Marking Shifts in Human Research Ethics in the Development of Biobanking
Published 2014 View Full Article
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Title
Marking Shifts in Human Research Ethics in the Development of Biobanking
Authors
Keywords
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Journal
Public Health Ethics
Volume 8, Issue 1, Pages 63-71
Publisher
Oxford University Press (OUP)
Online
2014-09-06
DOI
10.1093/phe/phu023
References
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Related references
Note: Only part of the references are listed.- Dynamic consent: a patient interface for twenty-first century research networks
- (2014) Jane Kaye et al. EUROPEAN JOURNAL OF HUMAN GENETICS
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- (2013) Dorit T. Stein et al. Genetic Testing and Molecular Biomarkers
- Characterizing biobank organizations in the U.S.: results from a national survey
- (2013) Gail E Henderson et al. Genome Medicine
- On Sharing Quantitative Trait GWAS Results in an Era of Multiple-omics Data and the Limits of Genomic Privacy
- (2012) Hae Kyung Im et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Managing incidental findings and research results in genomic research involving biobanks and archived data sets
- (2012) Susan M. Wolf et al. GENETICS IN MEDICINE
- Bayesian method to predict individual SNP genotypes from gene expression data
- (2012) Eric E Schadt et al. NATURE GENETICS
- From patients to partners: participant-centric initiatives in biomedical research
- (2012) Jane Kaye et al. NATURE REVIEWS GENETICS
- ELSI 2.0 for Genomics and Society
- (2012) J. Kaye et al. SCIENCE
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- From consent to institutions: Designing adaptive governance for genomic biobanks
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- Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium
- (2010) Ellen Wright Clayton et al. GENETICS IN MEDICINE
- International network of cancer genome projects
- (2010) Thomas J. Hudson (Chairperson) et al. NATURE
- Developing a Simplified Consent Form for Biobanking
- (2010) Laura M. Beskow et al. PLoS One
- Meeting the Governance Challenges of Next-Generation Biorepository Research
- (2010) S. M. Fullerton et al. Science Translational Medicine
- Should post-trial provision of beneficial experimental interventions be mandatory in developing countries?
- (2008) Z. Zong JOURNAL OF MEDICAL ETHICS
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- (2008) Patrick Taylor NATURE
- The next steps for genomic medicine: challenges and opportunities for the developing world
- (2008) Billie-Jo Hardy et al. NATURE REVIEWS GENETICS
- ISBER: Best Practices for Repositories and Trends at the Institute for Problems of Cryobiology and Medicine
- (2008) J.G. Baust
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- (2008) Deborah Mascalzoni et al. PLOS MEDICINE
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