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Wuttke, M.* et al.: A catalog of genetic loci associated with kidney function from analyses of a million individuals. Nat. Genet. 51, 957-972 (2019)
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)
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)
Andlauer, T.F.* et al.: Novel multiple sclerosis susceptibility loci implicated in epigenetic regulation. Sci. Adv. 2:e1501678 (2016)
Peyrot, W.J.* et al.: The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25 000 subjects. Mol. Psychiatry 20, 735-743 (2015)
Köttgen, A.* et al.: Genome-wide association analyses identify 18 new loci associated with serum urate concentrations. Nat. Genet. 45, 145-154 (2013)
Menke, A.* et al.: Dexamethasone stimulated gene expression in peripheral blood is a sensitive marker for glucocorticoid receptor resistance in depressed patients. Neuropsychopharmacology 37, 1455-1464 (2012)
Cichon, S.* et al.: Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am. J. Hum. Genet. 88, 372-381 (2011)
Jourdan, C. et al.: Gene-PUFA interactions and obesity risk. Br. J. Nutr. 106, 1263-1272 (2011)
Anttila, V.* et al.: Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nat. Genet. 42, 869-873 (2010)
Liu, J.Z.* et al.: Meta-analysis and imputation refines the association of 15q25 with smoking quantity. Nat. Genet. 42, 436-440 (2010)
Rietschel, M.* et al.: Genome-wide association-, replication-, and neuroimaging study implicates HOMER1 in the etiology of major depression. Biol. Psychiatry 68, 589-601 (2010)
Baghai, T.C.* et al.: Polymorphisms in the angiotensin-converting enzyme gene are associated wit unipolar depression, ACE activity and hypercortisolism. Mol. Psychiatry 11, 1003-1015 (2006)
Binder, E.B.* et al.: Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nat. Genet. 36, 1319-1325 (2004)