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Zannas, A.S.* et al.: Epigenetic upregulation of FKBP5 by aging and stress contributes to NF-kappa B-driven inflammation and cardiovascular risk. Proc. Natl. Acad. Sci. U.S.A. 166, 11370-11379 (2019)
Salminen, A.V. et al.: Sleep disturbance by pramipexole is modified by Meis1 in mice. J. Sleep Res. 27:e12557 (2018)
Direk, N.* et al.: An analysis of two genome-wide association meta-analyses identifies a new locus for broad depression phenotype. Biol. Psychiatry 82, 322-329 (2017)
Power, R.A.* et al.: Genome-wide association for major depression through age at onset stratification: Major depressive disorder working group of the Psychiatric Genomics Consortium. Biol. Psychiatry 81, 325-335 (2017)
Schormair, B. et al.: Identification of novel risk loci for restless legs syndrome: A meta-analysis of genome-wide association studies in individuals of European ancestry: A meta-analysis. Lancet Neurol. 16, 898–907 (2017)
Amin, N.* et al.: Genetic variants in RBFOX3 are associated with sleep latency. Eur. J. Hum. Genet. 24, 1488-1495 (2016)
Andlauer, T.F.* et al.: Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci. Adv. 2:e1501678 (2016)
Fehringer, G.* et al.: Cross-cancer genome-wide analysis of lung, ovary, breast, prostate and colorectal cancer reveals novel pleiotropic associations. Cancer Res. 76, 5103-5114 (2016)
Gormley, P.* et al.: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)
Zhao, H.* et al.: Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia 36, 648-657 (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)
Dankowski, T.* et al.: Exome array GWAS in 10,000 Germans identifies association between MUC22 and multiple sclerosis. Hum. Hered. 79, 32-33 (2015)
Dankowski, T.* et al.: Successful replication of GWAS hits for multiple sclerosis in 10,000 Germans using the exome array. Genet. Epidemiol. 39, 601-608 (2015)
Nyholt, D.R.* et al.: Concordance of genetic risk across migraine subgroups: Impact on current and future genetic association studies. Cephalalgia 35, 489-499 (2015)
Aprile-Garcia, F.* et al.: P2RX7-a susceptibility gene for mood disorders? Purinergic Signal. 10, 718 (2014)
Khan, S.* et al.: MicroRNA related polymorphisms and breast cancer risk. PLoS ONE 9:e109973 (2014)
Opherk, C.* et al.: Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL. Stroke 45, 968-972 (2014)
Schulte, E.C. et al.: Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome. PLoS ONE 9:e98092 (2014)
Schulte, E.C. et al.: Targeted resequencing and systematic in vivo functional testing identifies rare variants in MEIS1 as significant contributors to restless legs syndrome. Am. J. Hum. Genet. 95, 85-95 (2014)