Evidence map›Paper›PMID 30546600›Full record

ArticleJournal of cardiology cases2016

Effective cascade screening through identification of a mutation in

Claire Bailey, Edward Blair, Clifford Garratt, William G Newman

Open access · bronzeAbstract read
In one paragraph

Article in Journal of cardiology cases, 2016. 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, top 87% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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 at 3 institutions in 1 country.

Claire BaileyManchester Centre for Genomic Medicine, University of Manchester, Manchester, UK.
Edward BlairDepartment of Clinical Genetics, Churchill Hospital, Old Road, Headington, Oxford, UK.
Clifford GarrattManchester Heart Centre, Central Manchester University Hospitals NHS Foundation Trust, & Institute of Cardiovascular Sciences, University of Manchester, Manchester, UK.
William G NewmanManchester Centre for Genomic Medicine, University of Manchester, Manchester, UK.
University of Manchester · GBChurchill Hospital · GBManchester University NHS Foundation Trust · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is an inherited arrhythmogenic disorder which usually presents in the first or second decade of life with syncope, which is typically induced by emotional stress or exercise. We describe a large family with a history of three sudden unexpected deaths. Investigations in the sibling of a deceased individual affected by emotion-induced syncope revealed ventricular bigeminy. Molecular genetic testing was performed on one symptomatic individual and a missense mutation in

Indexed as

Catecholaminergic polymorphic ventricular tachycardia (CPVT)RYR2Sudden death

Identifiers

PMID30546600
PMCPMC6281865
OpenAlexW2228079946

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.