Evidence map›Paper›PMID 41372126›Full record

ArticleNature communications2025

Transformer-based deep learning enhances discovery in migraine GWAS.

Ziang Meng, Yingchao Song, Yue Jiang, Xianjin Wang, Yang Zou, Xingyuan Li, Hakon Hakonarson, Xiao Chang

Abstract read
In one paragraph

Article in Nature communications, 2025. 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.

Ziang Meng *College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.
Yingchao Song *College of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.
Yue JiangCollege of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.
Xianjin WangCollege of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China.
Yang ZouSchool of Computer Science, Northwestern Polytechnical University, Shanxi, China.
Xingyuan LiCollege of Computer Science and Technology, Zhejiang University, Zhejiang, China.
Hakon HakonarsonCenter for Applied Genomics, The Children's Hospital of Philadelphia, Pennsylvania, PA, USA. hakonarson@email.chop.edu.ORCID http://orcid.org/0000-0003-2814-7461
Xiao ChangCollege of Medical Information and Artificial Intelligence, Shandong First Medical University, Shandong, China. changxiao@sdfmu.edu.cn.ORCID http://orcid.org/0000-0002-0230-0416

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Migraine is a complex neurological disorder with substantial heritability, yet genome-wide association studies (GWAS) have explained only a fraction of its genetic component. We developed InsightGWAS, a Transformer-based model, to enhance genetic discovery for migraine by integrating functional annotations and leveraging transfer learning from GWAS datasets of major depressive disorder (MDD). Applying InsightGWAS to migraine GWAS datasets comprising 53,109 cases and 230,876 controls, we identified 293 previously unreported loci, influencing genes such as CACNA1D, HTR3C, and NLGN1, respectively. Furthermore, two loci rs4320030 (SCN11A) and rs5763529 (HORMAD2) were validated in independent sequencing studies, demonstrating the model's precision in uncovering migraine-associated loci. Compared to traditional GWAS results, enrichment analyses of InsightGWAS-predicted loci uncovered new signaling pathways, including nitrogen compound metabolism and cation binding, offering novel insights into the metabolic and ionic mechanisms underlying migraine susceptibility. These findings demonstrate the impact of InsightGWAS in complementing conventional approaches and advancing our understanding of migraine genetics.

Indexed as

Deep LearningGenome-Wide Association StudyMigraine DisordersGenetic Predisposition to DiseaseHumansMajor Depressive DisorderPolymorphism, Single Nucleotide

Identifiers

PMID41372126
PMCPMC12696003

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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.