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Most common SNPs associated with rheumatoid arthritis in subjects of European ancestry confer risk of rheumatoid arthritis in African-Americans
Identification of a novel MYBPC3 gene variant in a patient with hypertrophic cardiomyopathy
ARMS2/HTRA1 locus can confer differential susceptibility to the advanced subtypes of age-related macular degeneration
Genome-wide association study identifies variants in the CFH region associated with host susceptibility to meningococcal disease
Association between the dopamine transporter gene and the inattentive subtype of attention deficit hyperactivity disorder in Taiwan
A new approach to imprinting mutation detection in GNAS by Sequenom EpiTYPER system
HOXB13, a target of DNMT3B, is methylated at an upstream CpG island, and functions as a tumor suppressor in primary colorectal tumors
Methylation profile of TP53 regulatory pathway and MtDNA alterations in breast cancer patients lacking TP53 mutations
Investigation of potential non-HLA rheumatoid arthritis susceptibility loci in a European cohort increases the evidence for nine markers
Assessing association of common variation in the C1Q gene cluster with systemic lupus erythematosus