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2,038 results on '"Krahn, Andrew D."'

3. Identification and in-silico characterization of splice-site variants from a large cardiogenetic national registry

Author

Rayani, Kaveh, Davies, Brianna, Cheung, Matthew, Comber, Drake, Roberts, Jason D., Tadros, Rafik, Green, Martin S., Healey, Jeffrey S., Simpson, Christopher S., Sanatani, Shubhayan, Steinberg, Christian, MacIntyre, Ciorsti, Angaran, Paul, Duff, Henry, Hamilton, Robert, Arbour, Laura, Leather, Richard, Seifer, Colette, Fournier, Anne, Atallah, Joseph, Kimber, Shane, Makanjee, Bhavanesh, Alqarawi, Wael, Cadrin-Tourigny, Julia, Joza, Jacqueline, Gardner, Martin, Talajic, Mario, Bagnall, Richard D., Krahn, Andrew D., and Laksman, Zachary W. M.

Published
2023
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5. 2023 ACC/AHA/ACCP/HRS Guideline for the Diagnosis and Management of Atrial Fibrillation: A Report of the American College of Cardiology/American Heart Association Joint Committee on Clinical Practice Guidelines

Author

Krahn, Andrew D., Andrade, Jason G., Beavers, Craig J., Bischoff, James M., Bunch, T. Jared, Campbell, Kristen Bova, Chen, Lin Yee, Dharia, Robin, Dorsch, Michael P., Gerstenfeld, Edward P., Jones, Aubrey E., Kaluzna, Stephanie Dwyer, Masha, Luke, Nault, Isabelle, Noseworthy, Peter A., Pellegrini, Cara N., Tzeis, Stylianos E., Volgman, Annabelle Santos, Zeitler, Emily P., Joglar, José A., Chung, Mina K., Armbruster, Anastasia L., Benjamin, Emelia J., Chyou, Janice Y., Cronin, Edmond M., Deswal, Anita, Eckhardt, Lee L., Goldberger, Zachary D., Gopinathannair, Rakesh, Gorenek, Bulent, Hess, Paul L., Hlatky, Mark, Hogan, Gail, Ibeh, Chinwe, Indik, Julia H., Kido, Kazuhiko, Kusumoto, Fred, Link, Mark S., Linta, Kathleen T., Marcus, Gregory M., McCarthy, Patrick M., Patel, Nimesh, Patton, Kristen K., Perez, Marco V., Piccini, Jonathan P., Russo, Andrea M., Sanders, Prashanthan, Streur, Megan M., Thomas, Kevin L., Times, Sabrina, Tisdale, James E., Valente, Anne Marie, and Van Wagoner, David R.

Published
2024
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8. 2024 HRS expert consensus statement on arrhythmias in the athlete: Evaluation, treatment, and return to play

Author

Lampert, Rachel, Chung, Eugene H., Ackerman, Michael J., Arroyo, Alonso Rafael, Darden, Douglas, Deo, Rajat, Dolan, Joe, Etheridge, Susan P., Gray, Belinda R., Harmon, Kimberly G., James, Cynthia A., Kim, Jonathan H., Krahn, Andrew D., La Gerche, Andre, Link, Mark S., MacIntyre, Ciorsti, Mont, Lluis, Salerno, Jack C., and Shah, Maully J.

Published
2024
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9. An international multicenter cohort study on implantable cardioverter-defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia

Author

Lamba, Avani, Roston, Thomas M., Peltenburg, Puck J., Kallas, Dania, Franciosi, Sonia, Lieve, Krystien V.V., Kannankeril, Prince J., Horie, Minoru, Ohno, Seiko, Brugada, Ramon, Aiba, Takeshi, Fischbach, Peter, Knight, Linda, Till, Jan, Kwok, Sit-Yee, Probst, Vincent, Backhoff, David, LaPage, Martin J., Batra, Anjan S., Drago, Fabrizio, Haugaa, Kristina, Krahn, Andrew D., Robyns, Tomas, Swan, Heikki, Tavacova, Terezia, van der Werf, Christian, Atallah, Joseph, Borggrefe, Martin, Rudic, Boris, Sarquella-Brugada, Georgia, Chorin, Ehud, Hill, Allison, Kammeraad, Janneke, Kamp, Anna, Law, Ian, Perry, James, Roberts, Jason D., Tisma-Dupanovic, Svjetlana, Semsarian, Christopher, Skinner, Jonathan R., Tfelt-Hansen, Jacob, Denjoy, Isabelle, Leenhardt, Antoine, Schwartz, Peter J., Ackerman, Michael J., Blom, Nico A., Wilde, Arthur A.M., and Sanatani, Shubhayan

Published
2024
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12. Clinical Management of Brugada Syndrome: Commentary From the Experts

Author

Cutler, Michael J., Eckhardt, Lee L., Kaufman, Elizabeth S., Arbelo, Elena, Behr, Elijah R., Brugada, Pedro, Cerrone, Marina, Crotti, Lia, deAsmundis, Carlo, Gollob, Michael H., Horie, Minoru, Huang, David T., Krahn, Andrew D., London, Barry, Lubitz, Steven A., Mackall, Judith A., Nademanee, Koonlawee, Perez, Marco V., Probst, Vincent, Roden, Dan M., Sacher, Frederic, Sarquella-Brugada, Georgia, Scheinman, Melvin M., Shimizu, Wataru, Shoemaker, Benjamin, Sy, Raymond W., Watanabe, Atsuyuki, and Wilde, Arthur A.M.

Published
2024
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13. The Prevalence and Characteristics of Arrhythmic Mitral Valve Prolapse in Patients With Unexplained Cardiac Arrest

Author

Alqarawi, Wael, Tadros, Rafik, Roberts, Jason D., Cheung, Christopher C., Green, Martin S., Burwash, Ian G., Steinberg, Christian, Healey, Jeffrey S., Khan, Habib, McIntyre, Ciorsti, Cadrin-Touringy, Julia, Laksman, Zachary W.M., Simpson, Christopher S., Sanatani, Shubhayan, Gardner, Martin, Angaran, Paul, Ilhan, Erkan, Talajic, Mario, Arbour, Laura, Leather, Richard, Seifer, Colette, Joza, Jacqueline, Lee, Felicity, Lau, Lawrence, Nair, Girish, Wells, George, and Krahn, Andrew D.

Published
2023
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14. Statement from the Asia Summit: Current state of arrhythmia care in Asia

Author

Shimizu, Wataru, Kusumoto, Fred M., Agbayani, Michael-Joseph F., Apiyasawat, Sirin, Chen, Minglong, Ching, Chi Keong, Choi, Jong-Il, Dan Do, Van Buu, Hanafy, Dicky A., Hurwitz, Jodie L., Johar, Sofian, Kalman, Jonathan M., Khan, Aamir Hameed H., Khmao, Pichmanil, Krahn, Andrew D., Ngarmukos, Tachapong, Binh Nguyen, Son Thai, Nwe, Nwe, Oh, Seil, Soejima, Kyoko, Stiles, Martin K., Tsao, Hsuan-Ming, and Tseveendee, Saruul

Published
2023
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18. Mode and Characteristics of Arrhythmia Initiation in Idiopathic Ventricular Fibrillation

Author

Belhassen, Bernard, primary, Conte, Giulio, additional, Steinberg, Christian, additional, Whitaker, John, additional, Khan, Habib R., additional, Laredo, Mikael, additional, Doldi, Florian, additional, Ho, Reginald, additional, Tadros, Rafik, additional, Dinov, Boris, additional, Chorin, Ehud, additional, Hansom, Simon, additional, Waintraub, Xavier, additional, Eckardt, Lars, additional, Jankelson, Lior, additional, Peichl, Petr, additional, Mellor, Greg, additional, Sy, Raymond W., additional, Rattanawong, Pattara, additional, Stojkovic, Stefan, additional, Garber, Leonid, additional, Suna, Gonca, additional, Kautzner, Josef, additional, Chan, Kim Hoe, additional, Srivathsan, Komandoor, additional, Tedrow, Usha, additional, Havranek, Stepan, additional, Murgatroyd, Francis, additional, Shauer, Ayelet, additional, Winkel, Bo Gregers, additional, Page, Stephen P., additional, Milman, Anat, additional, Lador, Adi, additional, Ayou, Romeo, additional, Sellal, Jean Marc, additional, Chevalier, Philippe, additional, García-Fernández, F. Javier, additional, Reichlin, Tobias, additional, Shah, Dipen, additional, Nazer, Babak, additional, Bermudez-Jimenez, Francisco, additional, Nagase, Satoshi, additional, Morita, Hiroshi, additional, Nam, Gi-Byoung, additional, Pappone, Carlo, additional, Lambiase, Pier D., additional, Strohmer, Bernhard, additional, Stuehlinger, Markus, additional, Gandjbakhch, Estelle, additional, Schulze-Bahr, Eric, additional, Krahn, Andrew D., additional, Tovia-Brodie, Oholi, additional, Asatryan, Babken, additional, Baskar, Shankar, additional, Berne, Paola, additional, Blommaert, Dominique, additional, Dormal, Fabien, additional, Boccellino, Antonio, additional, Ciconte, Giuseppe, additional, Giustetto, Carla, additional, Haqqani, Harris, additional, Jackson, Liang J., additional, DG, Latcu, additional, Lellouche, Nicolas, additional, Marai, Ibrahim, additional, Nakahara, Shiro, additional, Pannone, Luigi, additional, de Asmundis, Carlo, additional, Pavri, Behzad B., additional, Porretta, Alessandra Pia, additional, Pruvot, Etienne, additional, Rosu, Radu, additional, Scherr, Daniel, additional, Steinfurt, Johannes, additional, and Yagishita, Atsuhiko, additional

Published
2024
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20. An International Multicenter Evaluation of Inheritance Patterns, Arrhythmic Risks, and Underlying Mechanisms of CASQ2-Catecholaminergic Polymorphic Ventricular Tachycardia

Author

Ng, Kevin, Titus, Erron W, Lieve, Krystien V, Roston, Thomas M, Mazzanti, Andrea, Deiter, Frederick H, Denjoy, Isabelle, Ingles, Jodie, Till, Jan, Robyns, Tomas, Connors, Sean P, Steinberg, Christian, Abrams, Dominic J, Pang, Benjamin, Scheinman, Melvin M, Bos, J Martijn, Duffett, Stephen A, van der Werf, Christian, Maltret, Alice, Green, Martin S, Rutberg, Julie, Balaji, Seshadri, Cadrin-Tourigny, Julia, Orland, Kate M, Knight, Linda M, Brateng, Caitlin, Wu, Jeremy, Tang, Anthony S, Skanes, Allan C, Manlucu, Jaimie, Healey, Jeff S, January, Craig T, Krahn, Andrew D, Collins, Kathryn K, Maginot, Kathleen R, Fischbach, Peter, Etheridge, Susan P, Eckhardt, Lee L, Hamilton, Robert M, Ackerman, Michael J, Noguer, Ferran Rosés I, Semsarian, Christopher, Jura, Natalia, Leenhardt, Antoine, Gollob, Michael H, Priori, Silvia G, Sanatani, Shubhayan, Wilde, Arthur AM, Deo, Rahul C, and Roberts, Jason D

Subjects
Clinical Research, Cardiovascular, Genetics, Heart Disease, Aetiology, 2.1 Biological and endogenous factors, Calsequestrin, Female, Heterozygote, Homozygote, Humans, Male, Mutation, Missense, Risk Factors, Tachycardia, Ventricular, arrhythmias, cardiac, catecholaminergic polymorphic ventricular tachycardia, death, sudden, genetics, arrhythmias, cardiac, death, sudden, cardiac, Cardiorespiratory Medicine and Haematology, Clinical Sciences, Public Health and Health Services, Cardiovascular System & Hematology
Abstract

BackgroundGenetic variants in calsequestrin-2 (CASQ2) cause an autosomal recessive form of catecholaminergic polymorphic ventricular tachycardia (CPVT), although isolated reports have identified arrhythmic phenotypes among heterozygotes. Improved insight into the inheritance patterns, arrhythmic risks, and molecular mechanisms of CASQ2-CPVT was sought through an international multicenter collaboration.MethodsGenotype-phenotype segregation in CASQ2-CPVT families was assessed, and the impact of genotype on arrhythmic risk was evaluated using Cox regression models. Putative dominant CASQ2 missense variants and the established recessive CASQ2-p.R33Q variant were evaluated using oligomerization assays and their locations mapped to a recent CASQ2 filament structure.ResultsA total of 112 individuals, including 36 CPVT probands (24 homozygotes/compound heterozygotes and 12 heterozygotes) and 76 family members possessing at least 1 presumed pathogenic CASQ2 variant, were identified. Among CASQ2 homozygotes and compound heterozygotes, clinical penetrance was 97.1% and 26 of 34 (76.5%) individuals had experienced a potentially fatal arrhythmic event with a median age of onset of 7 years (95% CI, 6-11). Fifty-one of 66 CASQ2 heterozygous family members had undergone clinical evaluation, and 17 of 51 (33.3%) met diagnostic criteria for CPVT. Relative to CASQ2 heterozygotes, CASQ2 homozygote/compound heterozygote genotype status in probands was associated with a 3.2-fold (95% CI, 1.3-8.0; P=0.013) increased hazard of a composite of cardiac syncope, aborted cardiac arrest, and sudden cardiac death, but a 38.8-fold (95% CI, 5.6-269.1; P

Published
2020

22. An International Multicenter Evaluation of Type 5 Long QT Syndrome

Author

Roberts, Jason D, Asaki, S Yukiko, Mazzanti, Andrea, Bos, J Martijn, Tuleta, Izabela, Muir, Alison R, Crotti, Lia, Krahn, Andrew D, Kutyifa, Valentina, Shoemaker, M Benjamin, Johnsrude, Christopher L, Aiba, Takeshi, Marcondes, Luciana, Baban, Anwar, Udupa, Sharmila, Dechert, Brynn, Fischbach, Peter, Knight, Linda M, Vittinghoff, Eric, Kukavica, Deni, Stallmeyer, Birgit, Giudicessi, John R, Spazzolini, Carla, Shimamoto, Keiko, Tadros, Rafik, Cadrin-Tourigny, Julia, Duff, Henry J, Simpson, Christopher S, Roston, Thomas M, Wijeyeratne, Yanushi D, El Hajjaji, Imane, Yousif, Maisoon D, Gula, Lorne J, Leong-Sit, Peter, Chavali, Nikhil, Landstrom, Andrew P, Marcus, Gregory M, Dittmann, Sven, Wilde, Arthur AM, Behr, Elijah R, Tfelt-Hansen, Jacob, Scheinman, Melvin M, Perez, Marco V, Kaski, Juan Pablo, Gow, Robert M, Drago, Fabrizio, Aziz, Peter F, Abrams, Dominic J, Gollob, Michael H, Skinner, Jonathan R, Shimizu, Wataru, Kaufman, Elizabeth S, Roden, Dan M, Zareba, Wojciech, Schwartz, Peter J, Schulze-Bahr, Eric, Etheridge, Susan P, Priori, Silvia G, and Ackerman, Michael J

Subjects
Genetics, Cardiovascular, Clinical Trials and Supportive Activities, Heart Disease, Clinical Research, Human Genome, 2.1 Biological and endogenous factors, Aetiology, Adolescent, Adult, Death, Sudden, Cardiac, Electric Countershock, Electrocardiography, Female, Heart Arrest, Humans, Long QT Syndrome, Male, Middle Aged, Penetrance, Potassium Channels, Voltage-Gated, Registries, arrhythmia, genetics, long QT syndrome, penetrance, sudden cardiac death, Cardiorespiratory Medicine and Haematology, Clinical Sciences, Public Health and Health Services, Cardiovascular System & Hematology
Abstract

BackgroundInsight into type 5 long QT syndrome (LQT5) has been limited to case reports and small family series. Improved understanding of the clinical phenotype and genetic features associated with rare KCNE1 variants implicated in LQT5 was sought through an international multicenter collaboration.MethodsPatients with either presumed autosomal dominant LQT5 (N = 229) or the recessive Type 2 Jervell and Lange-Nielsen syndrome (N = 19) were enrolled from 22 genetic arrhythmia clinics and 4 registries from 9 countries. KCNE1 variants were evaluated for ECG penetrance (defined as QTc >460 ms on presenting ECG) and genotype-phenotype segregation. Multivariable Cox regression was used to compare the associations between clinical and genetic variables with a composite primary outcome of definite arrhythmic events, including appropriate implantable cardioverter-defibrillator shocks, aborted cardiac arrest, and sudden cardiac death.ResultsA total of 32 distinct KCNE1 rare variants were identified in 89 probands and 140 genotype positive family members with presumed LQT5 and an additional 19 Type 2 Jervell and Lange-Nielsen syndrome patients. Among presumed LQT5 patients, the mean QTc on presenting ECG was significantly longer in probands (476.9±38.6 ms) compared with genotype positive family members (441.8±30.9 ms, P

Published
2020

23. Ankyrin-B dysfunction predisposes to arrhythmogenic cardiomyopathy and is amenable to therapy

Author

Roberts, Jason D, Murphy, Nathaniel P, Hamilton, Robert M, Lubbers, Ellen R, James, Cynthia A, Kline, Crystal F, Gollob, Michael H, Krahn, Andrew D, Sturm, Amy C, Musa, Hassan, El-Refaey, Mona, Koenig, Sara, Aneq, Meriam Åström, Hoorntje, Edgar T, Graw, Sharon L, Davies, Robert W, Rafiq, Muhammad Arshad, Koopmann, Tamara T, Aafaqi, Shabana, Fatah, Meena, Chiasson, David A, Taylor, Matthew RG, Simmons, Samantha L, Han, Mei, van Opbergen, Chantal JM, Wold, Loren E, Sinagra, Gianfranco, Mittal, Kirti, Tichnell, Crystal, Murray, Brittney, Codima, Alberto, Nazer, Babak, Nguyen, Duy T, Marcus, Frank I, Sobriera, Nara, Lodder, Elisabeth M, van den Berg, Maarten P, Spears, Danna A, Robinson, John F, Ursell, Philip C, Green, Anna K, Skanes, Allan C, Tang, Anthony S, Gardner, Martin J, Hegele, Robert A, van Veen, Toon AB, Wilde, Arthur AM, Healey, Jeff S, Janssen, Paul ML, Mestroni, Luisa, van Tintelen, J Peter, Calkins, Hugh, Judge, Daniel P, Hund, Thomas J, Scheinman, Melvin M, and Mohler, Peter J

Subjects
Heart Disease, Cardiovascular, Clinical Research, Rare Diseases, 2.1 Biological and endogenous factors, Aetiology, Animals, Ankyrins, Arrhythmogenic Right Ventricular Dysplasia, Disease Models, Animal, Female, Humans, Indoles, Male, Maleimides, Mice, Mice, Knockout, Myocardium, Wnt Signaling Pathway, beta Catenin, Arrhythmias, Cardiology, Cardiovascular disease, Cell Biology, Genetic diseases, Medical and Health Sciences, Immunology
Abstract

Arrhythmogenic cardiomyopathy (ACM) is an inherited arrhythmia syndrome characterized by severe structural and electrical cardiac phenotypes, including myocardial fibrofatty replacement and sudden cardiac death. Clinical management of ACM is largely palliative, owing to an absence of therapies that target its underlying pathophysiology, which stems partially from our limited insight into the condition. Following identification of deceased ACM probands possessing ANK2 rare variants and evidence of ankyrin-B loss of function on cardiac tissue analysis, an ANK2 mouse model was found to develop dramatic structural abnormalities reflective of human ACM, including biventricular dilation, reduced ejection fraction, cardiac fibrosis, and premature death. Desmosomal structure and function appeared preserved in diseased human and murine specimens in the presence of markedly abnormal β-catenin expression and patterning, leading to identification of a previously unknown interaction between ankyrin-B and β-catenin. A pharmacological activator of the WNT/β-catenin pathway, SB-216763, successfully prevented and partially reversed the murine ACM phenotypes. Our findings introduce what we believe to be a new pathway for ACM, a role of ankyrin-B in cardiac structure and signaling, a molecular link between ankyrin-B and β-catenin, and evidence for targeted activation of the WNT/β-catenin pathway as a potential treatment for this disease.

Published
2019

24. Rationale and Design of the Randomized Bayesian Multicenter COME-TAVI Trial in Patients With a New Onset Left Bundle Branch Block

Author

Rivard, Lena, Nault, Isabelle, Krahn, Andrew D., Daneault, Benoit, Roux, Jean-Francois, Natarajan, Madhu, Healey, Jeffrey S., Quadros, Kenneth, Sandhu, Roopinder K., Kouz, Remi, Greiss, Isabelle, Leong-Sit, Peter, Gourraud, Jean Baptiste, Ben Ali, Walid, Asgar, Anita, Aguilar, Martin, Bonan, Raoul, Cadrin-Tourigny, Julia, Cartier, Raymond, Dorval, Jean-Francois, Dubuc, Marc, Dürrleman, Nicolas, Dyrda, Katia, Guerra, Peter, Ibrahim, Marina, Ibrahim, Reda, Macle, Laurent, Mondesert, Blandine, Moss, Emmanuel, Raymond-Paquin, Alexandre, Roy, Denis, Tadros, Rafik, Thibault, Bernard, Talajic, Mario, Nozza, Anna, Guertin, Marie-Claude, and Khairy, Paul

Published
2023
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25. Heart Rhythm Society’s survey assessing same-day discharge after electrophysiology procedures and implementation in ambulatory surgical centers

Author

Liu, Christopher F., primary, Hurwitz, Jodie L., additional, Krahn, Andrew D., additional, Ellenbogen, Kenneth A., additional, Slotwiner, David J., additional, Schoenfeld, Mark H., additional, Pelosi, Frank, additional, Mainigi, Sumeet K., additional, Berman, Adam E., additional, Rashba, Eric J., additional, Hao, Steven, additional, Sachdev, Molly, additional, Larsen, Timothy R., additional, Tsai, Shane, additional, Miller, Lisa, additional, Smith, Anne Marie, additional, and Shanker, Amit J., additional

Published
2024
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26. Deep Learning–Augmented ECG Analysis for Screening and Genotype Prediction of Congenital Long QT Syndrome

Author

Jiang, River, primary, Cheung, Christopher C., additional, Garcia-Montero, Marta, additional, Davies, Brianna, additional, Cao, Jason, additional, Redfearn, Damian, additional, Laksman, Zachary M., additional, Grondin, Steffany, additional, Atallah, Joseph, additional, Escudero, Carolina A., additional, Cadrin-Tourigny, Julia, additional, Sanatani, Shubhayan, additional, Steinberg, Christian, additional, Joza, Jacqueline, additional, Avram, Robert, additional, Tadros, Rafik, additional, and Krahn, Andrew D., additional

Published
2024
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28. Racial and ethnic disparities in arrhythmia care: A call for action

Author

Thomas, Kevin L., Garg, Jalaj, Velagapudi, Poonam, Gopinathannair, Rakesh, Chung, Mina K., Kusumoto, Fred, Ajijola, Olujimi, Jackson, Larry R., II, Turagam, Mohit K., Joglar, Jose A., Sogade, Felix O., Fontaine, John M., Krahn, Andrew D., Russo, Andrea M., Albert, Christine, and Lakkireddy, Dhanunjaya R.

Published
2022
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29. European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

Author

Wilde, Arthur A.M., Semsarian, Christopher, Márquez, Manlio F., Sepehri Shamloo, Alireza, Ackerman, Michael J., Ashley, Euan A., Sternick, Eduardo Back, Barajas-Martinez, Héctor, Behr, Elijah R., Bezzina, Connie R., Breckpot, Jeroen, Charron, Philippe, Chockalingam, Priya, Crotti, Lia, Gollob, Michael H., Lubitz, Steven, Makita, Naomasa, Ohno, Seiko, Ortiz-Genga, Martín, Sacilotto, Luciana, Schulze-Bahr, Eric, Shimizu, Wataru, Sotoodehnia, Nona, Tadros, Rafik, Ware, James S., Winlaw, David S., Kaufman, Elizabeth S., Aiba, Takeshi, Bollmann, Andreas, Choi, Jong-Il, Dalal, Aarti, Darrieux, Francisco, Giudicessi, John, Guerchicoff, Mariana, Hong, Kui, Krahn, Andrew D., MacIntyre, Ciorsti, Mackall, Judith A., Mont, Lluís, Napolitano, Carlo, Ochoa, Juan Pablo, Peichl, Petr, Pereira, Alexandre C., Schwartz, Peter J., Skinner, Jon, Stellbrink, Christoph, Tfelt-Hansen, Jacob, and Deneke, Thomas

Published
2022
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33. Return of Results Policies for Genomic Research: Current Practices and the Hearts in Rhythm Organization (HiRO) Approach

Author

Comber, Drake A., Davies, Brianna, Roberts, Jason D., Tadros, Rafik, Green, Martin S., Healey, Jeffrey S., Simpson, Christopher S., Sanatani, Shubhayan, Steinberg, Christian, MacIntyre, Ciorsti, Angaran, Paul, Duff, Henry, Hamilton, Robert, Arbour, Laura, Leather, Richard, Seifer, Colette, Fournier, Anne, Atallah, Joseph, Kimber, Shane, Makanjee, Bhavanesh, Alqarawi, Wael, Cadrin-Tourigny, Julia, Joza, Jacqueline, Gibbs, Karen, Robb, Laura, Zahavich, Laura, Gardner, Martin, Talajic, Mario, Virani, Alice, Krahn, Andrew D., Lehman, Anna, and Laksman, Zachary W.M.

Published
2022
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35. Brugada Syndrome

Author

Krahn, Andrew D., Behr, Elijah R., Hamilton, Robert, Probst, Vincent, Laksman, Zachary, and Han, Hui-Chen

Published
2022
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40. Evaluation of age at symptom onset, proband status, and sex as predictors of disease severity in pediatric catecholaminergic polymorphic ventricular tachycardia

Author

Kallas, Dania, Roston, Thomas M., Franciosi, Sonia, Brett, Laura, Lieve, Krystien V.V., Kwok, Sit-Yee, Kannankeril, Prince J., Krahn, Andrew D., LaPage, Martin J., Etheridge, Susan, Hill, Allison, Johnsrude, Christopher, Perry, James, Knight, Linda, Fischbach, Peter, Balaji, Seshadri, Tisma-Dupanovic, Svjetlana, Law, Ian, Atallah, Joseph, Backhoff, David, Kamp, Anna, Kubus, Peter, Kean, Adam, Aziz, Peter F., Kovach, Joshua, Lau, Yung, Kron, Jordana, Clur, Sally-Ann, Sarquella-Brugada, Georgia, Wilde, Arthur A.M., and Sanatani, Shubhayan

Published
2021
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42. Contributors

Author

Alomar, Mohammed, primary, Amarh, Enoch, additional, Baranchuk, Adrian, additional, Beach, Scott, additional, Boutjdir, Mohamed, additional, Campbell, Kristen Bova, additional, Capecchi, Pier Leopoldo, additional, Chandrasekhar, Sanjay, additional, Chung, Mina K., additional, Curtis, Michael J., additional, Fradley, Michael G., additional, Funk, Margo, additional, Haigney, Mark C.P., additional, Hancox, Jules C., additional, Kovacs, Richard J., additional, Krahn, Andrew D., additional, Krantz, Mori J., additional, Laghi-Pasini, Franco, additional, Laksman, Zachary W.M., additional, Lazzerini, Pietro Enea, additional, Overholser, Brian R., additional, Roberts, Jason D., additional, Roston, Thomas M., additional, Sowinski, Kevin M., additional, Tisdale, James E., additional, Wass, Sojin Youn, additional, Wilde, Arthur AM, additional, Woosley, Raymond L., additional, and Yeung, Cynthia, additional

Published
2022
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43. Implantable cardioverter defibrillator use in arrhythmogenic right ventricular cardiomyopathy in North America and Europe

Author

Carrick, Richard T, primary, De Marco, Corrado, additional, Gasperetti, Alessio, additional, Bosman, Laurens P, additional, Gourraud, Jean-Baptiste, additional, Trancuccio, Alessandro, additional, Mazzanti, Andrea, additional, Murray, Brittney, additional, Pendleton, Catherine, additional, Tichnell, Crystal, additional, Tandri, Harikrishna, additional, Zeppenfeld, Katja, additional, Wilde, Arthur A M, additional, Davies, Brianna, additional, Seifer, Colette, additional, Roberts, Jason D, additional, Healey, Jeff S, additional, MacIntyre, Ciorsti, additional, Alqarawi, Wael, additional, Tadros, Rafik, additional, Cutler, Michael J, additional, Targetti, Mattia, additional, Calò, Leonardo, additional, Vitali, Francesco, additional, Bertini, Matteo, additional, Compagnucci, Paolo, additional, Casella, Michela, additional, Dello Russo, Antonio, additional, Cappelletto, Chiara, additional, De Luca, Antonio, additional, Stolfo, Davide, additional, Duru, Firat, additional, Jensen, Henrik K, additional, Svensson, Anneli, additional, Dahlberg, Pia, additional, Hasselberg, Nina E, additional, Di Marco, Andrea, additional, Jordà, Paloma, additional, Arbelo, Elena, additional, Moreno Weidmann, Zoraida, additional, Borowiec, Karolina, additional, Delinière, Antoine, additional, Biernacka, Elżbieta K, additional, van Tintelen, J Peter, additional, Platonov, Pyotr G, additional, Olivotto, Iacopo, additional, Saguner, Ardan M, additional, Haugaa, Kristina H, additional, Cox, Moniek, additional, Tondo, Claudio, additional, Merlo, Marco, additional, Krahn, Andrew D, additional, te Riele, Anneline S J M, additional, Wu, Katherine C, additional, Calkins, Hugh, additional, James, Cynthia A, additional, and Cadrin-Tourigny, Julia, additional

Published
2024
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48. Driving Restrictions and Early Arrhythmias in Patients Receiving a Secondary Prevention Implantable Cardioverter-Defibrillator (DREAM-ICD- II study)

Author

Steinberg, Christian, Dognin, Nicolas, Sodhi, Amit, Champagne, Catherine, Staples, John A., Champagne, Jean, Laksman, Zachary, Sarrazin, Jean-François, Bennett, Matthew, Plourde, Benoit, Deyell, Marc W., Andrade, Jason G., Roy, Karine, Yeung-Lai-Wah, John A., Hawkins, Nathaniel M., Mondésert, Blandine, Blier, Louis, Nault, Isabelle, O’Hara, Gilles, Krahn, Andrew D., Philippon, François, and Chakrabarti, Santabhanu

Published
2022
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