To the barricades!

American Journal of Bioethics

Volumn 10, Issue 9, 2010, Pages 1-2

  Greely, Henry T ^a  

^a STANFORD LAW SCHOOL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMMERCIAL PHENOMENA; CONFIDENTIALITY; ETHICS; HUMAN; HUMAN EXPERIMENT; LABORATORY DIAGNOSIS; LEGISLATION AND JURISPRUDENCE; PERSONAL AUTONOMY; PERSONNEL; PRIVACY; RESEARCH SUBJECT; STANDARDS; TRUST; UNITED STATES;

COMMERCE; CONFIDENTIALITY; HUMAN EXPERIMENTATION; HUMANS; PERSONAL AUTONOMY; PRIVACY; RESEARCH PERSONNEL; RESEARCH SUBJECTS; SPECIMEN HANDLING; TRUST; UNITED STATES;

EID: 77956415308     PISSN: 15265161     EISSN: 15360075     Source Type: Journal    
DOI: 10.1080/15265161.2010.494229     Document Type: Editorial

References (11)

1. Clayton, E. W., K. K. Steinberg, M. J. Khoury, 1995. Informed consent for genetic research on stored tissue samples. Journal of the American Medical Association 274: 1786-1792.
2. Greely, H. T. 1998. Informed consent, stored tissue samples, and the Human Genome Diversity Project: Protecting the rights of research participants. In Ethical issues in stored tissue samples, ed. R. Weir, 89-110. Ames: University of Iowa Press.
3. Greely, H. T. 1999. Breaking the stalemate:Aprospective regulatory framework for unforeseen research uses of human tissue samples and health information. Wake Forest Law Review 34: 737-766
4. Greely, H. T. 2000. Ethical issues in the Human Genome Diversity Project. In The encyclopedia of ethical, legal, and policy issues in biotechnology, 552-566. New York: JohnWiley & Sons.
5. Greely, H. T. 2001. HumanGenomics Research: New Challenges for Research Ethics, Perspectives in Biology and Medicine 44(2): 221-229 (spring 2001).
6. Greely, H. T. 2007. The uneasy ethical and legal underpinnings of large-scale genomic biobanks. Annual Review of Genomics and Human Genetics 8: 343-364.
7. Greely, H. T. 2010. From Nuremberg to the human genome: The rights of humanresearch participants. In Medicine after theHolocaust: From themaster race to the human genome and beyond, ed. S. Rubenfeld, 185-200. New York: Palgrave.
8. Harmon,A. 2010. Dispute highlights risks in use of genetic material. New York Times April 22: A1.
9. North American Regional Committee, Human Genome Diversity Project. 1997. Proposed model ethical protocol for collecting DNA samples. Houston Law Review 33: 1431-1473.
10. Rothstein, M. 2010. Is deidentification sufficient to protect health privacy in research? American Journal of Bioethics 10(9): 3-11.
11. Skloot, R. 2010. The immortal life of Henrietta Lacks.NewYork:Crown.