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Identifying individuals at extreme risk of venous thromboembolism using polygenic risk scores
被引:0
|作者:
Chong, Michael
[1
,2
,3
,4
]
Pare, Guillaume
[1
,2
,3
,4
,5
]
机构:
[1] David Braley Cardiac Vasc & Stroke Res Inst, Populat Hlth Res Inst, Hamilton, ON, Canada
[2] David Braley Cardiac Vasc & Stroke Res Inst, Thrombosis & Atherosclerosis Res Inst, Hamilton, ON, Canada
[3] McMaster Univ, Michael G DeGroote Sch Med, Dept Pathol & Mol Med, Hamilton, ON, Canada
[4] McMaster Univ, Dept Biochem & Biomed Sci, Hamilton, ON, Canada
[5] McMaster Univ, Dept Hlth Res Methods Evidence & Impact, Hamilton, ON, Canada
关键词:
D O I:
10.1038/s41588-023-01330-0
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Current risk assessment and treatment strategies for venous thromboembolism (VTE) consider genetic factors only in a limited way. New work shows a more pervasive role of common variants in VTE risk, inspiring genetic predictors that surpass and complement individual clinical risk factors and monogenic thrombophilia testing.
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页码:358 / 360
页数:3
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