Public’s attitudes on participation in a biobank for research: an Italian survey

WPA guidance on how to combat stigmatization of psychiatry and psychiatrists

(2015) NORMAN SARTORIUS et al.   World Psychiatry

Factors influencing public participation in biobanking

(2013) Mamoun Ahram et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

The policies of ethics committees in the management of biobanks used for research: an Italian survey

(2013) Corinna Porteri et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Clinical trial sponsors’ refusal to communicate genetic research results to subjects

(2013) Corinna Porteri et al.   PATIENT EDUCATION AND COUNSELING

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

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

What does ‘respect for persons’ require? Attitudes and reported practices of genetics researchers in informing research participants about research

(2011) Fiona Alice Miller et al.   JOURNAL OF MEDICAL ETHICS

Connecting the public with biobank research: reciprocity matters

(2011) Herbert Gottweis et al.   NATURE REVIEWS GENETICS

Hypothetical and factual willingness to participate in biobank research

(2010) Linus Johnsson et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Biobank governance in the post-genomic age

(2010) Herbert Gottweis et al.   Personalized Medicine

Public Perspectives on Informed Consent for Biobanking

(2009) Juli Murphy et al.   AMERICAN JOURNAL OF PUBLIC HEALTH

Public Expectations for Return of Results from Large-Cohort Genetic Research

(2008) Juli Murphy et al.   AMERICAN JOURNAL OF BIOETHICS

Banking together. A unified model of informed consent for biobanking

(2008) Elena Salvaterra et al.   EMBO REPORTS