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Michael John Ackerman, MD, PhD, FACC

Professor

  • 32589 Citations
  • 100 h-Index
1991 …2020
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  • 12 Similar Profiles
Long QT Syndrome Medicine & Life Sciences
Hypertrophic Cardiomyopathy Medicine & Life Sciences
Mutation Medicine & Life Sciences
Sudden Cardiac Death Medicine & Life Sciences
Genetic Testing Medicine & Life Sciences
Cardiac Arrhythmias Medicine & Life Sciences
Channelopathies Medicine & Life Sciences
Sudden Death Medicine & Life Sciences

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Projects 2002 2020

Exercise in Genetic Cardiovascular Conditions

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

National Institutes of Health

2/1/15 → 1/31/20

Project: Research project

Exercise
Quality of Life
Long QT Syndrome
Sports
Patient Advocacy

Cardiac Channel Mutations in SIDS

Ackerman, M. J.

National Institutes of Health

6/7/02 → 5/31/18

Project: Research project

Sudden Infant Death
Mutation
Autonomic Nervous System
Genes
Macromolecular Substances

Research Output 1991 2019

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

Bains, S., Tester, D. J., Asirvatham, S. J., Noseworthy, P., Ackerman, M. J. & Giudicessi, J. R., Jan 1 2019, In : Mayo Clinic proceedings.

Research output: Contribution to journal › Article

Filamins
Mitral Valve Prolapse
Mothers
Exome
Haploinsufficiency
2 Citations (Scopus)

A pore-localizing CACNA1C-E1115K missense mutation, identified in a patient with idiopathic QT prolongation, bradycardia, and autism spectrum disorder, converts the L-type calcium channel into a hybrid nonselective monovalent cation channel

Ye, D., Tester, D. J., Zhou, W., Papagiannis, J. & Ackerman, M. J., Feb 1 2019, In : Heart Rhythm. 16, 2, p. 270-278 9 p.

Research output: Contribution to journal › Article

Monovalent Cations
L-Type Calcium Channels
Missense Mutation
Nifedipine
Bradycardia

Cost Efficacy of α-Galactosidase A Enzyme Screening for Fabry Disease

Newman, D. B., Miranda, W. R., Matern, D., Peck, D. S., Geske, J. B., Maleszewski, J., Ommen, S. R. & Ackerman, M. J., Jan 1 2019, In : Mayo Clinic Proceedings. 94, 1, p. 84-88 5 p.

Research output: Contribution to journal › Article

Galactosidases
Fabry Disease
Costs and Cost Analysis
Hypertrophic Cardiomyopathy
Enzymes

Induced Pluripotent Stem Cell–Derived Cardiomyocytes from a Patient with MYL2-R58Q-Mediated Apical Hypertrophic Cardiomyopathy Show Hypertrophy, Myofibrillar Disarray, and Calcium Perturbations

Zhou, W., Bos, J. M., Ye, D., Tester, D. J., Hrstka, S., Maleszewski, J., Ommen, S. R., Nishimura, R. A., Schaff, H. V., Kim, C. S. & Ackerman, M. J., Jan 1 2019, In : Journal of cardiovascular translational research.

Research output: Contribution to journal › Article

Hypertrophic Cardiomyopathy
Cardiac Myocytes
Hypertrophy
Calcium
Myosin Light Chains

International Triadin Knockout Syndrome Registry

Clemens, D. J., Tester, D. J., Giudicessi, J. R., Bos, J. M., Rohatgi, R. K., Abrams, D. J., Balaji, S., Crotti, L., Faure, J., Napolitano, C., Priori, S. G., Probst, V., Rooryck-Thambo, C., Roux-Buisson, N., Sacher, F., Schwartz, P. J., Silka, M. J., Walsh, M. A. & Ackerman, M. J., Feb 1 2019, In : Circulation. Genomic and precision medicine. 12, 2, p. e002419

Research output: Contribution to journal › Article

Registries
Heart Arrest
Genetic Therapy
Cardiac Arrhythmias
triadin