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dc.contributor.authorNaylor, Melissa G.
dc.contributor.authorWeiss, Scott Tillman
dc.contributor.authorLange, Christoph
dc.date.accessioned2014-02-21T14:59:54Z
dc.date.issued2009
dc.identifier.citationNaylor, Melissa G., Scott Tillman Weiss, Christoph Lange. 2009. Recommendations for using standardised phenotypes in genetic association studies. Human Genomics 3(4): 308-319.en_US
dc.identifier.issn1473-9542en_US
dc.identifier.issn1479-7364en_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:11726284
dc.description.abstractGenetic association studies of complex traits often rely on standardised quantitative phenotypes, such as percentage of predicted forced expiratory volume and body mass index to measure an underlying trait of interest (eg lung function, obesity). These phenotypes are appealing because they provide an easy mechanism for comparing subjects, although such standardisations may not be the best way to control for confounders and other covariates. We recommend adjusting raw or standardised phenotypes within the study population via regression. We illustrate through simulation that optimal power in both population- and family-based association tests is attained by using the residuals from within-study adjustment as the complex trait phenotype. An application of family-based association analysis of forced expiratory volume in one second, and obesity in the Childhood Asthma Management Program data, illustrates that power is maintained or increased when adjusted phenotype residuals are used instead of typical standardised quantitative phenotypes.en_US
dc.language.isoen_USen_US
dc.publisherBioMed Centralen_US
dc.relation.isversionofdoi:10.1186/1479-7364-3-4-308en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pubmed/19706362en_US
dash.licenseLAA
dc.subjectbody mass indexen_US
dc.subjectconfounding factorsen_US
dc.subjectcovariate adjustmenten_US
dc.subjectforced expiratory volumeen_US
dc.subjectheritable quantitative traitsen_US
dc.titleRecommendations for using standardised phenotypes in genetic association studiesen_US
dc.typeJournal Articleen_US
dc.description.versionVersion of Recorden_US
dc.relation.journalHuman Genomicsen_US
dash.depositing.authorLange, Christoph
dc.date.available2014-02-21T14:59:54Z
dc.identifier.doi10.1186/1479-7364-3-4-308*
dash.contributor.affiliatedLange, Christoph
dash.contributor.affiliatedWeiss, Scott


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