Biobanks, consent and claims of consensus

Qualitative thematic analysis of consent forms used in cancer genome sequencing

(2011) Clarissa Allen et al.   BMC Medical Ethics

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

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

Saudi views on consenting for research on medical records and leftover tissue samples

(2010) Mohammad M Al-Qadire et al.   BMC Medical Ethics

The Havasupai Indian Tribe Case — Lessons for Research Involving Stored Biologic Samples

(2010) Michelle M. Mello et al.   NEW ENGLAND JOURNAL OF MEDICINE

Stem cell banking: between traceability and identifiability

(2010) Bartha M Knoppers et al.   Genome Medicine

Public Opinion about the Importance of Privacy in Biobank Research

(2009) David J. Kaufman et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Patients attending tertiary referral urology clinics: willingness to participate in tissue banking

(2009) Patricia E. Fitzpatrick et al.   BJU INTERNATIONAL

Obtaining ‘fresh’ consent for genetic research with biological samples archived 10 years ago

(2009) Eric Vermeulen et al.   EUROPEAN JOURNAL OF CANCER

Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns

(2009) Aaro Tupasela et al.   SCANDINAVIAN JOURNAL OF PUBLIC HEALTH

“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

Ethics and biobanks

(2008) M G Hansson   BRITISH JOURNAL OF CANCER

Banking together. A unified model of informed consent for biobanking

(2008) Elena Salvaterra et al.   EMBO REPORTS

Opt-out plus, the patients' choice: preferences of cancer patients concerning information and consent regimen for future research with biological samples archived in the context of treatment

(2008) E Vermeulen et al.   JOURNAL OF CLINICAL PATHOLOGY