Prevalence of arrhythmia-associated gene mutations and risk of sudden cardiac death in the Finnish population

Circulation : Clinical Summaries

(2012)   CIRCULATION

Common Genetic Variants Associated with Sudden Cardiac Death: The FinSCDgen Study

(2012) Annukka M. Lahtinen et al.   PLoS One

Common Genetic Variants, QT Interval, and Sudden Cardiac Death in a Finnish Population-Based Study

(2011) Peter A. Noseworthy et al.   Circulation-Cardiovascular Genetics

Population-prevalent desmosomal mutations predisposing to arrhythmogenic right ventricular cardiomyopathy

(2011) Annukka M. Lahtinen et al.   HEART RHYTHM

Pathophysiology of arrhythmogenic cardiomyopathy

(2011) Cristina Basso et al.   Nature Reviews Cardiology

Allelic variant ofNOS1APeffects on cardiac alternans of repolarization during exercise testing

(2011) Jenni Koskela et al.   SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION

Recurrent and founder mutations in the Netherlands

(2011) P.A. van der Zwaag et al.   Netherlands Heart Journal

Sudden Cardiac Death Prediction and Prevention

(2010) Glenn I. Fishman et al.   CIRCULATION

Sudden cardiac death: epidemiology and risk factors

(2010) A. Selcuk Adabag et al.   Nature Reviews Cardiology

Etiology of sudden death in the community: Results of anatomical, metabolic, and genetic evaluation

(2009) A. Selcuk Adabag et al.   AMERICAN HEART JOURNAL

High prevalence of four long QT syndrome founder mutations in the Finnish population

(2009) Annukka Marjamaa et al.   ANNALS OF MEDICINE

Apolipoprotein E-dependent accumulation of Alzheimer disease-related lesions begins in middle age

(2009) Eloise Kok et al.   ANNALS OF NEUROLOGY

Arrhythmogenic Right Ventricular Cardiomyopathy Plakophilin-2 Mutations Disrupt Desmosome Assembly and Stability

(2009) Chad Hall et al.   CELL COMMUNICATION AND ADHESION

Prevalence of the Congenital Long-QT Syndrome

(2009) Peter J. Schwartz et al.   CIRCULATION

Clinical features, survival experience, and profile of plakophylin-2 gene mutations in participants of the Arrhythmogenic Right Ventricular Cardiomyopathy Registry of South Africa

(2009) David A. Watkins et al.   HEART RHYTHM

Ryanodine receptor (RyR2) mutations in sudden cardiac death: Studies in extended pedigrees and phenotypic characterization in vitro

(2009) Annukka Marjamaa et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Thirty-five-year trends in cardiovascular risk factors in Finland

(2009) E. Vartiainen et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Common candidate gene variants are associated with QT interval duration in the general population

(2009) A. Marjamaa et al.   JOURNAL OF INTERNAL MEDICINE

Post-Exercise Assessment of Cardiac Repolarization Alternans in Patients With Coronary Artery Disease Using the Modified Moving Average Method

(2009) Michael P. Slawnych et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Birthplace predicts risk for prehospital sudden cardiac death in middle-aged men who migrated to metropolitan area: The Helsinki Sudden Death Study

(2008) Petri Tyynelä et al.   ANNALS OF MEDICINE

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families

(2008) Elijah R. Behr et al.   EUROPEAN HEART JOURNAL

Gender and effects of a common genetic variant in the NOS1 regulator NOS1AP on cardiac repolarization in 3761 individuals from two independent populations

(2008) Martin D Tobin et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Long-QT Syndrome

(2008) Dan M. Roden   NEW ENGLAND JOURNAL OF MEDICINE

Epidemiology of Sudden Cardiac Death: Clinical and Research Implications

(2008) Sumeet S. Chugh et al.   PROGRESS IN CARDIOVASCULAR DISEASES

Effect of common KCNE1 and SCN5A ion channel gene variants on T-wave alternans, a marker of cardiac repolarization, during clinical exercise stress test: the Finnish Cardiovascular Study

(2008) Jenni Koskela et al.   Translational Research

Cardiac Sodium Channel Gene Variants and Sudden Cardiac Death in Women

(2007) Christine M. Albert et al.   CIRCULATION

Plakophilin-2 missense mutations in arrhythmogenic right ventricular cardiomyopathy

(2007) Annukka M. Lahtinen et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY