Genome-wide association studies for complex traits: consensus, uncertainty and challenges

dc.contributor.authorMcCarthy, M. I.en
dc.contributor.authorAbecasis, G. R.en
dc.contributor.authorCardon, L. R.en
dc.contributor.authorGoldstein, D. B.en
dc.contributor.authorLittle, J.en
dc.contributor.authorIoannidis, J. P.en
dc.contributor.authorHirschhorn, J. N.en
dc.date.accessioned2015-11-24T19:14:49Z
dc.date.available2015-11-24T19:14:49Z
dc.identifier.issn1471-0064-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/21396
dc.rightsDefault Licence-
dc.subjectAllelesen
dc.subjectAnimalsen
dc.subjectGenetic Diseases, Inborn/*geneticsen
dc.subject*Genetic Predisposition to Diseaseen
dc.subject*Genetic Variationen
dc.subject*Genome, Humanen
dc.subjectHumansen
dc.subject*Quantitative Trait Locien
dc.subject*Quantitative Trait, Heritableen
dc.titleGenome-wide association studies for complex traits: consensus, uncertainty and challengesen
heal.abstractThe past year has witnessed substantial advances in understanding the genetic basis of many common phenotypes of biomedical importance. These advances have been the result of systematic, well-powered, genome-wide surveys exploring the relationships between common sequence variation and disease predisposition. This approach has revealed over 50 disease-susceptibility loci and has provided insights into the allelic architecture of multifactorial traits. At the same time, much has been learned about the successful prosecution of association studies on such a scale. This Review highlights the knowledge gained, defines areas of emerging consensus, and describes the challenges that remain as researchers seek to obtain more complete descriptions of the susceptibility architecture of biomedical traits of interest and to translate the information gathered into improvements in clinical management.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primary10.1038/nrg2344-
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/18398418-
heal.journalNameNat Rev Geneten
heal.journalTypepeer-reviewed-
heal.languageen-
heal.publicationDate2008-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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