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Genome-wide association scan of Dupuytren's disease.
Association-heterogeneity mapping identifies an Asian-specific association of the GTF2I locus with rheumatoid arthritis.
Genetic admixture of European FRDA genes is the cause of Friedreich ataxia in the Mexican population.
Evaluation of imputation-based association in and around the integrin-alpha-M (ITGAM) gene and replication of robust association between a non-synonymous functional variant within ITGAM and systemic lupus erythematosus (SLE).
A polymorphism within IL21R confers risk for systemic lupus erythematosus.
Replication of association between a common variant near melanocortin-4 receptor gene and obesity-related traits in Asian Sikhs.
Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.
Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
PTPN22 association in systemic lupus erythematosus (SLE) with respect to individual ancestry and clinical sub-phenotypes.
Identifying the Vitiligo Related SLE Gene on 17p13
Identifying the novel SLE susceptibility gene on 5p15.3
Identification of Lupus Predisposing Variants by Comparing Multiple Populations