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Items: 1 to 20 of 90

1.

Consent to the use of stored DNA for genetics research: a survey of attitudes in the Jewish population.

Schwartz MD, Rothenberg K, Joseph L, Benkendorf J, Lerman C.

Am J Med Genet. 2001 Feb 1;98(4):336-42.

PMID:
11170078
2.

[Genetic research on blood samples stored for years in biobanks. Most people are willing to provide informed consent].

Stegmayr B, Asplund K.

Lakartidningen. 2003 Feb 20;100(8):618-20. Swedish.

PMID:
12640974
3.
4.

Public attitudes to the storage of blood left over from routine general practice tests and its use in research.

Treweek S, Doney A, Leiman D.

J Health Serv Res Policy. 2009 Jan;14(1):13-9. doi: 10.1258/jhsrp.2008.008016.

PMID:
19103912
5.

Public attitudes regarding willingness to participate in medical research studies.

Trauth JM, Musa D, Siminoff L, Jewell IK, Ricci E.

J Health Soc Policy. 2000;12(2):23-43.

PMID:
11184441
6.

Record linkage research and informed consent: who consents?

Huang N, Shih SF, Chang HY, Chou YJ.

BMC Health Serv Res. 2007 Feb 12;7:18.

7.

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
8.

Attitudes of emergency department patients and visitors regarding emergency exception from informed consent in resuscitation research, community consultation, and public notification.

McClure KB, DeIorio NM, Gunnels MD, Ochsner MJ, Biros MH, Schmidt TA.

Acad Emerg Med. 2003 Apr;10(4):352-9. Erratum in: Acad Emerg Med. 2003 Jun;10(6):690.

9.

Native Hawaiian preferences for informed consent and disclosure of results from genetic research.

Fong M, Braun KL, Chang RM.

J Cancer Educ. 2006 Spring;21(1 Suppl):S47-52.

PMID:
17020502
10.

Informed consent and biobanks: a population-based study of attitudes towards tissue donation for genetic research.

Hoeyer K, Olofsson BO, Mjörndal T, Lynöe N.

Scand J Public Health. 2004;32(3):224-9.

PMID:
15204184
11.

The debate over research on stored biological samples: what do sources think?

Wendler D, Emanuel E.

Arch Intern Med. 2002 Jul 8;162(13):1457-62.

PMID:
12090881
12.

Consent for genetic research in a general population: the NHANES experience.

McQuillan GM, Porter KS, Agelli M, Kington R.

Genet Med. 2003 Jan-Feb;5(1):35-42.

PMID:
12544474
13.

Informed consent in genetic research.

Williams ED.

Croat Med J. 2001 Aug;42(4):450-6. Review.

14.

Lay public's understanding of equipoise and randomisation in randomised controlled trials.

Robinson EJ, Kerr CE, Stevens AJ, Lilford RJ, Braunholtz DA, Edwards SJ, Beck SR, Rowley MG.

Health Technol Assess. 2005 Mar;9(8):1-192, iii-iv.

15.

Ethical challenges at the beginning of the millennium.

Steinberg KK.

Stat Med. 2001 May 15-30;20(9-10):1415-9.

PMID:
11343362
16.

Are subjects satisfied with the informed consent process? A survey of research participants.

Pope JE, Tingey DP, Arnold JM, Hong P, Ouimet JM, Krizova A.

J Rheumatol. 2003 Apr;30(4):815-24.

PMID:
12672205
17.

Informed consent for biorepositories: assessing prospective participants' understanding and opinions.

Beskow LM, Dean E.

Cancer Epidemiol Biomarkers Prev. 2008 Jun;17(6):1440-51. doi: 10.1158/1055-9965.EPI-08-0086.

18.

Communal discourse as a supplement to informed consent for genetic research.

Foster MW, Eisenbraun AJ, Carter TH.

Nat Genet. 1997 Nov;17(3):277-9.

PMID:
9354789
20.

Potential research participants' views regarding researcher and institutional financial conflicts of interest.

Kim SY, Millard RW, Nisbet P, Cox C, Caine ED.

J Med Ethics. 2004 Feb;30(1):73-9.

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