Evidence map›Paper›PMID 33381229›Full record

ReviewCardiovascular therapeutics2020

Inherited Cardiac Arrhythmia Syndromes: Focus on Molecular Mechanisms Underlying TRPM4 Channelopathies.

Mohamed-Yassine Amarouch, Jaouad El Hilaly

Abstract readReview
In one paragraph

Review in Cardiovascular therapeutics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Role of TRPM4 ion channel in pediatric arrhythmic syndromes.World journal of clinical pediatrics · 2026
    Review
  2. Article
  3. Genetic loci responsible for atrioventricular block in children.Frontiers in cell and developmental biology · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Two Transient Receptor Potential Channels at Focal Adhesions.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. The Role ofGenes · 2022
    Article
  18. Review
  19. Review
  20. 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

2 authors.

Mohamed-Yassine AmarouchR.N.E Laboratory, Multidisciplinary Faculty of Taza, University of Sidi Mohamed Ben Abdellah, Fez, Morocco.ORCID https://orcid.org/0000-0002-0523-1348
Jaouad El HilalyR.N.E Laboratory, Multidisciplinary Faculty of Taza, University of Sidi Mohamed Ben Abdellah, Fez, Morocco.ORCID https://orcid.org/0000-0002-3137-4975

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The Transient Receptor Potential Melastatin 4 (TRPM4) is a transmembrane N-glycosylated ion channel that belongs to the large family of TRP proteins. It has an equal permeability to Na

Indexed as

AnimalsArrhythmias, CardiacBrugada SyndromeChannelopathiesGenetic Predisposition to DiseaseHeart RateHeredityHumansLong QT SyndromePedigreePhenotypeTRPM Cation ChannelsTRPM4 protein, humanTRPM Cation Channels

Identifiers

PMID33381229
PMCPMC7759408

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.