Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionThe genetic structure of the Swedish populationCommon inherited variation in mitochondrial genes is not enriched for associations with type 2 diabetes or related glycemic traitsA six months exercise intervention influences the genome-wide DNA methylation pattern in human adipose tissueGenetic prediction of future type 2 diabetesThe association of a SNP upstream of INSIG2 with body mass index is reproduced in several but not all cohortsThe common PPARgamma Pro12Ala polymorphism is associated with decreased risk of type 2 diabetesOverexpression of alpha2A-adrenergic receptors contributes to type 2 diabetesMultiple environmental and genetic factors influence skeletal muscle PGC-1alpha and PGC-1beta gene expression in twinsCommon variants at 30 loci contribute to polygenic dyslipidemiaTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisGenetic variants in novel pathways influence blood pressure and cardiovascular disease riskGenome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetesCommon variants near MC4R are associated with fat mass, weight and risk of obesitySix new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humansIndependent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk cultureCommon missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrationsEpigenetic regulation of PPARGC1A in human type 2 diabetic islets and effect on insulin secretionEpigenetics: a molecular link between environmental factors and type 2 diabetesThe SLC6A14 gene shows evidence of association with obesityEPMA-World Congress 2015Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humansAuthors' ReplyA Variant of GJD2, Encoding for Connexin 36, Alters the Function of Insulin Producing β-CellsPolymorphisms in the gene encoding the voltage-dependent Ca(2+) channel Ca (V)2.3 (CACNA1E) are associated with type 2 diabetes and impaired insulin secretionThe -374 T/A polymorphism in the gene encoding RAGE is associated with diabetic nephropathy and retinopathy in type 1 diabetic patientsNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskEarly metabolic markers of the development of dysglycemia and type 2 diabetes and their physiological significanceExpression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivityAge-related clonal hematopoiesis associated with adverse outcomesThe diabetes susceptibility gene Clec16a regulates mitophagyDiscovery and Fine-Mapping of Glycaemic and Obesity-Related Trait Loci Using High-Density ImputationInfluence of Familial Renal Glycosuria Due to Mutations in the SLC5A2 Gene on Changes in Glucose Tolerance over TimeHarmonising and linking biomedical and clinical data across disparate data archives to enable integrative cross-biobank researchHuman hexokinase II gene: exon-intron organization, mutation screening in NIDDM, and its relationship to muscle hexokinase activityDesign and cohort description of the InterAct Project: an examination of the interaction of genetic and lifestyle factors on the incidence of type 2 diabetes in the EPIC StudyThe role of adiposity in cardiometabolic traits: a Mendelian randomization analysisA genome-wide association search for type 2 diabetes genes in African AmericansGenetic association analysis of LARS2 with type 2 diabetesGenetic variation in ATP5O is associated with skeletal muscle ATP50 mRNA expression and glucose uptake in young twins
P50
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1947-07-01T00:00:00Z