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DNA methylation differences after exposure to prenatal famine are common and timing- and sex-specific
Family-based association analysis of 42 hereditary prostate cancer families identifies the Apolipoprotein L3 region on chromosome 22q12 as a risk locus
DNA methylation analysis of multiple tissues from newborn twins reveals both genetic and intrauterine components to variation in the human neonatal epigenome
Fine scale mapping of the 6p25.3 chronic lymphocytic leukaemia susceptibility locus
Dissection of the genetics of Parkinson’s disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
A comprehensive study of the association between EGFR and ERBB2 genes and glioma risk
Association of the SLC22A1, SLC22A2, and SLC22A3 genes encoding organic cation transporters with diabetic nephtopathy and hypertension
Dysbindin gene (DTNBP1) in major depressive disorder (MDD) patients: Lack of association with clinical phenotypes
Detailed investigation of the role of common and low frequency WFS1 variants in type 2 diabetes risk
Fine-mapping quantitative trait loci for twinning rate on BTA14 in North American Holsteins