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  1. Genetic Moralism and Health.Tuija Takala - 2019 - Cambridge Quarterly of Healthcare Ethics 28 (2):225-235.
    :This article examines the moralistic language and arguments used in relation to genetics. The focus is on three practices: the claims that there is a duty to know about one’s own genetic makeup, assertions that genetic information should be used to inform reproductive decisions, and the proposition that there are moral reasons to participate in biobank research. With these three, the author contends that there are equally good, if not better, arguments to challenge them from a Millian perspective. Furthermore, especially (...)
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  • Editorial: Dogmas, Stigmas, and Questionable Arguments for Better Health.Johanna Ahola-Launonen, Tuija Takala & Matti Häyry - 2019 - Cambridge Quarterly of Healthcare Ethics 28 (2):191-199.
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  • The Nordic data imaginary.Heta Tarkkala, Karoliina Snell & Aaro Tupasela - 2020 - Big Data and Society 7 (1).
    The Nordic countries aim to have a unique place within the European and global health data economy. They have extensive nationally maintained and centralized health data records, as well as numerous biobanks where data from individuals can be connected based on personal identification numbers. Much of this phenomenon can be attributed to the emergence and development of the Nordic welfare state, where Nordic countries sought to systematically collect large amounts of population data to guide decision making and improve the health (...)
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