Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
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dc.contributor.author | Uitterlinden, AG | en_US |
dc.contributor.author | Wareham, NJ | en_US |
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dc.contributor.author | Larson, MG | en_US |
dc.contributor.author | Jarvelin, MR | en_US |
dc.contributor.author | Psaty, BM | en_US |
dc.contributor.author | Abecasis, GR | en_US |
dc.contributor.author | Chakravarti, A | en_US |
dc.contributor.author | Elliott, P | en_US |
dc.contributor.author | van Duijn, CM | en_US |
dc.contributor.author | Newton-Cheh, C | en_US |
dc.contributor.author | Levy, D | en_US |
dc.contributor.author | Caulfield, MJ | en_US |
dc.contributor.author | Johnson, T | en_US |
dc.contributor.author | Int Consortium Blood Pressure Geno | en_US |
dc.contributor.author | CARDIoGRAM Consortium | en_US |
dc.contributor.author | CKDGen Consortium | en_US |
dc.contributor.author | KidneyGen Consortium | en_US |
dc.contributor.author | EchoGen Consortium | en_US |
dc.contributor.author | CHARGE-HF Consortium | en_US |
dc.date.accessioned | 2016-08-03T13:53:56Z | |
dc.date.available | 2011-07-28 | en_US |
dc.date.issued | 2011-10-06 | en_US |
dc.date.submitted | 2016-06-03T10:00:59.323Z | |
dc.identifier.issn | 0028-0836 | en_US |
dc.identifier.other | 10.1038/nature10405 | |
dc.identifier.uri | http://qmro.qmul.ac.uk/xmlui/handle/123456789/13815 | |
dc.description.sponsorship | A number of the participating studies and authors are members of the CHARGE and Global BPgen consortia. Many funding mechanisms by NIH/NHLBI, European and private funding agencies contributed to this work and a full list is provided in section 21 of the Supplementary Materials. | en_US |
dc.format.extent | 103 - 109 | en_US |
dc.language.iso | en | en_US |
dc.relation.ispartof | NATURE | en_US |
dc.subject | GENOME-WIDE ASSOCIATION | en_US |
dc.subject | COMMON VARIANTS | en_US |
dc.subject | HYPERTENSION | en_US |
dc.subject | METAANALYSIS | en_US |
dc.subject | LOCI | en_US |
dc.subject | POPULATION | en_US |
dc.subject | RELEVANCE | en_US |
dc.subject | RECEPTOR | en_US |
dc.subject | CLONING | en_US |
dc.subject | HEALTH | en_US |
dc.title | Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | en_US |
dc.type | Article | |
dc.rights.holder | 2011 Macmillan Publishers Limited, part of Springer Nature. All rights reserved | |
dc.identifier.doi | 10.1038/nature10405 | en_US |
pubs.issue | 7367 | en_US |
pubs.notes | Not known | en_US |
pubs.volume | 478 | en_US |