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The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a...

The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2e9ea3ce2acd43b1ab8fe9b44430468c

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

About this item

Full title

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

Publisher

England: Wellcome Trust Limited

Journal title

Wellcome open research, 2018, Vol.3, p.138

Language

English

Formats

Publication information

Publisher

England: Wellcome Trust Limited

More information

Scope and Contents

Contents

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 provid...

Alternative Titles

Full title

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

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_2e9ea3ce2acd43b1ab8fe9b44430468c

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_2e9ea3ce2acd43b1ab8fe9b44430468c

Other Identifiers

ISSN

2398-502X

E-ISSN

2398-502X

DOI

10.12688/wellcomeopenres.14870.1

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