Evidence map›Paper›PMID 31731488›Full record

ReviewBiomolecules2019

Disease Associated Mutations in K

Eva-Maria Zangerl-Plessl, Muge Qile, Meye Bloothooft, Anna Stary-Weinzinger, Marcel A G van der Heyden

Open access · goldAbstract readReview
In one paragraph

Review in Biomolecules, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.6field-weighted citation impact, top 5% 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

17 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. NaFrontiers in physiology · 2023
    Article
  7. Article
  8. Tetramisole is a new IPharmacology research & perspectives · 2022
    Review
  9. Article
  10. Article
  11. Article
  12. KPhysiological reports · 2022
    Article
  13. Article
  14. Review
  15. Andersen-Tawil Syndrome With Novel Mutation inFrontiers in pediatrics · 2021
    Article
  16. Article
  17. 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

5 authors at 2 institutions in 2 countries.

Eva-Maria Zangerl-PlesslDepartment of Pharmacology and Toxicology, University of Vienna, 1090 Vienna, Austria.
Muge QileDepartment of Medical Physiology, Division of Heart & Lungs, University Medical Center Utrecht, 3584 CM Utrecht, The Netherlands.
Meye BloothooftDepartment of Medical Physiology, Division of Heart & Lungs, University Medical Center Utrecht, 3584 CM Utrecht, The Netherlands.
Anna Stary-WeinzingerDepartment of Pharmacology and Toxicology, University of Vienna, 1090 Vienna, Austria.
Marcel A G van der HeydenDepartment of Medical Physiology, Division of Heart & Lungs, University Medical Center Utrecht, 3584 CM Utrecht, The Netherlands.ORCID 0000-0002-4225-7942
University Medical Center Utrecht · NLUniversity of Vienna · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The ubiquitously expressed family of inward rectifier potassium (K

Indexed as

Genetic Predisposition to DiseaseHumansMutationPotassium Channels, Inwardly RectifyingProtein TransportSyndromePotassium Channels, Inwardly Rectifyingalignmentdiseaseinward rectifier channelKCNJKIRmutationstructuretrafficking

Identifiers

PMID31731488
PMCPMC6920955
OpenAlexW2981516656

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.