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Demontis, D.* et al.: Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder. Nat. Genet. 51, 63–75 (2019)
Hammerschlag, A.R.* et al.: Genome-wide association analysis of insomnia complaints identifies risk genes and genetic overlap with psychiatric and metabolic traits. Nat. Genet. 49, 1584-1592 (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)
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)
Desikan, R.S.* et al.: Genetic overlap between Alzheimer's disease and Parkinson's disease at the MAPT locus. Mol. Psychiatry 20, 1588-1595 (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)
AMD Gene Consortium et al.: Seven new loci associated with age-related macular degeneration. Nat. Genet. 45, 433-439 (2013)
Anttila, V.* et al.: Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat. Genet. 45, 912-917 (2013)
Holmans, P.* et al.: A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease. Hum. Mol. Genet. 22, 1039-1049 (2013)
Keller, M.F.* et al.: Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease. Hum. Mol. Genet. 21, 4996-5009 (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)
Hollingworth, P.* et al.: Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease. Nat. Genet. 43, 429-436 (2011)
Jacquemont, S.* et al.: Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature 478, 97-102 (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)
Thorgeirsson, T.E.* et al.: Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat. Genet. 42, 448-453 (2010)
Gudbjartsson, D.F.* et al.: Sequence variants affecting eosinophil numbers associate with asthma and myocardial infarction. Nat. Genet. 41, 342-347 (2009)