Projects per year
Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.
- 13 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
Network
Recent external collaboration on country level. Dive into details by clicking on the dots.
Projects 2002 2020
Exercise in Genetic Cardiovascular Conditions
Ackerman, M. J., Day, S. & Lampert, R.
2/1/15 → 1/31/20
Project: Research project
Exercise
Quality of Life
Long QT Syndrome
Sports
Patient Advocacy
Sudden Infant Death
Mutation
Autonomic Nervous System
Genes
Macromolecular Substances
Research Output 1991 2019
1
Citation
(Scopus)
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
Ambulatory Monitoring
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
Development and Validation of a Deep-Learning Model to Screen for Hyperkalemia from the Electrocardiogram
Galloway, C. D., Valys, A. V., Shreibati, J. B., Treiman, D. L., Petterson, F. L., Gundotra, V. P., Albert, D. E., Attia, Z. I., Carter, R. E., Asirvatham, S. J., Ackerman, M. J., Noseworthy, P., Dillon, J. J. & Friedman, P. A., Jan 1 2019, In : JAMA cardiology.Research output: Contribution to journal › Article
Hyperkalemia
Electrocardiography
Learning
Potassium
Chronic Renal Insufficiency
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