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| PMID |
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| TITLE |
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| Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk. |
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| ABSTRACT |
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| DATE PUBLISHED |
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| HISTORY |
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| PUBSTATUS |
PUBSTATUSDATE |
| aheadofprint |
2009/06/24 |
| entrez |
2009/06/26 09:00 |
| pubmed |
2009/06/26 09:00 |
| medline |
2009/12/16 06:00 |
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| AUTHORS |
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| NAME |
COLLECTIVENAME |
LASTNAME |
FORENAME |
INITIALS |
AFFILIATION |
AFFILIATIONINFO |
| Evans DM |
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Department of Social Medicine, MRC Centre for Causal Analyses in Translational Epidemiology, University of Bristol, Bristol, UK. dave.evans@bristol.ac.uk |
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| Visscher PM |
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| Wray NR |
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| INVESTIGATORS |
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| JOURNAL |
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| MEDLINE JOURNAL |
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| MEDLINETA: Hum Mol Genet |
| COUNTRY: England |
| ISSNLINKING: 0964-6906 |
| NLMUNIQUEID: 9208958 |
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| PUBLICATION TYPE |
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| PUBLICATIONTYPE TEXT |
| Journal Article |
| Research Support, Non-U.S. Gov't |
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| COMMENTS AND CORRECTIONS |
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| GRANTS |
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| GRANTID |
AGENCY |
COUNTRY |
| G0600705 |
Medical Research Council |
United Kingdom |
| G0800582 |
Medical Research Council |
United Kingdom |
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| GENERAL NOTE |
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| KEYWORDS |
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| MESH HEADINGS |
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| DESCRIPTORNAME |
QUALIFIERNAME |
| Computational Biology |
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| Genetic Testing |
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| Genome, Human |
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| Genome-Wide Association Study |
methods |
| Humans |
methods |
| Polymorphism, Single Nucleotide |
methods |
| Risk Factors |
methods |
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| SUPPLEMENTARY MESH |
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| GENE SYMBOLS |
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| CHEMICALS |
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| OTHER ID's |
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