PubRank

Alejandra Guerchicoff

Author PubWeight™ 35.67‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing. Heart Rhythm 2009 4.99
2 Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death. Circulation 2007 4.37
3 Sudden death associated with short-QT syndrome linked to mutations in HERG. Circulation 2003 3.68
4 Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death. Heart Rhythm 2010 2.79
5 Functional effects of KCNE3 mutation and its role in the development of Brugada syndrome. Circ Arrhythm Electrophysiol 2008 2.42
6 The homeodomain transcription factor Irx5 establishes the mouse cardiac ventricular repolarization gradient. Cell 2005 2.19
7 A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype. Circ Cardiovasc Genet 2009 1.87
8 Cryptic 5' splice site activation in SCN5A associated with Brugada syndrome. J Mol Cell Cardiol 2004 1.81
9 Functional expression of "cardiac-type" Nav1.5 sodium channel in canine intracardiac ganglia. Heart Rhythm 2006 1.50
10 Torsades de pointes following acute myocardial infarction: evidence for a deadly link with a common genetic variant. Heart Rhythm 2012 1.46
11 Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. Heart Rhythm 2008 1.27
12 Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations. Circulation 2004 1.14
13 Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction. Heart Rhythm 2007 1.04
14 Dual variation in SCN5A and CACNB2b underlies the development of cardiac conduction disease without Brugada syndrome. Pacing Clin Electrophysiol 2009 0.94
15 Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias. J Electrocardiol 2007 0.88
16 A novel mutation in KCNQ1 associated with a potent dominant negative effect as the basis for the LQT1 form of the long QT syndrome. J Cardiovasc Electrophysiol 2007 0.86
17 Complementary prognostic utility of myocardial blush grade and ST-segment resolution after primary percutaneous coronary intervention: analysis from the HORIZONS-AMI trial. Am Heart J 2013 0.80
18 Impact of scheduled angiographic follow-up in patients treated with primary percutaneous coronary intervention for ST-segment elevation myocardial infarction. J Interv Cardiol 2013 0.79
19 Susceptibility genes for coronary heart disease and myocardial infarction. Acute Card Care 2011 0.77
20 Characterization of Cyt2Bc toxin from Bacillus thuringiensis subsp. medellin. Appl Environ Microbiol 2002 0.76