PuSH - Publication Server of Helmholtz Zentrum München

30 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
1.
Lacruz, M.E.* et al.: Instability of personal human metabotype is linked to all-cause mortality. Sci. Rep. 8:9810 (2018)
2.
Barban, N.* et al.: Genome-wide analysis identifies 12 loci influencing human reproductive behavior. Nat. Genet. 48, 1462-1472 (2016)
3.
Jun, G.* et al.: A novel Alzheimer disease locus located near the gene encoding tau protein. Mol. Psychiatry 21, 108–117 (2016)
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.
Schulte, E.C. et al.: Excess of rare coding variants in PLD3 in late- but not early-onset Alzheimer’s disease. Hum. Genome Var. 2:14028 (2015)
6.
Altinigneli, C.* ; Konte, B.* ; Rujescu, D.* ; Böhm, C.* & Plant, C.: Identification of SNP interactions using data-parallel primitives on GPUs. In: Proceedings (IEEE International Conference on Big Data, 27-30 October 2014, Washington, DC, USA). Piscataway, NJ: IEEE, 2014.
7.
Boraska, V.* et al.: A genome-wide association study of anorexia nervosa. Mol. Psychiatry 19, 1085-1094 (2014)
8.
Sun, M. et al.: Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function. Mamm. Genome 24, 333-348 (2013)
9.
Tretter, F.* ; Pogarell, O.* ; Rujescu, D.* ; Meisenzahl, E.* & Mewes, H.-W.: Systems biology of oscillatory processes in sleep and mental disorders. Pharmacopsychiatry 46, S1 (2013)
10.
Gerrish, A.* et al.: The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease. J. Alzheimers Dis. 28, 377-387 (2012)
11.
Hartz, S.M.* et al.: Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers. JAMA psychiatry 69, 854-860 (2012)
12.
He, Y. et al.: Schizophrenia shows a unique metabolomics signature in plasma. Transl. Psychiatry 2:e149 (2012)
13.
Mühlau, M.* et al.: Variation within the Huntington's disease gene influences normal brain structure. PLoS ONE 7:e29809 (2012)
14.
Mühleisen, T.W.* et al.: Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr. Res. 138, 69-73 (2012)
15.
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)
16.
Tretter, F.* ; Pogarell, O.* ; Rujescu, D.* ; Meisenzahl, E.* & Mewes, H.-W.: Editorial. Pharmacopsychiatry 45, S1 (2012)
17.
Breitling, L.P.* et al.: Dopamine-related genes and spontaneous smoking cessation in ever-heavy smokers. Pharmacogenomics 12, 1099-1106 (2011)
18.
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)
19.
Tretter, F.* et al.: Affective disorders as complex dynamic diseases - a perspective from systems biology. Pharmacopsychiatry 44, Suppl 1, S2-S8 (2011)
20.
Jones, L.* et al.: Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease. PLoS ONE 5:e13950 (2010)