Functional and Clinical Significance of JIA-Specific Risk Alleles
Project Period:
2019-2021
Grant Category:
Large Grant
Disease Area:
Juvenile Idiopathic Arthritis (JIA)
This project is an important first step in our ability to use genetic information to guide how we monitor and treat juvenile idiopathic arthritis. In this study, we will examine 3 genetic variants associated with JIA and whose biological effects we have characterized. We will determine whether these genetic variants are associated with particular clinical features in JIA. If we are successful, this project will be the start of an ambitious second phase aimed to link genetic information to patient outcomes across the CARRA network.
Investigators
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James Jarvis, MD
The Research Foundation for The SUNY on behalf of University at BuffaloRelated Awarded Grants
Disease Area:
Juvenile Idiopathic Arthritis (JIA)
Assessment of juvenile idiopathic arthritis outcomes and place of residence in Canada: identifying disparities in care
Disease Area:
Juvenile Idiopathic Arthritis (JIA)
Genetic Ancestry Powered studies (GAPs) in JIA
Disease Area:
Juvenile Idiopathic Arthritis (JIA)