PuSH - Publication Server of Helmholtz Zentrum München

15 Records found.
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1.
Demontis, D.* et al.: Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat. Genet. 51, 63–75 (2019)
2.
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)
3.
Duncan, L.* et al.: Significant locus and metabolic genetic correlations revealed in genome-wide association study of anorexia nervosa. Am. J. Psychiatry 174, 850-858 (2017)
4.
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)
5.
Goyette, P.* et al.: High-density mapping of the MHC identifies a shared role for HLA-DRB1*01:03 in inflammatory bowel diseases and heterozygous advantage in ulcerative colitis. Nat. Genet. 47, 172-179 (2015)
6.
Locke, A.E.* et al.: Genetic studies of body mass index yield new insights for obesity biology. Nature 518, 197-206 (2015)
7.
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)
8.
Chan, Y.* et al.: An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases. Am. J. Hum. Genet. 94, 437-452 (2014)
9.
Wood, A.R.* et al.: Defining the role of common variation in the genomic and biological architecture of adult human height. Nat. Genet. 46, 1173-1186 (2014)
10.
AMD Gene Consortium et al.: Seven new loci associated with age-related macular degeneration. Nat. Genet. 45, 433-439 (2013)
11.
Jostins, L.* et al.: Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491, 119-124 (2012)
12.
Freilinger, T.* et al.: Genetic variation in the lymphotoxin-alpha pathway and the risk of ischemic stroke in European populations. Stroke 40, 970-972 (2009)
13.
Gschwendtner, A.* et al.: Genetic variation in soluble epoxide hydrolase (EPHX2) is associated with an increased risk of ischemic stroke in white Europeans. Stroke 39, 1593-1596 (2008)
14.
Schormair, B. et al.: PTPRD (protein tyrosine phosphatase receptor type delta) is associated with restless legs syndrome. Nat. Genet. 40, 946-948 (2008)
15.
Winkelmann, J. et al.: Genome-wide association study of restless legs syndrome identifies common variants in three genomic regions. Nat. Genet. 39, 1000-1006 (2007)