Literature DB >> 24077424

Returning genetic research results: study type matters.

Amy L McGuire1, Jill Oliver Robinson, Rachel B Ramoni, Debra S Morley, Steven Jofe, Sharon E Plon.   

Abstract

AIM: The return of individual genetic research results has been identified as one of the most pressing ethical challenges warranting immediate policy attention. We explored the practices and perspectives of genome-wide association studies (GWAS) investigators on this topic. MATERIALS &
METHODS: Corresponding authors of published GWAS were invited to participate in a semistructured interview. Interviews (n = 35) were transcribed and analyzed using conventional content analysis.
RESULTS: Most investigators had not returned GWAS results. Several had experience returning results in the context of linkage/family studies, and many felt that it will become a larger issue in whole-genome/-exome sequencing.
CONCLUSIONS: Research context and nature of the study are important considerations in the decision to return results. More nuanced ethical guidelines should take these contextual factors into account.

Entities:  

Keywords:  ethics; genome-wide association; genomics; policy; return of results; whole-genome sequencing

Year:  2013        PMID: 24077424      PMCID: PMC3783351          DOI: 10.2217/pme.12.109

Source DB:  PubMed          Journal:  Per Med        ISSN: 1741-0541            Impact factor:   2.512


  21 in total

1.  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
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2.  The incidentalome: a threat to genomic medicine.

Authors:  Isaac S Kohane; Daniel R Masys; Russ B Altman
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3.  Offering individual genetic research results: context matters.

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4.  Quality of informed consent in cancer clinical trials: a cross-sectional survey.

Authors:  S Joffe; E F Cook; P D Cleary; J W Clark; J C Weeks
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5.  Reporting genetic results in research studies: summary and recommendations of an NHLBI working group.

Authors:  Ebony B Bookman; Aleisha A Langehorne; John H Eckfeldt; Kathleen C Glass; Gail P Jarvik; Michael Klag; Greg Koski; Arno Motulsky; Benjamin Wilfond; Teri A Manolio; Richard R Fabsitz; Russell V Luepker
Journal:  Am J Med Genet A       Date:  2006-05-15       Impact factor: 2.802

6.  The emergence of an ethical duty to disclose genetic research results: international perspectives.

Authors:  Bartha Maria Knoppers; Yann Joly; Jacques Simard; Francine Durocher
Journal:  Eur J Hum Genet       Date:  2006-07-26       Impact factor: 4.246

7.  Informed consent and subject motivation to participate in a large, population-based genomics study: the Marshfield Clinic Personalized Medicine Research Project.

Authors:  Catherine A McCarty; Anuradha Nair; Diane M Austin; Philip F Giampietro
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8.  Taking aims seriously: repository research and limits on the duty to return individual research findings.

Authors:  Pilar Ossorio
Journal:  Genet Med       Date:  2012-03-08       Impact factor: 8.822

9.  The legal risks of returning results of genomics research.

Authors:  Ellen Wright Clayton; Amy L McGuire
Journal:  Genet Med       Date:  2012-02-09       Impact factor: 8.822

10.  Exploring concordance and discordance for return of incidental findings from clinical sequencing.

Authors:  Robert C Green; Jonathan S Berg; Gerard T Berry; Leslie G Biesecker; David P Dimmock; James P Evans; Wayne W Grody; Madhuri R Hegde; Sarah Kalia; Bruce R Korf; Ian Krantz; Amy L McGuire; David T Miller; Michael F Murray; Robert L Nussbaum; Sharon E Plon; Heidi L Rehm; Howard J Jacob
Journal:  Genet Med       Date:  2012-03-15       Impact factor: 8.822

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  16 in total

1.  Pediatric Cancer Genetics Research and an Evolving Preventive Ethics Approach for Return of Results after Death of the Subject.

Authors:  Sarah Scollon; Katie Bergstrom; Laurence B McCullough; Amy L McGuire; Stephanie Gutierrez; Robin Kerstein; D Williams Parsons; Sharon E Plon
Journal:  J Law Med Ethics       Date:  2015       Impact factor: 1.718

2.  Return of individual genomic research results: what do consent forms tell participants?

Authors:  Stacey Pereira; Jill Oliver Robinson; Amy L McGuire
Journal:  Eur J Hum Genet       Date:  2016-06-22       Impact factor: 4.246

3.  Challenges of coverage policy development for next-generation tumor sequencing panels: experts and payers weigh in.

Authors:  Julia R Trosman; Christine B Weldon; R Kate Kelley; Kathryn A Phillips
Journal:  J Natl Compr Canc Netw       Date:  2015-03       Impact factor: 11.908

4.  Confidentiality in Biobanking Research: A Comparison of Donor and Nondonor Families' Understanding of Risks.

Authors:  Laura A Siminoff; Maureen Wilson-Genderson; Maghboeba Mosavel; Laura Barker; Jennifer Trgina; Heather M Traino
Journal:  Genet Test Mol Biomarkers       Date:  2017-01-25

5.  The unintended implications of blurring the line between research and clinical care in a genomic age.

Authors:  Benjamin E Berkman; Sara Chandros Hull; Lisa Eckstein
Journal:  Per Med       Date:  2014       Impact factor: 2.512

Review 6.  Genome-Wide Sequencing for Prenatal Detection of Fetal Single-Gene Disorders.

Authors:  Ignatia B van den Veyver; Christine M Eng
Journal:  Cold Spring Harb Perspect Med       Date:  2015-08-07       Impact factor: 6.915

7.  Return of Value in the New Era of Biomedical Research-One Size Will Not Fit All.

Authors:  Dmitry Khodyakov; Alexandra Mendoza-Graf; Sandra Berry; Camille Nebeker; Elizabeth Bromley
Journal:  AJOB Empir Bioeth       Date:  2019-10-03

8.  A qualitative analysis of the attitudes of Irish patients towards participation in genetic-based research.

Authors:  T P McVeigh; K J Sweeney; M J Kerin; D J Gallagher
Journal:  Ir J Med Sci       Date:  2015-10-23       Impact factor: 1.568

9.  Processes and factors involved in decisions regarding return of incidental genomic findings in research.

Authors:  Robert Klitzman; Brigitte Buquez; Paul S Appelbaum; Abby Fyer; Wendy K Chung
Journal:  Genet Med       Date:  2013-09-26       Impact factor: 8.822

10.  Recommendations from the international stroke genetics consortium, part 1: standardized phenotypic data collection.

Authors:  Jennifer J Majersik; John W Cole; Jonathan Golledge; Natalia S Rost; Yu-Feng Yvonne Chan; M Edip Gurol; Arne G Lindgren; Daniel Woo; Israel Fernandez-Cadenas; Donna T Chen; Vincent Thijs; Bradford B Worrall; Ayeesha Kamal; Paul Bentley; Joanna M Wardlaw; Ynte M Ruigrok; Thomas W K Battey; Reinhold Schmidt; Joan Montaner; Anne-Katrin Giese; Jaume Roquer; Jordi Jiménez-Conde; Chaeyoung Lee; Hakan Ay; Juan Jose Martin; Jonathan Rosand; Jane Maguire
Journal:  Stroke       Date:  2014-12-09       Impact factor: 7.914

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