Broad consent versus dynamic consent in biobank research: Is passive participation an ethical problem?

Managing incidental findings and research results in genomic research involving biobanks and archived data sets

(2012) Susan M. Wolf et al.   GENETICS IN MEDICINE

Biobanks, consent and claims of consensus

(2012) Zubin Master et al.   NATURE METHODS

From patients to partners: participant-centric initiatives in biomedical research

(2012) Jane Kaye et al.   NATURE REVIEWS GENETICS

Consent and Research Governance in Biobanks: Evidence from Focus Groups with Medical Researchers

(2012) E.A. Whitley et al.   Public Health Genomics

Preventing overdiagnosis: how to stop harming the healthy

(2012) R. Moynihan et al.   BMJ-British Medical Journal

Power to the people: a wiki-governance model for biobanks

(2012) Edward S Dove et al.   GENOME BIOLOGY

Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research

(2011) Holly K. Tabor et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART A

In Defense of Broad Consent

(2011) GERT HELGESSON   CAMBRIDGE QUARTERLY OF HEALTHCARE ETHICS

Ethical Endgames: Broad Consent for Narrow Interests; Open Consent for Closed Minds

(2011) JAN REINERT KARLSEN et al.   CAMBRIDGE QUARTERLY OF HEALTHCARE ETHICS

Active choice but not too active: Public perspectives on biobank consent models

(2011) Christian M. Simon et al.   GENETICS IN MEDICINE

From single biobanks to international networks: developing e-governance

(2011) Jane Kaye   HUMAN GENETICS

Treat donors as partners in biobank research

(2011) Krishanu Saha et al.   NATURE

You never call, you never write: why return of ‘omic’ results to research participants is both a good idea and a moral imperative

(2011) Misha Angrist   Personalized Medicine

Biobanks--When is Re-consent Necessary?

(2011) K. S. Steinsbekk et al.   Public Health Ethics

Can Broad Consent be Informed Consent?

(2011) M. Sheehan   Public Health Ethics

Understanding the new digital divide—A typology of Internet users in Europe

(2010) Petter Bae Brandtzæg et al.   INTERNATIONAL JOURNAL OF HUMAN-COMPUTER STUDIES

Broadening consent--and diluting ethics?

(2009) B Hofmann   JOURNAL OF MEDICAL ETHICS

“Broad” consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose

(2009) Carlo Petrini   SOCIAL SCIENCE & MEDICINE