Evidence map›Paper›PMID 42662984›Full record

ArticleFrontiers in genetics2026

Genetic analysis of Behçet's disease using whole-exome sequencing and bioinformatics analysis in Korean patients.

Enkhjargal Bayarsaikhan, Hyunsoo Ahn, Sanguk Kim, Yong-Beom Park, Jae Hoon Lee

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Article in Frontiers in genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

5 authors.

Enkhjargal Bayarsaikhan *Department of Prosthodontics, College of Dentistry, Yonsei University, Seoul, Republic of Korea.
Hyunsoo Ahn *Graduate School of Artificial Intelligence, Pohang University of Science and Technology, Pohang, Republic of Korea.
Sanguk KimDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Republic of Korea.
Yong-Beom ParkDepartment of Internal Medicine, College of Medicine, Yonsei University, Seoul, Republic of Korea.
Jae Hoon LeeDepartment of Prosthodontics, College of Dentistry, Yonsei University, Seoul, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Behçet's disease (BD) is a rare autoimmune or autoinflammatory disorder characterized by various systemic manifestations, including mucocutaneous, ocular, and musculoskeletal symptoms. The etiology of BD involves a complex interplay between genetic predisposition and environmental factors. Methods: In this study, we conducted whole-exome sequencing of 20 Korean patients with BD to identify putative genetic markers and assess their association with the disease. Results: We identified six genes, namely Conclusion: Our findings shed light on the genetic basis of BD and provide insights into its molecular mechanisms, paving the way for further research and targeted therapeutic interventions.

Indexed as

Behçet’s diseasebioinformaticsexome sequencingfunctional enrichment analysisprotein-protein interaction networksusceptibility genes

Identifiers

PMID42662984
PMCPMC13521551

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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.