Influence of genetic modifiers on sudden cardiac death cases

Relevance of molecular testing in patients with a family history of sudden death

(2017) Silke Kauferstein et al.   FORENSIC SCIENCE INTERNATIONAL

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

(2017) T. Jenewein et al.   FORENSIC SCIENCE INTERNATIONAL

Electrophysiological characterization of a large set of novel variants in the SCN5A-gene: identification of novel LQTS3 and BrS mutations

(2016) Beatriz Ortiz-Bonnin et al.   PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY

Genetic and Clinical Advances in Congenital Long QT Syndrome

(2014) Yuka Mizusawa et al.   CIRCULATION JOURNAL

Genetic analysis of sudden unexplained death: A multidisciplinary approach

(2013) Silke Kauferstein et al.   FORENSIC SCIENCE INTERNATIONAL

Long QT syndrome: beyond the causal mutation

(2013) Ahmad S. Amin et al.   JOURNAL OF PHYSIOLOGY-LONDON

Cardiac channelopathy causing sudden death as revealed by molecular autopsy

(2012) Silke Kauferstein et al.   INTERNATIONAL JOURNAL OF LEGAL MEDICINE

Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes

(2012) John R. Giudicessi et al.   Translational Research

Derivation and Validation of a Simple Exercise-Based Algorithm for Prediction of Genetic Testing in Relatives of LQTS Probands

(2011) Raymond W. Sy et al.   CIRCULATION

Variants in the 3′ untranslated region of the KCNQ1-encoded Kv7.1 potassium channel modify disease severity in patients with type 1 long QT syndrome in an allele-specific manner

(2011) Ahmad S. Amin et al.   EUROPEAN HEART JOURNAL

Epidemiologic, molecular, and functional evidence suggest A572D-SCN5A should not be considered an independent LQT3-susceptibility mutation

(2010) David J. Tester et al.   HEART RHYTHM

A common SCN5A polymorphism modulates the biophysical defects of SCN5A mutations

(2010) Krekwit Shinlapawittayatorn et al.   HEART RHYTHM

Prevalence of the Congenital Long-QT Syndrome

(2009) Peter J. Schwartz et al.   CIRCULATION

Protective effect of KCNH2 single nucleotide polymorphism K897T in LQTS families and identification of novel KCNQ1 and KCNH2mutations

(2008) Xianqin Zhang et al.   BMC Medical Genetics

Age- and Genotype-Specific Triggers for Life-Threatening Arrhythmia in the Genotyped Long QT Syndrome

(2008) TOMOKO SAKAGUCHI et al.   JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY

Potassium channel KCNH2 K897T polymorphism and cardiac repolarization during exercise test: The Finnish Cardiovascular Study

(2008) J. Koskela et al.   SCANDINAVIAN JOURNAL OF CLINICAL & LABORATORY INVESTIGATION