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Czamara, D.* et al.: Integrated analysis of environmental and genetic influences on cord blood DNA methylation in new-borns. Nat. Commun. 10:2548 (2019)
Wiechmann, T.* et al.: Identification of dynamic glucocorticoid-induced methylation changes at the FKBP5 locus. Clin. Epigenet. 11:83 (2019)
Dedic, N.* et al.: Cross-disorder risk gene CACNA1C differentially modulates susceptibility to psychiatric disorders during development and adulthood. Mol. Psychiatry 23, 533-543 (2018)
Felix, J.F.* et al.: Cohort profile: Pregnancy and childhood epigenetics (PACE) consortium. Int. J. Epidemiol. 47, 22-23u (2018)
Andlauer, T.F.* et al.: Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci. Adv. 2:e1501678 (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)
Arloth, J.* et al.: Genetic differences in the immediate transcriptome response to stress predict risk-related brain function and psychiatric disorders. Neuron 86, 1189-1202 (2015)
Brenndörfer, J.* et al.: Connecting anxiety and genomic copy number variation: A genome-wide analysis in CD-1 mice. PLoS ONE 10:e0128465 (2015)
Aprile-Garcia, F.* et al.: P2RX7-a susceptibility gene for mood disorders? Purinergic Signal. 10, 718 (2014)
Spieler, D. et al.: Restless Legs Syndrome-associated intronic common variant in Meis1 alters enhancer function in the developing telencephalon. Genome Res. 24, 592-603 (2014)
Czamara, D.* et al.: Children with ADHD symptoms have a higher risk for reading, spelling and math difficulties in the GINIplus and LISAplus cohort studies. PLoS ONE 8:e63859 (2013)
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
Ludwig, K.U.* et al.: A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults. Transl. Psychiatry 3:e229 (2013)
Oexle, K.* et al.: Dilution of candidates: The case of iron-related genes in restless legs syndrome. Eur. J. Hum. Genet. 21, 410-414 (2013)
Schulte, E.C. et al.: Rare variants in PLXNA4 and Parkinson's disease. PLoS ONE 8:e79145 (2013)
Schormair, B. et al.: MEIS1 and BTBD9: Genetic association with restless leg syndrome in end stage renal disease. J. Med. Genet. 48, 462-466 (2011)
Winkelmann, J. et al.: Genome-wide association study identifies novel restless legs syndrome susceptibility loci on 2p14 and 16q12.1. PLoS Genet. 7:e1002171 (2011)