Evidence map›Paper›PMID 37868041›Full record

ReviewCell genomics2023

Equity, diversity, and inclusion at the Global Alliance for Genomics and Health.

Neerjah Skantharajah, Shakuntala Baichoo, Tiffany F Boughtwood, Esmeralda Casas-Silva, Subhashini Chandrasekharan, Sanjay M Dave, Khalid A Fakhro, Aida B Falcon de Vargas, Sylvia S Gayle, Vivek K Gupta and 15 more

Abstract readReview
PubMed Full text at PMC Publisher
In one paragraph

Review in Cell genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
–field-weighted citation impact
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

13 citing papers in PubMed.

  1. Article
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  6. Article
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  11. Review
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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

25 authors.

Neerjah SkantharajahOntario Institute for Cancer Research, Toronto, ON, Canada.
Shakuntala BaichooUniversity of Mauritius, Reduit, Mauritius.
Tiffany F BoughtwoodAustralian Genomics, Parkville, VIC, Australia.
Esmeralda Casas-SilvaNational Cancer Institute, Rockville, MD, USA.
Subhashini ChandrasekharanThe All of Us Research Program, National Institutes of Health, Bethesda, MD, USA.
Sanjay M DaveDepartment of Biotechnology, Hemchandracharya North Gujarat University, Patan, Gujarat, India.
Khalid A FakhroDepartment of Human Genetics, Sidra Medicine, Doha, Qatar.
Aida B Falcon de VargasHospital Vargas de Caracas, Vargas Medical School, Universidad Central de Venezuela, Caracas, Venezuela.
Sylvia S GayleNational Cancer Institute, Rockville, MD, USA.
Vivek K GuptaMacquarie Medical School, Faculty of Medicine, Health and Human Sciences, Macquarie University, Sydney, NSW, Australia.
Rachele Hendricks-SturrupDuke-Margolis Center for Health Policy, Washington, DC, USA.
Ashley E HobbDNAstack, Toronto, ON, Canada.
Stephanie LiGlobal Alliance for Genomics and Health, Toronto, ON, Canada.
Bastien LlamasAustralian Centre for Ancient DNA, School of Biological Sciences and The Environment Institute, University of Adelaide, Adelaide, SA, Australia.
Catalina Lopez-CorreaGenome Canada, Ottawa, ON, Canada.
Mavis MachiroriAda Lovelace Institute, London, UK.
Jorge Melendez-ZajglaInstituto Nacional de Medicina Genomica, Mexico City, Mexico.
Mareike A MillnerMaastricht University, Health Law and Governance Group, Maastricht, the Netherlands.
Angela J H PageGlobal Alliance for Genomics and Health, Toronto, ON, Canada.
Laura D PaglioneSpherical Cow Group, New York, NY, USA.
Maili C Raven-AdamsGlobal Alliance for Genomics and Health, Toronto, ON, Canada.
Lindsay SmithOntario Institute for Cancer Research, Toronto, ON, Canada.
Ericka M ThomasThe All of Us Research Program, National Institutes of Health, Bethesda, MD, USA.
Judit KumuthiniSouth African National Bioinformatics Institute, University of Western Cape, Cape Town, South Africa.
Manuel CorpasSchool of Life Sciences, University of Westminster, London, UK.

Funding

H3ABioNet: informatics solutions for H3AfricaU24HG006941 · NHGRI · UNIVERSITY OF CAPE TOWN · PI MULDER, NICOLA · 2017 to 2021
$12.9M
Tracking Ethical Provenance for Sharing Genomic and Health Related DataU24HG011025 · NHGRI · BROAD INSTITUTE, INC. · PI HEIDI L REHM · 2021 to 2026
$8.2M
Medical Research Council MC_PC_19024NHGRI NIH HHS U24 HG006941NHGRI NIH HHS U24 HG011025
6 · The paper itself

Abstract

A lack of diversity in genomics for health continues to hinder equitable leadership and access to precision medicine approaches for underrepresented populations. To avoid perpetuating biases within the genomics workforce and genomic data collection practices, equity, diversity, and inclusion (EDI) must be addressed. This paper documents the journey taken by the Global Alliance for Genomics and Health (a genomics-based standard-setting and policy-framing organization) to create a more equitable, diverse, and inclusive environment for its standards and members. Initial steps include the creation of two groups: the Equity, Diversity, and Inclusion Advisory Group and the Regulatory and Ethics Diversity Group. Following a framework that we call "Reflected in our Teams, Reflected in our Standards," both groups address EDI at different stages in their policy development process.

Indexed as

communitydiversityEDIequityGA4GHgenomicsinclusion

Identifiers

PMID37868041
PMCPMC10589617

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.