Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.

doi:10.1002/art.41637

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.

Arthritis & rheumatology (Hoboken, N.J.) - 1 Jul 2021

Ortiz Fernández Lourdes, Coit Patrick, Yilmaz Vuslat, Yentür Sibel P, Alibaz-Oner Fatma, Aksu Kenan, Erken Eren, Düzgün Nursen, Keser Gokhan, Cefle Ayse, Yazici Ayten, Ergen Andac, Alpsoy Erkan, Salvarani Carlo, Casali Bruno, Kısacık Bünyamin, Kötter Ina, Henes Jörg, Çınar Muhammet, Schaefer Arne, Nohutcu Rahime M, Zhernakova Alexandra, Wijmenga Cisca, Takeuchi Fujio, Harihara Shinji, Kaburaki Toshikatsu, Messedi Meriam, Song Yeong-Wook, Kaşifoğlu Timuçin, Carmona F David, Guthridge Joel M, James Judith A, Martin Javier, González Escribano María Francisca, Saruhan-Direskeneli Güher, Direskeneli Haner, Sawalha Amr H

Abstract excerpt

OBJECTIVE: Behçet's disease is a complex systemic inflammatory vasculitis of incompletely understood etiology. This study was undertaken to investigate genetic associations with Behçet's disease in a diverse multiethnic population. METHODS: A total of 9,444 patients and controls from 7 different populations were included in this study. Genotyping was performed using an Infinium ImmunoArray-24 v.1.0 or v.2.0...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Behcet Syndrome

Share to Chromosomes, Human, Pair 10

Share to DNA, Intergenic

Share to Gain of Function Mutation

Share to Interferon gamma Receptor

Share to Monocytes

Share to Receptors, Interferon

Share to RNA, Long Noncoding

Source

Open in PubMed Open full text

Identifiers

PMID: 33393726
DOI: 10.1002/art.41637
PMCID: PMC8238846

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic Association of a Gain-of-Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease.PMID 33393726Read ↗

Genetics of Behçet's Disease: Functional Genetic Analysis and Estimating Disease HeritabilitySemantic proximity Read ↗

Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement.Semantic proximity Read ↗

Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibility.Semantic proximity Read ↗

Genetics of Behçet's disease: lessons learned from genomewide association studies.Semantic proximity Read ↗

Genetics of Behçet's disease.Semantic proximity Read ↗

Identification of novel genetic susceptibility loci for Behçet's disease using a genome-wide association study.Semantic proximity Read ↗

The genetics of Behçet's disease in a Chinese population.Semantic proximity Read ↗

The immunogenetics of Behçet's disease: A comprehensive review.Semantic proximity Read ↗

Genetics of vasculitis.Semantic proximity Read ↗

Genetic analysis of innate immunity in Behcet's disease identifies an association with IL-37 and IL-18RAP.Semantic proximity Read ↗

Identification of multiple independent susceptibility loci in the HLA region in Behçet's disease.Semantic proximity Read ↗

Behçet disease, new insights in disease associations and manifestations: a next-generation sequencing study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.