PuSH - Publication Server of Helmholtz Zentrum München

13 Records found.
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1.
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)
2.
Cuellar-Partida, G.* et al.: Assessing the genetic predisposition of education on myopia: A mendelian randomization study. Genet. Epidemiol. 40, 66-72 (2016)
3.
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)
4.
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)
5.
McCarthy, S.* et al.: A reference panel of 64,976 haplotypes for genotype imputation. Nat. Genet. 48, 1279-1283 (2016)
6.
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)
7.
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)
8.
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)
9.
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)
10.
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)
11.
Huang, K.M.* et al.: Xcat, a novel mouse model for Nance-Horan syndrome inhibits expression of the cytoplasmic-targeted Nhs1 isoform. Hum. Mol. Genet. 15, 319-327 (2006)
12.
Wang, K.S.* ; Zahn, L.E.* ; Favor, J. ; Huang, K.M.* & Stambolian, D.*: Genetic and phenotypic analysis of Tcm, a mutation affecting early eye development. Mamm. Genome 16, 332-343 (2005)
13.
Huang, K.M.* et al.: Organization and annotation of the Xcat critical region: Elimination of seven positional candidate genes. Genomics 83, 893-901 (2004)