Genetic purgatory and the cardiac channelopathies: Exposing the variants of uncertain/unknown significance issue von Ackerman, Michael J., MD, PhD

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Urgent Guidance for Navigating and Circumventing the QTc-Prolonging and Torsadogenic Potential of Possible Pharmacotherapies for Coronavirus Disease 19 (COVID-19) von Giudicessi, John R., Noseworthy, Peter A., Friedman, Paul A., Ackerman, Michael J.

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Impact of Genetics on the Clinical Management of Channelopathies von Schwartz, Peter J., MD, Ackerman, Michael J., MD, PhD, George, Alfred L., MD, Wilde, Arthur A.M., MD, PhD

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An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome von Adler, Arnon, Novelli, Valeria, Amin, Ahmad S., Abiusi, Emanuela, Care, Melanie, Nannenberg, Eline A., Feilotter, Harriet, Amenta, Simona, Mazza, Daniela, Bikker, Hennie, Sturm, Amy C., Garcia, John, Ackerman, Michael J., Hershberger, Raymond E., Perez, Marco V., Zareba, Wojciech, Ware, James S., Wilde, Arthur A.M., Gollob, Michael H.

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Detection of Hypertrophic Cardiomyopathy Using a Convolutional Neural Network-Enabled Electrocardiogram von Ko, Wei-Yin, Siontis, Konstantinos C., Attia, Zachi I., Carter, Rickey E., Kapa, Suraj, Ommen, Steve R., Demuth, Steven J., Ackerman, Michael J., Gersh, Bernard J., Arruda-Olson, Adelaide M., Geske, Jeffrey B., Asirvatham, Samuel J., Lopez-Jimenez, Francisco, Nishimura, Rick A., Friedman, Paul A., Noseworthy, Peter A.

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Genetic Testing for Potentially Lethal, Highly Treatable Inherited Cardiomyopathies/Channelopathies in Clinical Practice von TESTER, David J, ACKERMAN, Michael J

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The genetic architecture of long QT syndrome: A critical reappraisal von Giudicessi, John R., Wilde, Arthur A.M., Ackerman, Michael J.

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Cardiac Channel Molecular Autopsy: Insights From 173 Consecutive Cases of Autopsy-Negative Sudden Unexplained Death Referred for Postmortem Genetic Testing von Tester, David J., BS, Medeiros-Domingo, Argelia, MD, PhD, Will, Melissa L., BS, Haglund, Carla M., HS, Ackerman, Michael J., MD, PhD

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Artificial Intelligence–Enabled Assessment of the Heart Rate Corrected QT Interval Using a Mobile Electrocardiogram Device von Giudicessi, John R., Schram, Matthew, Bos, J. Martijn, Galloway, Conner D., Shreibati, Jacqueline B., Johnson, Patrick W., Carter, Rickey E., Disrud, Levi W., Kleiman, Robert, Attia, Zachi I., Noseworthy, Peter A., Friedman, Paul A., Albert, David E., Ackerman, Michael J.

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Diagnostic, Prognostic, and Therapeutic Implications of Genetic Testing for Hypertrophic Cardiomyopathy von Bos, J. Martijn, MD, Towbin, Jeffrey A., MD, Ackerman, Michael J., MD, PhD

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MYBPC3 mutations are associated with a reduced super-relaxed state in patients with hypertrophic cardiomyopathy von McNamara, James W, Li, Amy, Lal, Sean, Bos, J Martijn, Harris, Samantha P, van der Velden, Jolanda, Ackerman, Michael J, Cooke, Roger, Dos Remedios, Cristobal G

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Classification and Reporting of Potentially Proarrhythmic Common Genetic Variation in Long QT Syndrome Genetic Testing von Giudicessi, John R, Roden, Dan M, Wilde, Arthur A M, Ackerman, Michael J

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Brugada syndrome and reduced right ventricular outflow tract conduction reserve: a final common pathway? von Behr, Elijah R, Ben-Haim, Yael, Ackerman, Michael J, Krahn, Andrew D, Wilde, Arthur A M

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Detection of hypertrophic cardiomyopathy by an artificial intelligence electrocardiogram in children and adolescents von Siontis, Konstantinos C., Liu, Kan, Bos, J. Martijn, Attia, Zachi I., Cohen-Shelly, Michal, Arruda-Olson, Adelaide M., Zanjirani Farahani, Nasibeh, Friedman, Paul A., Noseworthy, Peter A., Ackerman, Michael J.

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Determinants of incomplete penetrance and variable expressivity in heritable cardiac arrhythmia syndromes von Giudicessi, John R, Ackerman, Michael J

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A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT Syndrome von Limpitikul, Worawan B, Dick, Ivy E, Tester, David J, Boczek, Nicole J, Limphong, Pattraranee, Yang, Wanjun, Choi, Myoung Hyun, Babich, Jennifer, DiSilvestre, Deborah, Kanter, Ronald J, Tomaselli, Gordon F, Ackerman, Michael J, Yue, David T

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Mutation E169K in Junctophilin-2 Causes Atrial Fibrillation Due to Impaired RyR2 Stabilization von Beavers, David L., BS, Wang, Wei, PhD, Ather, Sameer, MD, PhD, Voigt, Niels, MD, Garbino, Alejandro, MD, PhD, Dixit, Sayali S., PhD, Landstrom, Andrew P., MD, PhD, Li, Na, PhD, Wang, Qiongling, PhD, Olivotto, Iacopo, MD, Dobrev, Dobromir, MD, Ackerman, Michael J., MD, PhD, Wehrens, Xander H.T., MD, PhD

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J-Wave syndromes expert consensus conference report: Emerging concepts and gaps in knowledge von Antzelevitch, Charles, PhD, FHRS, Yan, Gan-Xin, MD, PhD, Ackerman, Michael J., MD, PhD, Borggrefe, Martin, MD, Corrado, Domenico, MD, PhD, Guo, Jihong, MD, Gussak, Ihor, MD, PhD, Hasdemir, Can, MD, Horie, Minoru, MD, Huikuri, Heikki, MD, Ma, Changsheng, MD, Morita, Hiroshi, MD, PhD, Nam, Gi-Byoung, MD, PhD, Sacher, Frederic, MD, PhD, Shimizu, Wataru, MD, PhD, Viskin, Sami, MD, Wilde, Arthur A.M., MD, PhD, FHRS

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Left cardiac sympathetic denervation for the treatment of long QT syndrome and catecholaminergic polymorphic ventricular tachycardia using video-assisted thoracic surgery von Collura, Christopher A., MD, Johnson, Jonathan N., MD, Moir, Christopher, MD, Ackerman, Michael J., MD, PhD

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Incidence and Etiology of Sudden Cardiac Arrest and Death in High School Athletes in the United States von Harmon, Kimberly G., MD, Asif, Irfan M., MD, Maleszewski, Joseph J., MD, Owens, David S., MD, MS, Prutkin, Jordan M., MD, MHS, Salerno, Jack C., MD, Zigman, Monica L., MPH, Ellenbogen, Rachel, MS, Rao, Ashwin L., MD, Ackerman, Michael J., MD, PhD, Drezner, Jonathan A., MD

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