The tension between data sharing and the protection of privacy in genomics research.
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[1] Kelly Edwards,et al. From patients to partners: participant-centric initiatives in biomedical research , 2012, Nature Reviews Genetics.
[2] J. Kaye. Governing biobanks: understanding the interplay between law and practice , 2012 .
[3] Neil Pearce,et al. Data sharing: not as simple as it seems , 2011, Environmental health : a global access science source.
[4] M. Bamshad,et al. Genomics really gets personal: How exome and whole genome sequencing challenge the ethical framework of human genetics research , 2011, American journal of medical genetics. Part A.
[5] Mark Gerstein,et al. Genomics and Privacy: Implications of the New Reality of Closed Data for the Field , 2011, PLoS Comput. Biol..
[6] S. Holm. Withdrawing from Research: A Rethink in the Context of Research Biobanks , 2011, Health Care Analysis.
[7] A. Guttmacher,et al. Genomics, Health Care, and Society , 2011 .
[8] Andrew D. Johnson,et al. Temporal Trends in Results Availability from Genome-Wide Association Studies , 2011, PLoS genetics.
[9] R. Gallagher,et al. From consent to institutions: designing adaptive governance for genomic biobanks. , 2011, Social science & medicine.
[10] Jane Kaye,et al. From single biobanks to international networks: developing e-governance , 2011, Human Genetics.
[11] Heather A. Piwowar,et al. Who Shares? Who Doesn't? Factors Associated with Openly Archiving Raw Research Data , 2011, PloS one.
[12] Melissa A. Basford,et al. Ethical and practical challenges of sharing data from genome-wide association studies: the eMERGE Consortium experience. , 2011, Genome research.
[13] L. Ciaccia,et al. The Immortal Life of Henrietta Lacks , 2010, The Yale Journal of Biology and Medicine.
[14] Elaine R. Mardis,et al. A decade’s perspective on DNA sequencing technology , 2011, Nature.
[15] Stephanie M. Fullerton,et al. Research Practice and Participant Preferences: The Growing Gulf , 2011, Science.
[16] Jane Kaye,et al. Consent forms in genomics: the difference between law and practice. , 2011, European journal of health law.
[17] K. Hudson. Genomics, health care, and society. , 2011, The New England journal of medicine.
[18] Wendy A. Wolf,et al. The eMERGE Network: A consortium of biorepositories linked to electronic medical records data for conducting genomic studies , 2011, BMC Medical Genomics.
[19] Kelly Edwards,et al. Building a chain of trust: using policy and practice to enhance trustworthy clinical data discovery and sharing , 2010, GTIP '10.
[20] G. Laurie,et al. Managing Access to Biobanks: How Can We Reconcile Individual Privacy and Public Interests in Genetic Research? , 2010 .
[21] S. Fullerton,et al. Glad You Asked: Participants' Opinions of Re-Consent for DbGap Data Submission , 2010, Journal of empirical research on human research ethics : JERHRE.
[22] D. Butler. Human genome at ten: Science after the sequence , 2010, Nature.
[23] D. M. Gitter. The Challenges of Achieving Open Source Sharing of Biobank Data , 2010 .
[24] 王家志. Internet(互连网)简介 , 1994 .
[25] T. Lumley,et al. Potential for revealing individual-level information in genome-wide association studies. , 2010, JAMA.
[26] Bradley Malin,et al. Technical and Policy Approaches to Balancing Patient Privacy and Data Sharing in Clinical and Translational Research , 2010, Journal of Investigative Medicine.
[27] N. Hallowell,et al. An investigation of patients’ motivations for their participation in genetics-related research , 2009, Journal of Medical Ethics.
[28] F. Bowden. When two tribes go to war , 2009, The Medical journal of Australia.
[29] Jane Kaye,et al. Principles and Practice in Biobank Governance , 2009 .
[30] E. Mardis,et al. A focus on personal genomics. , 2009, Personalized medicine.
[31] G. Church,et al. Public Access to Genome-Wide Data: Five Views on Balancing Research with Privacy and Protection , 2009, PLoS genetics.
[32] Jane Kaye,et al. Broad Consent in Biobanking: Reflections on Seemingly Insurmountable Dilemmas , 2009 .
[33] Roger D. Cox,et al. A Mouse Model for the Metabolic Effects of the Human Fat Mass and Obesity Associated FTO Gene , 2009, PLoS genetics.
[34] Phil Andrews,et al. Recommendations from the 2008 International Summit on Proteomics Data Release and Sharing Policy: the Amsterdam principles. , 2009, Journal of proteome research.
[35] N. Hawkins,et al. Data sharing in genomics — re-shaping scientific practice , 2009, Nature Reviews Genetics.
[36] J. Gitschier,et al. Inferential genotyping of Y chromosomes in Latter-Day Saints founders and comparison to Utah samples in the HapMap project. , 2009, American journal of human genetics.
[37] N. Day. Commentary: How small is small? , 2009, International journal of epidemiology.
[38] P. Visscher,et al. On Jim Watson's APOE status: genetic information is hard to hide , 2009, European Journal of Human Genetics.
[39] klaguia. Prepublication Data Sharing , 2009 .
[40] J. Ioannidis,et al. Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement , 2009, European Journal of Epidemiology.
[41] K. Zatloukal,et al. [Biobanking and Biomolecular Resources Research Infrastructure (BBMRI). Implications for pathology]. , 2008, Der Pathologe.
[42] C. Viertler,et al. Biobanken und Biomolekulare Ressourcen Forschungsinfrastruktur (BBMRI) , 2008, Der Pathologe.
[43] S. Nelson,et al. Resolving Individuals Contributing Trace Amounts of DNA to Highly Complex Mixtures Using High-Density SNP Genotyping Microarrays , 2008, PLoS genetics.
[44] Jane Kaye,et al. Sample, data use and protection in biobanking in Europe: legal issues. , 2008, Pharmacogenomics.
[45] B. Ness,et al. Genomic Research and Incidental Findings , 2008 .
[46] Frances P Lawrenz,et al. Managing Incidental Findings in Human Subjects Research: Analysis and Recommendations , 2008, The Journal of law, medicine & ethics : a journal of the American Society of Law, Medicine & Ethics.
[47] G. Church,et al. From genetic privacy to open consent , 2008, Nature Reviews Genetics.
[48] S. Salzberg,et al. Bioinformatics challenges of new sequencing technology. , 2008, Trends in genetics : TIG.
[49] A. McGuire,et al. Research ethics and the challenge of whole-genome sequencing , 2008, Nature Reviews Genetics.
[50] Siobhan M. Dolan,et al. Assessment of cumulative evidence on genetic associations: interim guidelines. , 2008, International journal of epidemiology.
[51] Susanne B Haga,et al. Ethical, legal, and social implications of biobanks for genetics research. , 2008, Advances in genetics.
[52] R. Gertz. Withdrawing from participating in a biobank--a comparative study. , 2008, European journal of health law.
[53] A. McGuire,et al. DNA data sharing: research participants' perspectives , 2008, Genetics in Medicine.
[54] Muin J. Khoury,et al. Quantifying realistic sample size requirements for human genome epidemiology , 2008 .
[55] P. Donnelly,et al. New models of collaboration in genome-wide association studies: the Genetic Association Information Network , 2007, Nature Genetics.
[56] D. Winickoff. Partnership in U.K. Biobank: A Third Way for Genomic Property? , 2007, Journal of Law, Medicine & Ethics.
[57] B. Knoppers,et al. Our social genome? , 2007, Trends in biotechnology.
[58] Dirk Pilat,et al. OECD Principles and Guidelines for Access to Research Data from Public Funding , 2007, Data Sci. J..
[59] Simon C. Potter,et al. Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls , 2007, Nature.
[60] Russ B Altman,et al. Health-information altruists--a potentially critical resource. , 2005, The New England journal of medicine.
[61] R. Gibbs. Deeper into the genome , 2005, Nature.
[62] Mark I McCarthy,et al. What makes a good genetic association study? , 2005, The Lancet.
[63] John Gillott,et al. Genetic Databases: Socio-Ethical Issues in the Collection and Use of DNA , 2005 .
[64] Free genome databases finally defeat Celera , 2005, Nature.
[65] Anne Cambon-Thomsen,et al. The social and ethical issues of post-genomic human biobanks , 2004, Nature Reviews Genetics.
[66] H. Busby. Blood donation for genetic research: what can we learn from donors’ narratives? , 2004 .
[67] R. Tutton,et al. Genetic Databases : Socio-Ethical Issues in the Collection and Use of DNA , 2004 .
[68] B. Lo,et al. Untapped potential: IRB guidance for the ethical research use of stored biological materials. , 2004, IRB.
[69] Vilhjalmur Arnason,et al. Coding and Consent: Moral Challenges of the Database Project in Iceland , 2004, Bioethics.
[70] J. Otten,et al. The charitable trust as a model for genomic biobanks. , 2004, The New England journal of medicine.
[71] Christiane,et al. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. , 2004, Journal international de bioethique = International journal of bioethics.
[72] D. Winickoff,et al. The charitable trust as a model for genomic biobanks. , 2003, The New England journal of medicine.
[73] F. Collins,et al. The Human Genome Project: Lessons from Large-Scale Biology , 2003, Science.
[74] R. Tutton. Gift Relationships in Genetics Research , 2002, Science as culture.
[75] Wolzt,et al. World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects. , 2003, The Journal of the American College of Dentists.
[76] M Gwinn,et al. Informed consent for population-based research involving genetics. , 2001, JAMA.
[77] Human genomes, public and private , 2001, Nature.
[78] D. Mazur. Beyond Consent: Seeking Justice in Research , 1999 .
[79] J. D. Watson. The human genome project: past, present, and future. , 1990, Science.
[80] James M. Orten,et al. Trials of War Criminals Before the Nuremberg Military Tribunals , 1950 .