Evidence map›Paper›PMID 39251787›Full record

ArticleNature genetics2024

Defining and pursuing diversity in human genetic studies.

Maili C Raven-Adams, Tina Hernandez-Boussard, Yann Joly, Bartha Maria Knoppers, Subhashini Chandrasekharan, Adrian Thorogood, Judit Kumuthini, Calvin Wai Loon Ho, Ariana Gonzlez, Sarah C Nelson and 11 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
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

21 authors.

Maili C Raven-AdamsNuffield Council on Bioethics, London, UK.
Tina Hernandez-BoussardDepartment of Medicine, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0001-6553-3455
Yann JolyCentre of Genomics and Policy, Victor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0002-8775-2322
Bartha Maria KnoppersCentre of Genomics and Policy, Victor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montreal, Quebec, Canada.ORCID http://orcid.org/0000-0001-7004-2722
Subhashini ChandrasekharanNational Institutes of Health, Bethesda, MD, USA.
Adrian ThorogoodThe Terry Fox Research Institute, Vancouver, British Columbia, Canada.
Judit KumuthiniAfrican Biobanks and Longitudinal Epidemiologic Ecosystem, Ibadan, Nigeria.
Calvin Wai Loon HoFaculty of Law, Monash University, Melbourne, Victoria, Australia.ORCID http://orcid.org/0000-0002-8328-1308
Ariana GonzlezGenoox, Tel Aviv, Israel.
Sarah C NelsonDepartment of Biostatistics, University of Washington, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-2109-6465
Yvonne BombardInstitute of Health Policy, Management and Evaluation, University of Toronto, Ontario, Canada.ORCID http://orcid.org/0000-0002-9516-4539
Donrich ThaldarSchool of Law, University of KwaZulu-Natal, Durban, South Africa.
Hanshi LiuCentre of Genomics and Policy, Victor Phillip Dahdaleh Institute of Genomic Medicine, McGill University, Montreal, Quebec, Canada.
Alessia CostaConnecting Science, Wellcome Genome Campus, Hinxton, UK.
Vijaytha MuralidharanDepartment of Medicine, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-0226-8468
Sasha HenriquesConnecting Science, Wellcome Genome Campus, Hinxton, UK.
Jamal NasirLife Sciences, University of Northampton, Northampton, UK.
Aimé LumakaCentre for Human Genetics, University of Kinshasa, Kinshasa, Democratic Republic of the Congo.ORCID http://orcid.org/0000-0002-5468-8678
Beatrice KaiserDepartment of Medicine, Stanford University, Stanford, CA, USA.ORCID http://orcid.org/0000-0003-2227-9009
Saumya Shekhar JamuarSingHealth Duke-NUS Institute of Precision Medicine, Singapore, Singapore.ORCID http://orcid.org/0000-0003-2341-8349
Anna C F LewisDivision of Genetics, Brigham and Women's Hospital, Boston, MA, USA. aclewis@bwh.harvard.edu.ORCID http://orcid.org/0000-0002-1274-386X

Funding

African Rare Diseases Initiative (ARDI): Advancing Genomic Medicine through rare diseases research in AfricaR01HG012284 · NHGRI · CENTRE DE GENETIQUE HUMAINE · PI AIME LUMAKA ZOLA · 2023 to 2026
$2.5M
Identifying strategies to reveal genetic results over the lifespanK99HG012809 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI LEWIS, ANNA · 2023 to 2024
$360k
NHGRI NIH HHS R01 HG012284U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI) 1K99HG012809
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID39251787

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.