Evidence map›Paper›PMID 33256261›Full record

ArticleJournal of clinical medicine2020

Clinical Implications and Gender Differences of KCNQ1 p.Gly168Arg Pathogenic Variant in Long QT Syndrome.

Rebeca Lorca, Alejandro Junco-Vicente, Maria Martin-Fernandez, Isaac Pascual, Andrea Aparicio, Noemi Barja, Elias Cuesta-LLavona, Luis Roces, Pablo Avanzas, Cesar Moris and 3 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2020. 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
0.1field-weighted citation impact, top 44% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
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

13 authors at 2 institutions in 1 country.

Rebeca LorcaÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.
Alejandro Junco-VicenteHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-7003-3196
Maria Martin-FernandezHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Isaac PascualHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.ORCID 0000-0001-5433-1364
Andrea AparicioHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.
Noemi BarjaHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.ORCID 0000-0003-0806-7827
Elias Cuesta-LLavonaÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.
Luis RocesAnestesiología, Reanimación y terapéutica del dolor, Completo Asistencial Universitario de Salamanca, 37007 Salamanca, Spain.
Pablo AvanzasHeart Area, Hospital Universitario Central de Asturias, 33011 Oviedo, Spain.ORCID 0000-0002-4958-6108
Cesar MorisÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.ORCID 0000-0002-2871-190X
Eliecer CotoÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.
José Julían Rodríguez RegueroÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.
Juan GómezÁrea del Corazón y Departamento de Genética Molecular, Hospital Universitario Central Asturias, Unidad de Referencia de Cardiopatías Familiares-HUCA, 33011 Oviedo, Spain.ORCID 0000-0002-3318-4649
Hospital Universitario Central de Asturias · ESComplejo Hospitalario de Salamanca · ES

Funding

Spanish Ministerio de Economíıa y Competitividad-Instituto de Salud Carlos III and FondosEuropeos de Desarrollo Regional PI17/00648
6 · The paper itself

Abstract

backgroundLong QT syndrome (LQTS) is an inheritable arrhythmogenic disorder associated with life-threatening arrhythmic events (LAEs). In general, patients with LQTS2 (

methodswe identified all consecutive index cases referred for genetic testing with LQTS diagnosis carriers of

resultswe evaluated seven unrelated families, with a total 34

conclusions

Indexed as

genetic testinginheritable arrhythmogenic disorderlong QT syndrome

Identifiers

PMID33256261
PMCPMC7760054
OpenAlexW3107674367

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.