Kristian Paavonen

A founder mutation of the potassium channel KCNQ1 in long QT syndrome

Kirsi Piippo, Heikki Swan, Michael Pasternack et al. · Journal of the American College of Cardiology · 2001 · 131 citations

Founder Mutation, Long Qt Syndrome, Channelopathies +8

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

Heidi Fodstad, Heikki Swan, Päivi Laitinen et al. · Annals of Medicine · 2004 · 98 citations

Functional characterization of the common amino acid 897 polymorphism of the cardiac potassium channel KCNH2 (HERG)

Kristian Paavonen · Cardiovascular Research · 2003 · 77 citations · Full text

Predictors of Antihypertensive Drug Responses: Initial Data from a Placebo-Controlled, Randomized, Cross-Over Study With Four Antihypertensive Drugs (The GENRES Study)

Timo P. Hiltunen, Timo Suonsyrjä, Tuula Hannila‐Handelberg et al. · American Journal of Hypertension · 2007 · 71 citations

Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

Kirsi Piippo, Päivi Laitinen, Heikki Swan et al. · Journal of the American College of Cardiology · 2000 · 65 citations

Long Qt Syndrome, Channelopathies, Mendelian Disorder +9