Polygenic Risk Scoring

Polygenic Risk Scoring is a computational method in clinical genomics that quantifies an individual’s genetic predisposition to a specific trait or disease by aggregating the effects of numerous single nucleotide polymorphisms across the genome, weighted by their effect sizes derived from genome-wide association studies.

1K

Publications

73.6K

Citations

11.8K

Authors

2.5K

Institutions

Publications per year

2017–2026

907

Variants

Polygenic Risk ScorePrs

Authors

11.8K

  1. JW
    Jordan W. Smoller

    Massachusetts General Hospital, United States

    31 publications · 6.6K citations

    26

    h-index

  2. AM
    Andrew M. McIntosh

    University of Edinburgh, United Kingdom

    32 publications · 3.6K citations

    25

    h-index

  3. OA
    Ole A. Andreassen

    University of Oslo, Norway

    30 publications · 3.7K citations

    23

    h-index

  4. PK
    Peter Kraft

    Harvard University, United States

    25 publications · 6K citations

    21

    h-index

  5. NR
    Naomi R. Wray

    The University of Queensland, Australia

    24 publications · 3.4K citations

    21

    h-index

1–5 of 11.8K

Venues

  1. Translational Psychiatry

    51 publications · 2.6K citations

    32

    h-index

  2. Nature Communications

    37 publications · 5.8K citations

    29

    h-index

  3. The American Journal of Human Genetics

    AJHG · 25 publications · 5K citations

    22

    h-index

  4. Scientific Reports

    25 publications · 958 citations

    18

    h-index

  5. Circulation Genomic and Precision Medicine

    19 publications · 994 citations

    18

    h-index

1–5