Christiaan Scott

Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

Gillian Rice, Yoandris del Toro Duany, Emma M. Jenkinson et al. · Nature Genetics · 2014 · 591 citations · Full text

Life Sciences, Genetics, Molecular Biology +16

Treating juvenile idiopathic arthritis to target: recommendations of an international task force

Angelo Ravelli, Alessandro Consolaro, Gerd Horneff et al. · Annals of the Rheumatic Diseases · 2018 · 357 citations · Full text

Medicine, Clinical Sciences, Pediatrics +13

Distinct interferon signatures and cytokine patterns define additional systemic autoinflammatory diseases

Adriana A. de Jesus, Yangfeng Hou, Stephen R. Brooks et al. · Journal of Clinical Investigation · 2019 · 239 citations · Full text

Life Sciences, Immunology, Internal Medicine +17

Phenotypic variability and disparities in treatment and outcomes of childhood arthritis throughout the world: an observational cohort study

Alessandro Consolaro, Gabriella Giancane, Alessandra Alongi et al. · The Lancet Child & Adolescent Health · 2019 · 214 citations · Full text

Medicine, Child Health, Pediatrics +16

cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing

Carolina Uggenti, Alice Lepelley, Marine Depp et al. · Nature Genetics · 2020 · 197 citations · Full text

Life Sciences, Immunology, Molecular Biology +16