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Dupuis, J.* et al.: New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk. Nat. Genet. 42, 105-116 (2010)
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
Kestenbaum, B.* et al.: Common genetic variants associate with serum phosphorus concentration. J. Am. Soc. Nephrol. 21, 1223-1232 (2010)
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
Pfeufer, A. et al.: Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)
Saxena, R.* et al.: Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat. Genet. 42, 142-148 (2010)
Soranzo, N.* et al.: Common variants at 10 genomic loci influence hemoglobin A₁C levels via glycemic and nonglycemic pathways. Diabetes 59, 3229-3239 (2010)
Sotoodehnia, N.* et al.: Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. Nat. Genet. 42, 1068-1076 (2010)
Voight, B.F.* et al.: Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis. Nat. Genet. 42, 579-589 (2010)
Benjamin, E.J.* et al.: Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry. Nat. Genet. 41, 879-81 (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)
Pfeufer, A. et al.: Common variants at ten loci modulate the QT interval duration in the QTSCD Study. Nat. Genet. 41, 407-414 (2009)