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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Diagnostic miscues in congenital long-QT syndrome von TAGGART, Nathaniel W, HAGLUND, Carla M, TESTER, David J, ACKERMAN, Michael J

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Compendium of cardiac channel mutations in 541 consecutive unrelated patients referred for long QT syndrome genetic testing von Tester, David J., Will, Melissa L., Haglund, Carla M., Ackerman, Michael J.

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Effect of Clinical Phenotype on Yield of Long QT Syndrome Genetic Testing von Tester, David J., Will, Melissa L., Haglund, Carla M., Ackerman, Michael J.

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Spectrum and frequency of cardiac channel defects in swimming-triggered arrhythmia syndromes von CHOI, Grace, KOPPLIN, Laura J, TESTER, David J, WILL, Melissa L, HAGLUND, Carla M, ACKERMAN, Michael J

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Implantable cardioverter defibrillator therapy for congenital long QT syndrome: A single-center experience von Horner, Justin M., MD, MPH, Kinoshita, Masayoshi, MD, Webster, Tracy L., RN, Haglund, Carla M, Friedman, Paul A., MD, FHRS, Ackerman, Michael J., MD, PhD

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Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testing von Tester, David J., Arya, Puneeta, Will, Melissa, Haglund, Carla M., Farley, Amanda L., Makielski, Jonathan C., Ackerman, Michael J.

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Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant von Tobert, Kathryn E., Tester, David J., Zhou, Wei, Haglund-Turnquist, Carla M., Giudicessi, John R., Ackerman, Michael J.

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Elucidation of ALG10B as a Novel Long-QT Syndrome–Susceptibility Gene von Zhou, Wei, Ye, Dan, Tester, David J., Bains, Sahej, Giudicessi, John R., Haglund-Turnquist, Carla M., Orland, Kate M., January, Craig T., Eckhardt, Lee L., Maginot, Kathleen R., Ackerman, Michael J.

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Molecular characterization of the calcium release channel deficiency syndrome von Tester, David J, Kim, C S John, Hamrick, Samantha K, Ye, Dan, O'Hare, Bailey J, Bombei, Hannah M, Fitzgerald, Kristi K, Haglund-Turnquist, Carla M, Atkins, Dianne L, Nunez, Luis A Ochoa, Law, Ian, Temple, Joel, Ackerman, Michael J

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MP-470543-001 GENOME SEQUENCING IN MULTIPLE AUTOSOMAL DOMINANT PEDIGREES OF CONGENITAL LONG QT SYNDROME AND A NEGATIVE CLINICAL GENETIC TEST YIELD PATHOGENIC DEEP INTRONIC VARIANTS... von Tester, David, Haglund-Turnquist, Carla, Neves, Raquel A., Giudicessi, John R., Ackerman, Michael J.

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Abstract 14385: Genome Sequencing and Re-Engineered Heart Cell-Disease Modeling Identifies a Novel Deep Intronic Variant in a Multi-Generational Long QT Syndrome Pedigree von Tobert, Kathryn E, Tester, David J, Zhou, Wei, Haglund-Turnquist, Carla, Giudicessi, John, Ackerman, Michael J

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B-PO05-027 GENOME SEQUENCING IN A GENETICALLY ELUSIVE MULTI-GENERATIONAL LONG QT SYNDROME PEDIGREE IDENTIFIES A NOVEL PATHOGENIC CAUSE von Tobert, Kathryn E., Tester, David, Zhou, Wei, Haglund-Turnquist, Carla, Ackerman, Michael John

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PO-630-04 ELUCIDATION OF ALG10B AS A NOVEL LONG QT SYNDROME SUSCEPTIBILITY GENE von Zhou, Wei, Ye, Dan, Tester, David, Bains, Sahej, Giudicessi, John R., Haglund-Turnquist, Carla, Orland, Kate, January, Craig T., Eckhardt, L. Lee, Maginot, Kathleen R., Ackerman, Michael John

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Vigorous Exercise in Patients With Congenital Long-QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study von Lampert, Rachel, Day, Sharlene, Ainsworth, Barbara, Burg, Matthew, Marino, Bradley S, Salberg, Lisa, Tome Esteban, Maria Teresa, Abrams, Dominic J, Aziz, Peter F, Barth, Cheryl, Behr, Elijah R, Bell, Cheyanne, Berul, Charles I, Bos, Johan M, Bradley, David, Cannom, David S, Cannon, Bryan C, Concannon, Maryann Anandi, Cerrone, Marina, Czosek, Richard J, Dubin, Anne M, Dziura, James, Erickson, Christopher C, Estes, 3rd, N A Mark, Etheridge, Susan P, Goldenberg, Ilan, Gray, Belinda, Haglund-Turnquist, Carla, Harmon, Kimberly, James, Cynthia A, Johnsrude, Christopher, Kannankeril, Prince, Lara, Alice, Law, Ian H, Li, Fangyong, Link, Mark S, Molossi, Silvana M, Olshansky, Brian, Noseworthy, Peter A, Saarel, Elizabeth V, Sanatani, Shubhayan, Shah, Maully, Simone, Laura, Skinner, Jonathan, Tomaselli, Gordon F, Ware, James Simon, Webster, Gregory, Zareba, Wojciech, Zipes, Douglas P, Ackerman, Michael J

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LB-469807-01 IMPACT OF VIGOROUS EXERCISE IN THE LONG QT SYNDROME BY GENOTYPE, AGE, AND SEX: DATA FROM THE LIFESTYLE AND EXERCISE IN LONG QT SYNDROME REGISTRY (LIVE-LQTS) von Lampert, Rachel, Day, Sharlene, Ainsworth, Barbara, Burg, Mathew, Marino, Bradley, Salberg, Lisa R., Tome Esteban, Maria Teresa, Abrams, Dominic J., Aziz, Peter F., Barth, Cheryl, Behr, Elijah, Bell, Cheyenne, Berul, Charles I., Bos, Johan M., Bradley, David J., Cannom, David S., Cannon, Bryan C., Concannon, Maryann, Cerrone, Marina, Czosek, Richard J., Dubin, Anne M., Dziura, James, Erickson, Christopher C., Estes, Mark, Etheridge, Susan P., Goldenberg, Ilan, Gray, Belinda R., Haglund-Turnquist, Carla, Harmon, Kimberly, James, Cynthia A., Johnsrude, Christopher L., Kannankeril, Prince J., Lara, Alice, Law, Ian H., Li, Fangyong, Link, Mark S., Molossi, Silvana, Olshansky, Brian, Noseworthy, Peter A., Saarel, Elizabeth V., Sanatani, Shubhayan, Shah, Maully J., Simone, Laura, Skinner, Jonathan, Tomaselli, Gordon F., Ware, James S., Webster, Gregory, Zareba, Wojciech, Zipes, Douglas P., Ackerman, Michael J.

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EN-452414-5 VENTRICULAR CONDUCTION IS A MARKER FOR ARRHYTHMIC RISK IN OVERLAP SODIUM CHANNEL DISEASE von Wijeyeratne, Yanushi D., Tanck, Michael, Barc, Julien, Muir, Alison, Aiba, Takeshi, Bos, Johan M., Veltmann, Christian, Galvin, Joseph M., Crotti, Lia, Ishikawa, Taisuke, Ohno, Seiko, Page, Stephen, Denjoy, Isabelle, Tester, David, Muggenthaler, Martina, Takahashi, Kazuhiro, Raju, Hari, GOURRAUD, JEAN BAPTISTE, Redon, Richard, Schott, Jean-Jacques, Kyndt, Florence, Haglund-Turnquist, Carla, Pedrazzini, Matteo, Torchio, Margherita, Dagradi, Frederica, Papadakis, Michael, Sharma, Sanjay, Petzer, Edward, Roden, Dan M., Horie, Minoru, Schwartz, Peter J., Makita, Naomasa, Borggrefe, Martin M., Ackerman, Michael J., Shimizu, Wataru, McKeown, Pascal, PROBST, VINCENT, Behr, Elijah

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Abstract 3094: Implantable Cardioverter Defibrillator Therapy for Congenital Long QT Syndrome: a Single Center Experience von Horner, Justin M, Kinoshita, Masayoshi, Haglund, Carla, Friedman, Paul, Ackerman, Michael J

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Abstract 3091: The Clinical and Electrocardiographic Phenotype of Unrelated Patients with Genotype-Negative Long QT Syndrome von El Yaman, Malek M, Tester, David J, Domingo, Argelia Medeiros, Haglund, Carla M, Ackerman, Michael J

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Elucidation of ALG10B as a Novel Long-QT Syndrome–Susceptibility Gene von Zhou, Wei, Ye, Dan, Tester, David J., Bains, Sahej, Giudicessi, John R., Haglund-Turnquist, Carla M., Orland, Kate M., January, Craig T., Eckhardt, Lee L., Maginot, Kathleen R., Ackerman, Michael J.

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