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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)
Confirmation of TNIP1 and IL23A as susceptibility loci for psoriatic arthritis
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