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Items: 20

1.

The Public Population Project in Genomics (P3G): a proof of concept?

Knoppers BM, Fortier I, Legault D, Burton P.

Eur J Hum Genet. 2008 Jun;16(6):664-5. doi: 10.1038/ejhg.2008.55. Epub 2008 Apr 2. No abstract available.

2.

The OBO Foundry: coordinated evolution of ontologies to support biomedical data integration.

Smith B, Ashburner M, Rosse C, Bard J, Bug W, Ceusters W, Goldberg LJ, Eilbeck K, Ireland A, Mungall CJ; OBI Consortium, Leontis N, Rocca-Serra P, Ruttenberg A, Sansone SA, Scheuermann RH, Shah N, Whetzel PL, Lewis S.

Nat Biotechnol. 2007 Nov;25(11):1251-5.

3.

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls.

Wellcome Trust Case Control Consortium.

Nature. 2007 Jun 7;447(7145):661-78.

4.

Toward a national framework for the secondary use of health data: an American Medical Informatics Association White Paper.

Safran C, Bloomrosen M, Hammond WE, Labkoff S, Markel-Fox S, Tang PC, Detmer DE, Expert Panel.

J Am Med Inform Assoc. 2007 Jan-Feb;14(1):1-9. Epub 2006 Oct 31.

5.

Who owns your body? A patient's perspective on Washington University v. Catalona.

Andrews L.

J Law Med Ethics. 2006 Summer;34(2):398-407. No abstract available.

PMID:
16789962
6.

Protecting genomic sequence anonymity with generalization lattices.

Malin BA.

Methods Inf Med. 2005;44(5):687-92.

PMID:
16400377
7.

Health-information altruists--a potentially critical resource.

Kohane IS, Altman RB.

N Engl J Med. 2005 Nov 10;353(19):2074-7. No abstract available.

PMID:
16282184
8.

Realizing the promise of genomics in biomedical research.

Guttmacher AE, Collins FS.

JAMA. 2005 Sep 21;294(11):1399-402. No abstract available.

PMID:
16174701
9.

The Babel of genetic data terminology.

Knoppers BM, Saginur M.

Nat Biotechnol. 2005 Aug;23(8):925-7. No abstract available.

PMID:
16082354
10.

Navigating an ethical patchwork--human gene banks.

Maschke KJ.

Nat Biotechnol. 2005 May;23(5):539-45. No abstract available. Erratum in: Nat Biotechnol. 2005 Jul;23(7):896.

PMID:
15877066
11.

Protecting medical record information: start your research registries today.

Vates JR, Hetrick JL, Lavin KL, Sharma GK, Wagner RL, Johnson JT.

Laryngoscope. 2005 Mar;115(3):441-4.

PMID:
15744154
12.

Ownership and use of tissue specimens for research.

Hakimian R, Korn D.

JAMA. 2004 Nov 24;292(20):2500-5.

PMID:
15562130
13.
14.

When two tribes go to war.

Dalton R.

Nature. 2004 Jul 29;430(6999):500-2. No abstract available.

PMID:
15282577
15.

Genetics. Genomic research and human subject privacy.

Lin Z, Owen AB, Altman RB.

Science. 2004 Jul 9;305(5681):183. No abstract available.

PMID:
15247459
16.
17.

DNA databanks and consent: a suggested policy option involving an authorization model.

Caulfield T, Upshur RE, Daar A.

BMC Med Ethics. 2003 Jan 3;4:E1.

18.

Using binning to maintain confidentiality of medical data.

Lin Z, Hewett M, Altman RB.

Proc AMIA Symp. 2002:454-8.

19.

Principles, organization, and operation of a DNA bank for clinical trials: a Department of Veterans Affairs cooperative study.

Lavori PW, Krause-Steinrauf H, Brophy M, Buxbaum J, Cockroft J, Cox DR, Fiore L, Greely HT, Greenberg H, Holmes EW, Nelson LM, Sugarman J.

Control Clin Trials. 2002 Jun;23(3):222-39.

PMID:
12057876
20.

Public attitudes regarding the donation and storage of blood specimens for genetic research.

Wang SS, Fridinger F, Sheedy KM, Khoury MJ.

Community Genet. 2001;4(1):18-26.

PMID:
11493749

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