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Suhre, K. et al.: Human metabolic individuality in biomedical and pharmaceutical research. Nature 477, 54-60 (2011)
Wain, L.V.* et al.: Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005-1011 (2011)
Wild, P.S.* et al.: A genome-wide association study identifies LIPA as a susceptibility gene for coronary artery disease. Circ. Cardiovasc. Genet. 4, 403-412 (2011)
Allen, H.L.* et al.: Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838 (2010)
Assimes, T.L.* et al.: Lack of association between the Trp719Arg polymorphism in kinesin-like protein-6 and coronary artery disease in 19 case-control studies. J. Am. Coll. Cardiol. 56, 1552-1563 (2010)
Linsel-Nitschke, P.* et al.: Genetic variation at chromosome 1p13.3 affects sortilin mRNA expression, cellular LDL-uptake and serum LDL levels which translates to the risk of coronary artery disease. Atherosclerosis 208, 183-189 (2010)
Speliotes, E.K.* et al.: Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Nat. Genet. 42, 937-948 (2010)
Stark, K.* et al.: Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. PLoS Genet. 6:e1001167 (2010)
Teslovich, T.M.* et al.: Biological, clinical and population relevance of 95 loci for blood lipids. Nature 466, 707-713 (2010)
Teupser, D.* et al.: Genetic regulation of serum phytosterol levels and risk of coronary artery disease. Circ. Cardiovasc. Genet. 3, 331-339 (2010)
Amouyel, P.* et al.: Large scale association analysis of novel genetic loci for coronary artery disease. Arterioscler. Thromb. Vasc. Biol. 29, 774-780 (2009)
Erdmann, J.* et al.: New susceptibility locus for coronary artery disease on chromosome 3q22.3. Nat. Genet. 41, 280-282 (2009)
Hicks, A.A.* et al.: Genetic determinants of circulating sphingolipid concentrations in European populations. PLoS Genet. 5:e1000672 (2009)
Kathiresan, S.* et al.: Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. Nat. Genet. 41, 334-341 (2009)
Maas, R.* et al.: Polymorphisms in the promoter region of the dimethylarginine dimethylaminohydrolase 2 gene are associated with prevalence of hypertension. Pharmacol. Res. 60, (Sp. Iss. SI), 488-493 (2009)
Richards, J.B.* et al.: A genome-wide association study reveals variants in ARL15 that influence adiponectin levels. PLoS Genet. 5:e1000768 (2009)
Soranzo, N.* et al.: A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium. Nat. Genet. 41, 1182-1190 (2009)
Soranzo, N.* et al.: A novel variant on chromosome 7q22.3 associated with mean platelet volume, counts, and function. Blood 113, 3831-3837 (2009)
Stark, K.* et al.: Common polymorphisms influencing serum uric acid levels contribute to susceptibility to gout, but not to coronary artery disease. PLoS ONE 4:e7729 (2009)
Tregouet, D.A.* et al.: Genome-wide haplotype association study identifies the SLC22A3-LPAL2-LPA gene cluster as a risk locus for coronary artery disease. Nat. Genet. 41, 283-285 (2009)