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Circulation. Arrhythmia and Electrophysiology|August 13, 2016
Novel CPVT-Associated Calmodulin Mutation in CALM3 (CALM3-A103V) Activates Arrhythmogenic Ca Waves and SparksNieves Gomez-Hurtado, Nicole J Boczek, Dmytro O Kryshtal, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2021
De novo mutations in childhood cases of sudden unexplained death that disrupt intracellular Ca2+ regulationMatthew Halvorsen, Laura Gould, Xiaohan Wang, et al.
Plos One|September 4, 2014
A CACNA1C variant associated with reduced voltage-dependent inactivation, increased CaV1.2 channel window current, and arrhythmogenesisJessica A Hennessey, Nicole J Boczek, Yong-Hui Jiang, et al.
Circulation Research|October 22, 2016
A Precision Medicine Approach to the Rescue of Function on Malignant Calmodulinopathic Long-QT SyndromeWorawan B Limpitikul, Ivy E Dick, David J Tester, et al.
Journal of Molecular and Cellular Cardiology|May 19, 2007
Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humansAndrew P Landstrom, Noah Weisleder, Karin B Batalden, et al.
The Journal of Pediatrics|October 1, 2018
Exome-Wide Rare Variant Analyses in Sudden Infant Death SyndromeDavid J Tester, Leonie C H Wong, Pritha Chanana, et al.
Heart Rhythm|March 11, 2017
Vectorcardiography identifies patients with electrocardiographically concealed long QT syndromeDaniel Cortez, J Martijn Bos, Michael J Ackerman
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|October 10, 2020
Idiopathic ventricular fibrillation: the ongoing quest for diagnostic refinementGiulio Conte, John R Giudicessi, Michael J Ackerman
Biorxiv : the Preprint Server for Biology|March 11, 2024
A Multi-Omics Atlas of Sex-Specific Differences in Obstructive Hypertrophic CardiomyopathyRamin Garmany, Surendra Dasari, J Martijn Bos, et al.
Heart Rhythm|April 27, 2005
Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testingMichael J Ackerman, Igor Splawski, Jonathan C Makielski, et al.
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