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Cited by 860

The DOI matches its Crossref record; 18 of the 18 references it cites were found in a registry or an index.

Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci

Open access
International Genetics of Ankylosing Spondylitis Consortium (IGAS)·2013·Nature Genetics

Abstract

Ankylosing spondylitis is a common, highly heritable inflammatory arthritis affecting primarily the spine and pelvis. In addition to HLA-B*27 alleles, 12 loci have previously been identified that are associated with ankylosing spondylitis in populations of European ancestry, and 2 associated loci have been identified in Asians. In this study, we used the Illumina Immunochip microarray to perform a case-control association study involving 10,619 individuals with ankylosing spondylitis (cases) and 15,145 controls. We identified 13 new risk loci and 12 additional ankylosing spondylitis–associated haplotypes at 11 loci. Two ankylosing spondylitis–associated regions have now been identified encoding four aminopeptidases that are involved in peptide processing before major histocompatibility complex (MHC) class I presentation. Protective variants at two of these loci are associated both with reduced aminopeptidase function and with MHC class I cell surface expression.

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Metadata

Authors
International Genetics of Ankylosing Spondylitis Consortium (IGAS)
Venue
Nature Genetics
Published
2013-06-09
Volume
45
Issue
7
Pages
730-738
ISSN
  • 1061-4036 (ISSN-L)
  • 1546-1718
OpenAlex
W2026853694
Cited by
860
References
18
FWCI
49.18
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. https://app.cochat.ai/papers/10.1038/ng.2667
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International Genetics of Ankylosing Spondylitis Consortium (IGAS). (2013). Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci. Nature Genetics. https://doi.org/10.1038/ng.2667

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