Ethical and Practical Issues Associated with Aggregating Databases
article has not abstract
Vyšlo v časopise:
Ethical and Practical Issues Associated with Aggregating Databases. PLoS Med 5(9): e190. doi:10.1371/journal.pmed.0050190
Kategorie:
Guidelines and Guidance
prolekare.web.journal.doi_sk:
https://doi.org/10.1371/journal.pmed.0050190
Souhrn
article has not abstract
Zdroje
1. GuttmacherAECollinsFS
2005
Realizing the promise of genomics in biomedical research.
JAMA
294
1399
1402
2. Wellcome Trust Case Control Consortium
2007
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.
Nature
447
661
678
3. DaltonR
2004
When two tribes go to war.
Nature
430
500
502
4. SafranCBloomrosenMHammondWELabkoffSMarkel-FoxS
2007
Toward a national framework for the secondary use of health data: An American Medical Informatics Association White Paper.
J Am Med Inform Assoc
14
1
9
5. WangSSFridingerFSheedyKMKhouryMJ
2001
Public attitudes regarding the donation and storage of blood specimens for genetic research.
Community Genet
4
18
26
6. CaulfieldT
2007
Biobanks and blanket consent: The proper place of the public good and public perception rationales.
Kings Coll Law J
18
209
226
7. AndrewsL
2006
Who owns your body? A patient's perspective on Washington University v. Catalona.
J Law Med Ethics
34
398
407
8. HakimianRKornD
2004
Ownership and use of tissue specimens for research.
JAMA
292
2500
2505
9. ArnasonV
2004
Coding and consent: Moral challenges of the database project in Iceland.
Bioethics
18
27
49
10. CaulfieldTUpshurREDaarA
2003
DNA databanks and consent: A suggested policy option involving an authorization model.
BMC Med Ethics
4
E1
11. MaschkeKJ
2005
Navigating an ethical patchwork—Human gene banks.
Nat Biotechnol
23
539
545
12. LavoriPWKrause-SteinraufHBrophyMBuxbaumJCockroftJ
2002
Principles, organization, and operation of a DNA bank for clinical trials: A Department of Veterans Affairs cooperative study.
Control Clin Trials
23
222
239
13. VatesJRHetrickJLLavinKLSharmaGKWagnerRL
2005
Protecting medical record information: Start your research registries today.
Laryngoscope
115
441
444
14. KnoppersBMFortierILegaultDBurtonP
2008
The Public Population Project in Genomics (P(3)G): A proof of concept.
Eur J Hum Genet
16
664
665
15. SmithBAshburnerMRosseCBardJBugW
2007
The OBO Foundry: Coordinated evolution of ontologies to support biomedical data integration.
Nat Biotechnol
25
1251
1255
16. KnoppersBMSaginurM
2005
The Babel of genetic data terminology.
Nat Biotechnol
23
925
927
17. KohaneISAltmanRB
2005
Health-information altruists—A potentially critical resource.
N Engl J Med
353
2074
2077
18. LinZOwenABAltmanRB
2004
Genomic research and human subject privacy.
Science
305
183
19. MalinBA
2005
An evaluation of the current state of genomic data privacy protection technology and a roadmap for the future.
J Am Med Inform Assoc
12
28
34
20. LinZHewettMAltmanRB
2002
Using binning to maintain confidentiality of medical data.
Proc AMIA Sym
454
458
21. MalinBA
2005
Protecting genomic sequence anonymity with generalization lattices.
Methods Inf Med
44
687
692
Štítky
Interné lekárstvoČlánok vyšiel v časopise
PLOS Medicine
2008 Číslo 9
- Jak rozpoznat pacienty s familiární hypercholesterolémií ve své praxi
- Myasthenia gravis: kombinace chirurgie a farmakoterapie jako nejefektivnější modalita?
- Statinová intolerance
- Parazitičtí červi v terapii Crohnovy choroby a dalších zánětlivých autoimunitních onemocnění
- Mutace v genu PCSK9 zodpovědné za rozvoj familiární hypercholesterolémie
Najčítanejšie v tomto čísle
- Informed Consent in the Genomics Era
- Publication of Clinical Trials Supporting Successful New Drug Applications: A Literature Analysis
- A 50-Year-Old Woman with Recurrent Generalised Seizures
- Ethical and Practical Issues Associated with Aggregating Databases