Biobank research, informed consent and society. Towards a new alliance?

Research across the disciplines: a road map for quality criteria in empirical ethics research

(2014) Marcel Mertz et al.   BMC Medical Ethics

Dynamic consent: a patient interface for twenty-first century research networks

(2014) Jane Kaye et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Biobanking research on oncological residual material: a framework between the rights of the individual and the interest of society

(2013) Luciana Caenazzo et al.   BMC Medical Ethics

The Haystack Is Made of Needles

(2013) Sharon F. Terry et al.   Genetic Testing and Molecular Biomarkers

A SOLIDARITY-BASED APPROACH TO THE GOVERNANCE OF RESEARCH BIOBANKS

(2013) B. Prainsack et al.   Medical Law Review

Social Epigenetics and Equality of Opportunity

(2013) M. Loi et al.   Public Health Ethics

Publics and biobanks: Pan-European diversity and the challenge of responsible innovation

(2012) George Gaskell et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The Privacy-Reciprocity Connection in Biobanking: Comparing German with UK Strategies

(2012) A. Hobbs et al.   Public Health Genomics

Involving citizens in the ethics of biobank research: Informing institutional policy through structured public deliberation

(2012) Kieran C. O'Doherty et al.   SOCIAL SCIENCE & MEDICINE

Is the commercialisation of human tissue and body material forbidden in the countries of the European Union?

(2011) Christian Lenk et al.   JOURNAL OF MEDICAL ETHICS

Balancing the Risks and Benefits of Genomic Data Sharing: Genome Research Participants’ Perspectives

(2011) J.M. Oliver et al.   Public Health Genomics

Consent for Biobanking: Assessing the Understanding and Views of Cancer Patients

(2010) Julien Mancini et al.   JNCI-Journal of the National Cancer Institute

Biobank governance: a lesson in trust

(2010) A. K. Hawkins et al.   NEW GENETICS AND SOCIETY

Broadening consent--and diluting ethics?

(2009) B Hofmann   JOURNAL OF MEDICAL ETHICS