Heidi Fodstad

association between HERG K897T polymorphism and QT interval in middle-aged finnish women

E M Pietilä, Heidi Fodstad, Elmo Niskasaari et al. · Journal of the American College of Cardiology · 2002 · 103 citations

Life Sciences, Genetics, Molecular Genetics +6

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

Life Sciences, Genetics, Molecular Genetics +14

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

Medicine, Cardiology, Genetics +14

Genotype–phenotype correlations in recessive titinopathies

Marco Savarese, Anna Vihola, Emily C. Oates et al. · Genetics in Medicine · 2020 · 80 citations · Full text

Life Sciences, Genetics, Molecular Genetics +13

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

Tuula Hannila‐Handelberg, Kimmo Kontula, Ilkka Tikkanen et al. · BMC Medical Genetics · 2005 · 74 citations · Full text

Life Sciences, Cardiology, Genetics +15