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The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practice

2018-10-31

Abstract excerpt

Initial genomewide association studies were exceptional owing to an ability to yield novel and reliable evidence for heritable contributions to complex disease and phenotype. However the top results alone were certainly not responsible for a wave of new predictive tools. Despite this, even studies small by contemporary standards were able to provide estimates of the relative contribution of all recorded genetic va...

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Literature Corpus work
2e40d9eb-0bbd-5a8e-bc48-9030e57ea1f1
DOI
10.12688/wellcomeopenres.14870.1
Open publication

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The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practiceDOI 10.12688/wellcomeopenres.14870.1
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