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Improved detection of common variants in coronary artery disease and blood pressure using a pleiotropy cFDR method
Plenty of genome-wide association studies (GWASs) have identified numerous single nucleotide polymorphisms (SNPs) for coronary artery disease (CAD) and blood pressure (BP). However, these SNPs only explain a small proportion of the heritability of two traits/diseases. Although high BP is a major ris...
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| 出版年: | Sci Rep |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Nature Publishing Group UK
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6637206/ https://ncbi.nlm.nih.gov/pubmed/31316127 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-019-46808-2 |
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