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Ehret, G.B.* et al.: The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat. Genet. 48, 1171-1184 (2016)
Draisma, H.H.* et al.: Genome-wide association study identifies novel genetic variants contributing to variation in blood metabolite levels. Nat. Commun. 6:7208 (2015)
Claussnitzer, M. et al.: Leveraging cross-species transcription factor binding site patterns: From diabetes risk loci to disease mechanisms. Cell 156, 343-358 (2014)
Hara, K.* et al.: Genome-wide association study identifies three novel loci for type 2 diabetes. Hum. Mol. Genet. 23, 239-246 (2014)
Jourdan, C. et al.: Associations between thyroid hormones and serum metabolite profiles in an euthyroid population. Catal. Lett. 10, 152-164 (2014)
Keildson, S.* et al.: Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity. Diabetes 63, 1154-1165 (2014)
Petersen, A.-K. et al.: Epigenetics meets metabolomics: An epigenome-wide association study with blood serum metabolic traits. Hum. Mol. Genet. 23, 534-545 (2014)
Shin, S.-Y.* et al.: Interrogating causal pathways linking genetic variants, small molecule metabolites and circulating lipids. Genome Med. 6:25 (2014)
Shin, S.Y.* et al.: An atlas of genetic influences on human blood metabolites. Nat. Genet. 46, 543-550 (2014)
Spyroglou, A.* et al.: Diastrophic dysplasia sulfate transporter (SLC26A2) is expressed in the adrenal cortex and regulates aldosterone secretion. Hypertension 63, 1102-1109 (2014)
Global Lipids Genetics Consortium et al.: Discovery and refinement of loci associated with lipid levels. Nat. Genet. 45, 1274-1283 (2013)
Albrechtsen, A.* et al.: Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes. Diabetologia 56, 298-310 (2013)
Do, R.* et al.: Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat. Genet. 45, 1345-1352 (2013)
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
Lam, V.K.* et al.: Genetic associations of type 2 diabetes with islet amyloid polypeptide processing and degrading pathways in asian populations. PLoS ONE 8:e62378 (2013)
Li, H.* et al.: A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. Diabetes 62, 291-298 (2013)
Ma, R.C.* et al.: Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4. Diabetologia 56, 1291-1305 (2013)
Menni, C.* et al.: Metabolomic markers reveal novel pathways of ageing and early development in human populations. Int. J. Epidemiol. 42, 1111-1119 (2013)
Menni, C.* et al.: Biomarkers for type 2 diabetes and impaired fasting glucose using a non-targeted metabolomics approach. Diabetes 62, 4270-4276 (2013)
Prudente, S.* et al.: The SH2B1 obesity locus and abnormal glucose homeostasis: Lack of evidence for association from a meta-analysis in individuals of European ancestry. Nutr. Metab. Cardiovasc. Dis. 23, 1043-1049 (2013)