Literature DB >> 11067631

Involving study populations in the review of genetic research.

R R Sharp1, M W Foster.   

Abstract

Genetic research can present risks to all members of a study population, not just those who choose to participate in research. The authors suggest that community-based reviews of research protocols can help identify and minimize such research-related risks.

Keywords:  Biomedical and Behavioral Research; Genetics and Reproduction

Mesh：

Year:  2000        PMID： 11067631     DOI： 10.1111/j.1748-720x.2000.tb00315.x

Source DB:  PubMed          Journal:  J Law Med Ethics        ISSN： 1073-1105            Impact factor:   1.718


  32 in total

1.  Nondirectiveness and its lay interpretations: the effect of counseling style, ethnicity and culture on attitudes towards genetic counseling among Jewish and Bedouin respondents in Israel.

Authors:  Aviad E Raz; Marcela Atar
Journal:  J Genet Couns       Date:  2003-08       Impact factor: 2.537

Review 2.  Establishing ethical trials for treatment and prevention of AIDS in developing countries.

Authors:  Bernard Lo; Ronald Bayer
Journal:  BMJ       Date:  2003-08-09

Review 3.  Integrating ethics and science in the International HapMap Project.

Authors: 
Journal:  Nat Rev Genet       Date:  2004-06       Impact factor: 53.242

4.  Caught in Collaboration.

Authors:  Deepa S Reddy
Journal:  Collab Anthropol       Date:  2008

5.  Research on environmental health interventions: ethical problems and solutions.

Authors:  David B Resnik; Darryl C Zeldin; Richard R Sharp
Journal:  Account Res       Date:  2005 Apr-Jun       Impact factor: 2.622

6.  Research with groups: group rights, group consent, and collaborative research commentary on "Protecting the Navajo People through tribal regulation of research".

Authors:  Brian Schrag
Journal:  Sci Eng Ethics       Date:  2006-07       Impact factor: 3.525

Review 7.  The routinisation of genomics and genetics: implications for ethical practices.

Authors:  M W Foster; C D M Royal; R R Sharp
Journal:  J Med Ethics       Date:  2006-11       Impact factor: 2.903

8.  The informed consent aftermath of the genetic revolution. An Italian example of implementation.

Authors:  Federica Artizzu
Journal:  Med Health Care Philos       Date:  2007-07-19

9.  GOOD GIFTS FOR THE COMMON GOOD: Blood and Bioethics in the Market of Genetic Research.

Authors:  Deepa S Reddy
Journal:  Cult Anthropol       Date:  2007-08

10.  Ethics in public health research: protecting human subjects: the role of community advisory boards.

Authors:  Sandra Crouse Quinn
Journal:  Am J Public Health       Date:  2004-06       Impact factor: 9.308
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