PuSH - Publication Server of Helmholtz Zentrum München

12 Records found.
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1.
Amin, N.* et al.: Genetic variants in RBFOX3 are associated with sleep latency. Eur. J. Hum. Genet. 24, 1488-1495 (2016)
2.
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
3.
Huffman, J.E.* et al.: Modulation of genetic associations with serum urate levels by body-mass-index in humans. PLoS ONE 10:e0119752 (2015)
4.
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
5.
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
6.
O'Seaghdha, C.M.* et al.: Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations. PLoS Genet. 9:e1003796 (2013)
7.
Manning, A.K.* et al.: A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance. Nat. Genet. 44, 659-669 (2012)
8.
Pattaro, C.* et al.: Genome-wide association and functional follow-up reveals new loci for kidney function. PLoS Genet. 8:e1002584 (2012)
9.
Saxena, R.* et al.: Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci. Am. J. Hum. Genet. 90, 410-425 (2012)
10.
Speliotes, E.K.* et al.: Genome-wide association analysis identifies variants associated with nonalcoholic fatty liver disease that have distinct effects on metabolic traits. PLoS Genet. 7:e1001324 (2011)
11.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)
12.
Arking, D.E.* et al.: A common genetic variant in the NOS1 regulator NOS1AP modulates cardiac repolarization. Nat. Genet. 38, 644-651 (2006)