Common Variant Analysis

Common Variant Analysis is a methodological framework in genetic association studies that identifies and evaluates the contribution of genetic variants with minor allele frequencies typically exceeding 1% to phenotypic traits or disease susceptibility within populations.

226

Publications

17.3K

Citations

3.2K

Authors

940

Institutions

Publications per year

2017–2026

62

Authors

3.2K

  1. LG
    Leif Groop

    Lund University, Sweden

    6 publications · 1.7K citations

    6

    h-index

  2. PK
    Peter Kraft

    Harvard University, United States

    6 publications · 561 citations

    6

    h-index

  3. AV
    Amit V. Khera

    Massachusetts General Hospital, United States

    5 publications · 629 citations

    5

    h-index

  4. EB
    Eric Boerwinkle

    The University of Texas Health Science Center at Houston, United States

    5 publications · 300 citations

    5

    h-index

  5. AM
    Alison M. Dunning

    University of Cambridge, United Kingdom

    5 publications · 764 citations

    5

    h-index

1–5 of 3.2K

Venues

  1. Nature Genetics

    12 publications · 3.9K citations

    12

    h-index

  2. PLoS ONE

    9 publications · 480 citations

    9

    h-index

  3. The American Journal of Human Genetics

    AJHG · 6 publications · 659 citations

    6

    h-index

  4. Nature Communications

    6 publications · 647 citations

    6

    h-index

  5. Human Molecular Genetics

    6 publications · 317 citations

    6

    h-index

1–5