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Spracklen, C.N.* et al.: Exome-derived adiponectin-associated variants implicate obesity and lipid biology. Am. J. Hum. Genet., accepted (2019)
Tedja, M.S.* et al.: IMI - Myopia genetics report. Invest. Ophthalmol. Vis. Sci. 60, M89-M105 (2019)
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)
Cuellar-Partida, G.* et al.: Assessing the genetic predisposition of education on myopia: A mendelian randomization study. Genet. Epidemiol. 40, 66-72 (2016)
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)
Joshi, P.K.* et al.: Directional dominance on stature and cognition in diverse human populations. Nature 523, 459-462 (2015)
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)
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)
Sim, X.* et al.: Genetic loci for retinal arteriolar microcirculation. PLoS ONE 8:e65804 (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)
Verhoeven, V.J.M.* et al.: Large scale international replication and meta-analysis study confirms association of the 15q14 locus with myopia. The CREAM consortium. Hum. Genet. 131, 1467-1480 (2012)
Ikram, M.K.* et al.: Four novel Loci (19q13, 6q24, 12q24, and 5q14) influence the microcirculation in vivo. PLoS Genet. 6:e1001184 (2010)
Tischfield, M.A.* et al.: Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell 140, 74-87 (2010)