Evidence map›Paper›PMID 36091819›Full record

ArticleFrontiers in pharmacology2022

Diagnostic yield and variant reassessment in the genes encoding Nav1.5 channel in Russian patients with Brugada syndrome.

Elena Zaklyazminskaya, Anna Shestak, Dmitry Podolyak, Vera Komoliatova, Leonid Makarov, Anna Novitskaya, Amiran Revishvili

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. 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

7 authors at 3 institutions in 1 country.

Elena ZaklyazminskayaPetrovsky National Research Centre of Surgery, Moscow, Russia.
Anna ShestakPetrovsky National Research Centre of Surgery, Moscow, Russia.
Dmitry PodolyakPetrovsky National Research Centre of Surgery, Moscow, Russia.
Vera KomoliatovaCentre of Syncope and Cardiac Arrhythmias in Children and Adolescents, Moscow, Russia.
Leonid MakarovCentre of Syncope and Cardiac Arrhythmias in Children and Adolescents, Moscow, Russia.
Anna NovitskayaSechenov First Medical State University, Moscow, Russia.
Amiran RevishviliVishnevsky Institute of Surgery, Moscow, Russia.
Russian Scientific Center of Surgery · RUInstitute of Surgery named after A. V. Vishnevskogo · RUSechenov University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brugada syndrome (BrS) is an inherited cardiac arrhythmia characterized by ST-elevation, negative T-wave, and a high risk of sudden cardiac death (SCD) due to ventricular tachycardia. It is associated with mutations in over 20 genes but only

Indexed as

Brugada syndromeBrugada syndrome comorbiditycardiac channelopathyNav1.5 channelSCN5A

Identifiers

PMID36091819
PMCPMC9449364
OpenAlexW4293211852

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.