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1.
Karasik, D.* et al.: Disentangling the genetics of lean mass. Am. J. Clin. Nutr. 109, 276-287 (2019)
2.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 5:180002 (2018)
3.
Karch, C.M.* et al.: Selective genetic overlap between amyotrophic lateral sclerosis and diseases of the frontotemporal dementia spectrum. JAMA Neurol. 75, 860-875 (2018)
4.
Kesselmeier, M.* et al.: High-throughput DNA methylation analysis in anorexia nervosa confirms TNXB hypermethylation. World J. Biol. Psychiatry 19, 187-199 (2018)
5.
Sulkava, M.* et al.: Formyl peptide receptors 1-3 and annexin 1 in atherosclerotic plaques  - tampere vascular study. Atherosclerosis 275, E104-E105 (2018)
6.
Akmatov, M.F.* et al.: Determination of nasal and oropharyngeal microbiomes in a multicenter population-based study - findings from Pretest 1 of the German National Cohort. Sci. Rep. 7:1855 (2017)
7.
Chen, G.B.* et al.: Across-cohort QC analyses of GWAS summary statistics from complex traits. Eur. J. Hum. Genet. 25, 137-146 (2017)
8.
Flannick, J.* et al.: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls. Sci. Data 4:170179 (2017)
9.
Hinney, A.* et al.: Evidence for three genetic loci involved in both anorexia nervosa risk and variation of body mass index. Mol. Psychiatry 22, 192-201 (2017)
10.
Jansen, I.E.* et al.: Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing. Genome Biol. 18:22 (2017)
11.
Laaksonen, J.* et al.: Blood pathway analyses reveal differences between prediabetic subjects with or without dyslipidaemia. The Cardiovascular Risk in Young Finns Study. Diabetes Metab. Res. Rev. 33:e2914 (2017)
12.
Manning, A.* et al.: A low-frequency inactivating Akt2 variant enriched in the Finnish population is associated with fasting insulin levels and type 2 diabetes risk. Diabetes 66, 2019-2032 (2017)
13.
Oksala, N.K.J.* et al.: Synergistic expression of histone deacetylase 9 and matrix metalloproteinase 12 in M4 macrophages in advanced carotid plaques. Eur. J. Vasc. Endovasc. Surg. 53, 632-640 (2017)
14.
Pecanka, J.* ; Jonker, M.A.* ; Bochdanovits, Z.* & International Parkinson's Disease Genomics Consortium (IPDGC) (Illig, T. ; Lichtner, P.): A powerful and efficient two-stage method for detecting gene-to-gene interactions in GWAS. Biostatistics 18, 477-494 (2017)
15.
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)
16.
Robak, L.A.* et al.: Excessive burden of lysosomal storage disorder gene variants in Parkinson's disease. Brain 140, 3191-3203 (2017)
17.
Rotter, M. et al.: Stability of targeted metabolite profiles of urine samples under different storage conditions. Metabolomics 13:4 (2017)
18.
Stratmann, B.* et al.: Metabolomic signature of coronary artery disease in type 2 diabetes mellitus. Int. J. Endocrinol. 2017:7938216 (2017)
19.
Sulkava, M.* et al.: Differentially expressed genes and canonical pathway expression in human atherosclerotic plaques-Tampere Vascular Study. Sci. Rep. 7:41483 (2017)
20.
Sulkava, M.* et al.: Differentially expressed genes and canonical pathways in the ascending thoracic aortic aneurysm - The Tampere Vascular Study. Sci. Rep. 7:12127 (2017)