Evidence map›Paper›PMID 42123196›Full record

ArticleJournal of clinical medicine2026

Familial Short QT Syndrome: Phenotypic Variability and Challenges in Risk Stratification.

Paula Bouzón, Alberto Alen, María Salgado, Francisco González-Urbistondo, Lorena María Vega-Prado, Eliecer Coto, José Julián Rodríguez-Reguero, Juan Gomez, Barbara Fernández-Barrio, Pablo Avanzas and 1 more

Abstract read
In one paragraph

Article in Journal of clinical medicine, 2026. 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

11 authors.

Paula BouzónÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Alberto AlenÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-0771-4650
María SalgadoÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-6697-6274
Francisco González-UrbistondoÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Lorena María Vega-PradoUnidad de Cardiopatías Familiares, Área del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Eliecer CotoUnidad de Cardiopatías Familiares, Área del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-8649-9150
José Julián Rodríguez-RegueroÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.
Juan GomezUnidad de Cardiopatías Familiares, Área del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-3318-4649
Barbara Fernández-BarrioUnidad de Cardiopatías Familiares, Área del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-9843-1025
Pablo AvanzasÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-4958-6108
Rebeca LorcaÁrea del Corazón, Hospital Universitario Central Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-7803-4011

Funding

ISCIII PI22/00705SEC SECARIT-INV-MUL 24/01
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

channelopathyinherited arrhythmiaKCNJ2risk stratificationshort QT syndromesudden cardiac death

Identifiers

PMID42123196
PMCPMC13163790

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.