Evidence map›Paper›PMID 31889767›Full record

ArticleEthnicity & disease2019

How Can Law Support Development of Genomics and Precision Medicine to Advance Health Equity and Reduce Disparities?

Susan M Wolf, Vence L Bonham, Marino A Bruce

Open access · bronzeAbstract readEditorial
In one paragraph

Article in Ethnicity & disease, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 20% 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

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Review
  3. Increasing access to individualized medicine: a matched-cohort study examining Latino participant experiences of genomic screening.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Article
  4. 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 at 3 institutions in 2 countries.

Susan M WolfConsortium on Law and Values in Health, Environment & the Life Sciences; Law School; Medical School, University of Minnesota, Minneapolis, MN.
Vence L BonhamSocial and Behavioral Research Branch, Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD.
Marino A BruceProgram for Research on Faith and Health, Vanderbilt Center for Research on Men's Health, Center for Medicine, Health, and Society, Vanderbilt University, Nashville, TN.
National Human Genome Research Institute · USUniversity of Minnesota Medical Center · USVanderbilt Health · US

Funding

Training and Mentoring CoreU54MD010722 · NIMHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI DENNY, JOSHUA C. · 2016 to 2020
$11.9M
LawSeq: Building a Sound Legal Foundation for Translating Genomics into Clinical ApplicationR01HG008605 · NHGRI · UNIVERSITY OF MINNESOTA · PI CLAYTON, ELLEN WRIGHT, LAWRENZ, FRANCES PATRICIA · 2016 to 2018
$2.2M
NHGRI NIH HHS R01 HG008605NIMHD NIH HHS U54 MD010722
6 · The paper itself

Abstract

There is growing recognition that the genomic and precision medicine revolution in health care can deepen health disparities. This has produced urgent calls to prioritize inclusion of historically underrepresented populations in research and to make genomic databases more inclusive. Answering the call to address health care disparities in the delivery of genomic and precision medicine requires a consideration of important, yet understudied, legal issues that have blocked progress. This article introduces a special issue of

Indexed as

Delivery of Health Care, IntegratedHealth EquityPrecision MedicineEthnicityGenomicsHealthcare DisparitiesHumansBiomedical EthicsGenomic MedicineHealth DisparitiesHealth EquityLawPrecision Medicine

Identifiers

PMID31889767
PMCPMC6919974
OpenAlexW2995315822

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.