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
132
Research Ethics Recommendations for Whole-Genome Research: Consensus Statement
Timothy Caulfield, Amy L. McGuire, Mildred K. Cho et al. · PLoS Biology · 2008 · 241 citations · Full text
Ethical issues in human genomics research in developing countries
Jantina de Vries, Susan Bull, Ogobara K. Doumbo et al. · BMC Medical Ethics · 2011 · 172 citations · Full text
Public Health, Biology, Genetics +17
1–5 of 132
382
11
h-index
6
h-index
University of North Carolina at Chapel Hill, United States
5 publications · 428 citations
5
h-index
3
h-index
3
h-index
1–5 of 382
223

University of Cape Town
Rondebosch, South Africa
11 h-index
24 publications
733 citations
Université de Montréal
Montreal, Canada
8 h-index
14 publications
608 citations
University of Washington
Seattle, United States
6 h-index
7 publications
441 citations
Baylor College of Medicine
Houston, United States
5 h-index
7 publications
602 citations
National Human Genome Research Institute
Bethesda, United States
4 h-index
5 publications
591 citations
University of Oxford
Oxford, United Kingdom
4 h-index
8 publications
1K citations
Case Western Reserve University
Cleveland, United States
4 h-index
4 publications
371 citations

University of the Witwatersrand
Johannesburg, South Africa
4 h-index
11 publications
322 citations
1–8 of 223
Repository · 10 publications · 276 citations
10
h-index
5 publications · 238 citations
5
h-index
GIM · 5 publications · 234 citations
5
h-index
CRO · 4 publications · 141 citations
4
h-index
4 publications · 290 citations
4
h-index
1–5