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dc.contributor.authorBreeyear, JH
dc.contributor.authorMautz, BS
dc.contributor.authorKeaton, JM
dc.contributor.authorHellwege, JN
dc.contributor.authorTorstenson, ES
dc.contributor.authorLiang, J
dc.contributor.authorBray, MJ
dc.contributor.authorGiri, A
dc.contributor.authorWarren, HR
dc.contributor.authorMunroe, PB
dc.contributor.authorVelez Edwards, DR
dc.contributor.authorZhu, X
dc.contributor.authorLi, C
dc.contributor.authorEdwards, TL
dc.date.accessioned2024-04-17T08:01:59Z
dc.date.available2024-03-22
dc.date.available2024-04-17T08:01:59Z
dc.date.issued2024-04-12
dc.identifier.citationJoseph H. Breeyear, Brian S. Mautz, Jacob M. Keaton, Jacklyn N. Hellwege, Eric S. Torstenson, Jingjing Liang, Michael J. Bray, Ayush Giri, Helen R. Warren, Patricia B. Munroe, Digna R. Velez Edwards, Xiaofeng Zhu, Chun Li, Todd L. Edwards, A new test for trait mean and variance detects unreported loci for blood-pressure variation, The American Journal of Human Genetics, 2024, , ISSN 0002-9297, https://doi.org/10.1016/j.ajhg.2024.03.014. (https://www.sciencedirect.com/science/article/pii/S0002929724000879) Abstract: Summary Variability in quantitative traits has clinical, ecological, and evolutionary significance. Most genetic variants identified for complex quantitative traits have only a detectable effect on the mean of trait. We have developed the mean-variance test (MVtest) to simultaneously model the mean and log-variance of a quantitative trait as functions of genotypes and covariates by using estimating equations. The advantages of MVtest include the facts that it can detect effect modification, that multiple testing can follow conventional thresholds, that it is robust to non-normal outcomes, and that association statistics can be meta-analyzed. In simulations, we show control of type I error of MVtest over several alternatives. We identified 51 and 37 previously unreported associations for effects on blood-pressure variance and mean, respectively, in the UK Biobank. Transcriptome-wide association studies revealed 633 significant unique gene associations with blood-pressure mean variance. MVtest is broadly applicable to studies of complex quantitative traits and provides an important opportunity to detect novel loci. Keywords: variability; genetic association; interaction; canalization; estimating equations; blood pressureen_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/96181
dc.description.abstractVariability in quantitative traits has clinical, ecological, and evolutionary significance. Most genetic variants identified for complex quantitative traits have only a detectable effect on the mean of trait. We have developed the mean-variance test (MVtest) to simultaneously model the mean and log-variance of a quantitative trait as functions of genotypes and covariates by using estimating equations. The advantages of MVtest include the facts that it can detect effect modification, that multiple testing can follow conventional thresholds, that it is robust to non-normal outcomes, and that association statistics can be meta-analyzed. In simulations, we show control of type I error of MVtest over several alternatives. We identified 51 and 37 previously unreported associations for effects on blood-pressure variance and mean, respectively, in the UK Biobank. Transcriptome-wide association studies revealed 633 significant unique gene associations with blood-pressure mean variance. MVtest is broadly applicable to studies of complex quantitative traits and provides an important opportunity to detect novel loci.en_US
dc.languageeng
dc.publisherElsevieren_US
dc.relation.ispartofAm J Hum Genet
dc.rights© 2024. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectblood pressureen_US
dc.subjectcanalizationen_US
dc.subjectestimating equationsen_US
dc.subjectgenetic associationen_US
dc.subjectinteractionen_US
dc.subjectvariabilityen_US
dc.titleA new test for trait mean and variance detects unreported loci for blood-pressure variation.en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.ajhg.2024.03.014
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38614075en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2024-03-22
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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