Michael J.AckermanMDPhD

Pediatric Cardiac Genetics, Pediatric Electrophysiology

Genetic Cardiologist at the Mayo Clinic Windland Smith Rice Cardiovascular Genomics Research Professor Professor of Medicine, Pediatrics, and Pharmacology Director, Windland Smith Rice Genetic Heart Rhythm Clinic President of the Sudden Arrhythmia Death Syndromes (SADS) Foundation

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Office
200 1st St SW
Rochester, MN 55905
Phone+1 507-284-2511

Summary

Dr. Michael J. Ackerman is a genetic cardiologist in Rochester, MN. He received his medical degree from the Mayo Clinic Alix School of Medicine and his PhD from the Mayo Clinic Graduate School of Biomedical Sciences in 1995. After residency training in Pediatrics and fellowship training in pediatric cardiology at Mayo Clinic, he joined Mayo Clinic's faculty in 2000. He specializes in genetic cardiology and takes care of patients and families at risk of premature sudden cardiac death from a variety of genetic heart diseases like long QT syndrome and hypertrophic cardiomyopathy in the Windland Smith Rice Genetic Heart Rhythm Clinic. His research team is devoted to "healing the sick and advancing the science" as it relates to these genetic channelopathies and cardiomyopathies.

The Mayo Clinic Windland Smith Rice Genetic Heart Rhythm Clinic

Welcome to the Mayo Clinic Windland Smith Rice Genetic Heart Rhythm Clinic and Sudden Death Genomics Laboratory directed by Michael J. Ackerman, MD, PhD

Education & Training

Mayo Clinic College of Medicine and Science (Rochester)Fellowship, Pediatric Cardiology, 1998 - 2000
Mayo Clinic College of Medicine and Science (Rochester)Residency, Pediatrics, 1995 - 1998
Mayo Clinic College of MedicineClass of 1995, MD, PhD
Luther CollegeB.A., Chemistry and Mathematics, Summa Cum Laude, 1984 - 1988

Certifications & Licensure

AZ State Medical License 2022 - 2026
FL State Medical License 2020 - 2025
MN State Medical License 1996 - 2025
American Board of Pediatrics Pediatric Cardiology

Awards, Honors, & Recognition

Distinguished Scientist Award Heart Rhythm Society, 2018
America's Top Doctors Castle Connolly, 2005-2016
Distinguished Clinician Award Mayo Clinic, 2015
Dean's Recognition Award Mayo Clinic School of Medicine, 2013
Department of Medicine Outstanding Investigator Award Mayo Clinic, 2011
Center for Individualized Medicine Award 2012
Elected Member The American Society for Clinical Investigation, 2010
Inductee American Society of Clinical Investigation, 2010
Teacher of the Year Mayo Medical School 1st Year Class, 2009
Distinguished Service Award Luther College, 2008
25th Young Investigator Award Society for Pediatric Research, 2007
Medical School Continuing Medical Education Faculty of the Year 2004
Young Investigator Award (Section on Perinatal Pediatrics) American Academy of Pediatrics, 2002
15th Annual Niland Lecturer University of Michigan, 2002
Travel Award Society for Pediatric Research, 2002
Young Investigator Award Finalist American College of Cardiology, 2001
Best Pediatric Poster Award Mayo Clinic Research Forum, 2001
Young Investigator Award Finalist North American Society of Pacing and Electrophysiology, 2001
Clinical Fellow Research Award Society for Pediatric Research, 2000
Donald C. Balfour Research Award Mayo Alumni Association, 2000
Pediatric Resident Research Award American Academy of Pediatrics, 1999
Outstanding Presentation Award Midwest Pediatric Cardiology Society, 1999
Best Poster Award 25th Mayo Clinic Pediatric Days, 1998
Distinguished Fellowship Award Mayo Brothers, 1997
Best Poster Award 24th Mayo Clinic Pediatric Days, 1997
Molecular Medicine Award Harold W. Siebens, 1997
Medical Student Award American Federation for Clinical Research, 1995
Karis Award Mayo Foundation, 1994
International TaeKwonDo Club of the Year 1990, 1992, 2000
Phi Beta Kappa 1988
Torrison Research Scholarship 1988
Regional TaeKwonDo Instructor of the Year 1987
Fellow (FACC) American College of Cardiology
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Publications & Presentations

PubMed

Artificial intelligence electrocardiography for the evaluation of cardiac involvement in Fabry disease.
Muhannad A Abbasi, Elias Akiki, Edward A El-Am, Jeffrey B Geske, J Martijn Bos
Current Problems in Cardiology. 2025-01-01
Novel risk predictor of arrhythmias for patients with potassium channel related congenital Long-QT Syndrome.
Christian Krijger Juarez, Virginnio M Proost, Michael W Tanck, Sven Dittmann, J Martijn Bos
Heart Rhythm. 2024-12-13
Unexplained sudden cardiac arrest and sudden cardiac death in the young: What is killing these young people when nothing is found?
Andrew S Tseng, Mayank Sardana, John R Giudicessi, Michael J Ackerman
Trends in Cardiovascular Medicine. 2024-11-20

Journal Articles

Electromechanical Window Negativity in Genotyped Long-QT Syndrome Patients: Relation to Arrhythmia Risk
Ter Bekke RM, Haugaa KH, van den Wijngaard A, Bos JM, Ackerman MJ, Edvardsen T, Volders PG, Eur Heart Journal, 9/8/2014
Reduced Junctional Na/Ca2+-exchanger Activity Contributes to Sarcoplasmic Reticulum Ca2+ Leak in Junctophilin-2 Deficient Mice
Wang W, Landstrom AP, Wang Q, Munro ML, Beavers D, Ackerman MJ, Soeller C, Wehrens XH, Am J Physiol Heart Circ Physiol, 9/5/2014
Compound Heterozygous Mutations in the SCN5A-Encoded Nav15 Cardiac Sodium Channel Resulting in Atrial Standstill and His-Purkinje System Disease
Baskar S, Ackerman MJ, Clements D, Mayuga KA, Aziz PF, J Pediatr, 8/27/2014
Epilepsy Misdiagnosed as Long QT Syndrome: It Can Go Both Ways
Medford BA, Bos JM, Ackerman MJ, Congenit Heart Dis, 1/1/2014
A KCNQ1 Mutation Contributes to the Concealed Type 1 Long QT Phenotype by Limiting the Kv71 Channel Conformational Changes Associated with Protein Kinase a Phosphoryla...
Bartos DC, Giudicessi JR, Tester DJ, Ackerman MJ, Ohno S, Horie M, Gollob MH, Burgess DE, Delisle BP, Heart Rhythm, 1/1/2014
Confirmation of Cause and Manner of Death via a Comprehensive Cardiac Autopsy Including Whole Exome Next-Generation Sequencing
Loporcaro CG, Tester DJ, Maleszewski JJ, Kruisselbrink T, Ackerman MJ, Arch Pathol Lab Med, 1/1/2014
Sympathetic Nerve Activity and Simulated Diving in Healthy Humans
Shamsuzzaman A, Ackerman MJ, Kuniyoshi FS, Accurso V, Davison D, Amin RS, Somers VK, Autonomic Neuroscience, 1/1/2014
Surgical Myectomy Improves Pulmonary Hypertension in Obstructive Hypertrophic Cardiomyopathy
Geske JB, Konecny T, Ommen SR, Nishimura RA, Sorajja P, Schaff HV, Ackerman MJ, Gersh BJ, Eur Heart Journal, 1/1/2014
Is Sudden Unexplained Nocturnal Death Syndrome in Southern China a Cardiac Sodium Channel Dysfunction Disorder?
Liu C, Tester DJ, Hou Y, Wang W, Lv G, Ackerman MJ, Makielski JC, Cheng J, Forensic Sci Int, 1/1/2014
Pathogeneses of Sudden Cardiac Death in National Collegiate Athletic Association Athletes
Harmon KG, Drezner JA, Maleszewski JJ, Lopez-Anderson M, Owens D, Prutkin JM, Asif IM, Klossner D, Ackerman MJ, Circ Arrhythm Electrophysiol, 1/1/2014
Association of Common Variants in NOS1AP Gene with Sudden Unexplained Nocturnal Death Syndrome in the Southern Chinese Han Population
Huang L, Yu Y, Chen Y, Tester DJ, Tang S, Ackerman MJ, Yuan Z, Cheng J, Int J Legal Med, 1/1/2014
Characterization of a Phenotype-Based Genetic Test Prediction Score for Unrelated Patients with Hypertrophic Cardiomyopathy
Bos JM, Will ML, Gersh BJ, Kruisselbrink TM, Ommen SR, Ackerman MJ, Mayo Clin Proc, 1/1/2014
Response to Letters regarding Article, "Stroke or Transient Ischemic Attack in Patients with Transvenous Pacemaker or Defibrillator and Echocardiographically Detected ...
DeSimone CV, Friedman PA, Noheria A, Ackerman MJ, Asirvatham SJ, DeSimone DC, Aakre CA, Vaidya VR, Noheria A, Patel NA, Bdeir S, Slusser JP, Hodge DO, Rabinstein AA, Circulation, 1/1/2014
Characterization of SEMA3A-encoded Semaphorin as a Naturally Occurring Kv43 Protein Inhibitor and Its Contribution to Brugada Syndrome
Boczek NJ, Ye D, Johnson EK, Wang W, Crotti L, Tester DJ, Dagradi F, Mizusawa Y, Torchio M, Alders M, Giudicessi JR, Wilde AA, Schwartz PJ, Nerbonne JM, Ackerman MJ, Circ Res, 1/1/2014
Congenital Long QT Syndrome and Concomitant Early Repolarization Pattern: A Benign Association or an ICD-worthy One?
DeSimone CV, Ackerman MJ, Heart Rhythm, 1/1/2014
Beta-Blockers in the Treatment of Congenital Long QT Syndrome: Is One Beta-Blocker Superior to Another?
Wilde AA, Ackerman MJ, J Am Coll Cardiol, 1/1/2014
Unctophilin-2 Is Necessary for T-tubule Maturation during Mouse Heart Development
Reynolds JO, Chiang DY, Wang W, Beavers DL, Dixit SS, Skapura DG, Landstrom AP, Song LS, Ackerman MJ, Wehrens XH, Cardiovasc Res, 7/1/2013
Left Cardiac Sympathetic Denervation in Long QT Syndrome: Analysis of Therapeutic Non-Responders
Bos JM, Bos KM, Johnson JN, Moir C, Ackerman MJ, Circ Arrhythm Electrophysiol, 5/31/2013
Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome
Boczek NJ, Best JM, Tester DJ, Giudicessi JR, Middha S, Evans JM, Kamp TJ, Ackerman MJ, Circ Cardiovasc Genet, 5/15/2013
Sudden Cardiac Arrest in a Young Patient with Hypertrophic Cardiomyopathy and Zero Canonical Risk Factors: The Inherent Limitations of Risk Stratification in Hypertrop...
Kohorst JJ, Bos JM, Hagler DJ, Ackerman MJ, Congenit Heart Dis, 5/7/2013
The Long QT Syndrome: A Transatlantic Clinical Approach to Diagnosis and Therapy
Schwartz PJ, Ackerman MJ, Eur Heart J, 3/18/2013
A KCNQ1 Mutation Causes a High Penetrance for Familial Atrial Fibrillation
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP, JCE, 1/1/2013
Institution-Wide QT Alert System Identifies Patients With a High Risk of Mortality
Haugaa KH, Bos JM, Tarrell RF, Morlan BW, Caraballo PJ, Ackerman MJ, Mayo Clin Proc, 1/1/2013
Prevention of Sudden Cardiac Death with Implantable Cardioverter-defibrillators in Children and Adolescents with Hypertrophic Cardiomyopathy
Maron BJ, Spirito P, Ackerman MJ, Casey SA, Semsarian C, Estes NA 3rd, Shannon KM, Ashley EA, Day SM, Pacileo G, Formisano F, Devoto E, Anastasakis A, Bos JM, Woo A, A..., J Am Coll Cardiol, 1/1/2013
Personalized Medicine: Genetic Diagnosis for Inherited Cardiomyopathies/Channelopathies
Ackerman MJ, Marcou CA, Tester DJ, Rev Esp Cardiol, 1/1/2013
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Books/Book Chapters

Forensic Pathology of Infancy and Childhood
Chapter: Chaper 31 Cardiac Channelopathies and the Molecular Autopsy
Page 899 - 942Tester DJ, Ackerman MJSpringer Publishing, New York, NY2014
Management of Cardiac Arrhythmias
Chapter: Chapter 19, Long QT Syndrome
Page 419 - 440Johnson JN, Ackerman MJSpringer Publishing, New York, NYEdition 2nd,2010
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Chapter: Chapter 62. Sudden Cardiac Death in Infancy: Focus on Prolonged Repolarization
Page 924 - 933Schwartz PJ, Stramba-Badiale M, Crotti L, Ackerman MJSpringer Publishing, New York, NY2008
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Chapter: Chapter 40. Arrhythmogenic Malignancies in Hypertrophic Cardiomyopathy
Page 610 - 626Menon SC, Bos, JM, Ommen SR, Ackerman MJSpringer Publishing, New York, NY2008
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Chapter: Chapter 31. Congenital Long QT Syndrome
Page 462 - 482Ackerman MJ, Khositseth A, Tester DJ, Schwartz PJSpringer Publishing, New York, NY2008
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Chapter: Chapter 30: Genetic Testing
Page 444 - 458Tester DJ and Ackerman MJSpringer Publishing, New York, NY2008
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Chapter: Chapter 28: Provocative testing in Inherited Arrhythmias
Page 424 - 433Shimizu W and Ackerman MJSpringer Publishing, New York, NY2008
Electrical Diseases of the Heart; Genetics, Mechanisms, Treatment, Prevention
Gussak I, Antzelevitch C, Ackerman MJ, Friedman PA, Shen WKSpringer Publishing, New York, NY2008
Mayo Clinic Cardiology: Concise Textbook
Chapter: Cardiac Channelopathies
Page 335 - 344Bunch TJ and Ackerman MJMayo Clinic Scientific Press: Informa Healthcare, Rochester, MNEdition 3rd,2007
Mayo Clinic Cardiology: Concise Textbook
Chapter: Heritable Cardiomyopathyies
Page 425 - 442Menon SC, Ommen SR, Ackerman MJMayo Clinic Scientific Press: Informa Healthcare, Rochester, MNEdition 3rd,2007
Molecular Pathology in Clinical Practice
Chapter: Chapter 14: Cardiovascular Disease
Page 161 - 177Khositseth A and Ackerman MJSpringer Publishing, New York, NY2007
Cardiovascular Disease: Methods and Protocols
Chapter: Chapter 13: Mutation Detection in Congenital Long QT Syndrome
Page 181 - 207Tester DJ, Will ML, Ackerman MJEditors: Wang QK.Humana Press Inc., Totowa, New Jersey2006
Cardiac Electrophysiology: From Cell to Bedside
Chapter: Chapter 4. Intracellular Signaling and Regulation of Cardiac Ion Channels
Page 33 - 41Khositseth A, Clapham DE, and Ackerman MJEditors: Zipes DP, Jalife J.W.B. Saunders, Philadelphia2004
Molecular Basis of Cardiovascular Disease: A Companion to Braunwald's Heart Disease
Chapter: Excitability and Conduction
Page 311 - 335Ackerman MJ and Clapham DEEditors: Kenneth R. Chien.W.B. Saunders, PhiladelphiaEdition Seco,2004
Cardiac Repolarization: Bridging Basic and Clinical Science
Chapter: Clinical Evaluation, Risk Stratification, and Management of Congenital Long QT Syndrome
Page 447 - 480Khositseth A and Ackerman MJEditors: Gussak I and Antzelevitch C.Humana Press, Totowa NJ2003
Cardiac Electrophysiology: From Cell to Bedside
Chapter: G Proteins and Ion Channels
Page 112 - 118Ackerman MJ and Clapham DEEditors: Zipes DP, Jalife J.W.B. Saunders, Philadelphia2000
Molecular Basis of Cardiovascular Disease: A Companion to Braunwald's Heart Disease
Chapter: Normal Cardiac Electrophysiology. Understanding the Action Potential in the Human Heart
Page 281 - 301Ackerman MJ and Clapham DEEditors: Chien KR and Braunwald E.W.B. Saunders, Philadelphia1999
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Abstracts/Posters

Automatic External Defibrillator Rescues Among Children with Diagnosed and Treated Long QT Syndrome
Pundi KN, Bos JM, Cannon BC, Ackerman MJ, Heart Rhythm, 1/1/2014
Minimally Invasive Epicardial ICD Placement: An Effective Alternative to the Transvenous Approach
Schneider A, Burkhard H, Ackerman MJ, Dearani JA, Cannon BC, Heart Rhythm, 1/1/2014
Personal Wearable Defibrillators for Adults with Long QT Syndrome
Owen HJ, Bos JM, Ackerman MJ, Heart Rhythm, 1/1/2014
Short and Long-Term ECG Changes After Left Cardiac Sympathetic Denervation in Patients with Long QT Syndrome
DeSimone CV, Bos JM, Patel N, Liang J, Hodge D, Noheria A, Asirvatham SJ, Ackerman MJ, Heart Rhythm, 1/1/2014
Functional Characterization of a Novel Long QT Syndrome-Susceptibility Mutation, E141G, in CALM1-Encoded Calmodulin
Boczek NJ, Ye D, Will M, Tester D, Shah MJ, Ackerman MJ, Heart Rhythm, 1/1/2014
LMNA-Mediated Arrhythmogenic Right Ventricular Cardiomyopathy and Charcot-Marie Tooth Type 2B1: A Patient Discovered Unifying Diagnosis
Liang JJ, Goodsell K, Grogan M, Ackerman MJ, Heart Rhythm, 1/1/2014
Left Cardiac Sympathetic Denervation for CPVT
Dusi, Veronica, De Ferrari GM, Bos JM, Moir C, Shkolnikova MA, Abrams DJ, Crotti L, Wilde AAM, Ackerman MJ, Schwartz PJ, Heart Rhythm, 1/1/2014
Sudden Cardiac Arrest During Sex in Patients with either CPVT or LQTS: A Rare but Shocking Experience
Loar R, Bos JM, Cannon BC, Ackerman MJ, Heart Rhythm, 1/1/2014
Sudden Arrhythmic Death Syndrome and the Impact on Insurability: A North American Survey
Mohammed S, Lim Z, Potts JE, Etheridge SP, Lara A, Husband PR, Sherwin ED, Ackerman MJ, Sanatani S, Heart Rhythm, 1/1/2014
In-Silico Tools Including the Probability of Pathogenicity Calculator and the Identification of SCN5A Variants with Aberrant Functional Properties
Kapplinger JD, Ye D, Giudicessi JR, Tester DJ, Valdivia CR, Makielski JC, Wilde AAM, Ackerman MJ, Heart Rhythm, 1/1/2014
Whole Exome Sequencing Coverage Analysis of Genes Associated with Life-threatening Metabolic Disorders, Cardiac Channelopathies, and Cardiomyopathies
Middha S, Tester DJ, Kapplinger JD, Boczek NJ, Ackerman MJ., Heart Rhythm, 1/1/2014
Outcome of Left Cardiac Sympathetic Denervation (LCSD) as Monotherapy in Patients with Long QT Syndrome
Bos JM, Owen H, Moir C, Ackerman MJ, Heart Rhythm, 1/1/2014
Breath Holding Spells in Children with Long QT Syndrome
Robinson JA, Bos JM, Etheridge SP, Ackerman MJ, Heart Rhythm, 1/1/2014
Characterization of SEMA3A-Encoded Semaphorin as a Naturally Occurring KV4.3 Protein Inhibitor and its Contribution to Brugada Syndrome
Boczek NJ, Ye D, Wang D, Crotti L, Tester D, Nerbonne JM, Schwartz PJ, Ackerman MJ, Heart Rhythm, 1/1/2014
Spectrum and Prevalence of Mutations Involving BRS1-12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing
Kellen CA, Crotti L, Tester DJ, Castelletti S, Giudicessi JR, Torchio M, Medeiros-Domingo A, Will ML, Dagradi F, Schwartz PJ, Ackerman MJ, Heart Rhythm, 1/1/2012
Comparison of Rare Genetic Variation in Cases and Controls in Minor Long QT Syndrome (LQTS)-Susceptibility Genes Reveals a Low Signal-to-Noise Ratio
Callis TE, Pollevik GD, Tester DJ, Ackerman MJ, Salisbury BA, Heart Rhythm, 1/1/2012
Videoscopic Left Cardiac Sympathetic Denervation for Patients with Recurrent Ventricular Fibrillation of Malignant Ventricular Arrhythmia Syndromes Besides Autosomal D...
Coleman M, Johnson JN, Bos JM, Owen HJ, Deschamps C, Moir C, Ackerman MJ, Heart Rhythm, 1/1/2012
Competitive Sports Participation in Athletes with Congenital Long QT Syndrome and an Implantable Cardioverter Defibrillator
Johnson JN, Cannon BC, Ackerman MJ, Heart Rhythm, 1/1/2012
Electrophysiological Mechanisms by Which Quinidine Reduces the Genetic Enhancement of the Transient Outward KV4.3 Current in KCND3-Mediated Brugada Syndrome
Ye D, Giudicessi JR, Tester DJ, Ackerman MJ, Heart Rhythm, 1/1/2012
Assessment of Variants Identified in ARVC-Associated Genes in Samples From the 1000 Genome Project and the Exome Chip Design Project
Kapplinger JD, Salisbury BA, Tester DJ, Callis TE, Pollevik GD, van Tintelen P, Calkins, H, Judge DP, Wilde AAM, Ackerman MJ, Heart Rhythm, 1/1/2012
RYR2-Mediated Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) in Patients with Hypertrophic Cardiomyopathy
Kellen CA, Bos JM, Will ML, Medeiros-Domingo A, Gersh BJ, Ommen SR, Ackerman MJ, Heart Rhythm, 1/1/2012
Conservation Analysis of the C-Terminal Region of KCNQ1-Encoded KV7.1 Potassium Channel Identifies Regions of High and Low Probability of Pathogenicity for Type 1 Long...
Salisbury B, Callis TE, Susswein L, Pollevik GD, Kapplinger JD, Tester DJ, Alders M, Wilde AAM, Ackerman MJ, Heart Rhythm, 1/1/2012
Identification of Putative Sudden Death Predisposing Mutations in Antepartum Intrauterine Detal Demise: A Cardiac Channel Molecular Autopsy of 98 Stillbirths
Tester DJ, Crotti L, White WM, Bartos DC, Will ML, Velasco EJ, Bair JJ, Insolia R, Ghidoni A, Facchinetti F, Cetin I, Pfeufer A, Van Dyke DL, Wick MJ, Brost BC, Delisl..., Heart Rhythm, 1/1/2012
Maternal Mosaicism Confounds the Neonatal Diagnosis of Type 1 Timothy Syndrome
Dufendach KA, Giudicessi JR, Boczek NJ, Tester DJ, Ackerman MJ, Heart Rhythm, 1/1/2012
The KCNQ1 Variant R231H Confers a High Risk for Early Onset Atrial Fibrillation
Bartos DC, Anderson JB, Burgess DE, Johnson JN, Tester DJ, Bastiaenen R, Behr ER, Ackerman MJ, Guicheney P, Delisle BP, Heart Rhythm, 1/1/2012
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Lectures

The Cardiac Channelopathies
Moscow, Russia - 6/12/2014
The Molecular Autopsy for Sudden Unexplained Death in the Young
Moscow, Russia - 6/12/2014
Latest Diagnostic and Treatment Strategies for the Congenital Long QT Syndromes
MA General Hospital for Children, Boston, MA - 5/15/2014
Videoscopic Left Cardiac Sympathetic Denervation for LQTS and CPVT
San Francisco, CA - 5/9/2014
Presention Title: Getting out of Genetic Purgatory: Resolving the VUS Issue
San Francisco, CA - 5/8/2014
State of the Art: The Cardiac Channelopathies
Manhattan, NY - 4/11/2014
State of Postmortem Genetic Testing for Autopsy Negative Sudden Unexplained Death (aka, The Molecular Autopsy
Lancaster General, Lancaster, Philadelphia, PA - 3/27/2014
The Cardiac Channelopathies: Who needs an ICD?
Salt Lake City, UT - 3/7/2014
Update on Management of Long QT Syndrome and Brugada Syndrome: Role of ICD, Pharmacologic Therapy, and Genetic Testing
Cancun, Mexico - 2/28/2014
ECGS for Experts I
Cancun, Mexico - 2/28/2014
The Cardiac Channelopathies: Who Needs and ICD?
Kauai, HI - 1/28/2014
Arrhythmias in Athletes: When are Sports Not Worth the Risk?
Kauai, HI - 1/28/2014
Denervation Therapy for VF Syndromes
Kauai, HI - 1/28/2014
Update on Management of Long QT Syndrome and Brugada Syndrome: Role of ICD, Pharmacologic Therapy, and Genetic Testing
Nanjing, China - 1/8/2014
Electrophysiology Review for Boards and Recertification
Mayo School of Continuous Professional Development, Rochester, Minnesota - 8/23/2013
MMVR20 / NextMed (Medicine Meets Virtual Reality) 2013
Aligned Management Associates, Inc., San Diego, California - 2/20/2013
Hypertrophic Cardiomyopathy Diagnosis and Treatment
Tulsa, OK - 2/8/2013
Is Genetic Testing for Cardiomyopathies/Channelopathies Ready for the Big Screen?
Tulsa, OK - 2/8/2013
Cardiac Channelopathies for the Boards
Rochester, MN - 2/7/2013
Videoscopic Left Cardiac Sympathetic Denervation for Potentially Lethal VF Syndromes
Minneapolis, MN - 12/3/2012
Athletes with Heart Diseases: The ESC Guidelines Are Too Strict
Los Angeles - 11/4/2012
What Explains the Rest of Congenital LQTS?, Grand Rounds
UCLA, Los Angeles, CA - 11/2/2012
The Latest Treatment Strategies for Channelopathies,Grand Rounds
CHOC Children's Hospital, Orange, CA - 11/2/2012
From Detassling Corn to Decoding Sudden Death - Who/What Should I Be/Do When I Grow Up?
Rochester, MN - 10/16/2012
Latest Treatment Strategies for SADS Conditions
Salt Lake City, UT - 10/13/2012
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Other

Medical Edge
WCCO Lifeline: SUDs
Lifeline: Discovery Health
Medical Mysteries: ABC Primetime
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Press Mentions

At Least One Person Seriously Injured in a Car Accident in BrentwoodAugust 17th, 2024
Mayo Clinic Q&A: Are Energy Drinks Bad for Your Health? – Post BulletinAugust 17th, 2024
Energy Drinks May Trigger Cardiac Arrhythmias in Patients with Genetic Heart DiseaseJuly 25th, 2024
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Grant Support

Cardiac Channel Mutations In Sudden Infant Death Syndrome (SIDS)Eunice Kennedy Shriver National Institute Of Child Health &Human Development2007–2011
Cardiac Channel Mutations In SIDSEunice Kennedy Shriver National Institute Of Child Health &Human Development2004–2005
Cardiac Channel Mutations In SIDSEunice Kennedy Shriver National Institute Of Child Health &Human Development2002–2003