Evidence map›Paper›PMID 41852683›Full record

ArticleThe British journal of cardiology2024

Sudden cardiac death associated with a pathogenic genetic variant in

Gokul Parameswaran, Edward Blair, Hugh C Watkins, Julian Om Ormerod

Abstract readCase Reports
In one paragraph

Article in The British journal of cardiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Gokul ParameswaranMedical Student, Oxford University Medical School, Oxford.
Edward BlairConsultant Clinical Geneticist, Oxford Centre for Genomic Medicine, Oxford University Hospitals NHS Foundation Trust, Oxford.
Hugh C WatkinsProfessor of Cardiovascular Medicine.
Julian Om OrmerodConsultant Cardiologist, Division of Cardiovascular Medicine, Radcliffe Department of Medicine, John Radcliffe Hospital, Oxford.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pathogenic genetic variants in the

Indexed as

arrythmiasgenetic variantsHCN4 genesinus node dysfunction

Identifiers

PMID41852683
PMCPMC12993991

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.