Evidence map›Paper›PMID 20622878›Full record

ArticleNature genetics2010

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease.

Elaine F Remmers, Fulya Cosan, Yohei Kirino, Michael J Ombrello, Neslihan Abaci, Colleen Satorius, Julie M Le, Barbara Yang, Benjamin D Korman, Aris Cakiris and 27 more

Open access · greenAbstract read
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 317 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
317citing papers in PubMed, 9 pooled it
21.5field-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

317 citing papers in PubMed, 9 syntheses or guidelines pooled it, 670 citations in OpenAlex.

  1. Pooled it
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  3. 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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  15. Shared Genetics of Hypertension and Preeclampsia Converges on Immune Regulation.medRxiv : the preprint server for health sciences · 2026
    Article
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257 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

37 authors at 12 institutions in 6 countries.

Elaine F RemmersNational Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, USA. remmerse@mail.nih.gov
Fulya Cosan
Yohei Kirino
Michael J Ombrello
Neslihan Abaci
Colleen Satorius
Julie M Le
Barbara Yang
Benjamin D Korman
Aris Cakiris
Oznur Aglar
Zeliha Emrence
Hulya Azakli
Duran Ustek
Ilknur Tugal-Tutkun
Gulsen Akman-Demir
Wei Chen
Christopher I Amos
Michael B Dizon
Afet Akdag Kose
Gulsevim Azizlerli
Burak Erer
Oliver J Brand
Virginia G Kaklamani
Phaedon Kaklamanis
Eldad Ben-Chetrit
Miles Stanford
Farida Fortune
Marwen Ghabra
William E R Ollier
Young-Hun Cho
Dongsik Bang
John O'Shea
Graham R Wallace
Massimo Gadina
Daniel L Kastner
Ahmet Gül
Istanbul University · TRNational Institute of Arthritis and Musculoskeletal and Skin Diseases · USOffice of Science · USThe University of Texas MD Anderson Cancer Center · USUniversity of Birmingham · GBAthens Medical Center · GRHadassah Medical Center · ILKing's College London · GBKorea Advanced Institute of Science and Technology · KRNorthwestern University · USUniversity of Manchester · GBYonsei University · KR

Funding

Translational Immunology research: a support for clinical immunological researchZICAR041181 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI GADINA, MASSIMO · 2009 to 2025
$31.5M
TRANSCRIPTIONAL REGULATION OF WT-1P01CA034936 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI STRONG, LOUISE C · 1985 to 2010
$26.4M
NARAC The Genetics of Rheumatoid ArthritisR01AR044422 · NIAMS · NORTH SHORE UNIVERSITY HOSPITAL · PI GREGERSEN, PETER K. · 1997 to 2011
$6.0M
Targeting Janus kinases in the treatment of autoimmune diseaseZIAAR041106 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN · 2009 to 2024
$4.8M
Positional Gene Identification of Complex TraitsR01ES009912 · NIEHS · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AMOS, CHRISTOPHER I. · 1999 to 2006
$3.3M
Genetics Of Familial Mediterranean Fever/ Related ConditZ01AR041083 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KASTNER, DANIEL L · 1990 to 2008
$3.3M
Genetics, Natural History, and Pathophysiology of Behcet's DiseaseZIAAR041162 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KASTNER, DANIEL · 2009 to 2010
$3.0M
Genetic Analysis of Complex Inflammatory DisordersZ01AR041139 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KASTNER, DANIEL L · 2003 to 2008
$2.8M
Targeting Jak3 in the treatment of autoimmune diseaseZ01AR041106 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI O'SHEA, JOHN J. · 1995 to 2008
$2.7M
Genetics Of Familial Mediterranean Fever and Related ConditionsZIAAR041083 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KASTNER, DANIEL · 2009 to 2010
$2.4M
Genetic Analysis of Complex Inflammatory DisordersZIAAR041139 · NIAMS · NATIONAL INSTITUTE OF ARTHRITIS AND MUSCULOSKELETAL AND SKIN DISEASES · PI KASTNER, DANIEL · 2009 to 2010
$1.2M
Intramural NIH HHS Z01 AR041083Intramural NIH HHS Z01 AR041106Intramural NIH HHS Z01 AR041139Intramural NIH HHS Z99 AR999999Intramural NIH HHS Z99 HG999999Intramural NIH HHS ZIC AR041181NCI NIH HHS P01 CA034936NCI NIH HHS PC30CA016772NIAMS NIH HHS AR44422NIEHS NIH HHS R01 ES009912
6 · The paper itself

Abstract

Behçet's disease is a genetically complex disease of unknown etiology characterized by recurrent inflammatory attacks affecting the orogenital mucosa, eyes and skin. We performed a genome-wide association study with 311,459 SNPs in 1,215 individuals with Behçet's disease (cases) and 1,278 healthy controls from Turkey. We confirmed the known association of Behçet's disease with HLA-B*51 and identified a second, independent association within the MHC Class I region. We also identified an association at IL10 (rs1518111, P = 1.88 x 10(-8)). Using a meta-analysis with an additional five cohorts from Turkey, the Middle East, Europe and Asia, comprising a total of 2,430 cases and 2,660 controls, we identified associations at IL10 (rs1518111, P = 3.54 x 10(-18), odds ratio = 1.45, 95% CI 1.34-1.58) and the IL23R-IL12RB2 locus (rs924080, P = 6.69 x 10(-9), OR = 1.28, 95% CI 1.18-1.39). The disease-associated IL10 variant (the rs1518111 A allele) was associated with diminished mRNA expression and low protein production.

Indexed as

Genome-Wide Association StudyAllelesAsiaBehcet SyndromeCase-Control StudiesEuropeGenes, MHC Class IHLA-B AntigensHumansInterleukin-10Middle EastPolymorphism, Single NucleotideTurkeyHLA-B AntigensInterleukin-10

Identifiers

PMID20622878
PMCPMC2923807
OpenAlexW2065059951

What OpenQuestion holds

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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.