Associated Papers
A highly prevalent lupus risk haplotype increases IRF7-dependent induction of IFN-α, enhancing antiviral defense and exacerbating autoimmunity.
Virolainen SJ et al.
Medrxiv : the Preprint Server for Health Sciences, 2026
Start codon variant in LAG3 is associated with decreased LAG-3 expression and increased risk of autoimmune thyroid disease.
Saevarsdottir S et al.
Nature Communications, 2024
38982041 (PubMed )
Supplement: 41467_2024_50007_MOESM4_ESM.xlsx › SD3
Respiratory viral infections in otherwise healthy humans with inherited IRF7 deficiency.
Campbell TM et al.
The Journal of Experimental Medicine, 2022
Evaluation of the peripheral blood T and B cell subsets and IRF-7 variants in adult patients with severe influenza virus infection.
Çalık Başaran N et al.
Health Science Reports, 2022
Mutation analysis of adenomas and carcinomas of the colon: Early and late drivers.
Wolff RK et al.
Genes, Chromosomes & Cancer, 2018
29575536 (PubMed )
Supplement: GCC-57-366-s004.xlsx › MSI
Whole-exome sequencing of pancreatic cancer defines genetic diversity and therapeutic targets.
Witkiewicz AK et al.
Nature Communications, 2015
25855536 (PubMed )
Supplement: ncomms7744-s2.xlsx › MUTATIONS_ALL_CASES
Association of PHRF1-IRF7 region polymorphism with clinical manifestations of systemic lupus erythematosus in a Japanese population.
Kawasaki A et al.
Lupus, 2012
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