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Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
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)
Macé, A.* et al.: CNV-association meta-analysis in 191,161 European adults reveals new loci associated with anthropometric traits. Nat. Commun. 8:744 (2017)
Nolte, I.M.* et al.: Genetic loci associated with heart rate variability and their effects on cardiac disease risk. Nat. Commun. 8:15805 (2017)
Pasutto, F.* et al.: Pseudoexfoliation syndrome-associated genetic variants affect transcription factor binding and alternative splicing of LOXL1. Nat. Commun. 8:15466 (2017)
Okbay, A.* et al.: Genome-wide association study identifies 74 loci associated with educational attainment. Nature 533, 539-542 (2016)
Pattaro, C.* et al.: Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. Nat. Commun. 7:10023 (2016)
Ried, J.S. et al.: A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape. Nat. Commun. 7:13357 (2016)
Gorski, M.* et al.: Genome-wide association study of kidney function decline in individuals of European descent. Kidney Int. 87, 1017–1029 (2015)
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
Hoggart, C.J.* et al.: Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on Body Mass Index. PLoS Genet. 10, 1-12:e1004508 (2014)
Koumakis, E.* et al.: Brief report: A regulatory variant in CCR6 is associated with susceptibility to antitopoisomerase-positive systemic sclerosis. Arthritis Rheum. 65, 3202-3208 (2013)
Boraska, V.* et al.: Genome-wide association study to identify common variants associated with brachial circumference: A meta-analysis of 14 cohorts. PLoS ONE 7:e31369 (2012)
Allanore, Y.* et al.: Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis. PLoS Genet. 7:e1002091 (2011)
Dieudé, P.* et al.: Evidence of the contribution of the X chromosome to systemic sclerosis susceptibility: Association with the functional IRAK1 196Phe/532Ser haplotype. Arthritis Rheum. 63, 3979-3987 (2011)
Johnson, T.* et al.: Blood pressure loci identified with a gene-centric array. Am. J. Hum. Genet. 89, 688-700 (2011)
Allen, H.L.* et al.: Hundreds of variants clustered in genomic loci and biological pathways affect human height. Nature 467, 832-838 (2010)