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Mild Folate Deficiency Induces Genetic and Epigenetic Instability and Phenotype Changes in Prostate Cancer Cells
Methylation of novel markers of fragile X alleles is inversely correlated with FMRP expression and FMR1 activation ratio
Assessment of SNPs associated with the human glucocorticoid receptor in primary open-angle glaucoma and steroid responders
Robust Replication of Genotype-Phenotype Associations across Multiple Diseases in an Electronic Medical Record
Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
Common variants at 19p13 are associated with susceptibility to ovarian cancer
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
Genetic variability in the MTHFR gene and colorectal cancer risk using the colorectal cancer family registry