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JAMA Dermatology|May 21, 2015
Stimulator of Interferon Genes-Associated Vasculopathy With Onset in Infancy: A Mimic of Childhood Granulomatosis With PolyangiitisJustine Munoz, Michel Rodière, Nadia Jeremiah, et al.
Nature Immunology|July 28, 2014
The SKIV2L RNA exosome limits activation of the RIG-I-like receptorsSterling C Eckard, Gillian I Rice, Alexandre Fabre, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|November 19, 2016
Expression of Cyclic GMP-AMP Synthase in Patients With Systemic Lupus ErythematosusJie An, Laura Durcan, Reynold M Karr, et al.
Plos One|February 1, 2020
Genetic polymorphism in C3 is associated with progression in chronic kidney disease (CKD) patients with IgA nephropathy but not in other causes of CKDSara T Ibrahim, Rajkumar Chinnadurai, Ibrahim Ali, et al.
Orphanet Journal of Rare Diseases|June 16, 2026
Refining Human Phenotype Ontology (HPO) to enable better phenotype-genotype integration in systemic autoimmune rheumatic diseasesAnastasia-Vasiliki Madenidou, Gillian I Rice, Sarah Dyball, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 9, 2016
Brief Report: Vitamin D Deficiency Is Associated With Endothelial Dysfunction and Increases Type I Interferon Gene Expression in a Murine Model of Systemic Lupus ErythematosusJohn A Reynolds, Avi Z Rosenberg, Carolyne K Smith, et al.
Human Mutation|September 8, 2011
A functional XPNPEP2 promoter haplotype leads to reduced plasma aminopeptidase P and increased risk of ACE inhibitor-induced angioedemaAmy L Cilia La Corte, Angela M Carter, Gillian I Rice, et al.
Clinical Genetics|April 26, 2020
Expanding the clinical spectrum of Fowler syndrome: Three siblings with survival into adulthood and systematic review of the literatureChiara De Luca, Yanick J Crow, Mathieu Rodero, et al.
Journal of Immunology (Baltimore, Md. : 1950)|February 13, 2015
Characterization of samhd1 morphant zebrafish recapitulates features of the human type I interferonopathy Aicardi-Goutières syndromePaul R Kasher, Emma M Jenkinson, Valérie Briolat, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
A de novo p.Asp18Asn mutation in TREX1 in a patient with Aicardi-Goutières syndromeCharlotte A Haaxma, Yanick J Crow, Maurice A M van Steensel, et al.
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