Michael John Ackerman, MD, PhD, FACC

  • 35048 Citations
  • 103 Scopus h-Index
1991 …2020
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Research Output 1991 2019

2018
13 Citations (Scopus)

Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing

Giudicessi, J. R., Roden, D. M., Wilde, A. A. M. & Ackerman, M. J., Feb 6 2018, In : Circulation. 137, 6, p. 619-630 12 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Genetic Testing
Cardiac Arrhythmias
Macromolecular Substances
Genetic Predisposition to Disease
2 Citations (Scopus)

Clinical Significance of Early Repolarization in Long QT Syndrome

Sugrue, A., Rohatgi, R. K., Bos, M., Vaidya, V. R., Asirvatham, S. J., Noseworthy, P. & Ackerman, M. J., Sep 1 2018, In : JACC: Clinical Electrophysiology. 4, 9, p. 1238-1244 7 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Sudden Cardiac Death
Electrocardiography
Implantable Defibrillators
Syncope
3 Citations (Scopus)

Common Phenotype in Patients With Mitral Valve Prolapse Who Experienced Sudden Cardiac Death

Hourdain, J., Clavel, M. A., Deharo, J. C., Asirvatham, S. J., Avierinos, J. F., Habib, G., Franceschi, F., Probst, V., Sadoul, N., Martins, R., Leclercq, C., Chauvin, M., Pasquie, J. L., Maury, P., Laurent, G., Ackerman, M. J., Hodge, D. O. & Sarano, M. E., Sep 4 2018, In : Circulation. 138, 10, p. 1067-1069 3 p.

Research output: Contribution to journalLetter

Mitral Valve Prolapse
Sudden Cardiac Death
Phenotype
17 Citations (Scopus)

Dysfunction of NaV1.4, a skeletal muscle voltage-gated sodium channel, in sudden infant death syndrome: a case-control study

Männikkö, R., Wong, L., Tester, D. J., Thor, M. G., Sud, R., Kullmann, D. M., Sweeney, M. G., Leu, C., Sisodiya, S. M., FitzPatrick, D. R., Evans, M. J., Jeffrey, I. J. M., Tfelt-Hansen, J., Cohen, M. C., Fleming, P. J., Jaye, A., Simpson, M. A., Ackerman, M. J., Hanna, M. G., Behr, E. R. & 1 others, Matthews, E., Apr 14 2018, In : The Lancet. 391, 10129, p. 1483-1492 10 p.

Research output: Contribution to journalArticle

Voltage-Gated Sodium Channels
Sudden Infant Death
Case-Control Studies
Skeletal Muscle
National Institutes of Health (U.S.)
2 Citations (Scopus)

Effect of Ascertainment Bias on Estimates of Patient Mortality in Inherited Cardiac Diseases

Nannenberg, E. A., van Rijsingen, I. A. W., van der Zwaag, P. A., van den Berg, M. P., van Tintelen, J. P., Tanck, M. W. T., Ackerman, M. J., Wilde, A. A. M. & Christiaans, I., Oct 1 2018, In : Circulation. Genomic and precision medicine. 11, 10, p. e001797

Research output: Contribution to journalArticle

Heart Diseases
Survival
Mortality
Mutation
Genetic Testing
2 Citations (Scopus)

Effect of Body Mass Index on Exercise Capacity in Patients With Hypertrophic Cardiomyopathy

Larsen, C. M., Ball, C. A., Hebl, V. B., Ong, K. C., Siontis, K. C., Olson, T. P., Ackerman, M. J., Ommen, S. R., Allison, T. G. & Geske, J. B., Jan 1 2018, In : American Journal of Cardiology. 121, 1, p. 100-106 7 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Body Mass Index
Exercise
Exercise Test
Tertiary Care Centers
Romano-Ward Syndrome
Long QT Syndrome
Heart Arrest
Cardiac Arrhythmias
Pediatrics
2 Citations (Scopus)

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome

Tester, D. J., Wong, L. C. H., Chanana, P., Gray, B., Jaye, A., Evans, J. M., Evans, M., Fleming, P., Jeffrey, I., Cohen, M., Tfelt-Hansen, J., Simpson, M. A., Behr, E. R. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : Journal of Pediatrics.

Research output: Contribution to journalArticle

Exome
Sudden Infant Death
Genes
Glucocorticoids
Research
1 Citation (Scopus)

Functional Invalidation of Putative Sudden Infant Death Syndrome-Associated Variants in the KCNH2-Encoded Kv11.1 Channel

Smith, J. L., Tester, D. J., Hall, A. R., Burgess, D. E., Hsu, C. C., Elayi, S. C., Anderson, C. L., January, C. T., Luo, J. Z., Hartzel, D. N., Mirshahi, U. L., Murray, M. F., Mirshahi, T., Ackerman, M. J. & Delisle, B. P., May 1 2018, In : Circulation. Arrhythmia and electrophysiology. 11, 5, p. e005859

Research output: Contribution to journalArticle

Sudden Infant Death
Long QT Syndrome
Electronic Health Records
Action Potentials
Validation Studies

Genetic testing in athletes

Tester, D. J. & Ackerman, M. J., Apr 20 2018, Exercise Risks, Cardiac Arrhythmias and Unusual Problems in Athletes. World Scientific Publishing Co. Pte Ltd, Vol. 3-3. p. 41-74 34 p.

Research output: Chapter in Book/Report/Conference proceedingChapter

Genetic Testing
Athletes
1 Citation (Scopus)

Idiopathic Restrictive Cardiomyopathy in Children and Young Adults

Anderson, H. N., Cetta, F., Driscoll, D. J., Olson, T. M., Ackerman, M. J. & Johnson, J. N., Jan 1 2018, (Accepted/In press) In : American Journal of Cardiology.

Research output: Contribution to journalArticle

Restrictive Cardiomyopathy
Young Adult
Heart Transplantation
Survival
Transplantation
8 Citations (Scopus)

Implantable cardioverter-defibrillator use in catecholaminergic polymorphic ventricular tachycardia: A systematic review

Roston, T. M., Jones, K., Hawkins, N. M., Bos, J. M., Schwartz, P. J., Perry, F., Ackerman, M. J., Laksman, Z. W. M., Kaul, P., Lieve, K. V. V., Atallah, J., Krahn, A. D. & Sanatani, S., Dec 1 2018, In : Heart Rhythm. 15, 12, p. 1791-1799 9 p.

Research output: Contribution to journalArticle

Implantable Defibrillators
Shock
Primary Prevention
Flecainide
Guideline Adherence
8 Citations (Scopus)

Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case Series

Shanks, G. W., Tester, D. J., Ackerman, J. P., Simpson, M. A., Behr, E. R., White, S. M. & Ackerman, M. J., Jun 19 2018, In : Circulation. 137, 25, p. 2705-2715 11 p.

Research output: Contribution to journalArticle

Exome
Sudden Death
Autopsy
Population
Cardiomyopathies
48 Citations (Scopus)

International recommendations for electrocardiographic interpretation in athletes

Sharma, S., Drezner, J. A., Baggish, A., Papadakis, M., Wilson, M. G., Prutkin, J. M., La Gerche, A., Ackerman, M. J., Borjesson, M., Salerno, J. C., Asif, I. M., Owens, D. S., Chung, E. H., Emery, M. S., Froelicher, V. F., Heidbuchel, H., Adamuz, C., Asplund, C. A., Cohen, G., Harmon, K. G. & 13 others, Marek, J. C., Molossi, S., Niebauer, J., Pelto, H. F., Perez, M. V., Riding, N. R., Saarel, T., Schmied, C. M., Shipon, D. M., Stein, R., Vetter, V. L., Pelliccia, A. & Corrado, D., Apr 21 2018, In : European Heart Journal. 39, 16, p. 1466-1480 15 p.

Research output: Contribution to journalArticle

Athletes
9 Citations (Scopus)

Irritable bowel syndrome patients have SCN5A channelopathies that lead to decreased Nav1.5 current and mechanosensitivity

Strege, P. R., Mazzone, A., Bernard, C. E., Neshatian, L., Gibbons, S. J., Saito Loftus, Y. A., Tester, D. J., Calvert, M. L., Mayer, E. A., Chang, L., Ackerman, M. J., Beyder, A. & Farrugia, G., Apr 1 2018, In : American Journal of Physiology - Gastrointestinal and Liver Physiology. 314, 4, p. G494-G503

Research output: Contribution to journalArticle

Channelopathies
Irritable Bowel Syndrome
Mutation
Missense Mutation
Smooth Muscle
1 Citation (Scopus)

Left axis deviation in children without previously known heart disease

Schneider, A. E., Cannon, B. C., Johnson, J. N., Ackerman, M. J. & Wackel, P. L., Mar 1 2018, In : Pediatrics. 141, 3, e20171970.

Research output: Contribution to journalArticle

Heart Diseases
Electrocardiography
Hypertrophy
Physical Examination
Pediatrics
1 Citation (Scopus)

Left Ventricular Isovolumetric Relaxation Time Is Prolonged in Fetal Long-QT Syndrome

Clur, S. A. B., Vink, A. S., Etheridge, S. P., Robles De Medina, P. G., Rydberg, A., Ackerman, M. J., Wilde, A. A., Blom, N. A., Benson, D. W., Herberg, U., Donofrio, M. T. & Cuneo, B. F., Apr 1 2018, In : Circulation: Arrhythmia and Electrophysiology. 11, 4, e005797.

Research output: Contribution to journalArticle

Long QT Syndrome
Fetal Heart Rate
Fetus
Gestational Age
Fetal Mortality
3 Citations (Scopus)

Localization and functional consequences of a direct interaction between TRIOBP-1 and hERG proteins in the heart

Jones, D. K., Johnson, A. C., Roti, E. C. R., Liu, F., Uelmen, R., Ayers, R. A., Baczko, I., Tester, D. J., Ackerman, M. J., Trudeau, M. C. & Robertson, G. A., Mar 1 2018, In : Journal of Cell Science. 131, 6, jcs206730.

Research output: Contribution to journalArticle

HEK293 Cells
Cardiac Myocytes
Proteins
Energy Transfer
Sudden Cardiac Death
9 Citations (Scopus)

Localized Structural Alterations Underlying a Subset of Unexplained Sudden Cardiac Death

Haïssaguerre, M., Hocini, M., Cheniti, G., Duchateau, J., Sacher, F., Puyo, S., Cochet, H., Takigawa, M., Denis, A., Martin, R., Derval, N., Bordachar, P., Ritter, P., Ploux, S., Pambrun, T., Klotz, N., Massoullié, G., Pillois, X., Dallet, C., Schott, J. J. & 19 others, Scouarnec, S., Ackerman, M. J., Tester, D., Piot, O., Pasquié, J. L., Leclerc, C., Hermida, J. S., Gandjbakhch, E., Maury, P., Labrousse, L., Coronel, R., Jais, P., Benoist, D., Vigmond, E., Potse, M., Walton, R., Nademanee, K., Bernus, O. & Dubois, R., Jul 1 2018, In : Circulation: Arrhythmia and Electrophysiology. 11, 7, e006120.

Research output: Contribution to journalArticle

Sudden Cardiac Death
Ventricular Fibrillation
Heart Ventricles
Epicardial Mapping
Catheter Ablation
4 Citations (Scopus)

Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variant

Lane, C. M., Giudicessi, J. R., Ye, D., Tester, D. J., Rohatgi, R. K., Bos, J. M. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : Heart Rhythm.

Research output: Contribution to journalArticle

Long QT Syndrome
Phenotype
Genetic Testing
Pedigree
Exome

Mexiletine rescues a mixed biophysical phenotype of the cardiac sodium channel arising from the SCN5a mutation, N406K, found in LQT3 patients

Hu, R. M., Tester, D. J., Li, R., Sun, T., Peterson, B. Z., Ackerman, M. J., Makielski, J. C. & Tan, B. H., Jan 1 2018, In : Channels. 12, 1, p. 176-186 11 p.

Research output: Contribution to journalArticle

Mexiletine
Sodium Channels
Phenotype
Mutation
Torsades de Pointes
1 Citation (Scopus)

Noncardiac genetic predisposition in sudden infant death syndrome

Gray, B., Tester, D. J., Wong, L. C., Chanana, P., Jaye, A., Evans, J. M., Baruteau, A. E., Evans, M., Fleming, P., Jeffrey, I., Cohen, M., Tfelt-Hansen, J., Simpson, M. A., Ackerman, M. J. & Behr, E. R., Jan 1 2018, (Accepted/In press) In : Genetics in Medicine.

Research output: Contribution to journalArticle

Sudden Infant Death
Genetic Predisposition to Disease
Genes
Gene Frequency
Exome
1 Citation (Scopus)
electrocardiography
Electric network analysis
Electrocardiography
neural networks
learning
2 Citations (Scopus)

Perioperative management of patients with congenital or acquired disorders of the QT interval

O'Hare, M., Maldonado, Y., Munro, J., Ackerman, M. J., Ramakrishna, H. & Sorajja, D., Apr 1 2018, In : British Journal of Anaesthesia. 120, 4, p. 629-644 16 p.

Research output: Contribution to journalReview article

Torsades de Pointes
Perioperative Period
Sudden Cardiac Death
Syncope
Ventricular Tachycardia
1 Citation (Scopus)

Platelet Function Analyzer 100 and Brain Natriuretic Peptide as Biomarkers in Obstructive Hypertrophic Cardiomyopathy

Blackshear, J. L., Safford, R. E., Thomas, C. S., Bos, J. M., Ackerman, M. J., Geske, J. B., Ommen, S. R., Shapiro, B. P. & Johns, G. S., Mar 15 2018, In : American Journal of Cardiology. 121, 6, p. 768-774 7 p.

Research output: Contribution to journalArticle

Brain Natriuretic Peptide
Hypertrophic Cardiomyopathy
Blood Platelets
Biomarkers
Electrocardiography
1 Citation (Scopus)

Potentially modifiable factors of dofetilide-associated risk of torsades de pointes among hospitalized patients with atrial fibrillation

Naksuk, N., Sugrue, A. M., Padmanabhan, D., Kella, D., DeSimone, C. V., Kapa, S., Asirvatham, S. J., Lee, H. C., Ackerman, M. J. & Noseworthy, P., Jan 1 2018, (Accepted/In press) In : Journal of Interventional Cardiac Electrophysiology.

Research output: Contribution to journalArticle

Torsades de Pointes
Atrial Fibrillation
Diuretics
Heart Failure
Odds Ratio
1 Citation (Scopus)

Prevalence and clinical phenotype of concomitant long QT syndrome and arrhythmogenic bileaflet mitral valve prolapse

Giudicessi, J. R., Rohatgi, R. K., Bos, J. M. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : International Journal of Cardiology.

Research output: Contribution to journalArticle

Long QT Syndrome
Mitral Valve Prolapse
Phenotype
Cardiac Arrhythmias
3 Citations (Scopus)

QT prolongation and sudden cardiac death risk in hypertrophic cardiomyopathy

Patel, S. I., Ackerman, M. J., Shamoun, F. E., Geske, J. B., Ommen, S. R., Love, W. T., Cha, S. S., Bos, J. M. & Lester, S. J., Mar 6 2018, (Accepted/In press) In : Acta Cardiologica. p. 1-6 6 p.

Research output: Contribution to journalArticle

Hypertrophic Cardiomyopathy
Sudden Cardiac Death
Bundle-Branch Block
Implantable Defibrillators
Logistic Models
39 Citations (Scopus)

Reappraisal of Reported Genes for Sudden Arrhythmic Death

National Institutes of Health Clinical Genome Resource Consortium, Sep 18 2018, In : Circulation. 138, 12, p. 1195-1205 11 p.

Research output: Contribution to journalArticle

Sudden Death
Brugada Syndrome
Genes
Causality
Inborn Genetic Diseases
Athletes
Sports
Heart Diseases
Decision Making
Ryanodine Receptor Calcium Release Channel
Genetic Testing
Ventricular Tachycardia
Polymorphic catecholergic ventricular tachycardia
2 Citations (Scopus)

Return-to-play for athletes with genetic heart diseases

Turkowski, K. L., Martijn Bos, J., Ackerman, N. C., Rohatgi, R. K. & Ackerman, M. J., Mar 1 2018, In : Circulation. 137, 10, p. 1086-1088 3 p.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Athletes
Heart Diseases
Return to Sport
4 Citations (Scopus)

Role of genetic heart disease in sentinel sudden cardiac arrest survivors across the age spectrum

Giudicessi, J. R. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : International Journal of Cardiology.

Research output: Contribution to journalArticle

Inborn Genetic Diseases
Sudden Cardiac Death
Survivors
Heart Diseases
Referral and Consultation
1 Citation (Scopus)

Safety of Sports for Young Patients With Implantable Cardioverter-Defibrillators

Saarel, E. V., Law, I., Berul, C. I., Ackerman, M. J., Kanter, R. J., Sanatani, S., Cohen, M. I., Berger, S., Fischbach, P. S., Burton, D. A., Dziura, J., Brandt, C., Simone, L., Li, F., Olshansky, B., Cannom, D. S. & Lampert, R. J., Nov 1 2018, In : Circulation. Arrhythmia and electrophysiology. 11, 11, p. e006305

Research output: Contribution to journalArticle

Open Access
Implantable Defibrillators
Sports
Safety
Shock
Athletes
6 Citations (Scopus)

SCN5A mutations in 442 neonates and children: Genotype-phenotype correlation and identification of higher-risk subgroups

Baruteau, A. E., Kyndt, F., Behr, E. R., Vink, A. S., Lachaud, M., Joong, A., Schott, J. J., Horie, M., Denjoy, I., Crotti, L., Shimizu, W., Bos, J. M., Stephenson, E. A., Wong, L., Abrams, D. J., Davis, A. M., Winbo, A., Dubin, A. M., Sanatani, S., Liberman, L. & 31 others, Kaski, J. P., Rudic, B., Kwok, S. Y., Rieubland, C., Tfelt-Hansen, J., Van Hare, G. F., Guyomarc'h-Delasalle, B., Blom, N. A., Wijeyeratne, Y. D., Gourraud, J. B., Marec, H. L., Ozawa, J., Fressart, V., Lupoglazoff, J. M., Dagradi, F., Spazzolini, C., Aiba, T., Tester, D. J., Zahavich, L. A., Beauséjour-Ladouceur, V., Jadhav, M., Skinner, J. R., Franciosi, S., Krahn, A. D., Abdelsayed, M., Ruben, P. C., Yung, T. C., Ackerman, M. J., Wilde, A. A., Schwartz, P. J. & Probst, V., Aug 1 2018, In : European Heart Journal. 39, 31, p. 2879-2887 9 p.

Research output: Contribution to journalArticle

Genetic Association Studies
Newborn Infant
Mutation
Phenotype
Genotype
2 Citations (Scopus)

Supraventricular tachycardias, conduction disease, and cardiomyopathy in 3 families with the same rare variant in TNNI3K (p.Glu768Lys)

Podliesna, S., Delanne, J., Miller, L., Tester, D. J., Uzunyan, M., Yano, S., Klerk, M., Cannon, B. C., Khongphatthanayothin, A., Laurent, G., Bertaux, G., Falcon-Eicher, S., Wu, S., Yen, H. Y., Gao, H., Wilde, A. A. M., Faivre, L., Ackerman, M. J., Lodder, E. M. & Bezzina, C. R., Jan 1 2018, (Accepted/In press) In : Heart Rhythm.

Research output: Contribution to journalArticle

Supraventricular Tachycardia
Cardiomyopathies
Phosphotransferases
Dilated Cardiomyopathy
Troponin I
12 Citations (Scopus)

The genetic architecture of long QT syndrome: A critical reappraisal

Giudicessi, J. R., Wilde, A. A. M. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : Trends in Cardiovascular Medicine.

Research output: Contribution to journalArticle

Long QT Syndrome
Genes
Exome
Human Genome Project
Genetic Testing
8 Citations (Scopus)

Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benign

Clemens, D. J., Lentino, A. R., Kapplinger, J. D., Ye, D., Zhou, W., Tester, D. J. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : Heart Rhythm.

Research output: Contribution to journalArticle

Romano-Ward Syndrome
Virulence
Genome
Databases
Mutation
5 Citations (Scopus)

Wearable cardioverter defibrillators for patients with long QT syndrome

Owen, H. J., Bos, J. M. & Ackerman, M. J., Jan 1 2018, (Accepted/In press) In : International Journal of Cardiology.

Research output: Contribution to journalArticle

Long QT Syndrome
Defibrillators
Implantable Defibrillators
Romano-Ward Syndrome
Channelopathies
10 Citations (Scopus)

Yield of the RYR2 Genetic Test in Suspected Catecholaminergic Polymorphic Ventricular Tachycardia and Implications for Test Interpretation

Kapplinger, J. D., Pundi, K. N., Larson, N., Callis, T. E., Tester, D. J., Bikker, H., Wilde, A. A. M. & Ackerman, M. J., Feb 1 2018, In : Circulation. Genomic and precision medicine. 11, 2, p. e001424

Research output: Contribution to journalArticle

Genetic Testing
Computer Simulation
Exome
Phenotype
Polymorphic catecholergic ventricular tachycardia
2017
2 Citations (Scopus)

A modifier screen identifies DNAJB6 as a cardiomyopathy susceptibility gene

Ding, Y., Long, P. A., Bos, J. M., Shih, Y. H., Ma, X., Sundsbak, R. S., Chen, J., Jiang, Y., Zhao, L., Hu, X., Wang, J., Shi, Y., Ackerman, M. J., Lin, X., Ekker, S. C., Redfield, M. M., Olson, T. M. & Xu, X. H., Apr 20 2017, In : JCI insight. 2, 8

Research output: Contribution to journalArticle

Open Access
Cardiomyopathies
Genes
42 Citations (Scopus)

A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome

Limpitikul, W. B., Dick, I. E., Tester, D. J., Boczek, N. J., Limphong, P., Yang, W., Choi, M. H., Babich, J., Disilvestre, D., Kanter, R. J., Tomaselli, G. F., Ackerman, M. J. & Yue, D. T., Jan 6 2017, In : Circulation Research. 120, 1, p. 39-48 10 p.

Research output: Contribution to journalArticle

Long QT Syndrome
Precision Medicine
Calmodulin
Induced Pluripotent Stem Cells
Clustered Regularly Interspaced Short Palindromic Repeats
1 Citation (Scopus)

Architectural T-Wave Analysis and Identification of On-Therapy Breakthrough Arrhythmic Risk in Type 1 and Type 2 Long-QT Syndrome

Sugrue, A., Rohatgi, R. K., Noseworthy, P., Kremen, V., Bos, J. M., Qiang, B., Sapir, Y., Attia, Z. I., Scott, C. G., Brady, P., Asirvatham, S. J., Friedman, P. A. & Ackerman, M. J., Nov 1 2017, In : Circulation. Arrhythmia and electrophysiology. 10, 11

Research output: Contribution to journalArticle

Romano-Ward Syndrome
Long QT Syndrome
Electrocardiography
Therapeutics
Gravitation
2 Citations (Scopus)

Automated T-wave analysis can differentiate acquired QT prolongation from congenital long QT syndrome

Sugrue, A., Noseworthy, P., Kremen, V., Bos, J. M., Qiang, B., Rohatgi, R. K., Sapir, Y., Attia, Z. I., Brady, P., Caraballo, P., Asirvatham, S. J., Friedman, P. A. & Ackerman, M. J., 2017, (Accepted/In press) In : Annals of Noninvasive Electrocardiology.

Research output: Contribution to journalArticle

Long QT Syndrome
Electrocardiography
Electrolytes
Physicians
Gravitation
18 Citations (Scopus)

Beta-blocker therapy for long QT syndrome and catecholaminergic polymorphic ventricular tachycardia: Are all beta-blockers equivalent?

Ackerman, M. J., Priori, S. G., Dubin, A. M., Kowey, P., Linker, N. J., Slotwiner, D., Triedman, J., Van Hare, G. F. & Gold, M. R., Jan 1 2017, In : Heart Rhythm. 14, 1, p. e41-e44

Research output: Contribution to journalArticle

Nadolol
Long QT Syndrome
Sudden Death
Therapeutics
Polymorphic catecholergic ventricular tachycardia
4 Citations (Scopus)

Cardiac transplantation in children and adolescents with long QT syndrome

Kelle, A. M., Bos, J. M., Etheridge, S. P., Cannon, B. C., Bryant, R. M., Johnson, J. N. & Ackerman, M. J., 2017, (Accepted/In press) In : Heart Rhythm.

Research output: Contribution to journalArticle

Long QT Syndrome
Heart Transplantation
Romano-Ward Syndrome
Channelopathies
Transplants
7 Citations (Scopus)

Channelopathies as Causes of Sudden Cardiac Death

Schwartz, P. J., Ackerman, M. J. & Wilde, A. A. M., Dec 1 2017, In : Cardiac Electrophysiology Clinics. 9, 4, p. 537-549 13 p.

Research output: Contribution to journalReview article

Channelopathies
Brugada Syndrome
Long QT Syndrome
Sudden Cardiac Death
Genetic Therapy
9 Citations (Scopus)

Clinical Outcomes and Modes of Death in Timothy Syndrome. A Multicenter International Study of a Rare Disorder

Dufendach, K. A., Timothy, K., Ackerman, M. J., Blevins, B., Pflaumer, A., Etheridge, S., Perry, J., Blom, N. A., Temple, J., Chowdhury, D., Skinner, J. R., Johnsrude, C., Bratincsak, A., Bos, J. M. & Shah, M., Jan 1 2017, (Accepted/In press) In : JACC: Clinical Electrophysiology.

Research output: Contribution to journalArticle

Multicenter Studies
Hypoglycemia
Cardiac Arrhythmias
Syndactyly
Timothy syndrome
15 Citations (Scopus)

Competitive sport participation among athletes with heart disease: A call for a paradigm shift in decision making

Baggish, A. L., Ackerman, M. J. & Lampert, R., Jan 1 2017, In : Circulation. 136, 17, p. 1569-1571 3 p.

Research output: Contribution to journalArticle

Athletes
Sports
Heart Diseases
Decision Making
8 Citations (Scopus)

Congenital myopathy associated with the triadin knockout syndrome

Engel, A. G., Redhage, K. R., Tester, D. J., Ackerman, M. J. & Selcen, D., Mar 21 2017, In : Neurology. 88, 12, p. 1153-1156 4 p.

Research output: Contribution to journalArticle

Myotonia Congenita
Skeletal Muscle
Sarcoplasmic Reticulum
Electron Microscopy
Deltoid Muscle