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13 Records found.
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1.
Milano, A.* et al.: Sudden cardiac arrest and rare genetic variants in the community. Circ. Cardiovasc. Genet. 9, 147-153 (2016)
2.
Wilde, A.A.* et al.: Clinical aspects of type 3 long QT syndrome: An international multicenter study. Circulation 134, 872-882 (2016)
3.
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)
4.
de Ferrari, G.M.* et al.: Clinical management of catecholaminergic polymorphic ventricular tachycardia: The role of left cardiac sympathetic denervation. Circulation 131, 2185-2193 (2015)
5.
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)
6.
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)
7.
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)
8.
Amin, A.S.* et al.: Variants in the 3' untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner. Eur. Heart J. 33, 714-723 (2012)
9.
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)
10.
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)
11.
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)
12.
Watanabe, H.* et al.: Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans. J. Clin. Invest. 118, 2260-2268 (2008)
13.
Yang, P.* et al.: Polymorphisms in the cardiac sodium channel promoter displaying variant in vitro expression activity. Eur. J. Hum. Genet. 16, 350-357 (2008)