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Genetic variation in neuroendocrine genes associates with somatic symptoms in the general population: Results from the EPIFUND study
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plama
Investigation of type 1 diabetes and celiac disease susceptibility loci for association with juvenile idiopathic arthritis
Methylation at 5HTT Mediates the Impact of Child Sex Abuse on Women’s Antisocial Behavior: An Examination of the Iowa Adoptee Sample
Insulin promoter DNA methylation correlates negatively with insulin gene expression and positively with HbA1c levels in human pancreatic islets
Influence of candidate genes on attention problems in children: a longitudinal study
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
Germ-line variation at a functional p53 binding site increases susceptibility to breast cancer development
A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinurea in patients with type 2 diabetes