Michael John Ackerman, MD, PhD, FACC

  • 33922 Citations
  • 101 Scopus h-Index
1991 …2020
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Fingerprint Dive into the research topics where Michael John Ackerman is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 13 Similar Profiles
Long QT Syndrome Medicine & Life Sciences
Hypertrophic Cardiomyopathy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Sudden Cardiac Death Medicine & Life Sciences
Cardiac Arrhythmias Medicine & Life Sciences
Genetic Testing Medicine & Life Sciences
Channelopathies Medicine & Life Sciences
Sudden Death Medicine & Life Sciences

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Projects 2002 2020

Exercise in Genetic Cardiovascular Conditions

Day, S., Lampert, R. & Ackerman, M. J.

National Institutes of Health


Project: Research project

Quality of Life
Long QT Syndrome
Patient Advocacy
Sudden Infant Death
Autonomic Nervous System
Macromolecular Substances

Research Output 1991 2019

1 Citation (Scopus)
Mitral Valve Prolapse
Ambulatory Monitoring
2 Citations (Scopus)
Monovalent Cations
L-Type Calcium Channels
Missense Mutation

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

Giudicessi, J. R., Lieve, K. V. V., Rohatgi, R. K., Koca, F., Tester, D. J., van der Werf, C., Martijn Bos, J., Wilde, A. A. M. & Ackerman, M. J., May 1 2019, In : Circulation. Genomic and precision medicine. 12, 5, p. e002510

Research output: Contribution to journalArticle

Genetic Testing
Multicenter Studies
Retrospective Studies
1 Citation (Scopus)

Cardiac hypertrophy and arrhythmia in mice induced by a mutation in ryanodine receptor 2

Alvarado, F. J., Bos, J. M., Yuchi, Z., Valdivia, C. R., Hernandez, J. J., Zhao, Y. T., Henderlong, D. S., Chen, Y., Booher, T. R., Marcou, C. A., Van Petegem, F., Ackerman, M. J. & Valdivia, H. H., Mar 5 2019, In : JCI insight. 5

Research output: Contribution to journalArticle

Ryanodine Receptor Calcium Release Channel
Cardiac Arrhythmias
Hypertrophic Cardiomyopathy
Long QT Syndrome
Induced Pluripotent Stem Cells
L-Type Calcium Channels
Missense Mutation
Cardiac Myocytes