Wade, N. (2010). A new way to look for diseases’ genetic roots. The New York Times. Available: http://www.nytimes.com/2010/01/26/science/26gene.html [accessed March 29, 2010].

Weir, R.F., and Olick, R.S. (2004). The Stored Tissue Issue: Biomedical Research, Ethics, and Law in the Era of Genomic Medicine. New York: Oxford University Press.

Wellcome Trust. (2003). Sharing Data from Large-Scale Biological Research Projects: A System of Tripartite Responsibility. Report of a meeting organized by the Wellcome Trust and held on January 14–15, Fort Lauderdale, FL. Available: http://www.genome.gov/Pages/Research/WellcomeReport0303.pdf [accessed June 22, 2010].

Westin, A.F. (2007). How the Public Views Privacy and Health Research. Available: http://www.iom.edu/Object.File/Master/48/528/%20Westin%20IOM%20Srvy%20Rept%2011-1107.pdf [accessed November 11, 2008].

Westin, A.F. (2008, November). Americans’ Changing Concerns About Health Privacy. Presentation at the Workshop on Collecting, Storing, Protecting, and Accessing Biological Data Collected in Social Surveys, November 17–18, National Research Council, Washington, DC.

Widom, C.S., and Brzustowicz, L.M. (2006). MAOA and the “cycle of violence”: Childhood abuse and neglect, MAOA genotype, and risk for violent and antisocial behavior. Biological Psychiatry, 60(7), 684–689.

Wolf, L.E., Croughan, M., and Lo, B. (2002). The challenges of IRB review and human subjects protections in practice-based research. Medical Care, 40(6), 521–529.

World Health Organization. (1998). Proposed International Guidelines on Ethical Issues in Medical Genetics and Genetic Services. Report of a WHO meeting on ethical issues in medical genetics. Geneva: Author. Available: http://www.who.int/genomics/publications/en/ethicalguidelines1998.pdf [accessed June 16, 2009].

World Medical Association. (1964). Declaration of Helsinki: Recommendations Guiding Physicians in Biomedical Research Involving Human Subjects. Available: http://www.cirp.org/library/ethics/helsinki/ [accessed June 17, 2009].

Zimmern, R.L., and Kroese, M. (2007). The evaluation of genetic tests. Journal of Public Health, 29(3), 246–250.

The National Academies | 500 Fifth St. N.W. | Washington, D.C. 20001
Copyright © National Academy of Sciences. All rights reserved.
Terms of Use and Privacy Statement