PuSH - Publication Server of Helmholtz Zentrum München

20 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
1.
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)
2.
Malik, R.* et al.: Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes. Nat. Genet. 50, 524-537 (2018)
3.
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)
4.
Malik, R.* et al.: Common coding variant in SERPINA1 increases the risk for large artery stroke. Proc. Natl. Acad. Sci. U.S.A. 114, 3613-3618 (2017)
5.
Rannikme, K.* et al.: COL4A2 is associated with lacunar ischemic stroke and deep ICH: Meta-analyses among 21,500 cases and 40,600 controls. Neurology 89, 1829-1839 (2017)
6.
Wierer, M.* et al.: Compartment-resolved proteomic analysis of mouse aorta during atherosclerotic plaque formation reveals osteoclast-specific protein expression. Mol. Cell. Proteomics 17, 321-334 (2017)
7.
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)
8.
Gormley, P.* et al.: Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine. Nat. Genet. 48, 856-866 (2016)
9.
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)
10.
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
11.
International Stroke Genetics Consortium (Pulit, S.L.* ; McArdle, P.F.* ; Wong, Q.* ; Malik, R.* ; Gieger, C. ; Meisinger, C. ; Müller-Nurasyid, M. ; Peters, A. ; Strauch, K. ; Waldenberger, M. ; Rosand, J.*): Loci associated with ischaemic stroke and its subtypes (SiGN): A genome-wide association study. Lancet Neurol. 15, 174-184 (2016)
12.
van der Laan, S.W.* et al.: Cystatin C and cardiovascular disease: A mendelian randomization study. J. Am. Coll. Cardiol. 68, 934-945 (2016)
13.
Zhao, H.* et al.: Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia 36, 648-657 (2016)
14.
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)
15.
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)
16.
Opherk, C.* et al.: Genome-wide genotyping demonstrates a polygenic risk score associated with white matter hyperintensity volume in CADASIL. Stroke 45, 968-972 (2014)
17.
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
18.
Anttila, V.* et al.: Genome-wide meta-analysis identifies new susceptibility loci for migraine. Nat. Genet. 45, 912-917 (2013)
19.
Ganesh, S.K.* et al.: Loci influencing blood pressure identified using a cardiovascular gene-centric array. Hum. Mol. Genet. 22, 1663-1678 (2013)
20.
Freilinger, T.* et al.: Genome-wide association analysis identifies susceptibility loci for migraine without aura. Nat. Genet. 44, 777-782 (2012)