Public preferences regarding informed consent models for participation in population-based genomic research.

Platt, Jodyn; Bollinger, Juli; Dvoskin, Rachel; Kardia, Sharon L R; Kaufman, David

Platt, Jodyn; Bollinger, Juli; Dvoskin, Rachel; Kardia, Sharon L R; Kaufman, David.

Affiliation

Platt J; 1] Life Sciences and Society Program, University of Michigan School of Public Health, Ann Arbor, Michigan, USA [2] Department of Health Management and Policy, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Bollinger J; Genetics and Public Policy Center, Berman Institute of Bioethics, Johns Hopkins University, Washington, DC, USA.
Dvoskin R; Genetics and Public Policy Center, Berman Institute of Bioethics, Johns Hopkins University, Washington, DC, USA.
Kardia SL; 1] Life Sciences and Society Program, University of Michigan School of Public Health, Ann Arbor, Michigan, USA [2] Department of Epidemiology, University of Michigan School of Public Health, Ann Arbor, Michigan, USA.
Kaufman D; Genetics and Public Policy Center, Berman Institute of Bioethics, Johns Hopkins University, Washington, DC, USA.

Genet Med ; 16(1): 11-8, 2014 Jan.

Article in En | MEDLINE | ID: mdl-23660530

Subject(s)

Biological Specimen Banks/ethics; Genetic Research/ethics; Genomics/ethics; Informed Consent; Adult; Cohort Studies; Data Collection; Demography; Humans; Internet; Public Opinion; United States

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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Biological Specimen Banks / Genomics / Genetic Research / Informed Consent Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Humans Country/Region as subject: America do norte Language: En Journal: Genet Med Journal subject: GENETICA MEDICA Year: 2014 Type: Article Affiliation country: United States

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