Polygenic scores (PGS) are primed for use in personalized risk assessments for common,
complex conditions and population health screening. Although there is growing evidence …

As common low penetrance variants associated with diseases are uncovered, attempts
continue to be made to harness this knowledge for improving healthcare. Polygenic scores …

Polygenic scores (PGS) can be used for risk stratification by quantifying individuals' genetic
predisposition to disease, and many potentially clinically useful applications have been …

Considerable progress continues to be made with regards to the value and use of disease
associated polygenic scores (PGS). PGS aim to capture a person's genetic liability to a …

Polygenic risk scores (PRSs) are heralded as useful tools for risk stratification and
personalized preventive care, but they are clinically useful only if they can be translated into …

Has the Genome Granted Our Wish Yet? Interpretation of polygenic risk scores will someday
become an accepted part of clinical practice—but not just yet. It is, however, time to evaluate …

Polygenic risk scores (PRS) have potential to improve health care by identifying individuals
that have elevated risk for common complex conditions. Use of PRS in clinical practice …

Polygenic risk scores (PRSs), which often aggregate results from genome-wide association
studies, can bridge the gap between initial discovery efforts and clinical applications for the …

The genotyping of millions of human samples has made it possible to evaluate variants
across the human genome for their possible association with risks for numerous diseases …

Polygenic inheritance is a non-Mendelian form of inheritance in which the risk of a trait,
disorder, or disease results from the combined contribution of variants from multiple genes …