Evidence map›Paper›PMID 41166152›Full record

ArticleNucleic acids research2026

GENEasso: a curated resource of credible disease-gene associations across complex diseases from GWAS summary statistics.

Tao Jiang, Mengting Shao, Junjie Wang, Pengze Wu, Changhui Zhu, Ranran Tang, Chen Cao, Ning Gu

Abstract read
In one paragraph

Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Tao JiangJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Mengting ShaoJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.ORCID 0009-0001-7443-7542
Junjie WangDepartment of Medical Informatics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.ORCID 0000-0003-0732-051X
Pengze WuJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Changhui ZhuJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.
Ranran TangNanjing Women and Children's Healthcare Institute, Women's Hospital of Nanjing Medical University, Nanjing Women and Children's Healthcare Hospital, Nanjing, Jiangsu 210004, China.
Chen CaoJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.ORCID 0000-0001-5343-808X
Ning GuJiangsu Key Laboratory for Biomedical Electromagnetic Precision Theranostics, School of Biomedical Engineering and Informatics, Nanjing Medical University, Nanjing, Jiangsu 211166, China.ORCID 0000-0003-0047-337X

Funding

Frontier Fundamental Research Program of Jiangsu Province for Leading Technology BK20222002National Natural Science Foundation of China 62471240
6 · The paper itself

Abstract

Gene-based association analysis has become a powerful strategy to improve the biological interpretability of genome-wide association studies (GWAS) by aggregating variant-level signals at the gene level. Although several transcriptome-wide association study (TWAS)-specific databases have been developed, TWAS represents only one class of gene-based association methods and relies primarily on expression-mediated effects, whereas other gene-based approaches also play critical roles in identifying disease-associated genes. To address this limitation, we present GENEasso, a comprehensive platform that integrates multiple gene-level statistical frameworks to enable robust exploration of disease-gene associations across complex diseases. GENEasso systematically applies seven representative methods to 8226 curated GWAS summary statistics, generating 716 122 high-confidence disease-gene associations. The platform supports cross-method consensus scoring, tissue-specific enrichment prioritization, and ancestry-stratified analyses across five populations. Results can be interactively explored through Manhattan plots and ontology-based navigation, with full transparency and unrestricted access to data. A web server module allows users to upload their own GWAS summary statistics, select gene-based methods, and benchmark their findings against the GENEasso reference database. Concordance across methods increases the credibility of associations, improving reproducibility and supporting user-defined gene prioritization workflows. GENEasso is freely available as an open-access resource at https://www.geneasso.net.

Indexed as

Databases, GeneticDiseaseGenetic Predisposition to DiseaseGenome-Wide Association StudySoftwareHumansInternetPolymorphism, Single Nucleotide

Identifiers

PMID41166152
PMCPMC12807607

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.