Community-Based Partnership to Identify Keys to Biospecimen Research Participation

Author:

Erwin Deborah O.,Moysich Kirsten,Kiviniemi Marc T.,Saad-Harfouche Frances G.,Davis Warren,Clark-Hargrave Nikia,Ciupak Gregory L.,Ambrosone Christine B.,Walker Charles

Publisher

Springer Science and Business Media LLC

Subject

Public Health, Environmental and Occupational Health,Oncology

Reference20 articles.

1. National Institutes of Health. 2012. National Human Genome Research Institute: the National Human Genome Research Institute strategic plan for reducing health disparities. http://www.genome.gov/10001493 . Accessed 06/20/2012

2. National Human Genome Research Institute. 2011. The cancer genome atlas. http://cancergenome.nih.gov/ . Accessed 06/20/2011.

3. Murphy J, Scott J, Kaufman D, Geller G, LeRoy L, Hudson K (2009) Public perspectives on informed consent for biobanking. Am J Public Health 99:2128–2134

4. Secko DM, Preto N, Niemeyer S, Burgess MM (2009) Informed consent in biobank research: a deliberative approach to the debate. Social Science & Medicine 68:781–789

5. Beskow LM, Dean E (2008) Informed consent for biorepositories: assessing prospective participants’ understanding and opinions. Cancer Epidemiology Biomarkers Prevention 17:1440–1451

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