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In Defence of informed consent for health record research - why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail

BMC medical ethics, 2020-08, Vol.21 (1), p.1-75, Article 75

Ploug, Thomas

2020

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Population preferences for AI system features across eight different decision-making contexts

PloS one, 2023-12, Vol.18 (12), p.e0295277-e0295277

2023

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Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)

PloS one, 2017, Vol.12 (7), p.e0179935-e0179935

2017

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Population Preferences for Performance and Explainability of Artificial Intelligence in Health Care: Choice-Based Conjoint Survey

Journal of medical Internet research, 2021-12, Vol.23 (12), p.e26611-e26611

2021

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The right to refuse diagnostics and treatment planning by artificial intelligence

Medicine, health care, and philosophy, 2020-03, Vol.23 (1), p.107-114

2020

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Ethics in Cyberspace: How Cyberspace May Influence Interpersonal Interaction

Ploug, Thomas

1. Aufl., 2009

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Informed consent and registry-based research - the case of the Danish circumcision registry

BMC medical ethics, 2017-09, Vol.18 (1), p.53-53, Article 53

2017

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The Right Not to Be Subjected to AI Profiling Based on Publicly Available Data—Privacy and the Exceptionalism of AI Profiling

Philosophy & technology, 2023-03, Vol.36 (1), p.14, Article 14

Ploug, Thomas

2023

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People Should Have a Right Not to Be Subjected to AI Profiling Based on Publicly Available Data! A Reply to Holm

Philosophy & technology, 2023-09, Vol.36 (3), p.49, Article 49

Ploug, Thomas

2023

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Should all medical research be published? The moral responsibility of medical journal editors

Journal of medical ethics, 2018-10, Vol.44 (10), p.690

Ploug, Thomas

2018

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Easy Resistible, Means-Paternalist Nudging in the Clinical Context is an Untenable Proposal

American journal of bioethics, 2019-05, Vol.19 (5), p.64-66

Ploug, Thomas

2019

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The four dimensions of contestable AI diagnostics - A patient-centric approach to explainable AI

Artificial intelligence in medicine, 2020-07, Vol.107, p.101901-101901, Article 101901

2020

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The biobank consent debate: why 'meta-consent' is still the solution

Journal of medical ethics, 2019-05, Vol.45 (5), p.295

2019

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Genome studies reveal flaws in broad consent

Science (American Association for the Advancement of Science), 2019-12, Vol.366 (6472), p.1460-1461

2019

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Population preferences for AI system features across eight different decision-making contexts

PloS one, 2023-01, Vol.18 (12)

2023

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Meta Consent - A Flexible Solution to the Problem of Secondary Use of Health Data

Bioethics, 2016-11, Vol.30 (9), p.721-732

2016

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Pharmaceutical information systems and possible implementations of informed consent -- developing an heuristic

BMC medical ethics, 2012-11, Vol.13 (1), p.30-30, Article 30

2012

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Informed consent and routinisation

Journal of medical ethics, 2013-04, Vol.39 (4), p.214-218

2013

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Doctors, Patients, and Nudging in the Clinical Context-Four Views on Nudging and Informed Consent

American journal of bioethics, 2015-10, Vol.15 (10), p.28-38

2015

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The right to a second opinion on Artificial Intelligence diagnosis—Remedying the inadequacy of a risk‐based regulation

Bioethics, 2023-03, Vol.37 (3), p.303-311

2023

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Meta consent: a flexible and autonomous way of obtaining informed consent for secondary research

BMJ (Online), 2015-05, Vol.350, p.h2146

2015

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The Right to Contest AI Profiling Based on Social Media Data

American journal of bioethics, 2021-07, Vol.21 (7), p.21-23

2021

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Persuasive Technology: 5th International Conference, PERSUASIVE 2010, Copenhagen, Denmark, June 7-10, 2010, Proceedings

2010 edition., 2010

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To nudge or not to nudge: cancer screening programmes and the limits of libertarian paternalism

Journal of Epidemiology and Community Health, 2012-12, Vol.66 (12), p.1193-1196

2012

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Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes .(Research Article)

PloS one, 2017-07, Vol.12 (7), p.e0179935

2017

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In Defence of informed consent for health record research - why arguments from ‘easy rescue’, ‘no harm’ and ‘consent bias’ fail

Population preferences for AI system features across eight different decision-making contexts

Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes (MAGs) to patient actionable genes (PAGs)

Population Preferences for Performance and Explainability of Artificial Intelligence in Health Care: Choice-Based Conjoint Survey

The right to refuse diagnostics and treatment planning by artificial intelligence

Ethics in Cyberspace: How Cyberspace May Influence Interpersonal Interaction

Informed consent and registry-based research - the case of the Danish circumcision registry

The Right Not to Be Subjected to AI Profiling Based on Publicly Available Data—Privacy and the Exceptionalism of AI Profiling

People Should Have a Right Not to Be Subjected to AI Profiling Based on Publicly Available Data! A Reply to Holm

Should all medical research be published? The moral responsibility of medical journal editors

Easy Resistible, Means-Paternalist Nudging in the Clinical Context is an Untenable Proposal

The four dimensions of contestable AI diagnostics - A patient-centric approach to explainable AI

The biobank consent debate: why 'meta-consent' is still the solution

Genome studies reveal flaws in broad consent

Population preferences for AI system features across eight different decision-making contexts

Meta Consent - A Flexible Solution to the Problem of Secondary Use of Health Data

Pharmaceutical information systems and possible implementations of informed consent -- developing an heuristic

Informed consent and routinisation

Doctors, Patients, and Nudging in the Clinical Context-Four Views on Nudging and Informed Consent

The right to a second opinion on Artificial Intelligence diagnosis—Remedying the inadequacy of a risk‐based regulation

Meta consent: a flexible and autonomous way of obtaining informed consent for secondary research

The Right to Contest AI Profiling Based on Social Media Data

Persuasive Technology: 5th International Conference, PERSUASIVE 2010, Copenhagen, Denmark, June 7-10, 2010, Proceedings

To nudge or not to nudge: cancer screening programmes and the limits of libertarian paternalism

Clinical genome sequencing and population preferences for information about 'incidental' findings-From medically actionable genes .(Research Article)

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