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The American Journal of Bioethics Volume 13, 2013 - Issue 4
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Open Peer Commentaries

A Thick Opt-Out Is Often Sufficient

Noor A. A. Giesbertz University Medical Center Utrecht
,
Annelien L. Bredenoord University Medical Center Utrecht
&
Johannes J. M. van Delden University Medical Center Utrecht
Pages 44-46 | Published online: 20 Mar 2013

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MarkA. Rothstein & AbigailB. Shoben. (2013) An Unbiased Response to the Open Peer Commentaries on “Does Consent Bias Research?”. The American Journal of Bioethics 13:4, pages W1-W4.
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Articles from other publishers (6)

Miriam Beusink, Annegien BroeksFolkert J. van KemenadeKing H. LamMarjanka K. SchmidtSusanne Rebers. (2022) Barriers and Facilitators for Implementing a National Guideline to Foster the Responsible Use of Residual Biospecimens and Data in Health Research. Biopreservation and Biobanking 20:1, pages 67-74.
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Jennifer Viberg Johansson, Heidi Beate Bentzen, Nisha Shah, Eik Haraldsdóttir, Guðbjörg Andrea Jónsdóttir, Jane Kaye, Deborah Mascalzoni & Jorien Veldwijk. (2021) Preferences of the Public for Sharing Health Data: Discrete Choice Experiment. JMIR Medical Informatics 9:7, pages e29614.
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Roel H. P. Wouters, Rieke van der Graaf, Tessel Rigter, Eline M. Bunnik, M. Corrette Ploem, Guido M. W. R. de Wert, Wybo J. Dondorp, Martina C. Cornel & Annelien L. Bredenoord. (2021) Towards a Responsible Transition to Learning Healthcare Systems in Precision Medicine: Ethical Points to Consider. Journal of Personalized Medicine 11:6, pages 539.
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Deborah Mascalzoni, Angelo Paradiso & Matts Hansson. (2014) Rare disease research: Breaking the privacy barrier. Applied & Translational Genomics 3:2, pages 23-29.
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Ian N Olver. (2014) Opting in for opt‐out consent. Medical Journal of Australia 200:4, pages 201-202.
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Evert-Ben van Veen. (2013) Europe and tissue research: a regulatory patchwork. Diagnostic Histopathology 19:9, pages 331-336.
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