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  1. 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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  • Withholding conflicts of interest: the many flaws of the new ICMJE disclosure form.David Shaw - 2022 - Journal of Medical Ethics 48 (1):19-21.
    In this article, I describe and analyse the proposed new International Committee of Medical Journal Editors form for disclosing conflicts of interest and conclude that it has many flaws. The form does not mention ‘conflicts of interest’ even once in either its body or its title, it introduces a conceptually confused categorisation of different potential conflicts and it ignores future conflicts and intellectual biases. Finally, many of the authors of the new form have themselves failed to declare relevant potential conflicts (...)
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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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  • 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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  • Addressing polarisation in science.Brian D. Earp - 2015 - Journal of Medical Ethics 41 (9):782-784.
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  • Fake facts and alternative truths in medical research.Bjørn Hofmann - 2018 - BMC Medical Ethics 19 (1):4.
    Fake news and alternative facts have become commonplace in these so-called “post-factual times.” What about medical research - are scientific facts fake as well? Many recent disclosures have fueled the claim that scientific facts are suspect and that science is in crisis. Scientists appear to engage in facting interests instead of revealing interesting facts. This can be observed in terms of what has been called polarised research, where some researchers continuously publish positive results while others publish negative results on the (...)
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