Rare Variants in the Functional Domains of Complement Factor H Are Associated With Age-Related Macular Degeneration.
Interactions between amino acid-defined major histocompatibility complex class II variants and smoking in seropositive rheumatoid arthritis.
An argument for early genomic sequencing in atypical cases: a WISP3 variant leads to diagnosis of progressive pseudorheumatoid arthropathy of childhood.
Disproportionate Contributions of Select Genomic Compartments and Cell Types to Genetic Risk for Coronary Artery Disease.
Functional implications of disease-specific variants in loci jointly associated with coeliac disease and rheumatoid arthritis.
Polymorphisms of large effect explain the majority of the host genetic contribution to variation of HIV-1 virus load.
HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis.
Rheumatoid Factor Is Associated With the Distribution of Hand Joint Destruction in Rheumatoid Arthritis.
