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Items: 1 to 20 of 106

1.

Ethical use of tissue samples in genetic research.

Azarow KS, Olmstead FL, Hume RF, Myers J, Calhoun BC, Martin LS.

Mil Med. 2003 Jun;168(6):437-41.

PMID:
12834131
2.

Informed consent for genetic research on stored tissue samples.

Clayton EW, Steinberg KK, Khoury MJ, Thomson E, Andrews L, Kahn MJ, Kopelman LM, Weiss JO.

JAMA. 1995 Dec 13;274(22):1786-92. Review.

PMID:
7500511
3.

Ethical issues in genetic research: disclosure and informed consent.

Reilly PR, Boshar MF, Holtzman SH.

Nat Genet. 1997 Jan;15(1):16-20.

PMID:
8988163
4.

American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility.

American Society of Clinical Oncology.

J Clin Oncol. 2003 Jun 15;21(12):2397-406. Epub 2003 Apr 11.

PMID:
12692171
5.
6.

Why the use of anonymous samples for research matters.

Clayton EW.

J Law Med Ethics. 1995 Winter;23(4):375-7. No abstract available.

PMID:
8715059
7.

Legal and ethical issues in psychiatric genetic research.

Shore D, Berg K, Wynne D, Folstein MF.

Am J Med Genet. 1993 May 1;48(1):17-21.

PMID:
8357032
8.

American Society of Clinical Oncology policy statement: oversight of clinical research.

American Society of Clinical Oncology.

J Clin Oncol. 2003 Jun 15;21(12):2377-86. Epub 2003 Apr 29.

PMID:
12721281
9.
10.

Drafting the Genetic Privacy Act: science, policy, and practical considerations.

Annas GJ, Glantz LH, Roche PA.

J Law Med Ethics. 1995 Winter;23(4):360-6. No abstract available.

PMID:
8715056
11.

Research and stored tissues. Persons as sources, samples as persons?

Knoppers BM, Laberge CM.

JAMA. 1995 Dec 13;274(22):1806-7. No abstract available.

PMID:
7500515
12.

Genetic research, adolescents, and informed consent.

Weir RF, Horton JR.

Theor Med. 1995 Dec;16(4):347-73. Review.

PMID:
8820748
13.

Pathologists enter debate on consent for genetic research on stored tissue.

Stephenson J.

JAMA. 1996 Feb 21;275(7):503-4. No abstract available.

PMID:
8606455
14.

Nonconsensual participation in genetic studies.

Lippman A.

Am J Public Health. 1996 Jul;86(7):1030. No abstract available.

15.

Ethical and legal implications of whole genome and whole exome sequencing in African populations.

Wright GE, Koornhof PG, Adeyemo AA, Tiffin N.

BMC Med Ethics. 2013 May 28;14:21. doi: 10.1186/1472-6939-14-21.

16.

Ethical aspects of participation in the database of genotypes and phenotypes of the National Center for Biotechnology Information: the Cancer and Leukemia Group B Experience.

Peppercorn J, Shapira I, Deshields T, Kroetz D, Friedman P, Spears P, Collyar DE, Shulman LN, Dressler L, Bertagnolli MM.

Cancer. 2012 Oct 15;118(20):5060-8. doi: 10.1002/cncr.27515. Epub 2012 Mar 13.

17.

Privacy issues in second stage genomics.

Robertson JA.

Jurimetrics. 1999 Fall;40:59-76.

PMID:
14621715
18.

Privacy and confidentiality in the publication of pedigrees: a survey of investigators and biomedical journals.

Botkin JR, McMahon WM, Smith KR, Nash JE.

JAMA. 1998 Jun 10;279(22):1808-12.

PMID:
9628712
19.

Patients' views on identifiability of samples and informed consent for genetic research.

Hull SC, Sharp RR, Botkin JR, Brown M, Hughes M, Sugarman J, Schwinn D, Sankar P, Bolcic-Jankovic D, Clarridge BR, Wilfond BS.

Am J Bioeth. 2008 Oct;8(10):62-70. doi: 10.1080/15265160802478404.

20.

Cancer risk research: what should we tell subjects?

Kodish E, Murray TH, Shurin S.

Clin Res. 1994 Oct;42(3):396-402. No abstract available.

PMID:
7955901

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