相关参考文献
注意：仅列出部分参考文献，下载原文获取全部文献信息。Broad consent, exceptions to consent and the question of using biological samples for research purposes different from the initial collection purpose
Carlo Petrini
SOCIAL SCIENCE & MEDICINE (2010)
Consent for use of personal information for health research: Do people with potentially stigmatizing health conditions and the general public differ in their opinions?
Donald J. Willison et al.
BMC MEDICAL ETHICS (2009)
Obtaining 'fresh' consent for genetic research with biological samples archived 10 years ago
Eric Vermeulen et al.
EUROPEAN JOURNAL OF CANCER (2009)
Researchers' preferences and attitudes on ethical aspects of genomics research: a comparative study between the USA and Spain
M. Ruiz-Canela et al.
JOURNAL OF MEDICAL ETHICS (2009)
Public attitudes to the storage of blood left over from routine general practice tests and its use in research
Shaun Treweek et al.
JOURNAL OF HEALTH SERVICES RESEARCH & POLICY (2009)
Patients' Views on Identifiability of Samples and Informed Consent for Genetic Research
Sara Chandros Hull et al.
AMERICAN JOURNAL OF BIOETHICS (2008)
Informed consent for biorepositories: Assessing prospective participants' understanding and opinions
Laura M. Beskow et al.
CANCER EPIDEMIOLOGY BIOMARKERS & PREVENTION (2008)
Obstacles to European research projects with data and tissue: Solutions and further challenges
Evert-Ben van Veen
EUROPEAN JOURNAL OF CANCER (2008)
Improvement of informed consent and the quality of consent documents
Michael Jefford et al.
LANCET ONCOLOGY (2008)
Participation in clinical trials as viewed by the patient: Understanding cultural and emotional aspects which influence choice
Chiara Catania et al.
ONCOLOGY (2008)
Rhode Islanders' attitudes towards the development of a statewide genetic biobank
Roberta E. Goldman et al.
PERSONALIZED MEDICINE (2008)
Participant characteristics that influence consent for genetic research in a population-based survey: The Baltimore epidemiologic catchment area follow-up
Briana Mezuk et al.
COMMUNITY GENETICS (2008)
Attitudes and perceptions of patients towards methods of establishing a DNA biobank
Jill M. Pulley et al.
CELL AND TISSUE BANKING (2008)
Cancer patients' attitudes toward future research uses of stored human biological materials
Paul R. Helft et al.
JOURNAL OF EMPIRICAL RESEARCH ON HUMAN RESEARCH ETHICS (2007)
Attitudes toward research participation and investigator conflicts of interest among advanced cancer patients participating in early phase clinical trials
Stacy W. Gray et al.
JOURNAL OF CLINICAL ONCOLOGY (2007)
Trends in ethical and legal frameworks for the use of human biobanks
A. Cambon-Thomsen et al.
EUROPEAN RESPIRATORY JOURNAL (2007)
Solidarity and justice as guiding principles in genomic research
Rogeer Hoedemaekers et al.
BIOETHICS (2007)
Attitudes towards clinical research among cancer trial participants and non-participants: an interview study using a Grounded Theory approach
S. M. Madsen et al.
JOURNAL OF MEDICAL ETHICS (2007)
Biobanking for epidemiological research and public health
Angela M. Brand et al.
PATHOBIOLOGY (2007)
Perceptions of potential donors in the Swedish public towards information and consent procedures in relation to use of human tissue samples in biobanks: A population-based study
Asa Kettis-Lindblad et al.
SCANDINAVIAN JOURNAL OF PUBLIC HEALTH (2007)
Genetic research and donation of tissue samples to biobanks.: What do potential sample donors in the Swedish general public think?
Asa Kettis-Lindblad et al.
EUROPEAN JOURNAL OF PUBLIC HEALTH (2006)
Should donors be allowed to give broad consent to future biobank research?
MG Hansson et al.
LANCET ONCOLOGY (2006)
Informed consent, participation in, and withdrawal from a population based cohort study involving genetic analysis
K Matsui et al.
JOURNAL OF MEDICAL ETHICS (2005)
Science and society - Human genetic research: emerging trends in ethics
BM Knoppers et al.
NATURE REVIEWS GENETICS (2005)
Science and society - The social and ethical issues of post-genomic human biobanks
A Cambon-Thomsen
NATURE REVIEWS GENETICS (2004)
Informed consent and biobanks:: a population-based study of attitudes towards tissue donation for genetic research
K Hoeyer et al.
SCANDINAVIAN JOURNAL OF PUBLIC HEALTH (2004)
Consent for genetic research in a general population: The NHANES experience
GM McQuillan et al.
GENETICS IN MEDICINE (2003)
Genomic medicine - A primer
AE Guttmacher et al.
NEW ENGLAND JOURNAL OF MEDICINE (2002)
Human tissue research in the genomic era of medicine -: Balancing individual and societal interests
TT Ashburn et al.
ARCHIVES OF INTERNAL MEDICINE (2000)
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