (p-adj = 0.005). The genetic findings, combined with previous evidence, indicate that the two identified GWAS loci may be considered novel genetic rare determinants for AF. Considering additionally the association of lysoPC a C20:3 with AF by metabolic screening, our results demonstrate the valuable contribution of the combined genomic and metabolomic approach in studying AF in large-scale population studies.
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  • Resultat 1-7 av 7

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