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Publications by David J. Tester

Gain-Of-Function Mutation S422L in the KCNJ8-encoded Cardiac KATP Channel Kir6.1 as a Pathogenic Substrate for J-Wave Syndromes

Heart Rhythm

Cardiovascular Medicine

Physiology

Cardiology

2010

English

Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance

Circulation. Genomic and precision medicine

Genetics

Cardiovascular Medicine

Cardiology

2019

English

A Novel Truncating Variant in FLNC-Encoded Filamin C May Serve as a Proarrhythmic Genetic Substrate for Arrhythmogenic Bileaflet Mitral Valve Prolapse Syndrome

Mayo Clinic Proceedings

Medicine

2019

English

Long QT Syndrome-Associated F97C and S141R CaV-3 Mutations Exert Pleiotropic Effects on Cardiac L-Type Calcium Channels

Biophysical Journal

Biophysics

2012

English

Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends Upon Splice Variant Background and Intracellular Acidosis

PLoS ONE

Multidisciplinary

2015

English

Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-Qt Syndrome

Circulation: Cardiovascular Genetics

2012

English

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

2015

English

Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome

Circulation: Cardiovascular Genetics

2013

English

Physiological Properties of hERG 1a/1b Heteromeric Currents and a hERG 1b-Specific Mutation Associated With Long-Qt Syndrome

Circulation Research

Cardiovascular Medicine

Physiology

Cardiology

2008

English

KCNJ2 Mutations in Arrhythmia Patients Referred for LQT Testing: A Mutation T305A With Novel Effect on Rectification Properties

Heart Rhythm

Cardiovascular Medicine

Physiology

Cardiology

2007

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by David J. Tester

Gain-Of-Function Mutation S422L in the KCNJ8-encoded Cardiac KATP Channel Kir6.1 as a Pathogenic Substrate for J-Wave Syndromes

Assessment and Validation of a Phenotype-Enhanced Variant Classification Framework to Promote or Demote RYR2 Missense Variants of Uncertain Significance

A Novel Truncating Variant in FLNC-Encoded Filamin C May Serve as a Proarrhythmic Genetic Substrate for Arrhythmogenic Bileaflet Mitral Valve Prolapse Syndrome

Long QT Syndrome-Associated F97C and S141R CaV-3 Mutations Exert Pleiotropic Effects on Cardiac L-Type Calcium Channels

Arrhythmogenic Biophysical Phenotype for SCN5A Mutation S1787N Depends Upon Splice Variant Background and Intracellular Acidosis

Phylogenetic and Physicochemical Analyses Enhance the Classification of Rare Nonsynonymous Single Nucleotide Variants in Type 1 and 2 Long-Qt Syndrome

Enhanced Classification of Brugada Syndrome–Associated and Long-Qt Syndrome–Associated Genetic Variants in theSCN5A-Encoded Nav1.5 Cardiac Sodium ChannelCLINICAL PERSPECTIVE

Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome

Physiological Properties of hERG 1a/1b Heteromeric Currents and a hERG 1b-Specific Mutation Associated With Long-Qt Syndrome

KCNJ2 Mutations in Arrhythmia Patients Referred for LQT Testing: A Mutation T305A With Novel Effect on Rectification Properties