Päivi J. Laitinen-Forsblom

<i>SCN5A</i> Mutation Associated with Cardiac Conduction Defect and Atrial Arrhythmias

Päivi J. Laitinen-Forsblom, Pekka J. Mäkynen, Heikki Mäkynen et al. · Journal of Cardiovascular Electrophysiology · 2006 · 90 citations

Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug–associated torsades de pointes

Annukka Lehtonen, Heidi Fodstad, Päivi J. Laitinen-Forsblom et al. · Heart Rhythm · 2007 · 90 citations

Genetics, Antiarrhythmic Drug–associated Torsades, Congenital Heart Defect +5

Mutant ryanodine receptors in catecholaminergic polymorphic ventricular tachycardia generate delayed afterdepolarizations due to increased propensity to Ca2+ waves

Jere Paavola, Matti Viitasalo, Päivi J. Laitinen-Forsblom et al. · European Heart Journal · 2007 · 81 citations · Full text

Gain-of-Function Mutation of the <i>SCN5A</i> Gene Causes Exercise-Induced Polymorphic Ventricular Arrhythmias

Heikki Swan, Mohamed‐Yassine Amarouch, Jaakko T. Leinonen et al. · Circulation Cardiovascular Genetics · 2014 · 62 citations

Search for cardiac calcium cycling gene mutations in familial ventricular arrhythmias resembling catecholaminergic polymorphic ventricular tachycardia

Annukka Marjamaa, Päivi J. Laitinen-Forsblom, Annukka M. Lahtinen et al. · BMC Medical Genetics · 2009 · 61 citations · Full text