Literature DB >> 19833988

Public perspectives on informed consent for biobanking.

Juli Murphy1, Joan Scott, David Kaufman, Gail Geller, Lisa LeRoy, Kathy Hudson.   

Abstract

The National Institutes of Health and other federal health agencies are considering establishing a national biobank to study the roles of genes and environment in health. We assessed the public's attitudes toward the proposed biobank, including preferences for providing informed consent. Sixteen focus groups were conducted, and themes arising from the focus groups were tested in a large, representative survey (n=4659) of the general population. Our research demonstrates that when considering participating in a genomic biobank, individuals want ongoing choices and control over access to their samples and information.

Mesh:

Year:  2009        PMID: 19833988      PMCID: PMC2775766          DOI: 10.2105/AJPH.2008.157099

Source DB:  PubMed          Journal:  Am J Public Health        ISSN: 0090-0036            Impact factor:   9.308


  15 in total

1.  Proposed international guidelines on ethical issues in medical genetics and genetic services (part I).

Authors: 
Journal:  Rev Derecho Genoma Hum       Date:  1998 Jan-Jun

2.  Consent and anonymization in research involving biobanks: differing terms and norms present serious barriers to an international framework.

Authors:  Bernice S Elger; Arthur L Caplan
Journal:  EMBO Rep       Date:  2006-07       Impact factor: 8.807

3.  Merging and emerging cohorts: necessary but not sufficient.

Authors:  Francis S Collins; Teri A Manolio
Journal:  Nature       Date:  2007-01-18       Impact factor: 49.962

Review 4.  Genes, environment and the value of prospective cohort studies.

Authors:  Teri A Manolio; Joan E Bailey-Wilson; Francis S Collins
Journal:  Nat Rev Genet       Date:  2006-10       Impact factor: 53.242

5.  Biobank research and the right to privacy.

Authors:  Lars Oystein Ursin
Journal:  Theor Med Bioeth       Date:  2008-10-15

6.  Attitudes and perceptions of patients towards methods of establishing a DNA biobank.

Authors:  Jill M Pulley; Margaret M Brace; Gordon R Bernard; Dan R Masys
Journal:  Cell Tissue Bank       Date:  2007-10-25       Impact factor: 1.522

7.  Ethical implications of including children in a large biobank for genetic-epidemiologic research: a qualitative study of public opinion.

Authors:  David Kaufman; Gail Geller; Lisa Leroy; Juli Murphy; Joan Scott; Kathy Hudson
Journal:  Am J Med Genet C Semin Med Genet       Date:  2008-02-15       Impact factor: 3.908

8.  Informed consent for biorepositories: assessing prospective participants' understanding and opinions.

Authors:  Laura M Beskow; Elizabeth Dean
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2008-06       Impact factor: 4.254

9.  The case for a US prospective cohort study of genes and environment.

Authors:  Francis S Collins
Journal:  Nature       Date:  2004-05-27       Impact factor: 49.962

10.  Subjects matter: a survey of public opinions about a large genetic cohort study.

Authors:  David Kaufman; Juli Murphy; Joan Scott; Kathy Hudson
Journal:  Genet Med       Date:  2008-11       Impact factor: 8.822

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  78 in total

1.  Donation intentions for cancer genetics research among African Americans.

Authors:  Jasmine A McDonald; Benita Weathers; Frances K Barg; Andrea B Troxel; Judy A Shea; Deborah Bowen; Carmen E Guerra; Chanita Hughes Halbert
Journal:  Genet Test Mol Biomarkers       Date:  2012-01-06

2.  Disclosing pathogenic genetic variants to research participants: quantifying an emerging ethical responsibility.

Authors:  Christopher A Cassa; Sarah K Savage; Patrick L Taylor; Robert C Green; Amy L McGuire; Kenneth D Mandl
Journal:  Genome Res       Date:  2012-01-06       Impact factor: 9.043

3.  Research ethics in the era of personalized medicine: updating science's contract with society.

Authors:  Eric M Meslin; Mildred K Cho
Journal:  Public Health Genomics       Date:  2010-08-31       Impact factor: 2.000

4.  The value of using top-down and bottom-up approaches for building trust and transparency in biobanking.

Authors:  Eric M Meslin
Journal:  Public Health Genomics       Date:  2010-04-15       Impact factor: 2.000

5.  A genetic counselor's guide to using next-generation sequencing in clinical practice.

Authors:  Flavia M Facio; Kristy Lee; Julianne M O'Daniel
Journal:  J Genet Couns       Date:  2013-10-24       Impact factor: 2.537

6.  Public perspectives on biospecimen procurement: what biorepositories should consider.

Authors:  Jamie L'Heureux; Jeffrey C Murray; Elizabeth Newbury; Laura Shinkunas; Christian M Simon
Journal:  Biopreserv Biobank       Date:  2013-05-29       Impact factor: 2.300

7.  Public Attitudes toward Consent and Data Sharing in Biobank Research: A Large Multi-site Experimental Survey in the US.

Authors:  Saskia C Sanderson; Kyle B Brothers; Nathaniel D Mercaldo; Ellen Wright Clayton; Armand H Matheny Antommaria; Sharon A Aufox; Murray H Brilliant; Diego Campos; David S Carrell; John Connolly; Pat Conway; Stephanie M Fullerton; Nanibaa' A Garrison; Carol R Horowitz; Gail P Jarvik; David Kaufman; Terrie E Kitchner; Rongling Li; Evette J Ludman; Catherine A McCarty; Jennifer B McCormick; Valerie D McManus; Melanie F Myers; Aaron Scrol; Janet L Williams; Martha J Shrubsole; Jonathan S Schildcrout; Maureen E Smith; Ingrid A Holm
Journal:  Am J Hum Genet       Date:  2017-02-09       Impact factor: 11.025

Review 8.  An Introduction to Starting a Biobank.

Authors:  Mitra D Harati; Ryan R Williams; Masoud Movassaghi; Amin Hojat; Gregory M Lucey; William H Yong
Journal:  Methods Mol Biol       Date:  2019

9.  Understanding participation by African Americans in cancer genetics research.

Authors:  Jasmine A McDonald; Frances K Barg; Benita Weathers; Carmen E Guerra; Andrea B Troxel; Susan Domchek; Deborah Bowen; Judy A Shea; Chanita Hughes Halbert
Journal:  J Natl Med Assoc       Date:  2012 Jul-Aug       Impact factor: 1.798

10.  Genetics specialists' perspectives on disclosure of genomic incidental findings in the clinical setting.

Authors:  Nancy R Downing; Janet K Williams; Sandra Daack-Hirsch; Martha Driessnack; Christian M Simon
Journal:  Patient Educ Couns       Date:  2012-10-12
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