Evidence map›Paper›PMID 39767645›Full record

ArticleBiomedicines2024

Expanding the Molecular Genetic Landscape of Dystrophinopathies and Associated Phenotypes.

Katja Neuhoff, Ozge Aksel Kilicarslan, Corinna Preuße, Ann-Kathrin Zaum, Heike Kölbel, Hanns Lochmüller, Ulrike Schara-Schmidt, Kiran Polavarapu, Andreas Roos, Andrea Gangfuß

Abstract read
In one paragraph

Article in Biomedicines, 2024. 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
–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

1 citing paper in PubMed.

  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

10 authors.

Katja NeuhoffDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, 45122 Essen, Germany.
Ozge Aksel KilicarslanChildren's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 5B2, Canada.
Corinna PreußeDepartment of Neuropathology, Charité-University Medicine Berlin, 10117 Berlin, Germany.ORCID 0000-0002-5494-8150
Ann-Kathrin ZaumInstitute of Human Genetics, University of Würzburg, 97074 Würzburg, Germany.
Heike KölbelDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, 45122 Essen, Germany.ORCID 0000-0001-9629-7053
Hanns LochmüllerChildren's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 5B2, Canada.
Ulrike Schara-SchmidtDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, 45122 Essen, Germany.
Kiran PolavarapuChildren's Hospital of Eastern Ontario Research Institute, Ottawa, ON K1H 5B2, Canada.
Andreas RoosDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, 45122 Essen, Germany.ORCID 0000-0003-2833-0928
Andrea GangfußDepartment of Pediatric Neurology, Centre for Neuromuscular Disorders, Centre for Translational Neuro- and Behavioral Sciences, University Duisburg-Essen, 45122 Essen, Germany.ORCID 0000-0002-9975-0092

Funding

Canada Foundation for Innovation CFI-JELF 38412Canada Research Chairs program 950-232279Canada Research Coordinating Committee New Frontiers in Research Fund NFRFG-2022-00033Canadian Institutes of Health Research (CIHR) FDN-167281CIHR Postdoctoral fellowship 202210MFE-491707-404816European Commission Grant #101080249European Regional Development Fund (ERDF) NME-GPS grantGovernment of Canada Canada First Research Excellence Fund (CFREF) CFREF-2022-00007Network Grant OR2-189333Transnational Team Grant ERT-174211
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Becker muscular dystrophyBMDDMDDuchenne muscular dystrophydystrophinmolecular diagnosisnovel pathogenic variants

Identifiers

PMID39767645
PMCPMC11727156

What Socratic 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 Socratic graph.