Evidence map›Paper›PMID 37735453›Full record

ArticleMolecular brain2023

Electrophysiological characterization of a Ca

Robin N Stringer, Leos Cmarko, Gerald W Zamponi, Michel De Waard, Norbert Weiss

Open access · goldAbstract readCase Reports
In one paragraph

Article in Molecular brain, 2023. 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 36% 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

5 authors at 3 institutions in 3 countries.

Robin N Stringer *Department of Pathophysiology, Third Faculty of Medicine, Charles University, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-0887-7670
Leos Cmarko *Institute of Organic Chemistry and Biochemistry, Czech Academy of Sciences, Prague, Czech Republic.ORCID http://orcid.org/0000-0003-4272-2784
Gerald W ZamponiDepartment of Clinical Neurosciences, Alberta Children's Hospital Research Institute, Hotchkiss Brain Institute, Cumming School of Medicine, University of Calgary, Calgary, Canada.ORCID http://orcid.org/0000-0002-0644-9066
Michel De WaardNantes Université, CNRS, INSERM, l'Institut du Thorax, Nantes, France.ORCID http://orcid.org/0000-0002-2782-9615
Norbert WeissDepartment of Pathophysiology, Third Faculty of Medicine, Charles University, Prague, Czech Republic. nalweiss@gmail.com.ORCID http://orcid.org/0000-0002-0040-1109
Centre National de la Recherche Scientifique · FRCharles University · CZUniversity of Calgary · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-type calcium channelopathies encompass a group of human disorders either caused or exacerbated by mutations in the genes encoding different T-type calcium channels. Recently, a new heterozygous missense mutation in the CACNA1H gene that encodes the Ca

Indexed as

EpilepsyHearing LossCalcium ChannelsHumansMutationMutation, MissenseCalcium ChannelsCACNA1HCalcium channelsCav3.2ChannelopathyEpilepsyHearingIon channelsMutationT-type channels

Identifiers

PMID37735453
PMCPMC10515227
OpenAlexW4386925889

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.