Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test
Kapplinger, Jamie D, Tester, David J, Salisbury, Benjamin A, Carr, Janet L, Harris-Kerr, Carole, Pollevick, Guido D, Wilde, Arthur A M, Ackerman, Michael J
Published in Heart rhythm (01.09.2009)
Published in Heart rhythm (01.09.2009)
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Pathogenic and likely pathogenic variant prevalence among the first 10,000 patients referred for next-generation cancer panel testing
Susswein, Lisa R., Marshall, Megan L., Nusbaum, Rachel, Vogel Postula, Kristen J., Weissman, Scott M., Yackowski, Lauren, Vaccari, Erica M., Bissonnette, Jeffrey, Booker, Jessica K., Cremona, M. Laura, Gibellini, Federica, Murphy, Patricia D., Pineda-Alvarez, Daniel E., Pollevick, Guido D., Xu, Zhixiong, Richard, Gabi, Bale, Sherri, Klein, Rachel T., Hruska, Kathleen S., Chung, Wendy K.
Published in Genetics in medicine (01.08.2016)
Published in Genetics in medicine (01.08.2016)
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Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death
ANTZELEVITCH, Charles, POLLEVICK, Guido D, GELBER, Philip, BONAROS, Elias P, BURASHNIKOV, Elena, YUESHENG WU, SARGENT, John D, SCHICKEL, Stefan, OBERHEIDEN, Ralf, BHATIA, Atul, HSU, Li-Fern, HÄÏSSAGUERRE, Michel, CORDEIRO, Jonathan M, SCHIMPF, Rainer, BORGGREFE, Martin, WOLPERT, Christian, CASIS, Oscar, SANGUINETTI, Michael C, AIZAWA, Yoshiyasu, GUERCHICOFF, Alejandra, PFEIFFER, Ryan, OLIVA, Antonio, WOLLNIK, Bernd
Published in Circulation (New York, N.Y.) (30.01.2007)
Published in Circulation (New York, N.Y.) (30.01.2007)
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Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death
Burashnikov, Elena, Pfeiffer, Ryan, Barajas-Martinez, Héctor, Delpón, Eva, Hu, Dan, Desai, Mayurika, Borggrefe, Martin, Häissaguerre, Michel, Kanter, Ronald, Pollevick, Guido D, Guerchicoff, Alejandra, Laiño, Ruben, Marieb, Mark, Nademanee, Koonlawee, Nam, Gi-Byoung, Robles, Roberto, Schimpf, Rainer, Stapleton, Dwight D, Viskin, Sami, Winters, Stephen, Wolpert, Christian, Zimmern, Samuel, Veltmann, Christian, Antzelevitch, Charles
Published in Heart rhythm (01.12.2010)
Published in Heart rhythm (01.12.2010)
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The Homeodomain Transcription Factor Irx5 Establishes the Mouse Cardiac Ventricular Repolarization Gradient
Costantini, Danny L., Arruda, Eric P., Agarwal, Pooja, Kim, Kyoung-Han, Zhu, Yonghong, Zhu, Wei, Lebel, Melanie, Cheng, Chi Wa, Park, Chong Y., Pierce, Stephanie A., Guerchicoff, Alejandra, Pollevick, Guido D., Chan, Toby Y., Kabir, M. Golam, Cheng, Shuk Han, Husain, Mansoor, Antzelevitch, Charles, Srivastava, Deepak, Gross, Gil J., Hui, Chi-chung, Backx, Peter H., Bruneau, Benoit G.
Published in Cell (21.10.2005)
Published in Cell (21.10.2005)
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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation
Ravn, Lasse S, Aizawa, Yoshiyasu, Pollevick, Guido D, Hofman-Bang, Jacob, Cordeiro, Jonathan M, Dixen, Ulrik, Jensen, Gorm, Wu, Yuesheng, Burashnikov, Elena, Haunso, Stig, Guerchicoff, Alejandra, Hu, Dan, Svendsen, Jesper H, Christiansen, Michael, Antzelevitch, Charles
Published in Heart rhythm (01.03.2008)
Published in Heart rhythm (01.03.2008)
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Value of electrocardiographic parameters and ajmaline test in the diagnosis of Brugada syndrome caused by SCN5A mutations
Hong, Kui, Brugada, Josep, Oliva, Antonio, Berruezo-Sanchez, Antonio, Potenza, Domenico, Pollevick, Guido D, Guerchicoff, Alejandra, Matsuo, Kiyotaka, Burashnikov, Elena, Dumaine, Robert, Towbin, Jeffrey A, Nesterenko, Vladislav, Brugada, Pedro, Antzelevitch, Charles, Brugada, Ramon
Published in Circulation (New York, N.Y.) (09.11.2004)
Published in Circulation (New York, N.Y.) (09.11.2004)
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Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant
Crotti, Lia, MD, PhD, Hu, Dan, MD, PhD, Barajas-Martinez, Hector, PhD, De Ferrari, Gaetano M., MD, Oliva, Antonio, MD, PhD, Insolia, Roberto, PhD, Pollevick, Guido D., PhD, Dagradi, Federica, PhD, Guerchicoff, Alejandra, PhD, Greco, Federica, BSc, Schwartz, Peter J., MD, FACC, FAHA, FESC, FHRS, Viskin, Sami, MD, Antzelevitch, Charles, PhD, FHRS, FACC, FAHA
Published in Heart rhythm (01.07.2012)
Published in Heart rhythm (01.07.2012)
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Identification of genes regulated by chronic psychosocial stress and antidepressant treatment in the hippocampus
Alfonso, Julieta, Pollevick, Guido D., Van Der Hart, Marieke G., Flügge, Gabriele, Fuchs, Eberhard, Frasch, Alberto C. C.
Published in The European journal of neuroscience (01.02.2004)
Published in The European journal of neuroscience (01.02.2004)
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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction
Hu, Dan, Viskin, Sami, Oliva, Antonio, Carrier, Tabitha, Cordeiro, Jonathan M, Barajas-Martinez, Hector, Wu, Yuesheng, Burashnikov, Elena, Sicouri, Serge, Brugada, Ramon, Rosso, Rafael, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles
Published in Heart rhythm (01.08.2007)
Published in Heart rhythm (01.08.2007)
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An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing
Kapplinger, Jamie D, Tester, David J, Alders, Marielle, Benito, Begoña, Berthet, Myriam, Brugada, Josep, Brugada, Pedro, Fressart, Véronique, Guerchicoff, Alejandra, Harris-Kerr, Carole, Kamakura, Shiro, Kyndt, Florence, Koopmann, Tamara T, Miyamoto, Yoshihiro, Pfeiffer, Ryan, Pollevick, Guido D, Probst, Vincent, Zumhagen, Sven, Vatta, Matteo, Towbin, Jeffrey A, Shimizu, Wataru, Schulze-Bahr, Eric, Antzelevitch, Charles, Salisbury, Benjamin A, Guicheney, Pascale, Wilde, Arthur A M, Brugada, Ramon, Schott, Jean-Jacques, Ackerman, Michael J
Published in Heart rhythm (01.01.2010)
Published in Heart rhythm (01.01.2010)
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Distinguishing Arrhythmogenic Right Ventricular Cardiomyopathy/Dysplasia–Associated Mutations From Background Genetic Noise
Kapplinger, Jamie D., BA, Landstrom, Andrew P., BS, Salisbury, Benjamin A., PhD, Callis, Thomas E., PhD, Pollevick, Guido D., PhD, Tester, David J., BS, Cox, Moniek G.P.J., MD, Bhuiyan, Zahir, MD, PhD, Bikker, Hennie, PhD, Wiesfeld, Ans C.P., MD, PhD, Hauer, Richard N.W., MD, van Tintelen, J. Peter, MD, PhD, Jongbloed, Jan D.H., PhD, Calkins, Hugh, MD, Judge, Daniel P., MD, Wilde, Arthur A.M., MD, PhD, Ackerman, Michael J., MD, PhD
Published in Journal of the American College of Cardiology (07.06.2011)
Published in Journal of the American College of Cardiology (07.06.2011)
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A Mutation in the β3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype
Hu, Dan, Barajas-Martinez, Hector, Burashnikov, Elena, Springer, Michael, Wu, Yuesheng, Varro, Andras, Pfeiffer, Ryan, Koopmann, Tamara T, Cordeiro, Jonathan M, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles
Published in Circulation. Cardiovascular genetics (01.06.2009)
Published in Circulation. Cardiovascular genetics (01.06.2009)
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Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome
Delpón, Eva, Cordeiro, Jonathan M, Núñez, Lucía, Thomsen, Poul Erik Bloch, Guerchicoff, Alejandra, Pollevick, Guido D, Wu, Yuesheng, Kanters, Jørgen K, Larsen, Carsten Toftager, Hofman-Bang, Jacob, Burashnikov, Elena, Christiansen, Michael, Antzelevitch, Charles
Published in Circulation. Arrhythmia and electrophysiology (01.08.2008)
Published in Circulation. Arrhythmia and electrophysiology (01.08.2008)
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A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype
Hu, Dan, Barajas-Martinez, Hector, Burashnikov, Elena, Springer, Michael, Wu, Yuesheng, Varro, Andras, Pfeiffer, Ryan, Koopmann, Tamara T, Cordeiro, Jonathan M, Guerchicoff, Alejandra, Pollevick, Guido D, Antzelevitch, Charles
Published in Circulation. Cardiovascular genetics (01.06.2009)
Published in Circulation. Cardiovascular genetics (01.06.2009)
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Increased Carrier Detection With Expanded Carrier Screening in Multiple Ancestries [7O]
Griswold, Catherine, Yao, Xinxin (Shirley), Susswein, Lisa R, Fagbemi, Adebanke F, Pollevick, Guido D, Klein, Rachel T
Published in Obstetrics and gynecology (New York. 1953) (01.05.2019)
Published in Obstetrics and gynecology (New York. 1953) (01.05.2019)
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Sudden death associated with short-QT syndrome linked to mutations in HERG
BRUGADA, Ramon, HONG, Kui, BURASHNIKOV, Elena, MATSUO, Kiyotaka, YUE SHENG WU, GUERCHICOFF, Alejandra, BIANCHI, Francesca, GIUSTETTO, Carla, SCHIMPF, Rainer, BRUGADA, Pedro, ANTZELEVITCH, Charles, DUMAINE, Robert, CORDEIRO, Jonathan, GAITA, Fiorenzo, BORGGREFE, Martin, MENENDEZ, Teresa M, BRUGADA, Josep, POLLEVICK, Guido D, WOLPERT, Christian
Published in Circulation (New York, N.Y.) (06.01.2004)
Published in Circulation (New York, N.Y.) (06.01.2004)
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Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias
Hu, Dan, MD, PhD, Viskin, Sami, MD, Oliva, Antonio, MD, Cordeiro, Jonathan M., PhD, Guerchicoff, Alejandra, PhD, Pollevick, Guido D., PhD, Antzelevitch, Charles, PhD
Published in Journal of electrocardiology (01.11.2007)
Published in Journal of electrocardiology (01.11.2007)
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SPECTRUM AND PREVALENCE OF CARDIAC RYANODINE RECEPTOR (RYR2) AND KIR2.1 (KCNJ2) MUTATIONS IN PATIENTS REFERRED FOR FAMILION® CATECHOLAMINERGIC POLYMORPHIC VENTRICULAR TACHYCARDIA (CPVT) GENETIC TESTING
Callis, Thomas E, Carr, Janet L, Susswein, Lisa, Pollevick, Guido D, Ackerman, Michael, Salisbury, Benjamin S
Published in Journal of the American College of Cardiology (27.03.2012)
Published in Journal of the American College of Cardiology (27.03.2012)
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