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. 2010 Oct;12(10):616-20.
doi: 10.1097/GIM.0b013e3181efdbd0.

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

Ellen Wright Clayton  1 , Maureen Smith, Stephanie M Fullerton, Wylie Burke, Catherine A McCarty, Barbara A Koenig, Amy L McGuire, Laura M Beskow, Lynn Dressler, Amy A Lemke, Erin M Ramos, Laura Lyman Rodriguez; Consent and Community Consultation Working Group of the eMERGE Consortium
Collaborators, Affiliations

Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

Ellen Wright Clayton et al. Genet Med. 2010 Oct.
No abstract available

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References

    1. National Institutes of Health Policy for Sharing of Data Obtained in NIH Supported or Conducted Genome-Wide Association Studies (GWAS) [7/31/2009]; http://grants.nih.gov/grants/guide/notice-files/NOT-OD-07-088.html.
    1. National Institutes of Health Human Microbiome Project. [4/20/2101]; http://nihroadmap.nih.gov/hmp/.
    1. NHLBI. NHLBI LARGE-SCALE DNA SEQUENCING PROJECT POPULATION STUDIES [4/21/2010];2009 http://www.nhlbi.nih.gov/recovery/media/NHLBI_DNA_cohorts.htm.
    1. International HapMap Consortium Integrating ethics and science in the International HapMap Project. Nat Rev Genet. 2004 Jun;5(6):467–475. - PMC - PubMed
    1. Foster MW, Eisenbraun AJ, Carter TH. Communal discourse as a supplement to informed consent for genetic research. Nat Genet. 1997 Nov;17(3):277–279. - PubMed

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