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Nature Genetics|February 7, 2017
Dense genotyping of immune-related loci implicates host responses to microbial exposure in Behçet's disease susceptibilityMasaki Takeuchi, Nobuhisa Mizuki, Akira Meguro, et al.
The New England Journal of Medicine|September 7, 2007
STAT4 and the risk of rheumatoid arthritis and systemic lupus erythematosusElaine F Remmers, Robert M Plenge, Annette T Lee, et al.
Cell|August 7, 2021
Human TBK1 deficiency leads to autoinflammation driven by TNF-induced cell deathJustin Taft, Michael Markson, Diana Legarda, et al.
Arthritis and Rheumatism|April 11, 2003
Screening the genome for rheumatoid arthritis susceptibility genes: a replication study and combined analysis of 512 multicase familiesDamini Jawaheer, Michael F Seldin, Christopher I Amos, et al.
Frontiers in Immunology|January 31, 2022
The Spectrum of the Deficiency of Adenosine Deaminase 2: An Observational Analysis of a 60 Patient CohortKaryl S Barron, Ivona Aksentijevich, Natalie T Deuitch, et al.
Arthritis and Rheumatism|December 17, 2002
De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of pyrin-associated autoinflammatory diseasesIvona Aksentijevich, Miroslawa Nowak, Mustapha Mallah, et al.
The New England Journal of Medicine|September 7, 2007
TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide studyRobert M Plenge, Mark Seielstad, Leonid Padyukov, et al.
Annals of the Rheumatic Diseases|May 27, 2022
The 2021 EULAR/American College of Rheumatology points to consider for diagnosis, management and monitoring of the interleukin-1 mediated autoinflammatory diseases: cryopyrin-associated periodic syndromes, tumour necrosis factor receptor-associated periodic syndrome, mevalonate kinase deficiency, and deficiency of the interleukin-1 receptor antagonistMicol Romano, Z Serap Arici, David Piskin, et al.
Science Advances|February 1, 2021
Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variationDavid B Beck, Mohammed A Basar, Anthony J Asmar, et al.
Medicine|February 3, 2018
Clinical and serological features of systemic sclerosis in a multicenter African American cohort: Analysis of the genome research in African American scleroderma patients clinical databaseNadia D Morgan, Ami A Shah, Maureen D Mayes, et al.
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