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  1. Protecting groups from genetic research.Daniel Hausman - 2008 - Bioethics 22 (3):157–165.
    ABSTRACT Genetics research, like research in sociology and anthropology, creates risks for groups from which research subjects are drawn. This paper considers what sort of protection for groups from the risks of genetics research should be provided and by whom. The paper categorizes harms by distinguishing process‐related from outcome‐related harms and by distinguishing two kinds of group harms. It argues that calls for community engagement are justified with respect to some kinds of harms, but not with respect to others; and (...)
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  • Group risks, risks to groups, and group engagement in genetics research.Daniel M. Hausman - 2007 - Kennedy Institute of Ethics Journal 17 (4):351-369.
    : This essay distinguishes between two kinds of group harms: harms to individuals in virtue of their membership in groups and harms to "structured" groups that have a continuing existence, an organization, and interests of their own. Genetic research creates risks of causing both kinds of group harms, and engagement with the groups at risk can help to mitigate those harms. The two kinds of group harms call for different kinds of group engagement.
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  • Groups, Communities, and Contested Identities in Genetic Research.Dena S. Davis - 2000 - Hastings Center Report 30 (6):38-45.
    Obtaining community consent before conducting genetic research seems to be a way of ensuring that a whole community is not harmed against its wishes—that all Jews, or all African Americans, or all Hutterites are not forced to learn things about themselves they would rather not know, or are not forced into identities they would rather not have. Unfortunately, there are insurmountable problems both in identifying the right representatives of the community and in obtaining their consent.
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