Evidence map›Paper›PMID 38884101›Full record

ArticleFrontiers in pediatrics2024

A mild phenotype associated with

Simona Bene Watts, Barbara Gauthier, Anders C Erickson, Julie Morrison, Mavis Sebastian, Lawrence Gillman, Sarah McIntosh, Connie Ens, Elizabeth Sherwin, Rod McCormick and 2 more

Abstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pediatrics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Simona Bene WattsIsland Medical Program, University of British Columbia, Victoria, BC, Canada.
Barbara GauthierEpidemiology and Surveillance Unit, Interior Health Authority, Kelowna, BC, Canada.
Anders C EricksonHealth Protection Branch, Ministry of Health, Victoria, BC, Canada.
Julie MorrisonGitxsan Community Member, Hazelton, BC, Canada.
Mavis SebastianGitxsan Community Member, Hazelton, BC, Canada.
Lawrence GillmanDepartment of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Sarah McIntoshDepartment of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Connie EnsDepartment of Pediatrics, Division of Cardiology, British Columbia Children's Hospital, Vancouver, BC, Canada.
Elizabeth SherwinDepartment of Pediatrics, Children's National Hospital, Washington, DC, United States.
Rod McCormickDepartment of Education and Social Work, Thompson Rivers University, Kamloops, BC, Canada.
Shubhayan SanataniDepartment of Pediatrics, Division of Cardiology, British Columbia Children's Hospital, Vancouver, BC, Canada.
Laura ArbourIsland Medical Program, University of British Columbia, Victoria, BC, Canada.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Congenital Long QT Syndrome (LQTS) is common in a First Nations community in Northern British Columbia due to the founder variant Methods: As part of a larger study assessing those with LQTS and their relatives in a Northern BC First Nation, we assessed those entering the study from birth to age 18 years. We compared the corrected peak QTc and potential cardiac events (syncope/seizures) of 186 children from birth to 18 years, with and without the Results: Only the Conclusion: While the

Indexed as

carnitine palmitoyltransferase 1AFirst NationsIndigenousKCNQ1long QT syndrome (LQTS)long QT syndrome type 1

Identifiers

PMID38884101
PMCPMC11176454

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.