Back to search

Article

Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary disease

2017-11-15

Abstract excerpt

Identification of individuals at increased genetic risk for a complex disorder such as coronary disease can facilitate treatments or enhanced screening strategies. A rare monogenic mutation associated with increased cholesterol is present in ~1:250 carriers and confers an up to 4-fold increase in coronary risk when compared with non-carriers. Although individual common polymorphisms have modest predictive capacity...

Topics

Open a Topic to create a Post that cites this publication.

Identifiers and source

Literature Corpus work
9012828d-5cda-5b2c-bacc-a013a2bbfa9b
DOI
10.1101/218388
Open publication

Related research

Semantic proximity does not establish scientific evidence.

Click a neighbor to travelStep 1 · 12 closest
Interactive article relationship graphSelect a related publication card to move it into the centre and load its closest explainable connections. Solid lines are source-backed structured connections. Dashed lines are semantic discovery signals and are not scientific evidence.
Genome-wide polygenic score to identify a monogenic risk-equivalent for coronary diseaseDOI 10.1101/218388
Select a neighboring publication to make it the new centre.