Evidence map›Paper›PMID 40443611›Full record

ArticleCureus2025

Gene Duplication in a Patient With Usher Syndrome Type 2C: A Case Report.

Sebastián J Ruiz Matos, Krytsia A Negrón Lugo, Natalio Izquierdo

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. 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

3 authors.

Sebastián J Ruiz MatosDepartment of Ophthalmology, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.
Krytsia A Negrón LugoDepartment of Ophthalmology, Universidad Central del Caribe, School of Medicine, Bayamón, PRI.
Natalio IzquierdoDepartment of Ophthalmology, University of Puerto Rico, Medical Sciences Campus, San Juan, PRI.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Variants of the

Indexed as

adgrv1congenital hearing lossretinitis pigmentosaush2cusher syndrome

Identifiers

PMID40443611
PMCPMC12122117

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.