Common Genetic Variants

Common Genetic Variants is a type of genetic variant characterized by a minor allele frequency of 5% or greater in a given population, distinguishing it from rare variants by its higher prevalence and typically smaller individual effect size on disease susceptibility within the context of complex traits such as dementia.

6.3K

Publications

473.3K

Citations

51.4K

Authors

6.9K

Institutions

Publications per year

2017–2026

2K

Variants

Common Variants

Authors

51.4K

  1. SJ
    Stephen J. Chanock

    National Cancer Institute, United States

    115 publications · 9.1K citations

    51

    h-index

  2. NG
    Nicholas G. Martin

    QIMR Berghofer Medical Research Institute, Australia

    74 publications · 13.2K citations

    46

    h-index

  3. PD
    Paul D.P. Pharoah

    University of Cambridge, United Kingdom

    80 publications · 6.8K citations

    44

    h-index

  4. LL
    Loı̈c Le Marchand

    University of Hawaiʻi at Mānoa, United States

    71 publications · 6.4K citations

    43

    h-index

  5. DF
    Douglas F. Easton

    University of Cambridge, United Kingdom

    77 publications · 8K citations

    42

    h-index

1–5 of 51.4K

Venues

  1. Nature Genetics

    87 publications · 36.8K citations

    75

    h-index

  2. Human Molecular Genetics

    151 publications · 14.2K citations

    72

    h-index

  3. PLoS ONE

    359 publications · 18.2K citations

    65

    h-index

  4. PLoS Genetics

    91 publications · 15.7K citations

    64

    h-index

  5. Diabetes

    85 publications · 9.5K citations

    56

    h-index

1–5