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Epigenetic and genetic variation at the IGF2/H19 imprinting control region on 11p15.5 is associated with cerebellum weight
A distinct DNA methylation signature defines pediatric pre-B cell acute lymphoblastic leukemia
Mutations of complement lectin pathway genes MBL2 and MASP2 associated with placental malaria
Common TGF?2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma
Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa
The 1200 Patients Project: Creating a New Medical Model System for Clinical Implementation of Pharmacogenomics
Footprints of genetic susceptibility to pulmonary tuberculosis: Cytokine gene variants in north Indians
Differential association between the norepinephrine transporter gene and ADHD: role of sex and subtype
Space/Population and Time/Age in DNA methylation variability in humans: a study on IGF2/H19 locus in different Italian populations and in mono- and di-zygotic twins of different age
ANKRD7 and CYTL1 are novel risk genes for alcohol drinking behavior