Crossref Citations
This article has been cited by the following publications. This list is generated based on data provided by
Crossref.
Alper, Joseph S.
and
Beckwith, Jon
1999.
Racism: A Central Problem for the Human Genome Diversity Project.
Politics and the Life Sciences,
Vol. 18,
Issue. 2,
p.
285.
Paul, Diane B.
1999.
What is a genetic test, and why does it matter?.
Endeavour,
Vol. 23,
Issue. 4,
p.
159.
McInerney, Joseph D.
2000.
Encyclopedia of Ethical, Legal and Policy Issues in Biotechnology.
Alper, Joseph S.
and
Beckwith, Jon
2000.
On the philosophical analysis of genetic essentialism.
Science and Engineering Ethics,
Vol. 6,
Issue. 3,
p.
311.
Weiss, Marcia J.
2000.
Health Information Privacy: A Disappearing Concept.
Bulletin of Science, Technology & Society,
Vol. 20,
Issue. 2,
p.
115.
Field, Robert
2001.
Investing in Health: The Social and Economic Benefits of Health Care Innovation.
Vol. 14,
Issue. ,
p.
1.
Kulynych, Jennifer
and
Korn, David
2002.
Use and Disclosure of Health Information in Genetic Research: Weighing the Impact of the New Federal Medical Privacy Rule.
American Journal of Law & Medicine,
Vol. 28,
Issue. 2-3,
p.
309.
Rabino, Isaac
2003.
Genetic Testing and its Implications: Human Genetics Researchers Grapple with Ethical Issues.
Science, Technology, & Human Values,
Vol. 28,
Issue. 3,
p.
365.
Epps, Phyllis Griffin
2003.
Policy Before Practice.
American Journal of PharmacoGenomics,
Vol. 3,
Issue. 6,
p.
405.
Plantinga, Laura
Natowicz, Marvin R.
Kass, Nancy E.
Hull, Sara Chandros
Gostin, Lawrence O.
and
Faden, Ruth R.
2003.
Disclosure, confidentiality, and families: Experiences and attitudes of those with genetic versus nongenetic medical conditions.
American Journal of Medical Genetics Part C: Seminars in Medical Genetics,
Vol. 119C,
Issue. 1,
p.
51.
Taylor, Sandra D.
Otlowski, Margaret F.
Barlow‐Stewart, Kristine K.
Treloar, Susan A.
Stranger, Mark
and
Chenoweth, Kellie
2004.
Investigating genetic discrimination in Australia: opportunities and challenges in the early stages.
New Genetics and Society,
Vol. 23,
Issue. 2,
p.
225.
Birenbaum-Carmeli, D.
2004.
On the prevalence of population groups in the human-genetics research literature.
Politics and the Life Sciences,
Vol. 23,
Issue. 1,
p.
34.
Lemke, Thomas
and
Lohkamp, Christiane
2005.
Biopolitik.
p.
45.
Kakuk, Péter
2006.
Genetic Information in the Age of Genohype.
Medicine, Health Care and Philosophy,
Vol. 9,
Issue. 3,
p.
325.
McGleenan, Tony
2006.
Encyclopedia of Life Sciences.
Lemke, Thomas
2010.
Diskriminierung.
p.
323.
Kakuk, P.
2012.
Encyclopedia of Applied Ethics.
p.
445.
Otlowski, M.
Taylor, S.
and
Bombard, Y.
2012.
Genetic Discrimination: International Perspectives.
Annual Review of Genomics and Human Genetics,
Vol. 13,
Issue. 1,
p.
433.
2012.
Genetic Data and the Law.
p.
180.
Plümecke, Tino
2016.
Genes, symptoms, and the “asymptomatic ill”: toward a broader understanding of genetic discrimination.
New Genetics and Society,
Vol. 35,
Issue. 2,
p.
124.