Evidence map›Paper›PMID 34446835›Full record

ArticleEuropean journal of human genetics : EJHG2021

Australian human research ethics committee members' confidence in reviewing genomic research applications.

Ryan Pysar, Courtney K Wallingford, Jackie Boyle, Scott B Campbell, Lisa Eckstein, Rebekah McWhirter, Bronwyn Terrill, Chris Jacobs, Aideen M McInerney-Leo

Open access · bronzeAbstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
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  4. Genomics elucidates both common and rare disease aetiology.European journal of human genetics : EJHG · 2021
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 7 institutions in 1 country.

Ryan Pysar *Genetic Counseling, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia. Ryan.Pysar@health.nsw.gov.au.
Courtney K Wallingford *University of Queensland Diamantina Institute, University of Queensland, Dermatology Research Centre, Woolloongabba, QLD, Australia.
Jackie BoyleNSW Genetics of Learning Disability (GOLD) Service, Hunter Genetics, Waratah, NSW, Australia.
Scott B CampbellDepartment of Nephrology, Princess Alexandra Hospital, Woolloongabba, QLD, Australia.
Lisa EcksteinFaculty of Law University of Tasmania, Hobart, TAS, Australia.
Rebekah McWhirterSchool of Medicine, Faculty of Health, Deakin University, Geelong, VIC, Australia.
Bronwyn TerrillKinghorn Centre for Clinical Genomics, Garvan Institute of Medical Research, Darlinghurst, NSW, Australia.ORCID http://orcid.org/0000-0003-0263-363X
Chris JacobsGenetic Counseling, Graduate School of Health, University of Technology Sydney, Sydney, NSW, Australia.ORCID http://orcid.org/0000-0002-9557-9080
Aideen M McInerney-LeoUniversity of Queensland Diamantina Institute, University of Queensland, Dermatology Research Centre, Woolloongabba, QLD, Australia. a.mcinerney@uq.edu.au.ORCID http://orcid.org/0000-0002-0059-5732
The University of Queensland · AUUniversity of Technology Sydney · AUDeakin University · AUGarvan Institute of Medical Research · AUHunter Genetics · AUPrincess Alexandra Hospital · AUUniversity of Tasmania · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human research ethics committees (HRECs) are evaluating increasing quantities of genomic research applications with complex ethical considerations. Genomic confidence is reportedly low amongst many non-genetics-experts; however, no studies have evaluated genomic confidence levels in HREC members specifically. This study used online surveys to explore genomic confidence levels, predictors of confidence, and genomics resource needs of members from 185 HRECs across Australia. Surveys were fully or partially completed by 145 members. All reported having postgraduate 94 (86%) and/or bachelor 15 (14%) degrees. Participants consisted mainly of researchers (n = 45, 33%) and lay members (n = 41, 30%), affiliated with either public health services (n = 73, 51%) or public universities (n = 31, 22%). Over half had served their HREC [Formula: see text]3 years. Fifty (44%) reviewed genomic studies [Formula: see text]3 times annually. Seventy (60%) had undertaken some form of genomic education. While most (94/103, 91%) had high genomic literacy based on familiarity with genomic terms, average genomic confidence scores (GCS) were moderate (5.7/10, n = 119). Simple linear regression showed that GCS was positively associated with years of HREC service, frequency of reviewing genomic applications, undertaking self-reported genomic education, and familiarity with genomic terms (p < 0.05 for all). Conversely, lay members and/or those relying on others when reviewing genomic studies had lower GCSs (p < 0.05 for both). Most members (n = 83, 76%) agreed further resources would be valuable when reviewing genomic research applications, and online courses and printed materials were preferred. In conclusion, even well-educated HREC members familiar with genomic terms lack genomic confidence, which could be enhanced with additional genomic education and/or resources.

Indexed as

AdultAustraliaEducational StatusEthics CommitteesFemaleGenomicsHuman GeneticsHumansMaleMiddle AgedPeer Review

Identifiers

PMID34446835
PMCPMC8633339
OpenAlexW3194671791

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.