Kirsi Piippo
United Medix Laboratories (Finland)(FI)
Publications by Year
Research Areas
Cardiac electrophysiology and arrhythmias, Ion channel regulation and function, ECG Monitoring and Analysis, Ion Transport and Channel Regulation, Receptor Mechanisms and Signaling
Most-Cited Works
- → Mutations of the Cardiac Ryanodine Receptor (RyR2) Gene in Familial Polymorphic Ventricular Tachycardia(2001)733 cited
- → Arrhythmic disorder mapped to chromosome 1q42–q43 causes malignant polymorphic ventricular tachycardia in structurally normal hearts(1999)345 cited
- → Prevalence of recurrent pathogenic microdeletions and microduplications in over 9500 pregnancies(2015)311 cited
- → High Efficacy of β-Blockers in Long-QT Syndrome Type 1(2009)309 cited
- → Sinus node function and ventricular repolarization during exercise stress test in long QT syndrome patients with KvLQT1 and HERG potassium channel defects(1999)196 cited
- → A founder mutation of the potassium channel KCNQ1 in long QT syndrome(2001)131 cited
- → Four potassium channel mutations account for 73% of the genetic spectrum underlying long‐QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland(2004)98 cited
- → Common variants of the beta and gamma subunits of the epithelial sodium channel and their relation to plasma renin and aldosterone levels in essential hypertension(2005)74 cited
- → Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects(2000)73 cited
- → Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns(2000)65 cited