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  1. Informed consent and registry-based research - the case of the Danish circumcision registry.Thomas Ploug & Søren Holm - 2017 - BMC Medical Ethics 18 (1):53.
    Research into personal health data holds great potential not only for improved treatment but also for economic growth. In these years many countries are developing policies aimed at facilitating such research often under the banner of ‘big data’. A central point of debate is whether the secondary use of health data requires informed consent if the data is anonymised. In 2013 the Danish Minister of Health established a new register collecting data about all ritual male childhood circumcisions in Denmark. The (...)
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  • Female genital mutilation and male circumcision: toward an autonomy-based ethical framework.Brian Earp - forthcoming - Medicolegal and Bioethics:89.
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  • Binocularity in Bioethics—and Beyond: A Review of Erik Parens, Shaping Our Selves: On Technology, Flourishing, and a Habit of Thinking. [REVIEW]Brian D. Earp & Michael Hauskeller - 2016 - American Journal of Bioethics 16 (2):3-6.
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  • Circumcision, Autonomy and Public Health.Brian D. Earp & Robert Darby - 2019 - Public Health Ethics 12 (1):64-81.
    Male circumcision—partial or total removal of the penile prepuce—has been proposed as a public health measure in Sub-Saharan Africa, based on the results of three randomized control trials showing a relative risk reduction of approximately 60 per cent for voluntary, adult male circumcision against female-to-male human immunodeficiency virus transmission in that context. More recently, long-time advocates of infant male circumcision have argued that these findings justify involuntary circumcision of babies and children in dissimilar public health environments, such as the USA, (...)
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