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Heart Rhythm|May 1, 2007
Further evidence of inherited long QT syndrome gene mutations in antiarrhythmic drug-associated torsades de pointesAnnukka Lehtonen, Heidi Fodstad, Päivi Laitinen-Forsblom, et al.
International Journal of Legal Medicine|April 12, 2003
Molecular screening of selected long QT syndrome (LQTS) mutations in 165 consecutive bodies found in waterPhilippe Lunetta, Antti Levo, Päivi J Laitinen, et al.
American Journal of Hypertension|December 6, 2008
Renin-angiotensin system and alpha-adducin gene polymorphisms and their relation to responses to antihypertensive drugs: results from the GENRES studyTimo Suonsyrjä, Tuula Hannila-Handelberg, Heidi Fodstad, et al.
Journal of Molecular and Cellular Cardiology|July 28, 2004
Loss-of-function mutations of the K(+) channel gene KCNJ2 constitute a rare cause of long QT syndromeHeidi Fodstad, Heikki Swan, Muriel Auberson, et al.
Pharmacogenetics and Genomics|March 20, 2010
Common genetic variation of beta1- and beta2-adrenergic receptor and response to four classes of antihypertensive treatmentTimo Suonsyrjä, Kati Donner, Tuula Hannila-Handelberg, et al.
Annals of Medicine|June 5, 2004
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 FinlandHeidi Fodstad, Heikki Swan, Päivi Laitinen, et al.
Genes|September 28, 2021
CNV Detection from Exome Sequencing Data in Routine Diagnostics of Rare Genetic Disorders: Opportunities and LimitationsBeryl Royer-Bertrand, Katarina Cisarova, Florence Niel-Butschi, et al.
Revue Medicale Suisse|June 23, 2017
[Multidisciplinary cardiogenetic counselling]Florence Fellmann, Xavier Jeanrenaud, Nicole Sekarski, et al.
American Journal of Physiology. Renal Physiology|March 20, 2009
Effects of mineralocorticoid and K+ concentration on K+ secretion and ROMK channel expression in a mouse cortical collecting duct cell lineHeidi Fodstad, Elena Gonzalez-Rodriguez, Sylvian Bron, et al.
Analytical Biochemistry|April 25, 2003
Multiplex genotyping of the human beta2-adrenergic receptor gene using solid-phase capturable dideoxynucleotides and mass spectrometrySobin Kim, Shundi Shi, Tomás Bonome, et al.
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