Genetic Basis and Outcome in a Nationwide Study of Finnish Patients with Hypertrophic CardiomyopathyPertti Jääskeläinen, Johanna Kuusisto, Erkki Ilveskoski et al.|ESC Heart Failure|2019Cited by 46
Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish populationPertti Jääskeläinen, Mikko Pietilä, Tiina Heliö et al.|Annals of Medicine|2012Cited by 45
A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathyPertti Jääskeläinen, Tiina Heliö, Katriina Aalto‐Setälä et al.|Annals of Medicine|2014Cited by 17
Lamin A/C Mutation Affecting Primarily the Right Side of the HeartLaura Ollila, Tiina Heliö, Johanna Kuusisto et al.|Cardiogenetics|2013Cited by 4