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Items: 1 to 20 of 301

1.

Ethical issues arising from the participation of children in genetic research.

Burke W, Diekema DS.

J Pediatr. 2006 Jul;149(1 Suppl):S34-8.

PMID:
16829241
2.

Ethical issues raised by incorporation of genetics into the National Birth Defects Prevention Study.

Jenkins MM, Rasmussen SA, Moore CA, Honein MA.

Am J Med Genet C Semin Med Genet. 2008 Feb 15;148C(1):40-6. doi: 10.1002/ajmg.c.30157.

PMID:
18189287
3.

Handling ethical, legal and social issues in birth cohort studies involving genetic research: responses from studies in six countries.

Ries NM, LeGrandeur J, Caulfield T.

BMC Med Ethics. 2010 Mar 23;11:4. doi: 10.1186/1472-6939-11-4. Review.

4.
5.

Ethical issues associated with conducting genetic family studies of complex disease.

Arar NH, Hazuda H, Steinbach R, Arar MY, Abboud HE.

Ann Epidemiol. 2005 Oct;15(9):712-9.

PMID:
16157258
6.
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
9.

Ethics in population-based genetic research.

DeCamp M, Sugarman J.

Account Res. 2004 Jan-Mar;11(1):1-26. Review.

PMID:
15341044
10.

The adequacy of informed consent forms in genetic research in Oman: a pilot study.

Al-Riyami A, Jaju D, Jaju S, Silverman HJ.

Dev World Bioeth. 2011 Aug;11(2):57-62. doi: 10.1111/j.1471-8847.2010.00293.x. Epub 2011 Jan 25.

PMID:
21266001
11.
12.

Ethical and practical challenges surrounding genetic and genomic research in developing countries.

Nyika A.

Acta Trop. 2009 Nov;112 Suppl 1:S21-31. doi: 10.1016/j.actatropica.2009.07.034. Epub 2009 Aug 8. Review.

PMID:
19665983
13.

Untapped potential: IRB guidance for the ethical research use of stored biological materials.

Wolf LE, Lo B.

IRB. 2004 Jul-Aug;26(4):1-8. No abstract available.

PMID:
15449408
14.

Returning genetic research results to individuals: points-to-consider.

Renegar G, Webster CJ, Stuerzebecher S, Harty L, Ide SE, Balkite B, Rogalski-Salter TA, Cohen N, Spear BB, Barnes DM, Brazell C.

Bioethics. 2006 Feb;20(1):24-36. Review.

PMID:
16680905
15.

Safety: when infants and parents are research subjects.

Thomas KA.

J Perinat Neonatal Nurs. 2005 Jan-Mar;19(1):52-8. Review.

PMID:
15796425
16.

Experiences with community engagement and informed consent in a genetic cohort study of severe childhood diseases in Kenya.

Marsh VM, Kamuya DM, Mlamba AM, Williams TN, Molyneux SS.

BMC Med Ethics. 2010 Jul 15;11:13. doi: 10.1186/1472-6939-11-13.

17.

A consumer perspective on informed consent and third-party issues.

Terry SF, Terry PF.

J Contin Educ Health Prof. 2001 Fall;21(4):256-64.

PMID:
11803770
18.

Ethical issues in identifying and recruiting participants for familial genetic research.

Beskow LM, Botkin JR, Daly M, Juengst ET, Lehmann LS, Merz JF, Pentz R, Press NA, Ross LF, Sugarman J, Susswein LR, Terry SF, Austin MA, Burke W.

Am J Med Genet A. 2004 Nov 1;130A(4):424-31.

PMID:
15455364
19.

Ethical issues in psychiatric research on children and adolescents.

Hoop JG, Smyth AC, Roberts LW.

Child Adolesc Psychiatr Clin N Am. 2008 Jan;17(1):127-48, x. Review.

PMID:
18036483
20.

A qualitative study of subject recruitment for familial cancer research.

Kreiger N, Ashbury F, Cotterchio M, Macey J.

Ann Epidemiol. 2001 May;11(4):219-24.

PMID:
11306339
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