The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practice [version 1; referees: 2 approved, 1 approved with reservations]
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 s...
| 出版年: | Wellcome Open Research |
|---|---|
| 主要な著者: | , |
| フォーマット: | 論文 |
| 言語: | 英語 |
| 出版事項: |
Wellcome
2018-10-01
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| オンライン･アクセス: | https://wellcomeopenresearch.org/articles/3-138/v1 |