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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
DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status
Haplotype analysis reveals a possible founder effect of RET mutation R114H for HirschsprungÂ´s disease in the Chinese population
Targeted genome-wide investigation identifies novel SNPs associated with diabetic nephropathy
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index