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ACR Open Rheumatology|February 22, 2023
Geographic Variation in Disease Burden and Mismatch in Care of Patients With Rheumatoid Arthritis in the United StatesSharon Dowell, Huifeng Yun, Jeffrey R Curtis, et al.
Genes|February 27, 2026
Behavioral Features in Phelan-McDermid Syndrome: Characteristics and Genetic and Metabolic Contributions in a Cohort of 56 IndividualsEmily Payne, Bridgette A Moffitt, Lindsay M Oberman, et al.
The Journal of Rheumatology|July 30, 2021
Higher Serum Urate Levels Are Associated With an Increased Risk for Sudden Cardiac DeathLisandro D Colantonio, Richard J Reynolds, Tony R Merriman, et al.
Arthritis Care & Research|January 13, 2015
Comprehensive appraisal of magnetic resonance imaging findings in sustained rheumatoid arthritis remission: a substudyVeena K Ranganath, Kambiz Motamedi, Espen A Haavardsholm, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|February 6, 2020
Factors associated with the contemplative stage of readiness to initiate osteoporosis treatmentG Adami, K G Saag, A S Mudano, et al.
Pharmacoepidemiology and Drug Safety|September 16, 2011
Study design for a comprehensive assessment of biologic safety using multiple healthcare data systemsLisa J Herrinton, Jeffrey R Curtis, Lang Chen, et al.
ACR Open Rheumatology|May 1, 2023
Engaging Multistakeholder Perspectives to Identify Patient-Centered Research Priorities Regarding Vaccine Uptake Among Adults With Autoimmune ConditionsShilpa Venkatachalam, Kelly Gavigan, Shubhasree Banerjee, et al.
American Journal of Human Genetics|May 15, 2012
GPSM2 mutations cause the brain malformations and hearing loss in Chudley-McCullough syndromeDan Doherty, Albert E Chudley, Gail Coghlan, et al.
Rheumatology (Oxford, England)|December 28, 2018
Adjustment of the multi-biomarker disease activity score to account for age, sex and adiposity in patients with rheumatoid arthritisJeffrey R Curtis, Darl D Flake, Michael E Weinblatt, et al.
Nature Genetics|January 1, 1997
Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene familyQ Y Li, R A Newbury-Ecob, J A Terrett, et al.
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