PuSH - Publication Server of Helmholtz Zentrum München

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1.
Kunkle, B.W.* et al.: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing. Nat. Genet. 51, 414-430 (2019)
2.
Lacruz, M.E.* et al.: Instability of personal human metabotype is linked to all-cause mortality. Sci. Rep. 8:9810 (2018)
3.
Sedlmeier, A.* et al.: The human metabolic profile reflects macro- and micronutrient intake distinctly according to fasting time. Sci. Rep. 8:12262 (2018)
4.
Lacruz, M.E.* et al.: Cardiovascular risk factors associated with blood metabolite concentrations and their alterations over a 4-year period in a population-based cohort. Circ. Cardiovasc. Genet. 9, 487-494 (2016)
5.
Boraska, V.* et al.: A genome-wide association study of anorexia nervosa. Mol. Psychiatry 19, 1085-1094 (2014)
6.
Hartz, S.M.* et al.: Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. JAMA psychiatry 69, 854-860 (2012)
7.
He, Y. et al.: Schizophrenia shows a unique metabolomics signature in plasma. Transl. Psychiatry 2:e149 (2012)
8.
Mühlau, M.* et al.: Variation within the Huntington's disease gene influences normal brain structure. PLoS ONE 7:e29809 (2012)
9.
Rietschel, M.* et al.: Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe. Mol. Psychiatry 17, 906-917 (2012)
10.
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)
11.
Mobascher, A.* et al.: Association of a variant in the muscarinic acetylcholine receptor 2 gene (CHRM2) with nicotine addiction. Am. J. Med. Genet. B 153B, 684-690 (2010)
12.
Thorgeirsson, T.E.* et al.: Sequence variants at CHRNB3-CHRNA6 and CYP2A6 affect smoking behavior. Nat. Genet. 42, 448-453 (2010)
13.
Winterer, G.* et al.: Risk gene variants for nicotine dependence in the CHRNA5-CHRNA3-CHRNB4 cluster are associated with cognitive performance. Am. J. Med. Genet. B 158B, 1448-1458 (2010)
14.
Breitling, L.P.* et al.: Association of nicotinic acetylcholine receptor subunit α4 polymorphisms with nicotine dependence in 5500 Germans. Pharmacogenomics J. 9, 219-224 (2009)
15.
van Es, M.A.* et al.: Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis. Nat. Genet. 41, 1083-1087 (2009)