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Tedja, M.S.* et al.: Genome-wide association meta-analysis highlights light-induced signaling as a driver for refractive error. Nat. Genet. 50, 834-848 (2018)
van Zuydam, N.R.* et al.: A genome-wide association study of diabetic kidney disease in subjects with type 2 diabetes. Diabetes 67, 1414-1427 (2018)
Fan, Q.* et al.: Meta-analysis of gene-environment-wide association scans accounting for education level identifies additional loci for refractive error. Nat. Commun. 7:11008 (2016)
Fan, Q.* et al.: Childhood gene-environment interactions and age-dependent effects of genetic variants associated with refractive error and myopia: The CREAM Consortium. Sci. Rep. 6:25853 (2016)
Teumer, A.* et al.: Genome-wide association studies identify genetic loci associated with albuminuria in diabetes. Diabetes 65, 803-817 (2016)
Li, Q.* et al.: Genome-wide association study for refractive astigmatism reveals genetic co-determination with spherical equivalent refractive error: The CREAM consortium. Hum. Genet. 134, 131-146 (2015)
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)
Simpson, C.L.* et al.: Genome-wide meta-analysis of myopia and hyperopia provides evidence for replication of 11 loci. PLoS ONE 9:e107110 (2014)
Ashraf, S.* et al.: ADCK4 mutations promote steroid-resistant nephrotic syndrome through CoQ10 biosynthesis disruption. J. Clin. Invest. 123, 5179-5189 (2013)
Cheng, C.Y.* et al.: Nine loci for ocular axial length identified through genome-wide association studies, including shared loci with refractive error. Am. J. Hum. Genet. 93, 264-277 (2013)
Stambolian, D.* et al.: Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error. Hum. Mol. Genet. 22, 2754-2764 (2013)
Verhoeven, V.J.M.* et al.: Genome-wide meta-analyses of multiancestry cohorts identify multiple new susceptibility loci for refractive error and myopia. Nat. Genet. 45, 314-318 (2013)
Böger, C.A.* et al.: CUBN is a gene locus for albuminuria. J. Am. Soc. Nephrol. 22, 555-570 (2011)
Nolte, I.M.* et al.: Common genetic variation near the Phospholamban gene is associated with cardiac repolarisation: Meta-analysis of three genome-wide association studies. PLoS ONE 4:e6138 (2009)
Billingsley, G.* et al.: CRYBA4, a novel human cataract gene, is also involved in microphthalmia. Am. J. Hum. Genet. 79, 702-709 (2006)