How not to think about genetic information

'Take my kidneys but not my corneas'-Selective preferences as a hidden problem for 'opt-out' organ donation policy.

Bioethics·2022

The case against meta-consent: not only do Ploug and Holm not answer it, they make it even stronger.

Journal of medical ethics·2019

The ethics of biobanking: Assessing the right to control problem for broad consent.

Bioethics·2019

The biobank consent debate: Why 'meta-consent' is not the solution?

Journal of medical ethics·2018

Misleading by Omission: Rethinking the Obligation to Inform Research Subjects about Funding Sources.

The Journal of medicine and philosophy·2017

When is a Choice not a Choice? 'Sham Offers' and the Asymmetry of Adolescent Consent and Refusal.

Bioethics·2016

Harm Reduction as an Alternative to Mandated Drug Treatment.

The Hastings Center report·2026

Rethinking Mandated Drug Treatment: Why Expanding Freedom Requires Structural Drug Policy Reform.

The Hastings Center report·2026

Banning Gender-Affirming Treatment for Minors: The Supreme Court Speaks.

The Hastings Center report·2026

Making the Move to a Learning System of Research Ethics.

The Hastings Center report·2026

Musical Performance and Biomedical Human Enhancement: Ethnographic Perspectives on Bioethical Questions.

The Hastings Center report·2026

Transformed but Not Cured: The Ethics of Describing Gene-Editing Therapy for Sickle Cell Disease.

The Hastings Center report·2026

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

Scientific reports·2026

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

The Lancet. Microbe·2026

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

Frontiers in genetics·2026

A Novel FN1 Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

Journal of clinical medicine·2026

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

HLA·2026

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Molecular syndromology·2026

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How not to think about genetic information

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'Take my kidneys but not my corneas'-Selective preferences as a hidden problem for 'opt-out' organ donation policy.

The case against meta-consent: not only do Ploug and Holm not <i>answer</i> it, they make it <i>even stronger</i>.

The ethics of biobanking: Assessing the right to control problem for broad consent.

The biobank consent debate: Why 'meta-consent' is not the solution?

Misleading by Omission: Rethinking the Obligation to Inform Research Subjects about Funding Sources.

When is a Choice not a Choice? 'Sham Offers' and the Asymmetry of Adolescent Consent and Refusal.

Harm Reduction as an Alternative to Mandated Drug Treatment.

Rethinking Mandated Drug Treatment: Why Expanding Freedom Requires Structural Drug Policy Reform.

Banning Gender-Affirming Treatment for Minors: The Supreme Court Speaks.

Making the Move to a Learning System of Research Ethics.

Musical Performance and Biomedical Human Enhancement: Ethnographic Perspectives on Bioethical Questions.

Transformed but Not Cured: The Ethics of Describing Gene-Editing Therapy for Sickle Cell Disease.

MORF4L1, encoding a chromatin remodeler, is mutated in a recognizable dysmorphic neurodevelopmental disorder.

First nationwide full-genome characterisation of human-derived Andes virus in Chile: a retrospective genomic epidemiology study.

Integrated hearing and genetic screening for neonatal deafness in a resource-limited region: insights from Qingyuan, China.

A Novel <i>FN1</i> Nucleotide Variant c.3051G>C (p.Trp1017Cys) in a Pediatric Patient with Fibronectin Glomerulopathy: Case Report and Literature Review.

The Novel HLA-DQA1*01:204 Allele Identified in Asian Female Donor by Next-Generation Sequencing.

Detailed Clinical Report of Four Individuals from a Nusayri Family with a Rare TNXB Variant: Classical-Like and Hypermobile Types of Ehlers-Danlos Syndrome.

Related Experiment Videos

How not to think about genetic information

Related Concept Videos

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