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Malik, R.* et al.: Publisher Correction: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes (Nature Genetics, (2018), 50, 4, (524-537), 10.1038/s41588-018-0058-3). Nat. Genet. (2019)
Valdes-Marquez, E.* et al.: Relative effects of LDL-C on ischemic stroke and coronary disease: A Mendelian randomization study. Neurology 92, E1176-E1187 (2019)
Christophersen, I.E.* et al.: Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation. Nat. Genet. 49, 946-952 (2017)
Magosi, L.E.* ; Goel, A.* ; Hopewell, J.C.* ; Farrall, M.* & CARDIoGRAMplusC4D Consortium (Gieger, C. ; Peters, A. ; Meitinger, T.): Identifying systematic heterogeneity patterns in genetic association meta-analysis studies. PLoS Genet. 13:e1006755 (2017)
Cheng, Y.C.* et al.: Genome-wide association analysis of young onset stroke identifies a locus on chromosome 10q25 near HABP2. Stroke 47, 307-316 (2016)
Keenan, T.* et al.: Causal assessment of serum urate levels in cardiometabolic diseases through a mendelian randomization study. J. Am. Coll. Cardiol. 67, 407-416 (2016)
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
Interleukin 1 Genetics Consortium et al.: Cardiometabolic effects of genetic upregulation of the interleukin 1 receptor antagonist: A mendelian randomisation analysis. Lancet Diabet. Endocrinol. 3, 243-253 (2015)
Kato, N.* et al.: Trans-ancestry genome-wide association study identifies 12 genetic loci influencing blood pressure and implicates a role for DNA methylation. Nat. Genet. 47, 1282-1293 (2015)
Nelson, C.P.* et al.: Genetically determined height and coronary artery disease. N. Engl. J. Med. 372, 1608-1618 (2015)
Dichgans, M.* et al.: Shared genetic susceptibility to ischemic stroke and coronary artery disease: A genome-wide analysis of common variants. Stroke 45, 24-36 (2014)
Deloukas, P.* et al.: Large-scale association analysis identifies new risk loci for coronary artery disease. Nat. Genet. 45, 25-35 (2013)
Sabater-Lleal, M.* et al.: Multiethnic meta-analysis of genome-wide association studies in >100 000 subjects identifies 23 fibrinogen-associated loci but no strong evidence of a causal association between circulating fibrinogen and cardiovascular disease. Circulation 128, 1310-1324 (2013)
Asselbergs, F.W.* et al.: Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. Am. J. Hum. Genet. 91, 823-838 (2012)
Clarke, R.* et al.: Homocysteine and coronary heart disease: Meta-analysis of MTHFR case-control studies, avoiding publication bias. PLoS Med. 9:e1001177 (2012)
Huang, J.* et al.: Genome-wide association study for circulating levels of PAI-1 provides novel insights into its regulation. Blood 120, 4873-4881 (2012)
Strawbridge, R.J.* et al.: Genome-wide association identifies nine common variants associated with fasting proinsulin levels and provides new insights into the pathophysiology of type 2 diabetes. Diabetes 60, 2624-2634 (2011)
Wain, L.V.* et al.: Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure. Nat. Genet. 43, 1005-1011 (2011)
Sarwar, N.* et al.: Triglyceride-mediated pathways and coronary disease: Collaborative analysis of 101 studies. Lancet 375, 1634-1639 (2010)