Evidence map›Paper›PMID 41978382›Full record

ArticleBriefings in bioinformatics2026

GEiPRS: a fast and powerful machine learning method for polygenic risk score prediction by leveraging genotype-environment interactions.

Le Huang, Wujuan Zhong, Song Zhai, Judong Shen

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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. Methods for modeling gene-environment interplay using polygenic risk scores.Statistical applications in genetics and molecular biology · 2026
    Review
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

4 authors.

Le HuangCurriculum in Bioinformatics and Computational Biology, University of North Carolina at Chapel Hill, 120 Mason Farm Road, Chapel Hill, NC 27514, United States.
Wujuan ZhongBiostatistics and Research Decision Sciences, Merck & Co., Inc., 126 East Lincoln Avenue, Rahway, NJ 07065, United States.
Song ZhaiBiostatistics and Research Decision Sciences, Merck & Co., Inc., 126 East Lincoln Avenue, Rahway, NJ 07065, United States.
Judong ShenBiostatistics and Research Decision Sciences, Merck & Co., Inc., 126 East Lincoln Avenue, Rahway, NJ 07065, United States.ORCID 0000-0001-6150-1034

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Penalized regression methods are widely used for variant selection and polygenic risk score (PRS) analysis in disease genome-wide association studies (GWASs). However, the existing penalized regression-based PRS methods often neglect genotype-environment interaction (GEI) and struggles with high-dimensional GWAS data. To overcome these challenges, we propose a novel machine learning-based PRS method Genotype-Environment interaction-based Polygenic Risk Score (GEiPRS). GEiPRS simultaneously models both genotype (G) and GEI effects and efficiently handle high-dimensional GWAS data in terms of variant selection and PRS construction and prediction. A novel algorithm called Group ITerative LAsso with Batch Screening (GITLABS) is developed for efficiently calculating iterative Group Lasso (GL) or Sparse Group Lasso (SGL) solutions for variant selection in GEiPRS, enabling high-dimensional variant selection and PRS construction in a computationally efficient manner. GITLABS consists of three steps: screening variants using strong rules, fitting GL/SGL model with the selected variants, and checking validity of the model solutions based on safe rules. Extensive simulations show GEiPRS outperforms existing PRS methods in terms of GEI-PRS association P-values, prediction accuracy, subgroup risk stratification, and computational efficiency. We further apply the GEiPRS method to large-scale UK Biobank GWAS data for three pairs of quantitative traits and environment variables and the results demonstrate superior performance of GEiPRS over existing PRS methods and support the main conclusions from our simulations.

Indexed as

Gene-Environment InteractionGenome-Wide Association StudyMachine LearningMultifactorial InheritanceAlgorithmsGenetic Risk ScoreGenotypeHumansPolymorphism, Single NucleotidePrediction AlgorithmsGEiPRSgenotype–environment interactionGroup ITerative LAsso with batch screeningpenalized regressionpolygenic risk score

Identifiers

PMID41978382
PMCPMC13076946

What OpenQuestion holds

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LicenceCC BY
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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.