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(2009)
Genome-wide association study identifies eight loci associated with blood pressure.
NATURE GENETICS, 41 (6).
666 - 676 (11).
ISSN 1061-4036
https://doi.org/10.1038/ng.361
SGUL Authors: Strachan, David Peter Hadley, David
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| Item Type: |
Article
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| Additional Information: |
PubMed ID: 19430483 |
| Keywords: |
Blood Pressure, Cardiovascular Diseases, Chromosome Mapping, Cytochrome P-450 CYP1A2, DNA-Binding Proteins, Diastole, Europe, European Continental Ancestry Group, Fibroblast Growth Factor 5, Genetic Variation, Genome-Wide Association Study, Humans, India, Methylenetetrahydrofolate Reductase (NADPH2), Open Reading Frames, Phospholipase C delta, Polymorphism, Single Nucleotide, Proteins, Steroid 17-alpha-Hydroxylase, Systole, Science & Technology, Life Sciences & Biomedicine, Genetics & Heredity, METHYLENETETRAHYDROFOLATE REDUCTASE GENE, LOW-RENIN HYPERTENSION, COMMON VARIANTS, CELL-DIFFERENTIATION, BARTTERS-SYNDROME, PUBLIC-HEALTH, RISK, POLYMORPHISM, POPULATION, MUTATIONS |
| SGUL Research Institute / Research Centre: |
Academic Structure > Population Health Research Institute (INPH) |
| Journal or Publication Title: |
NATURE GENETICS |
| ISSN: |
1061-4036 |
| Related URLs: |
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| Dates: |
| Date | Event |
|---|
| 1 June 2009 | Published |
|
| Web of Science ID: |
WOS:000266411700015 |
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| URI: |
https://openaccess.sgul.ac.uk/id/eprint/2491 |
| Publisher's version: |
https://doi.org/10.1038/ng.361 |
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