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Bressin, A.* et al.: TriPepSVM: De novo prediction of RNA-binding proteins based on short amino acid motifs. Nucleic Acids Res. 47, 4406-4417 (2019)
Ortiz-Bonnin, B.* et al.: Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: Identification of novel LQTS3 and BrS mutations. Pflugers Arch. 468, 1375-1387 (2016)
Kolder, I.C.* et al.: Analysis for genetic modifiers of disease severity in patients with long QT syndrome type 2. Circ. Cardiovasc. Genet. 8, 447-456 (2015)
Arking, D.E.* et al.: Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nat. Genet. 46, 826-836 (2014)
Makita, N.* et al.: Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)
Bezzina, C.R.* et al.: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death. Nat. Genet. 45, 1044-1049 (2013)
Crotti, L. et al.: Calmodulin mutations associated with recurrent cardiac arrest in infants. Circulation 127, 1009-1017 (2013)
Chockalingam, P.* et al.: Not all beta-blockers are equal in the management of long QT syndrome types 1 and 2: Higher recurrence of events under metoprolol. J. Am. Coll. Cardiol. 60, 2092-2099 (2012)
Kääb, S.* et al.: A large candidate gene survey identifies the KCNE1 D85N polymorphism as a possible modulator of drug-induced torsades de pointes. Circ. Cardiovasc. Genet. 5, 91-99 (2012)
Sinner, M.F.* et al.: A meta-analysis of genome-wide association studies of the electrocardiographic early repolarization pattern. Heart Rhythm 9, 1627-1634 (2012)
Merkel, O.M.* et al.: Polymer-related off-target effects in non-viral siRNA delivery. Biomaterials 32, 2388-2398 (2011)
Sinner, M.F.* et al.: Lack of replication in polymorphisms reported to be associated with atrial fibrillation. Heart Rhythm 8, 403-409 (2011)
Ellinor, P.T.* et al.: Common variants in KCNN3 are associated with lone atrial fibrillation. Nat. Genet. 42, 240-244 (2010)
Pfeufer, A. et al.: Genome-wide association study of PR interval. Nat. Genet. 42, 153-159 (2010)
Sinner, M.F.* et al.: Association of early repolarization pattern on ECG with risk of cardiac and all-cause mortality: A population-based prospective cohort study (MONICA/KORA). PLoS Med. 7:e1000314 (2010)
Kääb, S.* et al.: Large scale replication and meta-analysis of variants on chromosome 4q25 associated with atrial fibrillation. Eur. Heart J. 30, 813-819 (2009)
Sinner, M.F.* et al.: Spontaneous Brugada electrocardiogram patterns are rare in the German general population: Results from the KORA study. Europace 11, 1338-1344 (2009)
Hinterseer, M.* et al.: Beat-to-beat variability of QT intervals is increased in patients with drug-induced long-QT syndrome: A case control pilot study. Eur. Heart J. 29, 185-190 (2008)
Kääb, S.* et al.: High density tagSNP candidate gene analysis identifies I-Ks as a major modulator of genetic susceptibility to drug induced long QT syndrome. Circulation 118, 2, S884-S884 (2008)
Sinner, M.F. et al.: The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: Results from a systematic candidate gene-based analysis of KCNH2 (HERG). Eur. Heart J. 29, 907-914 (2008)