Evidence map›Paper›PMID 31824576›Full record

ArticleFrontiers in genetics2019

Informing Integration of Genomic Medicine Into Primary Care: An Assessment of Current Practice, Attitudes, and Desired Resources.

June C Carroll, Judith Allanson, Shawna Morrison, Fiona A Miller, Brenda J Wilson, Joanne A Permaul, Deanna Telner

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 5 pooled it
7.7field-weighted citation impact, top 2% 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

52 citing papers in PubMed, 5 syntheses or guidelines pooled it, 71 citations in OpenAlex.

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  5. Effect of genetics clinical decision support tools on health-care providers' decision making: a mixed-methods systematic review.Genetics in medicine : official journal of the American College of Medical Genetics · 2021
    Pooled it
  6. Educational considerations based on medical student use of polygenic risk information and apparent race in a simulated consultation.Genetics in medicine : official journal of the American College of Medical Genetics · 2022
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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

7 authors at 4 institutions in 1 country.

June C CarrollSinai Health System, Department of Family and Community Medicine, University of Toronto, Toronto, ON, Canada.
Judith AllansonDepartment of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
Shawna MorrisonDepartment of Genetics, Children's Hospital of Eastern Ontario, Ottawa, ON, Canada.
Fiona A MillerInstitute of Health Policy, Management and Evaluation, University of Toronto, Toronto, ON, Canada.
Brenda J WilsonDivision of Community Health and Humanities, Memorial University of Newfoundland, St. John's, NL, Canada.
Joanne A PermaulSinai Health System, Ray D Wolfe Department of Family Medicine, Toronto, ON, Canada.
Deanna TelnerSouth East Toronto Family Health Team, Department of Family and Community Medicine, University of Toronto, Toronto, ON, Canada.
Children's Hospital of Eastern Ontario · CASinai Health System · CAUniversity of Toronto · CAMemorial University of Newfoundland · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

genetic servicesgenomicshealth services needsprimary health carequestionnaire

Identifiers

PMID31824576
PMCPMC6882282
OpenAlexW2989769862

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.