Evidence map›Paper›PMID 38142673›Full record

ArticlePublic health genomics2024

Improving Care for Marginalized Populations at Risk for Hereditary Cancer Syndromes: Innovations that Expanded Reach in the CHARM Study.

Marian J Gilmore, Sarah Knerr, Stephanie A Kraft, Joanna E Bulkley, Barbara B Biesecker, Heather Spencer Feigelson, Jessica Ezzell Hunter, Charisma L Jenkins, Tia L Kauffman, Sandra Soo-Jin Lee and 13 more

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Public health genomics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

23 authors.

Marian J GilmoreDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA, marian.j.gilmore@kpchr.org.
Sarah KnerrDepartment of Health Systems and Population Health, School of Public Health, University of Washington, Seattle, Washington, USA.
Stephanie A KraftTreuman Katz Center for Pediatric Bioethics and Palliative Care, Seattle Children's Research Institute, Seattle, Washington, USA.
Joanna E BulkleyDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Barbara B BieseckerRTI International, Washington, District of Columbia, USA.
Heather Spencer FeigelsonInstitute for Health Research, Kaiser Permanente, Aurora, Colorado, USA.
Jessica Ezzell HunterGenomics, Ethics, and Translational Research Program, RTI International, Research Triangle Park, North Carolina, USA.
Charisma L JenkinsDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Tia L KauffmanDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Sandra Soo-Jin LeeDivision of Ethics, Department of Medical Humanities and Ethics, Columbia University, New York, New York, USA.
Elizabeth G LilesKaiser Permanente Center for Health Research, Portland, Oregon, USA.
Kathleen F MittendorfDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Kristin R MuessigDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Kathryn M PorterTreuman Katz Center for Pediatric Bioethics and Palliative Care, Seattle Children's Research Institute, Seattle, Washington, USA.
Bradley A RolfDepartment of Medicine (Medical Genetics), University of Washington Medical Center, Seattle, Washington, USA.
Alan F RopeGenome Medical, South San Francisco, California, USA.
Jamilyn M ZeppDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Katherine Patrice AndersonAmbulatory Care Services, Denver Health, Denver, Colorado, USA.
Beth DevineThe Comparative Health Outcomes, Policy and Economics (CHOICE) Institute, School of Pharmacy, University of Washington, Seattle, Washington, USA.
Galen JosephDepartment of Humanities and Social Sciences, University of California, San Francisco, California, USA.
Michael C LeoKaiser Permanente Center for Health Research, Portland, Oregon, USA.
Katrina GoddardDepartment of Translational and Applied Genomics, Kaiser Permanente Center for Health Research, Portland, Oregon, USA.
Benjamin S WilfondTreuman Katz Center for Pediatric Bioethics and Palliative Care, Seattle Children's Research Institute, Seattle, Washington, USA.

Funding

Exome sequencing in Diverse Populations in Colorado & OregonU01HG007292 · NHGRI · KAISER FOUNDATION RESEARCH INSTITUTE · PI LEO, MICHAEL C, WILFOND, BENJAMIN SIMON · 2017 to 2021
$15.7M
Evolving Our Partnership: The CSER2 Centralized Support Coordinating CenterU24HG007307 · NHGRI · UNIVERSITY OF WASHINGTON · PI FULLERTON, STEPHANIE MALIA, JARVIK, GAIL PAIRITZ · 2017 to 2021
$5.8M
NHGRI NIH HHS U01 HG007292NHGRI NIH HHS U01HG007292NHGRI NIH HHS U24 HG007307NHGRI NIH HHS U24HG007307
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Neoplastic Syndromes, HereditaryQuality ImprovementGenetic CounselingGenetic Predisposition to DiseaseGenetic TestingHumansRisk FactorsGenetic counselingHealth systemsHereditary cancer syndromesMarginalized populations

Identifiers

PMID38142673
PMCPMC13290324

What OpenQuestion holds

Textmetadata
LicenceTDM
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.