Population Genomics Ethics

Population Genomics Ethics is a subfield of Genetic Research Ethics that systematically examines the ethical implications arising from the study of genetic variation within and across populations, particularly with respect to issues of informed consent, data privacy, equitable benefit sharing, and the potential for stigmatization or discrimination.

132

Publications

6K

Citations

382

Authors

223

Institutions

Publications per year

2017–2026

25

Authors

382

  1. JD
    Jantina de Vries

    University of Cape Town, South Africa

    11 publications · 497 citations

    11

    h-index

  2. BM
    Bartha Maria Knoppers

    McGill University, Canada

    6 publications · 372 citations

    6

    h-index

  3. ET
    Eric T. Juengst

    University of North Carolina at Chapel Hill, United States

    5 publications · 428 citations

    5

    h-index

  4. MR
    Michèle Ramsay

    University of the Witwatersrand, South Africa

    3 publications · 96 citations

    3

    h-index

  5. AC
    Anne Cambon‐Thomsen

    Inserm, France

    3 publications · 109 citations

    3

    h-index

1–5 of 382

Venues

  1. PubMed

    Repository · 10 publications · 276 citations

    10

    h-index

  2. Science

    5 publications · 238 citations

    5

    h-index

  3. Genetics in Medicine

    GIM · 5 publications · 234 citations

    5

    h-index

  4. Choice Reviews Online

    CRO · 4 publications · 141 citations

    4

    h-index

  5. Journal of Medical Ethics

    4 publications · 290 citations

    4

    h-index

1–5