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1.
Jiang, X.* et al.: Genome-wide association study in 79,366 European-ancestry individuals informs the genetic architecture of 25-hydroxyvitamin D levels. Nat. Commun. 9:260 (2018)
2.
Böger, C.A.* et al.: NFAT5 and SLC4A10 loci associate with plasma osmolality. J. Am. Soc. Nephrol. 28, 2311-2321 (2017)
3.
Li, M.* et al.: SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. J. Am. Soc. Nephrol. 28, 981-994 (2017)
4.
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
5.
Teumer, A.* et al.: Genome-wide association studies identify genetic loci associated with albuminuria in diabetes. Diabetes 65, 803-817 (2016)
6.
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
7.
Böger, C.A.* et al.: CUBN is a gene locus for albuminuria. J. Am. Soc. Nephrol. 22, 555-570 (2011)
8.
Kestenbaum, B.* et al.: Common genetic variants associate with serum phosphorus concentration. J. Am. Soc. Nephrol. 21, 1223-1232 (2010)
9.
Köttgen, A.* et al.: New loci associated with kidney function and chronic kidney disease. Nat. Genet. 42, 376-384 (2010)