Polygenic risk score as a possible tool for identifying familial monogenic causes of complex diseases
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical)
Reference40 articles.
1. What is the clinical utility of genetic testing?;Grosse;Genet Med,2006
2. Genomics in public health: perspective from the Office of Public Health Genomics at the Centers for Disease Control and Prevention (CDC);Green;Healthcare (Basel),2015
3. Clinical outcomes of a genomic screening program for actionable genetic conditions;Buchanan;Genet Med,2020
4. Penetrance and outcomes at 1-year following return of actionable variants identified by genome sequencing;Lee;Genet Med,2021
5. Genetic testing and screening recommendations for patients with hereditary breast cancer;Bharucha;Radiographics,2020
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