Evidence map›Paper›PMID 38002481›Full record

ArticleBrain sciences2023

Higher Prevalence of Nonsense Pathogenic

Vitor Lucas Lopes Braga, Danielle Pessoa Lima, Tamiris Carneiro Mariano, Pedro Lucas Grangeiro de Sá Barreto Lima, Ana Beatriz de Almeida Maia, Wallace William da Silva Meireles, Kécia Tavares de Oliveira Pessoa, Cristiane Mattos de Oliveira, Erlane Marques Ribeiro, Paulo Ribeiro Nóbrega and 1 more

Open access · goldAbstract read
In one paragraph

Article in Brain sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Molecular genetics of dystrophinopathy.Journal of human genetics · 2025
    Review
  2. Article
  3. Editorial forBrain sciences · 2024
    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

11 authors at 4 institutions in 1 country.

Vitor Lucas Lopes BragaDivision of Pediatry, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Danielle Pessoa LimaDivision of Geriatry, Walter Cantidio University Hospital, Federal University of Ceara, Fortaleza 60430-372, CE, Brazil.ORCID 0000-0003-4591-727X
Tamiris Carneiro MarianoDivision of Neurogenetics and Neuromuscular Disorders, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Pedro Lucas Grangeiro de Sá Barreto LimaFaculty of Medicine, Federal University of Ceara, Fortaleza 60020-181, CE, Brazil.ORCID 0000-0002-8517-2324
Ana Beatriz de Almeida MaiaDivision of Pediatry, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Wallace William da Silva MeirelesSecretaria Estadual de Saúde do Distrito Federal, Sobradinho 73010-124, DF, Brazil.
Kécia Tavares de Oliveira PessoaDivision of Nutrition, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Cristiane Mattos de OliveiraDivision of Physiotherapy, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Erlane Marques RibeiroDivision of Genetics, Hospital Infantil Albert Sabin, Fortaleza 60410-794, CE, Brazil.
Paulo Ribeiro NóbregaDivision of Neurology, Walter Cantidio University Hospital, Federal University of Ceara, Fortaleza 60430-372, CE, Brazil.
André Luiz Santos PessoaAlbert Sabin Children's Hospital, Fortaleza 60410-794, CE, Brazil.ORCID 0000-0003-0043-5373
Hospital Infantil Albert Sabin · BRUniversidade Federal do Ceará · BRSecretaria de Estado de Educação do Distrito Federal · BRUniversidade Estadual do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Dystrophinopathies are muscle diseases caused by pathogenic variants in

Indexed as

Duchenne muscular dystrophydystrophingenetic profilemuscular dystrophiesmyopathyneuromuscular diseasespathogenic varianttherapeutics

Identifiers

PMID38002481
PMCPMC10669865
OpenAlexW4388020669

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.