Liisa Hämäläinen

Arg506GIn Factor V Mutation (Factor V Leiden) in Patients with Ischaemic Cerebrovascular Disease and Survivors of Myocardial Infarction

Kimmo Kontula, Antti Ylikorkala, Helena E. Miettinen et al. · Thrombosis and Haemostasis · 1995 · 160 citations

Vascular Disease, Healthy Blood Donors, Factor V +26

Genetic Basis and Outcome in a Nationwide Study of Finnish Patients with Hypertrophic Cardiomyopathy

Pertti Jääskeläinen, Jagadish Vangipurapu, Joose Raivo et al. · ESC Heart Failure · 2019 · 45 citations · Full text

Two founder mutations in the alpha-tropomyosin and the cardiac myosin-binding protein C genes are common causes of hypertrophic cardiomyopathy in the Finnish population

Pertti Jääskeläinen, Tiina Heliö, Katriina Aalto‐Setälä et al. · Annals of Medicine · 2012 · 44 citations · Full text

Genetic Polymorphism of Platelet Glycoprotein IIIa in Patients with Acute Myocardial Infarction and Acute Ischaemic Stroke

Satu Kekomäki, Liisa Hämäläinen, Ritva Kauppinen‐Mäkelin et al. · European Journal of Cardiovascular Prevention & Rehabilitation · 1999 · 39 citations

A new common mutation in the cardiac beta-myosin heavy chain gene in Finnish patients with hypertrophic cardiomyopathy

Pertti Jääskeläinen, Tiina Heliö, Katriina Aalto‐Setälä et al. · Annals of Medicine · 2014 · 16 citations