Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing

David J. Tester, Melissa L. Will, Carla M. Haglund, +1

Heart Rhythm

ChannelopathiesGenetic DisorderGeneticsCardiac Channel MutationsCongenital Heart Defect +5

Myosin binding protein C mutations and compound heterozygosity in hypertrophic cardiomyopathy

Sara L. Van Driest, Vlad C. Vasile, Steve R. Ommen, +4

Journal of the American College of Cardiology

Cardiac MuscleCardiomyopathyHeart FailureMolecular PhysiologyGenetics +9

Most LQT2 Mutations Reduce Kv11.1 (hERG) Current by a Class 2 (Trafficking-Deficient) Mechanism

Corey L. Anderson, Brian P. Delisle, Blake D. Anson, +7

Circulation

Clinical Features and Outcome of Hypertrophic Cardiomyopathy Associated With Triple Sarcomere Protein Gene Mutations

Francesca Girolami, Carolyn Y. Ho, Christopher Semsarian, +8

Journal of the American College of Cardiology

Cardiac MuscleCardiomyopathyGeneticsPathologyClinical Features +5

Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome

Michael J. Ackerman, David J. Tester, Gregg S. Jones, +3

Mayo Clinic Proceedings

CardiomyopathyGenetic TestingCardiovascular DiseaseGeneticsPhysiology +10

Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: Implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing

Michael J. Ackerman, Igor Splawski, Jonathan C. Makielski, +11

Heart Rhythm

CardiomyopathyGenetic TestingEpidemiologyCardiovascular DiseaseGenetics +8

Spectrum and Frequency of Cardiac Channel Defects in Swimming-Triggered Arrhythmia Syndromes

Grace R. Choi, Laura J. Kopplin, David J. Tester, +3

Circulation

Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing

David J. Tester, Argelia Medeiros‐Domingo, Melissa L. Will, +2

Mayo Clinic Proceedings

ChannelopathiesCardiomyopathyCardiovascular DiseaseForensic MedicinePathology +7

Prevalence and age-dependence of malignant mutations in the beta-myosin heavy chain and troponin t genes in hypertrophic cardiomyopathy

Michael J. Ackerman, Sara L VanDriest, Steve R. Ommen, +4

Journal of the American College of Cardiology

Cardiac MuscleCardiomyopathyGeneticsGenetic EpidemiologyTroponin T Genes +6

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Lia Crotti, Cherisse A. Marcou, David J. Tester, +9

Journal of the American College of Cardiology

Genetic DisorderMedicineGeneticsGenetic EpidemiologyPathology +8