Literature DB >> 11700299

Informed consent and other ethical issues in human population genetics.

H T Greely1.   

Abstract

Human population genetics has entered a new era of public interest, of controversy, and of ethical problems. Population genetics raises novel ethical problems because both the individuals and the populations being studied are, in effect, "subjects" of the research. Those populations are collectively subject to possible benefits and harms from the research and have interests, somewhat different from those of the individuals, that must be considered from both ethical and practical standpoints. The chapter first describes the new setting for research in human population genetics. It then examines the most controversial ethical issue in population genetics-whether researchers must obtain the informed consent of both the individual subjects and the group as a collectivity. Other vexing issues, including special problems caused by researchers' commercial interests, confidentiality, control over research uses and materials, and return of information to the population are also considered.

Entities:  

Keywords:  Biomedical and Behavioral Research; Genetics and Reproduction

Mesh:

Year:  2001        PMID: 11700299     DOI: 10.1146/annurev.genet.35.102401.091453

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  7 in total

Review 1.  Ethics and neuropsychiatric genetics: a review of major issues.

Authors:  Steven K Hoge; Paul S Appelbaum
Journal:  Int J Neuropsychopharmacol       Date:  2012-01-25       Impact factor: 5.176

2.  Politics, Culture, and Governance in the Development of Prior Informed Consent in Indigenous Communities.

Authors:  Joshua P Rosenthal
Journal:  Curr Anthropol       Date:  2006-02-01

Review 3.  The Ethics of Consent in a Shifting Genomic Ecosystem.

Authors:  Sandra Soo-Jin Lee
Journal:  Annu Rev Biomed Data Sci       Date:  2021-07-20

Review 4.  Social and scientific motivations to move beyond groups in allele frequencies: The TOPMed experience.

Authors:  Sarah C Nelson; Stephanie M Gogarten; Stephanie M Fullerton; Carmen R Isasi; Braxton D Mitchell; Kari E North; Stephen S Rich; Matthew R G Taylor; Sebastian Zöllner; Tamar Sofer
Journal:  Am J Hum Genet       Date:  2022-09-01       Impact factor: 11.043

5.  Awareness and Acceptable Practices: IRB and Researcher Reflections on the Havasupai Lawsuit.

Authors:  Nanibaa' A Garrison; Mildred K Cho
Journal:  AJOB Prim Res       Date:  2013-10-01

6.  Race and ancestry in biomedical research: exploring the challenges.

Authors:  Timothy Caulfield; Stephanie M Fullerton; Sarah E Ali-Khan; Laura Arbour; Esteban G Burchard; Richard S Cooper; Billie-Jo Hardy; Simrat Harry; Robyn Hyde-Lay; Jonathan Kahn; Rick Kittles; Barbara A Koenig; Sandra Sj Lee; Michael Malinowski; Vardit Ravitsky; Pamela Sankar; Stephen W Scherer; Béatrice Séguin; Darren Shickle; Guilherme Suarez-Kurtz; Abdallah S Daar
Journal:  Genome Med       Date:  2009-01-21       Impact factor: 11.117

7.  Qualitative study of knowledge and attitudes to biobanking among lay persons in Nigeria.

Authors:  Michael A Igbe; Clement A Adebamowo
Journal:  BMC Med Ethics       Date:  2012-10-16       Impact factor: 2.652

  7 in total

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