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Leptin gene epigenetic adaption to impaired glucose metabolism during pregnancy
Genetic variation in GIPR influences the glucose and insulin responses to oral glucose challenge
Lack of association of the CIITA -168A/G promoter SNP with Myasthenia gravis and its role in autoimmunity
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
Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
DNA methylome of familial breast cancer identifies distinct profiles defined by mutation status
Haplotype analysis reveals a possible founder effect of RET mutation R114H for HirschsprungÂ´s disease in the Chinese population