Literature DB >> 33871839

Ethical, Legal, and Social Issues (ELSI) in Clinical Genetics Research.

Daryl Pullman1, Holly Etchegary2.   

Abstract

ELSI (Ethical, Legal, and Social Issues) is a widely used acronym in the bioethics literature that encompasses a broad range of research examining the various impacts of science and technology on society. In Canada, GE3LS (Genetics, Ethical, Economic, Environmental, Legal, Social issues) is the term used to describe ELSI studies in the context of genetics and genomics research. It is intentionally more expansive in that GE3LS explicitly brings economic and environmental issues under its purview. ELSI/GE3LS research is increasingly relevant in recent years as there has been a greater emphasis on "translational research" that moves genomic discoveries from the bench to the clinic. The purpose of this chapter is to outline a range of ELSI-related work that might be conducted as part of a large scale genetics or genomics research project, and to provide some practical insights on how a scientific research team might incorporate a strong and effective ELSI program within its broader research mandate. We begin by describing the historical context of ELSI research and the development of GE3LS research in the Canadian context. We then illustrate how some ELSI research might unfold by outlining a variety of GE3LS research questions or content domains and the methodologies that might be employed in studying them. We conclude with some practical suggestions about how to build an effective ELSI/GE3LS team and focus within a broader scientific research program.

Keywords:  Clinical genetics; Ethical; GE3LS; Genomics; Legal; Mixed methods; Social issues (ELSI)

Year:  2021        PMID: 33871839     DOI: 10.1007/978-1-0716-1138-8_5

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  35 in total

Review 1.  Consumers' views of direct-to-consumer genetic information.

Authors:  Colleen M McBride; Christopher H Wade; Kimberly A Kaphingst
Journal:  Annu Rev Genomics Hum Genet       Date:  2010       Impact factor: 8.929

2.  Biobanking in British Columbia: discussions of the future of personalized medicine through deliberative public engagement.

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Journal:  Per Med       Date:  2008-05       Impact factor: 2.512

3.  The integration of citizens into a science/policy network in genetics: governance arrangements and asymmetry in expertise.

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Journal:  Health Expect       Date:  2010-10-28       Impact factor: 3.377

4.  Seeking Genomic Knowledge: The Case for Clinical Restraint.

Authors:  Wylie Burke; Susan Brown Trinidad; Ellen Wright Clayton
Journal:  Hastings Law J       Date:  2013-08-01

5.  Defining translational research: implications for training.

Authors:  Doris McGartland Rubio; Ellie E Schoenbaum; Linda S Lee; David E Schteingart; Paul R Marantz; Karl E Anderson; Lauren Dewey Platt; Adriana Baez; Karin Esposito
Journal:  Acad Med       Date:  2010-03       Impact factor: 6.893

6.  Public and biobank participant attitudes toward genetic research participation and data sharing.

Authors:  A A Lemke; W A Wolf; J Hebert-Beirne; M E Smith
Journal:  Public Health Genomics       Date:  2010-01-15       Impact factor: 2.000

Review 7.  Clinical Applications of Next-Generation Sequencing in Cancer Diagnosis.

Authors:  Leila Sabour; Maryam Sabour; Saeid Ghorbian
Journal:  Pathol Oncol Res       Date:  2016-10-08       Impact factor: 3.201

8.  Patient and Family Advisory Councils (PFACs): Identifying Challenges and Solutions to Support Engagement in Research.

Authors:  James D Harrison; Wendy G Anderson; Maureen Fagan; Edmondo Robinson; Jeffrey Schnipper; Gina Symczak; Catherine Hanson; Martha B Carnie; Jim Banta; Sherry Chen; Jonathan Duong; Celene Wong; Andrew D Auerbach
Journal:  Patient       Date:  2018-08       Impact factor: 3.883

9.  The clinical application of genome-wide sequencing for monogenic diseases in Canada: Position Statement of the Canadian College of Medical Geneticists.

Authors:  Kym Boycott; Taila Hartley; Shelin Adam; Francois Bernier; Karen Chong; Bridget A Fernandez; Jan M Friedman; Michael T Geraghty; Stacey Hume; Bartha M Knoppers; Anne-Marie Laberge; Jacek Majewski; Roberto Mendoza-Londono; M Stephen Meyn; Jacques L Michaud; Tanya N Nelson; Julie Richer; Bekim Sadikovic; David L Skidmore; Tracy Stockley; Sherry Taylor; Clara van Karnebeek; Ma'n H Zawati; Julie Lauzon; Christine M Armour
Journal:  J Med Genet       Date:  2015-05-07       Impact factor: 6.318

10.  Perceptions of genetic discrimination among people at risk for Huntington's disease: a cross sectional survey.

Authors:  Yvonne Bombard; Gerry Veenstra; Jan M Friedman; Susan Creighton; Lauren Currie; Jane S Paulsen; Joan L Bottorff; Michael R Hayden
Journal:  BMJ       Date:  2009-06-09
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  1 in total

1.  Genetics and Genomics Teaching in Nursing Programs in a Latin American Country.

Authors:  Luís Carlos Lopes-Júnior; Emiliana Bomfim; Milena Flória-Santos
Journal:  J Pers Med       Date:  2022-07-12
  1 in total

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