Improving the utility of polygenic scores to predict and understand disease risk: a foundational resource.
Improving the utility of polygenic scores to predict and understand disease risk: a foundational resource.
提高多基因评分的实用性以预测和了解疾病风险：基础资源。
批准号：
412608
负责人：
Lambert Samuel A
金额：
$10.93万
依托单位国家：
加拿大
项目类别：
Fellowship Programs
财政年份：
2019
资助国家：
加拿大
项目状态：
已结题
起止时间：
2019-10-01 至 2022-10-01
中文摘要
翻译
如果我们知道谁的风险最大，许多疾病是可以通过早期发现和/或干预来预防的。对于冠状动脉疾病（CAD）等疾病，风险预测是基于年龄和性别以及已知的风险因素（如家族史）。
英文摘要
Many diseases are preventable by early detection and/or intervention if we knew who is most at risk. For diseases like coronary artery disease (CAD), risk predictions are made based on age and sex in combination with known risk factors (e.g. family histor
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