Evidence map›Paper›PMID 34068417›Full record

ArticleInternational journal of molecular sciences2021

Antonio F Martínez-Monseny, Albert Edo, Dídac Casas-Alba, Mercè Izquierdo-Serra, Mercè Bolasell, David Conejo, Loreto Martorell, Jordi Muchart, Laura Carrera, Carlos I Ortez and 4 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.9field-weighted citation impact, top 31% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Brain communications · 2026
    Article
  2. Article
  3. Article
  4. Phenotypic variability in cases with CACNA1A mutation.European journal of pediatrics · 2025
    Article
  5. Review
  6. The genotype-phenotype correlations of theFrontiers in molecular neuroscience · 2023
    Article
  7. 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

14 authors at 3 institutions in 1 country.

Antonio F Martínez-MonsenyDepartment of Genetic and Molecular Medicine, Institut de Recerca, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Albert EdoLaboratory of Molecular Physiology, Department of Experimental and Health Sciences, Universitat Pompeu Fabra, 08003 Barcelona, Spain.
Dídac Casas-AlbaDepartment of Genetic and Molecular Medicine, Institut de Recerca, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Mercè Izquierdo-SerraLaboratory of Molecular Physiology, Department of Experimental and Health Sciences, Universitat Pompeu Fabra, 08003 Barcelona, Spain.ORCID 0000-0002-3524-8052
Mercè BolasellDepartment of Genetic and Molecular Medicine, Institut de Recerca, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
David ConejoPediatric Department, Complejo Asistencial de Burgos, 09006 Burgos, Spain.
Loreto MartorellDepartment of Genetic and Molecular Medicine, Institut de Recerca, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Jordi MuchartPediatric Radiology Department, Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Laura CarreraNeuropediatric Department, Institut de Recerca Sant Joan de Déu, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Carlos I OrtezU-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, 08002 Barcelona, Spain.
Andrés NascimentoU-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, 08002 Barcelona, Spain.
Baldo OlivaStructural Bioinformatics Lab, Department of Experimental and Health Sciences, Universitat Pompeu Fabra, 08003 Barcelona, Spain.
José M Fernández-FernándezLaboratory of Molecular Physiology, Department of Experimental and Health Sciences, Universitat Pompeu Fabra, 08003 Barcelona, Spain.ORCID 0000-0003-2330-8449
Mercedes SerranoU-703 Centre for Biomedical Research on Rare Diseases (CIBER-ER), Instituto de Salud Carlos III, 08002 Barcelona, Spain.ORCID 0000-0002-2056-2428
Hospital Sant Joan de Déu Barcelona · ESUniversitat Pompeu Fabra · ESUniversidad de Burgos · ES

Funding

Agencia Estatal de Investigación CEX2018-000792-MAgencia Estatal de Investigación RTI2018-094809-B-I00Direcció General de Recerca, Generalitat de Catalunya PERIS SLT008/18/00194Instituto de Salud Carlos III PI17/00101
6 · The paper itself

Abstract

The

Indexed as

MutationAdultAmino Acid SequenceAtaxiaCalcium ChannelsCalcium Channels, N-TypeChildFemaleHumansMaleNeuroimagingPhenotypeProtein ConformationSequence HomologyStructure-Activity RelationshipYoung AdultCACNA1A protein, humanCalcium ChannelsCalcium Channels, N-TypeataxiaCACNA1A geneCaV2.1 (P/Q-type) voltage-dependent calcium channelcerebellar atrophydysmorphic traitsearly-onset cerebellar ataxia

Identifiers

PMID34068417
PMCPMC8153625
OpenAlexW3161134296

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.