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Publications by Jamie D. Kapplinger
Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-Qt Syndrome
Circulation: Cardiovascular Genetics
Enhanced Classification of Brugada Syndrome–Associated and Long-Qt Syndrome–Associated Genetic Variants in theSCN5A-Encoded Nav1.5 Cardiac Sodium ChannelCLINICAL PERSPECTIVE
Circulation: Cardiovascular Genetics
Related publications
Clinical and Molecular Genetic Risk Determinants in Adult Long QT Syndrome Type 1 and 2 Patients
BMC Medical Genetics
Genetics
Figure 2: Phylogenetic Relationship and Identification of Single-Nucleotide Variations for 105 CSVd Variants.
Long Qt Syndrome. Part 1
Journal of the Grodno State Medical University
Small Effective Population Sizes and Rare Nonsynonymous Variants in Potyviruses
Virology
Virology
R231C Mutation in KCNQ1 Causes Long QT Syndrome Type 1 and Familial Atrial Fibrillation
Heart Rhythm
Cardiovascular Medicine
Physiology
Cardiology
Statin Therapy in Long QT Syndrome Type II
Biophysical Journal
Biophysics
Rare Single‐nucleotide Variants in Oculo‐auriculo‐vertebral Spectrum (OAVS)
Molecular genetics & genomic medicine
Genetics
Molecular Biology
Association of a Congenital Long QT Syndrome Type 1 With Takotsubo Cardiomyopathy
Clinical Case Reports
Medicine
