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Items: 1 to 20 of 133

1.

Simplifying informed consent for biorepositories: stakeholder perspectives.

Beskow LM, Friedman JY, Hardy NC, Lin L, Weinfurt KP.

Genet Med. 2010 Sep;12(9):567-72. doi: 10.1097/GIM.0b013e3181ead64d.

2.

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.

3.

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
4.

Developing a simplified consent form for biobanking.

Beskow LM, Friedman JY, Hardy NC, Lin L, Weinfurt KP.

PLoS One. 2010 Oct 8;5(10):e13302. doi: 10.1371/journal.pone.0013302.

5.
7.

The privacy-reciprocity connection in biobanking: comparing German with UK strategies.

Hobbs A, Starkbaum J, Gottweis U, Wichmann HE, Gottweis H.

Public Health Genomics. 2012;15(5):272-84. doi: 10.1159/000336671. Epub 2012 Jun 20.

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10.

Qualitative thematic analysis of consent forms used in cancer genome sequencing.

Allen C, Foulkes WD.

BMC Med Ethics. 2011 Jul 19;12:14. doi: 10.1186/1472-6939-12-14.

11.

Emerging issues in paediatric health research consent forms in Canada: working towards best practices.

Dove ES, Avard D, Black L, Knoppers BM.

BMC Med Ethics. 2013 Jan 30;14:5. doi: 10.1186/1472-6939-14-5.

12.

Improvement of informed consent and the quality of consent documents.

Jefford M, Moore R.

Lancet Oncol. 2008 May;9(5):485-93. doi: 10.1016/S1470-2045(08)70128-1. Review.

PMID:
18452859
13.

To share or not to share: a randomized trial of consent for data sharing in genome research.

McGuire AL, Oliver JM, Slashinski MJ, Graves JL, Wang T, Kelly PA, Fisher W, Lau CC, Goss J, Okcu M, Treadwell-Deering D, Goldman AM, Noebels JL, Hilsenbeck SG.

Genet Med. 2011 Nov;13(11):948-55. doi: 10.1097/GIM.0b013e3182227589.

14.

Excluding particular information from consent forms.

Dickert N, Kass N, Paasche-Orlow M, Taylor H.

Account Res. 2005 Jan-Mar;12(1):33-45.

PMID:
16021790
15.

Information sheets and informed consent forms for clinical study participants: towards standardised recommendations?

Chassany O, Bernard-Harlaut M, Guy G, Billon N.

Therapie. 2009 May-Jun;64(3):161-86. doi: 10.2515/therapie/2009035. Epub 2009 Aug 13. Review. English, French.

16.

Views of US researchers about informed consent in international collaborative research.

Dawson L, Kass NE.

Soc Sci Med. 2005 Sep;61(6):1211-22. Epub 2005 Apr 9.

PMID:
15970232
17.

Medical records and privacy: empirical effects of legislation.

McCarthy DB, Shatin D, Drinkard CR, Kleinman JH, Gardner JS.

Health Serv Res. 1999 Apr;34(1 Pt 2):417-25.

19.

Informed consent for research participation in frail older persons.

Barron JS, Duffey PL, Byrd LJ, Campbell R, Ferrucci L.

Aging Clin Exp Res. 2004 Feb;16(1):79-85.

PMID:
15132296
20.
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