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Association of a melatonin receptor 1B (MTNR1B) gene variant with fasting glucose and HOMA-B in children and adolescents of high BMI-SDS groups
Association of variants in the glucose dependent insulinotropic peptide receptor gene (GIPR) with impaired glucose homeostasis in obese children and adolescents from Berlin
The role of ghrelin and ghrelin-receptor gene variants and promoter activity in type 2 diabetes
Evaluation of affinity-based genome-wide DNA methylation data: effects of CpG density, amplification bias, and copy number variation
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