Evidence map›Paper›PMID 42133706›Full record

ArticlePloS one2026

Multivariate genetic architecture of age-related eye disease.

Luqi Gao, Qihao Wang, Chao Zhu

Abstract read
In one paragraph

Article in PloS one, 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

3 authors.

Luqi GaoThe Second Hospital of Jilin University, Changchun, China.
Qihao WangThe Second Hospital of Jilin University, Changchun, China.
Chao ZhuThe Second Hospital of Jilin University, Changchun, China.ORCID https://orcid.org/0000-0002-1271-5500

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

At present, the genetic architecture underlying traits linked to Age-related eye disease (ARED) remains largely unexplored. We utilized Genomic Structural Equation Modeling (Genomic-SEM) and various Post-processing analysis of Genome-Wide Association Studies (GWAS) to identify statistically prioritized candidate single nucleotide polymorphisms (SNPs) associated with independent ARED variants. A total of 11 genome-wide significant loci were identified in the study. By applying diverse transcriptome-wide association approaches, we analyzed tissue-, cell layer-, and genomic element-associated gene signals reflecting age-related ocular vulnerabilities, alongside their functional annotations in relation to ARED. Through conducting a GWAS on a phenotype not directly measured, our research presents the first comprehensive genetic landscape of ARED.

Indexed as

AgingEye DiseasesGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansPhenotypePolymorphism, Single Nucleotide

Identifiers

PMID42133706
PMCPMC13175492

What OpenQuestion holds

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Registered trials

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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.