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  1.  80
    Reconsidering the value of consent in biobank research.Judy Allen & Beverley Mcnamara - 2011 - Bioethics 25 (3):155-166.
    Biobanks for long-term research pose challenges to the legal and ethical validity of consent to participate. Different models of consent have been proposed to answer some of these challenges. This paper contributes to this discussion by considering the meaning and value of consent to participants in biobanks. Empirical data from a qualitative study is used to provide a participant view of the consent process and to demonstrate that, despite limited understanding of the research, consent provides the research participants with some (...)
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  2.  91
    The Disclosure of Genetic Information: A Human Research Ethics Perspective.Danielle E. Dye, Leanne Youngs, Beverley McNamara, Jack Goldblatt & Peter O’Leary - 2010 - Journal of Bioethical Inquiry 7 (1):103-109.
    Increasing emphasis on genetic research means that growing numbers of human research projects in Australia will involve complex issues related to genetic privacy, familial information and genetic epidemiology. The Office of Population Health Genomics (Department of Health, Western Australia) hosted an interactive workshop to explore the ethical issues involved in the disclosure of genetic information, where researchers and members of human research ethics committees (HRECs) were asked to consider several case studies from an ethical perspective. Workshop participants used a variety (...)
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    The relationship between postnatal depression, sociodemographic factors, levels of partner support, and levels of physical activity.Maryam Saligheh, Rosanna M. Rooney, Beverley McNamara & Robert T. Kane - 2014 - Frontiers in Psychology 5.
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