Evidence map›Paper›PMID 41662355›Full record

ArticleBriefings in bioinformatics2026

Transfer learning-based two-sample Mendelian randomization method for heterogeneous population.

Yun Wei, Hao Chen, Xinhui Liu, Xiaoru Sun, Yuanyuan Yu, Lei Hou, Fuzhong Xue, Hongkai Li

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. 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

8 authors.

Yun WeiDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.ORCID 0000-0002-2623-0221
Hao ChenDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.ORCID 0000-0002-8739-289X
Xinhui LiuDepartment of Emergency Medicine, Qilu Hospital, Shandong University, No. 107 Wenhua Xi Road, Lixia District, Jinan 250000, Shandong, China.
Xiaoru SunDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.
Yuanyuan YuDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.
Lei HouDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.ORCID 0000-0002-5636-4028
Fuzhong XueDepartment of Biostatistics, School of Public Health, Cheeloo College of Medicine, Shandong University, No. 12550 Erhuan East Road, Shizhong District, Jinan 250000, Shandong, China.ORCID 0000-0003-0378-7956
Hongkai LiThe Second Qilu Hospital of Shandong University, Shandong University, No. 247 Beiyuan Street, Tianqiao District, Jinan 250000, Shandong, China.ORCID 0000-0003-1848-937X

Funding

2021 Shandong Medical Association Clinical Research Fund - Qilu Special Project YXH2022DZX02008General Program of the National Natural Science Foundation of China 8217120947Key Program of the National Natural Science Foundation of China 82330108Key R&D Program of Shandong Province 2024CXPT085National Key Research and Development Program of China 2022YFC3502100National Natural Science Foundation of China 82404378
6 · The paper itself

Abstract

Population heterogeneity presents a significant challenge for two-sample Mendelian randomization (MR), often leading to biased estimates of causal effects. This heterogeneity arises when covariate distributions differ across populations, especially when these covariates function both as confounders and effect modifiers. To address this issue, we propose a new method, transfer learning-based Mendelian randomization (TLMR) that leverages observable effect modifiers to transfer predicted exposures from a source population to a target population. This transfer enables causal effect estimation in the target population while properly accounting for population differences. TLMR is developed under minimal modeling assumptions, allowing flexible exposure modeling, and supporting both continuous and binary outcomes. We further extend TLMR to accommodate reverse transfer in the outcome model that broadens its applicability in practical settings. Through extensive simulations, we demonstrate that TLMR yields robust and consistent estimates in heterogeneous populations, outperforming eight widely used MR methods that exhibit substantial estimation bias. Even in homogeneous populations or in the absence of effect modification, TLMR performs comparably to existing approaches. Finally, we systematically evaluate the causal relationship between body mass index and pulmonary function, demonstrating the practical utility and improved accuracy of TLMR in real-world analysis.

Indexed as

Mendelian Randomization AnalysisBody Mass IndexComputer SimulationHumansTransfer Machine Learningeffect modifierheterogeneityMendelian randomizationtransfer learning

Identifiers

PMID41662355
PMCPMC12885102

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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.