PuSH - Publication Server of Helmholtz Zentrum München

61 Records found.
Zum Exportieren der Ergebnisse bitte einloggen.
Lay all publications on this page into basket
Lin, H.* et al.: Gene-gene interaction analyses for atrial fibrillation. Sci. Rep. 6:35371 (2016)
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)
van der Harst, P.* et al.: 52 Genetic loci influencing myocardial mass. J. Am. Coll. Cardiol. 68, 1435-1448 (2016)
Yousri, N.A.* et al.: Diagnostic and prognostic metabolites identified for joint symptoms in the KORA population. J. Proteome Res. 15, 554-562 (2016)
Behr, E.R.* et al.: Role of common and rare variants in SCN10A: Results from the Brugada syndrome QRS locus gene discovery collaborative study. Cardiovasc. Res. 106, 520-529 (2015)
Brandes, A. ; Sinner, M.F.* ; Kääb, S.* & Rogowski, W.H.: Early decision-analytic modeling - a case study on vascular closure devices. BMC Health Serv. Res. 15:486 (2015)
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)
Müller-Nurasyid, M. et al.: Genome-wide association analysis with multivariate ECG traits. Genet. Epidemiol. 39, 571 (2015)
Thiele, I. et al.: Associations between calcium and vitamin D supplement use as well as their serum concentrations and subclinical cardiovascular disease phenotypes. Atherosclerosis 241, 743-751 (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)
Lemaitre, R.N.* et al.: Common variation in fatty acid metabolic genes and risk of incident sudden cardiac arrest. Heart Rhythm 11, 471-477 (2014)
Lubitz, S.A.* et al.: Novel genetic markers associate with atrial fibrillation risk in Europeans and Japanese. J. Am. Coll. Cardiol. 63, 1200-1210 (2014)
Makita, N.* et al.: Novel calmodulin (CALM2) mutations associated with congenital arrhythmia susceptibility. Circ. Cardiovasc. Genet. 7, 466-474 (2014)
Meder, B.* et al.: A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. Eur. Heart J. 35, 1069-1077 (2014)
Röhrig, N.* et al.: Directed acyclic graphs helped to identify confounding in the association of disability and electrocardiographic findings: Results from the KORA-Age study. J. Clin. Epidemiol. 67, 199-206 (2014)
Sinner, M.F.* et al.: Integrating genetic, transcriptional, and functional analyses to identify five novel genes for atrial fibrillation. Circulation 130, 1225-1235 (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)
den Hoed, M.* et al.: Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders. Nat. Genet. 45, 621-631 (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)