Michael W. Beresford

Characterization of human disease phenotypes associated with mutations in <i>TREX1</i>, <i>RNASEH2A</i>, <i>RNASEH2B</i>, <i>RNASEH2C</i>, <i>SAMHD1</i>, <i>ADAR</i>, and <i>IFIH1</i>

Yanick J. Crow, Diana Chase, Johanna L. Schmidt et al. · American Journal of Medical Genetics Part A · 2015 · 613 citations · Full text

Life Sciences, Genetics, Molecular Genetics +9

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

Toward New Classification Criteria for Juvenile Idiopathic Arthritis: First Steps, Pediatric Rheumatology International Trials Organization International Consensus

Alberto Martini, Angelo Ravelli, Tadej Avčin et al. · The Journal of Rheumatology · 2018 · 546 citations · Full text

Medicine, Clinical Sciences, Pediatrics +15

Adalimumab plus Methotrexate for Uveitis in Juvenile Idiopathic Arthritis

Athimalaipet V Ramanan, Andrew D. Dick, Ashley P Jones et al. · New England Journal of Medicine · 2017 · 425 citations · Full text

Medicine, Immunology, Pharmacotherapy +15

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