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Metallothionein genes: no association with Crohnâ€™s disease in a New Zealand population
Glucose as a fetal nutrient: dynamic regulation of several glucose transporter genes by DNA methylation in the human placenta across gestation
Association between milk protein gene variants and protein composition traits in dairy cattle
Testing for the recurrent HOXB13 G84E germline mutation in men with clinical indications for prostate biopsy
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