Evidence map›Paper›PMID 32824506›Full record

ArticleInternational journal of molecular sciences2020

Novel

Michelle M Monasky, Emanuele Micaglio, Giuseppe Ciconte, Valeria Borrelli, Luigi Giannelli, Gabriele Vicedomini, Andrea Ghiroldi, Luigi Anastasia, Emanuela T Locati, Sara Benedetti and 3 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. Article
  3. Brugada Syndrome: Warning of a Systemic Condition?Frontiers in cardiovascular medicine · 2021
    Review
  4. 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.

Michelle M MonaskyArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
Emanuele MicaglioArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
Giuseppe CiconteArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
Valeria BorrelliArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.ORCID 0000-0002-7564-5677
Luigi GiannelliArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
Gabriele VicedominiArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
Andrea GhiroldiStem Cells for Tissue Engineering Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.ORCID 0000-0002-2896-7390
Luigi AnastasiaStem Cells for Tissue Engineering Laboratory, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.ORCID 0000-0002-0712-2161
Emanuela T LocatiArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.ORCID 0000-0002-4488-0455
Sara BenedettiClinical Genomics-SMEL, IRCCS San Raffaele Hospital, 20132 Milan, Italy.
Chiara Di RestaVita-Salute San Raffaele University, 20132 Milan, Italy.
Giorgio CasariVita-Salute San Raffaele University, 20132 Milan, Italy.
Carlo PapponeArrhythmology Department, IRCCS Policlinico San Donato, San Donato Milanese, 20097 Milan, Italy.
IRCCS Policlinico San Donato · ITVita-Salute San Raffaele University · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brugada syndrome (BrS) is diagnosed by the presence of an elevated ST-segment and can result in sudden cardiac death. The most commonly found mutated gene is

Indexed as

MutationAdultAgedBrugada SyndromeFemaleHeterozygoteHumansMaleMiddle AgedNAV1.5 Voltage-Gated Sodium ChannelPedigreeNAV1.5 Voltage-Gated Sodium ChannelSCN5A protein, humanarrhythmiaBrugada syndromechannelopathyfamilygenetic testinghumanmutationSCN5Asodium channelsudden cardiac deathvariant

Identifiers

PMID32824506
PMCPMC7460631
OpenAlexW3049060968

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.