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Arthritis & Rheumatology (Hoboken, N.J.)|May 8, 2018
Brief Report: Whole-Exome Sequencing to Identify Rare Variants and Gene Networks That Increase Susceptibility to Scleroderma in African AmericansPravitt Gourh, Elaine F Remmers, Steven E Boyden, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 25, 2019
HLA and autoantibodies define scleroderma subtypes and risk in African and European Americans and suggest a role for molecular mimicryPravitt Gourh, Sarah A Safran, Theresa Alexander, et al.
Research Square|March 30, 2023
Multiomics integration of 22 immune-mediated monogenic diseases reveals an emergent axis of human immune healthRachel Sparks, Nicholas Rachmaninoff, Dylan C Hirsch, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 2015
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritisMichael J Ombrello, Elaine F Remmers, Ioanna Tachmazidou, et al.
Nature Genetics|September 17, 2008
Common variants at CD40 and other loci confer risk of rheumatoid arthritisSoumya Raychaudhuri, Elaine F Remmers, Annette T Lee, et al.
Annals of the Rheumatic Diseases|December 9, 2016
Genetic architecture distinguishes systemic juvenile idiopathic arthritis from other forms of juvenile idiopathic arthritis: clinical and therapeutic implicationsMichael J Ombrello, Victoria L Arthur, Elaine F Remmers, et al.
Nature Medicine|July 3, 2024
A unified metric of human immune healthRachel Sparks, Nicholas Rachmaninoff, William W Lau, et al.
Annals of the Rheumatic Diseases|January 24, 2018
Aberrant tRNA processing causes an autoinflammatory syndrome responsive to TNF inhibitorsAngeliki Giannelou, Hongying Wang, Qing Zhou, et al.
Nature Immunology|April 12, 2024
Biallelic human SHARPIN loss of function induces autoinflammation and immunodeficiencyHirotsugu Oda, Kalpana Manthiram, Pallavi Pimpale Chavan, et al.
Annals of the Rheumatic Diseases|February 5, 2026
Gain of function NOTCH4 variants disrupt angiogenesis in systemic sclerosisUrvashi Kaundal, Pei-Suen Tsou, Mousumi Sahu, et al.
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