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Publications by Michael J. Ackerman

A Novel Mutation in TNNC1-ENCODED Cardiac Troponin C Predisposes to Hypertrophic Cardiomyopathy and Recurrent Episodes of Aborted Sudden Cardiac Death

Biophysical Journal

Biophysics

2011

English

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

PLoS ONE

Multidisciplinary

2015

English

Noninvasive Potassium Determination Using a Mathematically Processed ECG: Proof of Concept for a Novel “Blood-Less, Blood Test”

Journal of Electrocardiology

Cardiovascular Medicine

Cardiology

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

Green Tea Catechin Normalizes the Enhanced Ca2+Sensitivity of Myofilaments Regulated by a Hypertrophic Cardiomyopathy–Associated Mutation in Human Cardiac Troponin I (K206I)CLINICAL 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

Prevalence, Clinical Significance, and Natural History of Left Ventricular Apical Aneurysms in Hypertrophic Cardiomyopathy

Circulation

Cardiovascular Medicine

Physiology

Cardiology

2008

English

Risk of Aborted Cardiac Arrest or Sudden Cardiac Death During Adolescence in the Long-Qt Syndrome

JAMA - Journal of the American Medical Association

Medicine

2006

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

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Michael J. Ackerman

A Novel Mutation in TNNC1-ENCODED Cardiac Troponin C Predisposes to Hypertrophic Cardiomyopathy and Recurrent Episodes of Aborted Sudden Cardiac Death

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

Noninvasive Potassium Determination Using a Mathematically Processed ECG: Proof of Concept for a Novel “Blood-Less, Blood Test”

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

Green Tea Catechin Normalizes the Enhanced Ca2+Sensitivity of Myofilaments Regulated by a Hypertrophic Cardiomyopathy–Associated Mutation in Human Cardiac Troponin I (K206I)CLINICAL 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

Prevalence, Clinical Significance, and Natural History of Left Ventricular Apical Aneurysms in Hypertrophic Cardiomyopathy

Risk of Aborted Cardiac Arrest or Sudden Cardiac Death During Adolescence in the Long-Qt Syndrome

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