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A critique of the regulation of data science in healthcare research in the European Union
BMC Medical Ethics Open Access 08 April 2017
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References
Hirschfeld, D.J. President weighs in on data from genes. New York Times p.A15 (25 February 2016).
Skloot, R. The Immortal Life of Henrietta Lacks (Crown Publishers, New York, 2010).
International News Svc. v. Associated Press, 248 U.S. 215, 250 (1918) (Brandeis, J., dissenting).
Greenberg v. Miami Children's Hospital Research Institute, 264 F.Supp.2d 1064, 1076 (S.D. Fla. 2003).
Beleno v. Lakey, Order, Civ. Action No. SA-09-CA-188-FB (W.D. Tex. 17 September 2009).
Havasupai Tribe v. Ariz. Bd. of Regents, 220 Ariz. 214, 217 (2008).
US Department of Homeland Security et al. Fed. Reg. 80, 53933 (8 September 2015).
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Contreras, J. The president says patients should own their genetic data. He's wrong. Nat Biotechnol 34, 585–586 (2016). https://doi.org/10.1038/nbt.3608
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DOI: https://doi.org/10.1038/nbt.3608
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A critique of the regulation of data science in healthcare research in the European Union
BMC Medical Ethics (2017)