标题
Broad Consent for Research With Biological Samples: Workshop Conclusions
作者
关键词
-
出版物
AMERICAN JOURNAL OF BIOETHICS
Volume 15, Issue 9, Pages 34-42
出版商
Informa UK Limited
发表日期
2015-08-26
DOI
10.1080/15265161.2015.1062162
参考文献
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。- “It’s my blood”: ethical complexities in the use, storage and export of biological samples: perspectives from South African research participants
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- Broad versus Blanket Consent for Research with Human Biological Samples
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- Biobanks containing clinical specimens: Defining characteristics, policies, and practices
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- Publics and biobanks: Pan-European diversity and the challenge of responsible innovation
- (2012) George Gaskell et al. EUROPEAN JOURNAL OF HUMAN GENETICS
- Biobanking: shifting the analogy from consent to surrogacy
- (2012) Ann M. Mongoven et al. GENETICS IN MEDICINE
- From patients to partners: participant-centric initiatives in biomedical research
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- Two large-scale surveys on community attitudes toward an opt-out biobank
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- Active choice but not too active: Public perspectives on biobank consent models
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- (2011) Yann Joly et al. HUMAN GENETICS
- Autoantibodies predate the onset of systemic lupus erythematosus in northern Sweden
- (2011) Catharina Eriksson et al. ARTHRITIS RESEARCH & THERAPY
- Principles of Human Subjects Protections Applied in an Opt-Out, De-identified Biobank
- (2010) Jill Pulley et al. CTS-Clinical and Translational Science
- Attitudes towards biomedical use of tissue sample collections, consent, and biobanks among Finns
- (2009) Aaro Tupasela et al. SCANDINAVIAN JOURNAL OF PUBLIC HEALTH
- Community consultation and communication for a population-based DNA biobank: The Marshfield clinic personalized medicine research project
- (2008) Catherine A. McCarty et al. AMERICAN JOURNAL OF MEDICAL GENETICS PART A
- Participant Characteristics That Influence Consent for Genetic Research in a Population-Based Survey: The Baltimore Epidemiologic Catchment Area Follow-Up
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