When do genetic researchers have a duty to recontact study participants?

American Journal of Bioethics

Volumn 6, Issue 6, 2006, Pages 26-27

  Wade, Christopher H ^a   Kalfoglou, Andrea L ^a  

^a NATIONAL HUMAN GENOME RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPREHENSION; DECISION MAKING; DUTY TO RECONTACT; ETHICS; GENETICS; HUMAN; INTERPERSONAL COMMUNICATION; NOTE; PERSONNEL; RESEARCH ETHICS; RESEARCH SUBJECT;

COMPREHENSION; DECISION MAKING; DUTY TO RECONTACT; ETHICS, RESEARCH; GENETIC RESEARCH; HUMANS; RESEARCH PERSONNEL; RESEARCH SUBJECTS; TRUTH DISCLOSURE;

EID: 33750611619     PISSN: 15265161     EISSN: 15360075     Source Type: Journal    
DOI: 10.1080/15265160600935746     Document Type: Note

References (4)

1. Holtzman N. A., and M. S. Watson. 1997. Promoting safe and effective genetic testing in the United States: Final report of the task force on genetic testing. Bethesda, MD: National Institutes of Health.
2. Hunter, A. G. W., Sharpe, N., Mullen, M., and W. S. Meschino. 2001. Ethical, legal, and practical concerns about recontacting patients to inform them of new information: the case in medical genetics. American Journal of Medical Genetics 103(4): 265-276.
3. Knoppers, B. M. 2001. Duty to recontact: A legal harbinger? American Journal of Medical Genetics 103(4): 277
4. Ravitsky, V., and B. S. Wilfond. 2006. Disclosing individual genetic results to research participants. American Journal of Bioethics 6(6): 8-17.