Evidence map›Paper›PMID 41802284›Full record

ArticleBriefings in bioinformatics2026

An integrative association analysis for complex diseases in underrepresented groups by leveraging the trans-ethnic genetic similarity.

Shuo Zhang, Jike Qi, Yuchen Jiang, Hua Lin, Xinyi Wang, Ting Wang, Hongyan Cao, Ping Zeng

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 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Shuo ZhangDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Jike QiDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Yuchen JiangDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Hua LinDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Xinyi WangDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Ting WangDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.
Hongyan CaoDepartment of Health Statistics, Shanxi Provincial Key Laboratory of Major Diseases Risk Assessment, School of Public Health, Shanxi Medical Unive rsity, No. 56 South Xinjian Road, Yingze District, Taiyuan, Shanxi 030001, China.ORCID 0000-0002-0315-7156
Ping ZengDepartment of Biostatistics, School of Public Health, Xuzhou Medical University, No. 209 Tongshan Road, Yunlong District, Xuzhou, Jiangsu 221004, China.ORCID 0000-0003-2710-3440

Funding

Ministry of Education, China MEKLCEPP/SXMU-202415National Natural Science Foundation of China 82173630National Natural Science Foundation of China 82574203Natural Science Foundation of Jiangsu Province of China BK20241952Open Project Fund from Key Laboratory of Coal Environmental Pathogenicity and PreventionQingLan Research Project of Jiangsu Province for Young and Middle-aged Academic LeadersTraining Project for Youth Teams of Science and Technology Innovation at Xuzhou Medical University TD202008
6 · The paper itself

Abstract

Genome-wide association studies (GWASs) have been conducted primarily in European (EUR) populations, limiting insights into underrepresented groups such as East Asian (EAS), but cross-ancestry GWASs have demonstrated high trans-ethnic genetic similarity between EUR and non-EUR populations. To enhance association analysis power in EAS populations, we propose tranScore, a novel summary-statistics-based transfer learning method that leverages trans-ethnic genetic similarity through hierarchical modeling. By considering EUR as auxiliary population, tranScore performs joint testing of genetic effects in auxiliary and target populations via well-established P-value combination procedures. Simulations demonstrate that tranScore maintains control of type I error rates and provides substantial power gains for diverse genetic architectures, showing robustness against various challenges including incomplete SNP overlap and effect heterogeneity. In the real-data application of eight diseases from the China Kadoorie Biobank (CKB), after incorporating the genetic information of the EUR population, tranScore identified significantly more genes than the traditional score test which ignored such information. Approximately 41.9% of discovered genes were replicated in the Biobank Japan cohort. Overall, tranScore represents a flexible and powerful statistical approach for association analysis of complex diseases and traits through transfer learning of shared genetic similarities between the auxiliary and target populations.

Indexed as

Ethnic and Racial MinoritiesGenetic Predisposition to DiseaseGenome-Wide Association StudyEast Asian PeopleEuropean PeopleHumansPolymorphism, Single Nucleotidegenome-wide association studyhierarchical modelingintegrative analysisP-value combination proceduresummary statisticstrans-ethnic genetic similarity

Identifiers

PMID41802284
PMCPMC12971055

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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.