Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
Molecular basis for increased susceptibility of Indigenous North Americans to seropositive rheumatoid arthritis.
Leveraging blood and tissue CD4+ T cell heterogeneity at the single cell level to identify mechanisms of disease in rheumatoid arthritis.
Genetic landscape of interactive effects of HLA-DRB1 alleles on susceptibility to ACPA(+) rheumatoid arthritis and ACPA levels in Japanese population.
Heritability enrichment of specifically expressed genes identifies disease-relevant tissues and cell types.
