Genetic Privacy: Might There Be a Moral Duty to Share One's Genetic Information?

REFERENCES

• de Melo-Martin , I. 2008 . A duty to participate in research: Does social context matter? . The American Journal of Bioethics , 8 ( 10 ) : 28 – 36 .
   PubMed Web of Science ®Google Scholar
• Harris , J. 2005 . Scientific research is a moral duty . Journal of Medical Ethics , 31 : 242 – 248 .
   PubMed Web of Science ®Google Scholar
• Lee , S. S. and Crawley , L. 2009 . Research 2.0: Social networking and DTC genomics . American Journal of Bioethics , 9 ( 6–7 ) : 35 – 44 .
   PubMed Web of Science ®Google Scholar
• Malm , H. 2000 . Bad Samaritan laws: Harm, hype or help . Law and Philosophy , 19 ( 6 ) : 707 – 750 .
   Web of Science ®Google Scholar
• Resnik , D. 2009 . Direct-to-consumer genomics, social networking, and confidentiality . American Journal of Bioethics , 9 ( 6–7 ) : 45 – 46 .
   PubMed Web of Science ®Google Scholar
• Rhodes , R. Rethinking research ethics . American Journal of Bioethics , 5 ( 1 ) 7 – 28 .
   PubMedGoogle Scholar
• Shapshay , S. and Pimple , K. D. 2007 . Participation is biomedical research is an imperfect moral duty: A response to John Harris . Journal of Medical Ethics , 33 ( 7 ) : 414 – 417 .
   PubMedGoogle Scholar
• Sharp , R. R. and Yarborough , M. 2005 . Additional thought on rethinking research ethics . American Journal of Bioethics , 5 ( 1 ) : 40 – 42 .
   PubMed Web of Science ®Google Scholar
• Smith , P. 1998 . Liberalism and Affirmative Obligation , Oxford, , UK : Oxford Press .
   Google Scholar
• Wasson , K. 2009 . Direct-to-consumer genomics and research ethics: Should a more robust informed consent process be included? . American Journal of Bioethics , 9 ( 6–7 ) : 56 – 58 .
   PubMed Web of Science ®Google Scholar