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Items: 14

1.

The Adoption of Cloud Computing in the Field of Genomics Research: The Influence of Ethical and Legal Issues.

Charlebois K, Palmour N, Knoppers BM.

PLoS One. 2016 Oct 18;11(10):e0164347. doi: 10.1371/journal.pone.0164347. eCollection 2016.

2.

A practical field guide to conducting nursing research in low- and middle-income countries.

LeBaron VT, Iribarren SJ, Perri S, Beck SL.

Nurs Outlook. 2015 Jul-Aug;63(4):462-73. doi: 10.1016/j.outlook.2015.02.003. Epub 2015 Feb 14.

3.

Estimating the incidence, prevalence and true cost of asthma in the UK: secondary analysis of national stand-alone and linked databases in England, Northern Ireland, Scotland and Wales-a study protocol.

Mukherjee M, Gupta R, Farr A, Heaven M, Stoddart A, Nwaru BI, Fitzsimmons D, Chamberlain G, Bandyopadhyay A, Fischbacher C, Dibben C, Shields M, Phillips C, Strachan D, Davies G, McKinstry B, Sheikh A; Burden and True Cost of Asthma in the UK Research Team.

BMJ Open. 2014 Nov 4;4(11):e006647. doi: 10.1136/bmjopen-2014-006647.

4.

Genomic data-sharing: what will be our legacy?

Callier S, Husain R, Simpson R.

Front Genet. 2014 Mar 5;5:34. doi: 10.3389/fgene.2014.00034. eCollection 2014.

5.

Procedures of recruiting, obtaining informed consent, and compensating research participants in Qatar: findings from a qualitative investigation.

Killawi A, Khidir A, Elnashar M, Abdelrahim H, Hammoud M, Elliott H, Thurston M, Asad H, Al-Khal AL, Fetters MD.

BMC Med Ethics. 2014 Feb 4;15:9. doi: 10.1186/1472-6939-15-9.

6.

Integrating genomics into clinical oncology: ethical and social challenges from proponents of personalized medicine.

McGowan ML, Settersten RA Jr, Juengst ET, Fishman JR.

Urol Oncol. 2014 Feb;32(2):187-92. doi: 10.1016/j.urolonc.2013.10.009.

7.

Balancing the risks and benefits of genomic data sharing: genome research participants' perspectives.

Oliver JM, Slashinski MJ, Wang T, Kelly PA, Hilsenbeck SG, McGuire AL.

Public Health Genomics. 2012;15(2):106-14. doi: 10.1159/000334718. Epub 2011 Dec 30.

8.

Addressing the ethical, policy, and social challenges of preclinical Alzheimer disease.

Karlawish J.

Neurology. 2011 Oct 11;77(15):1487-93. doi: 10.1212/WNL.0b013e318232ac1a. Epub 2011 Sep 14.

9.

Ethical aspects of human biobanks: a systematic review.

Budimir D, Polasek O, Marusić A, Kolcić I, Zemunik T, Boraska V, Jeroncić A, Boban M, Campbell H, Rudan I.

Croat Med J. 2011 Jun;52(3):262-79. Review.

10.

The right to ignore genetic status of late onset genetic disease in the genomic era; Prenatal testing for Huntington disease as a paradigm.

Erez A, Plunkett K, Sutton VR, McGuire AL.

Am J Med Genet A. 2010 Jul;152A(7):1774-80. doi: 10.1002/ajmg.a.33432.

11.

The investigator and the IRB: a survey of depression and schizophrenia researchers.

Fischer BA, George P.

Schizophr Res. 2010 Sep;122(1-3):206-12. doi: 10.1016/j.schres.2009.12.019. Epub 2010 Jan 12.

12.

Current anti-doping policy: a critical appraisal.

Kayser B, Mauron A, Miah A.

BMC Med Ethics. 2007 Mar 29;8:2.

13.

Imaging or imagining? A neuroethics challenge informed by genetics.

Illes J, Racine E.

Am J Bioeth. 2005 Spring;5(2):5-18.

14.

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