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SNPs in miRNA binding sites and miRNA genes as breast/ovarian cancer risk modifiers in Jewish high risk women
Genetic association between intronic variants is AS3MT and arsenic methylation efficiency is focused on a large linkage disequilibrium cluster in chromosome 10
Association and Interaction Analyses of Eight Genes under Asthma Linkage Peaks
Genome-wide SNP genotyping study using pooled DNA to identify candidate markers mediating susceptibility to end-stage renal disease attributed to Type 1 diabetes
Lung Cancer Susceptibility Model Based on Age, Family History and Genetic Variants
Genetic analysis of coronary artery disease single-nucleotide polymorphisms in diabetic nephropathy
Folate Intake, Methylenetetrahydrofolate Reductase Polymorphisms, and Breast Cancer Risk in Women from the MalmÃ¶ Diet and Cancer Cohort
VEGF gene haplotypes are associated with sarcoidosis.
Utility of incorporating genetic variants for the early detection of prostate cancer.
A novel association between a SNP in CYBRD1 and serum ferritin levels in a cohort study of HFE hereditary haemochromatosis.