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Results: 18

PubMed Links for Books (Select 2375190)

1.

Beyond the HIPAA Privacy Rule: Enhancing Privacy, Improving Health Through Research.

Institute of Medicine (US) Committee on Health Research and the Privacy of Health Information: The HIPAA Privacy Rule; Nass SJ, Levit LA, Gostin LO, editors.

Washington (DC): National Academies Press (US); 2009.

2.

The SAIL databank: linking multiple health and social care datasets.

Lyons RA, Jones KH, John G, Brooks CJ, Verplancke JP, Ford DV, Brown G, Leake K.

BMC Med Inform Decis Mak. 2009 Jan 16;9:3. doi: 10.1186/1472-6947-9-3.

3.

Incidence and survival of childhood bone cancer in northern England and the West Midlands, 1981-2002.

Eyre R, Feltbower RG, Mubwandarikwa E, Jenkinson HC, Parkes S, Birch JM, Eden TO, James PW, McKinney PA, Pearce MS, McNally RJ.

Br J Cancer. 2009 Jan 13;100(1):188-93. doi: 10.1038/sj.bjc.6604837.

4.

National registries of systemic treatment for psoriasis and the European 'Psonet' initiative.

Lecluse LL, Naldi L, Stern RS, Spuls PI.

Dermatology. 2009;218(4):347-56. doi: 10.1159/000183757. Epub 2008 Dec 11.

PMID:
19077384
5.

Resolving individuals contributing trace amounts of DNA to highly complex mixtures using high-density SNP genotyping microarrays.

Homer N, Szelinger S, Redman M, Duggan D, Tembe W, Muehling J, Pearson JV, Stephan DA, Nelson SF, Craig DW.

PLoS Genet. 2008 Aug 29;4(8):e1000167. doi: 10.1371/journal.pgen.1000167.

6.

My sister's keeper?: genomic research and the identifiability of siblings.

Cassa CA, Schmidt B, Kohane IS, Mandl KD.

BMC Med Genomics. 2008 Jul 25;1:32. doi: 10.1186/1755-8794-1-32.

7.

The search for effective and safe disease control in psoriasis.

Naldi L.

Lancet. 2008 Apr 19;371(9621):1311-2. doi: 10.1016/S0140-6736(08)60571-1. No abstract available.

PMID:
18424307
8.

Genetic screening and disability insurance: what can we learn from the health insurance experience?

Kass N, Medley A.

J Law Med Ethics. 2007 Summer;35(2 Suppl):66-73.

PMID:
17543060
9.

Public willingness to participate in and public opinions about genetic variation research: a review of the literature.

Sterling R, Henderson GE, Corbie-Smith G.

Am J Public Health. 2006 Nov;96(11):1971-8. Epub 2006 Oct 3. Review.

10.

A secure protocol to distribute unlinkable health data.

Malin BA, Sweeney L.

AMIA Annu Symp Proc. 2005:485-9.

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13.

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
14.

Ethical, legal, and social implications of genomic medicine.

Clayton EW.

N Engl J Med. 2003 Aug 7;349(6):562-9. Review. No abstract available.

15.

Statistical perspectives on confidentiality and data access in public health.

Fienberg SE.

Stat Med. 2001 May 15-30;20(9-10):1347-56.

PMID:
11343356
16.

US employer agrees to stop genetic testing.

Gottlieb S.

BMJ. 2001 Feb 24;322(7284):449. No abstract available.

17.

Weaving technology and policy together to maintain confidentiality.

Sweeney L.

J Law Med Ethics. 1997 Summer-Fall;25(2-3):98-110, 82. Review.

PMID:
11066504
18.

Bounds for cell entries in contingency tables given marginal totals and decomposable graphs.

Dobra A, Fienberg SE.

Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11885-92.

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