Literature DB >> 20371468

Meeting the governance challenges of next-generation biorepository research.

Stephanie M Fullerton1, Nicholas R Anderson, Greg Guzauskas, Dena Freeman, Kelly Fryer-Edwards.   

Abstract

Advances in clinical translational research have led to an explosion of interest in infrastructure development and data sharing facilitated by biorepositories of specimens and linked health information. These efforts are qualitatively different from the single-center sample collections that preceded them and pose substantial new ethics and regulatory challenges for investigators and institutions. New research governance approaches, which can address current and anticipated challenges, promote high-quality research, and provide a robust basis for ongoing research participation, are urgently required.

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Year:  2010        PMID: 20371468      PMCID: PMC3038212          DOI: 10.1126/scitranslmed.3000361

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  31 in total

Review 1.  Solidarity and equity: new ethical frameworks for genetic databases.

Authors:  R Chadwick; K Berg
Journal:  Nat Rev Genet       Date:  2001-04       Impact factor: 53.242

Review 2.  Data storage and DNA banking for biomedical research: informed consent, confidentiality, quality issues, ownership, return of benefits. A professional perspective.

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Journal:  Eur J Hum Genet       Date:  2003-12       Impact factor: 4.246

3.  The charitable trust as a model for genomic biobanks.

Authors:  David E Winickoff; Richard N Winickoff
Journal:  N Engl J Med       Date:  2003-09-18       Impact factor: 91.245

4.  Governing UK Biobank: the importance of ensuring public trust.

Authors:  Richard Tutton; Jane Kaye; Klaus Hoeyer
Journal:  Trends Biotechnol       Date:  2004-06       Impact factor: 19.536

Review 5.  The social and ethical issues of post-genomic human biobanks.

Authors:  Anne Cambon-Thomsen
Journal:  Nat Rev Genet       Date:  2004-11       Impact factor: 53.242

6.  Genomics--the perfect information-seeking research problem.

Authors:  J David Johnson; Donald O Case; James E Andrews; Suzanne L Allard
Journal:  J Health Commun       Date:  2005-06

7.  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

8.  Genetics. No longer de-identified.

Authors:  Amy L McGuire; Richard A Gibbs
Journal:  Science       Date:  2006-04-21       Impact factor: 47.728

Review 9.  Human biological materials in research: ethical issues and the role of stewardship in minimizing research risks.

Authors:  B R Jeffers
Journal:  ANS Adv Nurs Sci       Date:  2001-12       Impact factor: 1.824

10.  A new statistic and its power to infer membership in a genome-wide association study using genotype frequencies.

Authors:  Kevin B Jacobs; Meredith Yeager; Sholom Wacholder; David Craig; Peter Kraft; David J Hunter; Justin Paschal; Teri A Manolio; Margaret Tucker; Robert N Hoover; Gilles D Thomas; Stephen J Chanock; Nilanjan Chatterjee
Journal:  Nat Genet       Date:  2009-10-04       Impact factor: 38.330

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  39 in total

Review 1.  Inactivated influenza vaccines: recent progress and implications for the elderly.

Authors:  Valentina Parodi; Daniela de Florentiis; Mariano Martini; Filippo Ansaldi
Journal:  Drugs Aging       Date:  2011-02-01       Impact factor: 3.923

Review 2.  Bioethical considerations in developing a biorepository for the Pneumonia Etiology Research for Child Health project.

Authors:  Andrea N DeLuca; Alan Regenberg; Jeremy Sugarman; David R Murdoch; Orin Levine
Journal:  Clin Infect Dis       Date:  2012-04       Impact factor: 9.079

3.  Secondary uses and the governance of de-identified data: lessons from the human genome diversity panel.

Authors:  Stephanie M Fullerton; Sandra S-J Lee
Journal:  BMC Med Ethics       Date:  2011-09-26       Impact factor: 2.652

4.  Data governance requirements for distributed clinical research networks: triangulating perspectives of diverse stakeholders.

Authors:  Katherine K Kim; Dennis K Browe; Holly C Logan; Roberta Holm; Lori Hack; Lucila Ohno-Machado
Journal:  J Am Med Inform Assoc       Date:  2013-12-03       Impact factor: 4.497

5.  Beyond Consent: Building Trusting Relationships With Diverse Populations in Precision Medicine Research.

Authors:  Stephanie A Kraft; Mildred K Cho; Katherine Gillespie; Meghan Halley; Nina Varsava; Kelly E Ormond; Harold S Luft; Benjamin S Wilfond; Sandra Soo-Jin Lee
Journal:  Am J Bioeth       Date:  2018-04       Impact factor: 11.229

6.  Reflexive governance in biobanking: on the value of policy led approaches and the need to recognise the limits of law.

Authors:  Graeme Laurie
Journal:  Hum Genet       Date:  2011-07-16       Impact factor: 4.132

7.  Access policies in biobank research: what criteria do they include and how publicly available are they? A cross-sectional study.

Authors:  Holger Langhof; Hannes Kahrass; Sören Sievers; Daniel Strech
Journal:  Eur J Hum Genet       Date:  2016-12-21       Impact factor: 4.246

8.  Reporting actionable research results: shared secrets can save lives.

Authors:  Lawrence E Hunter; Christian Hopfer; Sharon F Terry; Marilyn E Coors
Journal:  Sci Transl Med       Date:  2012-07-18       Impact factor: 17.956

Review 9.  Evolving approaches to the ethical management of genomic data.

Authors:  Jean E McEwen; Joy T Boyer; Kathie Y Sun
Journal:  Trends Genet       Date:  2013-02-28       Impact factor: 11.639

10.  A trade secret model for genomic biobanking.

Authors:  John M Conley; Robert Mitchell; R Jean Cadigan; Arlene M Davis; Allison W Dobson; Ryan Q Gladden
Journal:  J Law Med Ethics       Date:  2012       Impact factor: 1.718

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