Evidence map›Paper›PMID 37107612›Full record

ArticleGenes2023

Retinal Phenotyping of a Murine Model of Lafora Disease.

Ajoy Vincent, Kashif Ahmed, Rowaida Hussein, Zorana Berberovic, Anupreet Tumber, Xiaochu Zhao, Berge A Minassian

Open access · goldAbstract read
PubMed Full text at PMC Publisher
In one paragraph

Article in Genes, 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
0.2field-weighted citation impact, top 46% 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

7 authors at 4 institutions in 2 countries.

Ajoy VincentDepartment of Ophthalmology and Vision Sciences, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.ORCID 0000-0001-6446-3846
Kashif AhmedGenetics and Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Rowaida HusseinGenetics and Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Zorana BerberovicThe Center for Phenogenomics, Toronto, ON M5T 3H7, Canada.
Anupreet TumberDepartment of Ophthalmology and Vision Sciences, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada.
Xiaochu ZhaoGenetics and Genome Biology, Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.ORCID 0000-0002-0875-3133
Berge A MinassianDivision of Neurology, Department of Pediatrics, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
Hospital for Sick Children · CAThe University of Texas Southwestern Medical Center · USToronto Centre for Phenogenomics · CAUniversity of Toronto · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Lafora disease (LD) is a progressive neurologic disorder caused by biallelic pathogenic variants in

Indexed as

Lafora DiseaseMyoclonic Epilepsies, ProgressiveAnimalsDisease Models, AnimalElectroretinographyMiceRetinadiseaseelectroretinographyEPM2Ageneknock outsLaforaLafora body disorderoptical coherence tomographyperiodic acid Schiff reactionphenotype

Identifiers

PMID37107612
PMCPMC10137594
OpenAlexW3186655313

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.