Evidence map›Paper›PMID 20622879›Full record

ArticleNature genetics2010

Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behçet's disease susceptibility loci.

Nobuhisa Mizuki, Akira Meguro, Masao Ota, Shigeaki Ohno, Tomoko Shiota, Tatsukata Kawagoe, Norihiko Ito, Jiro Kera, Eiichi Okada, Keisuke Yatsu and 11 more

Abstract readComment
PubMed Publisher
In one paragraph

Article in Nature genetics, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 239 papers, 10 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
239citing papers in PubMed, 10 pooled it
42.8field-weighted citation impact, top 1% of its field
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

239 citing papers in PubMed, 10 syntheses or guidelines pooled it, 522 citations in OpenAlex.

  1. Pooled it
  2. Behçet's Disease: A Comprehensive Review on the Role ofInternational journal of molecular sciences · 2023
    Pooled it
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  6. Behҫet's Disease, and the Role of TNF-α and TNF-α Blockers.International journal of molecular sciences · 2020
    Pooled it
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  11. Trial
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  19. Article
  20. Ocular Manifestations of Pediatric Behçet's Disease.Clinical medicine & research · 2025
    Review

179 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

21 authors at 9 institutions in 3 countries.

Nobuhisa MizukiDepartment of Ophthalmology and Visual Science, Yokohama City University, Yokohama, Kanagawa, Japan. mizunobu@med.yokohama-cu.ac.jp
Akira Meguro
Masao Ota
Shigeaki Ohno
Tomoko Shiota
Tatsukata Kawagoe
Norihiko Ito
Jiro Kera
Eiichi Okada
Keisuke Yatsu
Yeong-Wook Song
Eun-Bong Lee
Nobuyoshi Kitaichi
Kenichi Namba
Yukihiro Horie
Mitsuhiro Takeno
Sunao Sugita
Manabu Mochizuki
Seiamak Bahram
Yoshiaki Ishigatsubo
Hidetoshi Inoko
Yokohama City University · JPHokkaido University · JPSeoul National University · KRTokai University · JPTokyo Medical and Dental University · JPHealth Sciences University of Hokkaido · JPHôpitaux Universitaires de Strasbourg · FRMinamiaoyama Eye Clinic · JPShinshu University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Behçet's disease is a chronic systemic inflammatory disorder characterized by four major manifestations: recurrent ocular symptoms, oral and genital ulcers and skin lesions. We conducted a genome-wide association study in a Japanese cohort including 612 individuals with Behçet's disease and 740 unaffected individuals (controls). We identified two suggestive associations on chromosomes 1p31.3 (IL23R-IL12RB2, rs12119179, P = 2.7 x 10(-8)) and 1q32.1 (IL10, rs1554286, P = 8.0 x 10(-8)). A meta-analysis of these two loci with results from additional Turkish and Korean cohorts showed genome-wide significant associations (rs1495965 in IL23R-IL12RB2, P = 1.9 x 10(-11), odds ratio = 1.35; rs1800871 in IL10, P = 1.0 x 10(-14), odds ratio = 1.45).

Indexed as

Genome-Wide Association StudyBehcet SyndromeCase-Control StudiesDisease SusceptibilityEyeHumansInterleukin-10Odds RatioSkin DiseasesTurkeyInterleukin-10

Identifiers

PMID20622879
OpenAlexW2025813691

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.