Evidence map›Paper›PMID 35690058›Full record

ArticleMed (New York, N.Y.)2022

Tailored community engagement to address the genetics diversity gap.

Neil A Hanchard, Maria Chahrour, Jantina de Vries

Abstract readLetter
PubMed Full text at PMC Publisher
In one paragraph

Article in Med (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

3 authors.

Neil A HanchardChildhood Complex Disease Genomics Section, Center for Personalized Health Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA. Electronic address: neil.hanchard@nih.gov.
Maria ChahrourEugene McDermott Center for Human Growth and Development, Departments of Neuroscience and Psychiatry, Center for the Genetics of Host Defense, Peter O'Donnell Jr. Brain Institute, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Jantina de VriesUCT Neuroscience Institute and Department of Medicine, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa.

Funding

Multiscale functional characterization of genomic variation in human developmental disordersUM1HG011996 · NHGRI · UT SOUTHWESTERN MEDICAL CENTER · PI Gary Chung Hon, WILLIAM Lee KRAUS · 2021 to 2026
$10.5M
Multi-omics Studies of Childhood Complex Traits in Diverse PopulationsZIAHG200412 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI HANCHARD, NEIL · 2021 to 2025
$8.2M
Genetics of childhood-onset hypertensionZIAHG200414 · NHGRI · NATIONAL HUMAN GENOME RESEARCH INSTITUTE · PI HANCHARD, NEIL · 2021 to 2025
$2.5M
Molecular mechanisms underlying vocal communicationR01HD099162 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI CHAHROUR, MARIA · 2020 to 2024
$2.0M
Intramural NIH HHS ZIA HG200412Intramural NIH HHS ZIA HG200414NHGRI NIH HHS UM1 HG011996NICHD NIH HHS R01 HD099162Wellcome Trust
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Identifiers

PMID35690058
PMCPMC10612127

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.