Jamie D. Kapplinger

An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Jamie D. Kapplinger, David J. Tester, Mariëlle Alders et al. · Heart Rhythm · 2009 · 753 citations · Full text

Channelopathies, Cardiomyopathy, Genetic Disorder +7

Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION® long QT syndrome genetic test

Jamie D. Kapplinger, David J. Tester, Benjamin A. Salisbury et al. · Heart Rhythm · 2009 · 465 citations · Full text

Genetic Testing, Mendelian Disorder, Genetic Disorder +11

Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise

Jamie D. Kapplinger, Andrew P. Landstrom, Benjamin A. Salisbury et al. · Journal of the American College of Cardiology · 2011 · 301 citations · Full text

Cardiomyopathy, Heart Failure, Genetic Disorder +6

Genotype-Phenotype Correlation of <i>SCN5A</i> Mutation for the Clinical and Electrocardiographic Characteristics of Probands With Brugada Syndrome

Kenichiro Yamagata, Minoru Horie, Takeshi Aiba et al. · Circulation · 2017 · 174 citations · Full text

Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records

Sara L. Van Driest, Quinn S. Wells, Sarah Stallings et al. · JAMA · 2016 · 171 citations · Full text