Evidence map›Paper›PMID 38468717›Full record

ArticleJournal of ophthalmology2024

Mutational Profile and Retinal Phenotypes of

Víctor R López-Rodríguez, Rocío Arce-González, Alan Martínez-Aguilar, Carlos E Rodríguez-López, Sergio Groman-Lupa, M Isabel Neria-González, Genaro Rodríguez-Uribe, Juan C Zenteno

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

Article in Journal of ophthalmology, 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, top 97% 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, 0 citations in OpenAlex.

  1. Cone-Rod DystrophyDiagnostics (Basel, Switzerland) · 2026
    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

8 authors at 4 institutions in 1 country.

Víctor R López-RodríguezDepartment of Genetics, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico.
Rocío Arce-GonzálezDepartment of Genetics, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico.
Alan Martínez-AguilarRetinal Dystrophies Clinic, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico.
Carlos E Rodríguez-LópezRetina Department, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico.
Sergio Groman-LupaCODET Vision Institute, Tijuana, Mexico.
M Isabel Neria-GonzálezLaboratory of Integrative Microbiology and Molecular Biology, Division of Chemical and Biochemical Engineering, TecNm: Tecnológico de Estudios Superiores de Ecatepec, Ecatepec de Morelos, Estado de México, Mexico.
Genaro Rodríguez-UribeCODET Vision Institute, Tijuana, Mexico.
Juan C ZentenoDepartment of Genetics, Institute of Ophthalmology "Conde de Valenciana", Mexico City, Mexico.ORCID https://orcid.org/0000-0002-9716-8146
Institute of Ophthalmology · MXCODET Vision Institute · MXUniversidad Autónoma de Baja California · MXUniversidad de Ecatepec · MX

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: The aim of the study is to describe the genotype and phenotype of a Mexican cohort with Methods: The study included 14 patients from 11 unrelated pedigrees with retinal dystrophies who were demonstrated to carry biallelic pathogenic variants in Results: According to the results of multimodal imaging and functional tests, all 14 patients were diagnosed with cone-rod dystrophy. Six different Conclusion: Our work expands the

Identifiers

PMID38468717
PMCPMC10927338
OpenAlexW4392384662

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.