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Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene
CXCR1 and CXCR2 haplotypes synergistically modulate cystic fibrosis lung disease
Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers
Genome-wide association study identifies breast cancer risk variant at 10q21.2: results from the Asia Breast Cancer Consortium
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF)
A common SNP in the CD40 region is associated with systemic lupus erythematosus and correlates with altered CD40 expression: implications for the pathogenesis
Integrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies
Association between genome-wide association studies reported SNPs and pediatric-onset CrohnÂ´s disease in Canadian children
Susceptibility loci reported in genome-wide association studies are associated with CrohnÂ´s disease in Canadian children