American journal of human genetics
Transethnic Genetic-Correlation Estimates from Summary Statistics.
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
CRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein.
Two functional lupus-associated BLK promoter variants control cell-type- and developmental-stage-specific transcription.
Unraveling multiple MHC gene associations with systemic lupus erythematosus: model choice indicates a role for HLA alleles and non-HLA genes in Europeans.
Identification of IRF8, TMEM39A, and IKZF3-ZPBP2 as susceptibility loci for systemic lupus erythematosus in a large-scale multiracial replication study.
Identification of a systemic lupus erythematosus susceptibility locus at 11p13 between PDHX and CD44 in a multiethnic study.
Gene expression and genetic variation in response to endoplasmic reticulum stress in human cells.
PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritis.
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.
