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Nature Communications|April 4, 2017
Loss of the Arp2/3 complex component ARPC1B causes platelet abnormalities and predisposes to inflammatory diseaseWalter H A Kahr, Fred G Pluthero, Abdul Elkadri, et al.
Circulation. Cardiovascular Genetics|November 24, 2016
Genetic Variation in the SLC8A1 Calcium Signaling Pathway Is Associated With Susceptibility to Kawasaki Disease and Coronary Artery AbnormalitiesChisato Shimizu, Hariklia Eleftherohorinou, Victoria J Wright, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|April 4, 2017
Early Outcomes in Children With Antineutrophil Cytoplasmic Antibody-Associated VasculitisKimberly A Morishita, Lakshmi N Moorthy, Joanna M Lubieniecka, et al.
Nature Genetics|November 15, 2011
Genome-wide association study identifies FCGR2A as a susceptibility locus for Kawasaki diseaseChiea Chuen Khor, Sonia Davila, Willemijn B Breunis, et al.
The Journal of Rheumatology|August 4, 2012
Access to biologic therapies in Canada for children with juvenile idiopathic arthritisClaire M A Leblanc, Bianca Lang, Alma Bencivenga, et al.
Arthritis Care & Research|March 21, 2017
Health-Related Quality of Life in an Inception Cohort of Children With Juvenile Idiopathic Arthritis: A Longitudinal AnalysisKiem Oen, Jaime Guzman, Brenden Dufault, et al.
Frontiers in Immunology|April 6, 2019
Extensive Ethnic Variation and Linkage Disequilibrium at the FCGR2/3 Locus: Different Genetic Associations Revealed in Kawasaki DiseaseSietse Q Nagelkerke, Carline E Tacke, Willemijn B Breunis, et al.
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