Evidence map›Paper›PMID 42792986›Full record

Observational studyGenes2026

Early Molecular Testing for Presumptive Genetic Eye Diseases.

Marisol Ibarra-Ramírez, Jibran Mohamed-Noriega, Joel Arenas-Estala, David Asael Rodríguez-Torres, Luis Daniel Campos-Acevedo, Marissa L Fernández-de-Luna

Abstract readObservational Study
In one paragraph

Observational study in Genes, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Marisol Ibarra-RamírezDepartment of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.ORCID 0000-0002-3875-4532
Jibran Mohamed-NoriegaDepartment of Ophthalmology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.ORCID 0000-0002-4234-7083
Joel Arenas-EstalaDepartment of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.ORCID 0000-0003-4312-0910
David Asael Rodríguez-TorresDepartment of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.
Luis Daniel Campos-AcevedoDepartment of Genetics, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.
Marissa L Fernández-de-LunaDepartment of Ophthalmology, University Hospital and Faculty of Medicine, Autonomous University of Nuevo León (UANL), Monterrey 64460, Mexico.ORCID 0000-0002-9398-6432

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Eye DiseasesEye Diseases, HereditaryGenetic TestingAdolescentAdultAgedChildChild, PreschoolFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedMutationMyosin VIIaRetrospective StudiesMyosin VIIagenetic eye diseasesmolecular diagnosismultigene panelnext-generation sequencingophthalmic geneticsprecision medicine

Identifiers

PMID42792986
PMCPMC13606511

What OpenQuestion holds

Textmetadata
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.