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  1. Is there a duty to share genetic information?S. Matthew Liao - 2009 - Journal of Medical Ethics 35 (5):306-309.
    A number of prominent bioethicists such as Mike Parker, Anneke Lucassen, and Bartha Maria Knoppers have called for the adoption of a system in which by default, genetic information is shared among family members. In this paper, I suggest that a main reason given in support of this call to share genetic information among family members is the idea that genetic information is essentially familial in nature. Upon examining this ‘familial nature of genetics’ argument, I show that most genetic information (...)
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  • Using biomarkers in acute medicine to prevent hearing loss: should this require specific consent?Peta Coulson-Smith & Anneke Lucassen - 2020 - Journal of Medical Ethics 46 (8):536-537.
    In this round table response, we discuss some of the problems inherent in insisting on specific consent for an activity that needs to happen rapidly as part of a package of care. The Human Tissue Authority consider that specific consent is mandatory to assess which antibiotics are appropriate on the neonatal unit, but this insistence may actually limit the autonomy which consent aims to promote. While genetic testing to determine which child will react adversely to particular antibiotics has been available (...)
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