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dc.contributor.authorInouye, Michael
dc.contributor.authorRipatti, Samuli
dc.contributor.authorKettunen, Johannes
dc.contributor.authorLyytikäinen, Leo-Pekka
dc.contributor.authorOksala, Niku
dc.contributor.authorLaurila, Pirkka-Pekka
dc.contributor.authorKangas, Antti J.
dc.contributor.authorSoininen, Pasi
dc.contributor.authorSavolainen, Markku J.
dc.contributor.authorViikari, Jorma
dc.contributor.authorKähönen, Mika
dc.contributor.authorPerola, Markus
dc.contributor.authorSalomaa, Veikko
dc.contributor.authorRaitakari, Olli
dc.contributor.authorLehtimäki, Terho
dc.contributor.authorTaskinen, Marja-Riitta
dc.contributor.authorJärvelin, Marjo-Riitta
dc.contributor.authorAla-Korpela, Mika
dc.contributor.authorPalotie, Aarno
dc.contributor.authorde Bakker, Paul I Wen
dc.date.accessioned2013-03-29T20:01:03Z
dc.date.issued2012
dc.identifier.citationInouye, Michael, Samuli Ripatti, Johannes Kettunen, Leo-Pekka Lyytikäinen, Niku Oksala, Pirkka-Pekka Laurila, Antti J. Kangas, et al. 2012. Novel loci for metabolic networks and multi-tissue expression studies reveal genes for atherosclerosis. PLoS Genetics 8(8): e1002907.en_US
dc.identifier.issn1553-7390en_US
dc.identifier.issn1553-7404en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:10482575
dc.description.abstractAssociation testing of multiple correlated phenotypes offers better power than univariate analysis of single traits. We analyzed 6,600 individuals from two population-based cohorts with both genome-wide SNP data and serum metabolomic profiles. From the observed correlation structure of 130 metabolites measured by nuclear magnetic resonance, we identified 11 metabolic networks and performed a multivariate genome-wide association analysis. We identified 34 genomic loci at genome-wide significance, of which 7 are novel. In comparison to univariate tests, multivariate association analysis identified nearly twice as many significant associations in total. Multi-tissue gene expression studies identified variants in our top loci, SERPINA1 and AQP9, as eQTLs and showed that SERPINA1 and AQP9 expression in human blood was associated with metabolites from their corresponding metabolic networks. Finally, liver expression of AQP9 was associated with atherosclerotic lesion area in mice, and in human arterial tissue both SERPINA1 and AQP9 were shown to be upregulated (6.3-fold and 4.6-fold, respectively) in atherosclerotic plaques. Our study illustrates the power of multi-phenotype GWAS and highlights candidate genes for atherosclerosis.en_US
dc.language.isoen_USen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.isversionofdoi:10.1371/journal.pgen.1002907en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3420921/pdf/en_US
dash.licenseLAA
dc.subjectBiologyen_US
dc.subjectGeneticsen_US
dc.subjectGene Expressionen_US
dc.subjectGenome-Wide Association Studiesen_US
dc.subjectSystems Biologyen_US
dc.subjectMedicineen_US
dc.subjectCardiovascularen_US
dc.subjectAtherosclerosisen_US
dc.titleNovel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosisen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalPLoS Geneticsen_US
dash.depositing.authorde Bakker, Paul I Wen
dc.date.available2013-03-29T20:01:03Z
dc.identifier.doi10.1371/journal.pgen.1002907*
dash.authorsorderedfalse
dash.contributor.affiliatedde Bakker, Paul


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