PuSH - Publication Server of Helmholtz Zentrum München

18 Records found.
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1.
Bihlmeyer, N.A.* et al.: ExomeChip-wide analysis of 95 626 individuals identifies 10 novel loci associated with QT and JT intervals. Circ. Genom. Precis. Med. 11:e001758 (2018)
2.
Lin, H.* et al.: Common and rare coding genetic variation underlying the electrocardiographic PR interval. Circ. Genom. Precis. Med. 11:e002037 (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.
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)
5.
van den Berg, M.* et al.: Discovery of novel heart rate-associated loci using the Exome Chip. Hum. Mol. Genet. 26, 2346-2363 (2017)
6.
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)
7.
Malik, R.* et al.: Low-frequency and common genetic variation in ischemic stroke: The METASTROKE collaboration. Neurology 86, 1217-1226 (2016)
8.
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)
9.
Bluher, A.* et al.: Heritability of young- and old-onset ischaemic stroke. Eur. J. Neurol. 22, 1488-1491 (2015)
10.
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)
11.
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)
12.
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (2014)
13.
Ellinor, P.T.* et al.: Meta-analysis identifies six new susceptibility loci for atrial fibrillation. Nat. Genet. 44, 670-675 (2012)
14.
Jeanne, M.* et al.: COL4A2 mutations impair COL4A1 and COL4A2 secretion and cause hemorrhagic stroke. Am. J. Hum. Genet. 90, 91-101 (2012)
15.
Sinner, M.F.* et al.: Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Heart Rhythm 8, 403-409 (2011)
16.
Lubitz, S.A.* et al.: Independent susceptibility markers for atrial fibrillation on chromosome 4q25. Circulation 122, 976-984 (2010)
17.
Nalls, M.A.* et al.: Failure to validate association between 12p13 variants and ischemic stroke. N. Engl. J. Med. 362, 1547-1550 (2010)
18.
Gschwendtner, A.* et al.: Sequence variants on chromosome 9p21.3 confer risk for atherosclerotic stroke. Ann. Neurol. 65, 531-539 (2009)