Mazzarotto, Francesco
Mazzarotto, Francesco
Dipartimento di Medicina Molecolare e Traslazionale
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy
2019-01-01 Horvat, C; Johnson, R; Lam, L; Munro, J; Mazzarotto, F; Roberts, Am; Herman, Ds; Parfenov, M; Haghighi, A; Mcdonough, B; Depalma, Sr; Keogh, Am; Macdonald, Ps; Hayward, Cs; Roberts, A; Barton, Pjr; Felkin, Le; Giannoulatou, E; Cook, Sa; Seidman, Jg; Seidman, Ce; Fatkin, D
A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy
2021-01-01 Smole, T.; Zunkovic, B.; Piculin, M.; Kokalj, E.; Robnik-Sikonja, M.; Kukar, M.; Fotiadis, D. I.; Pezoulas, V. C.; Tachos, N. S.; Barlocco, F.; Mazzarotto, F.; Popovic, D.; Maier, L.; Velicki, L.; Macgowan, G. A.; Olivotto, I.; Filipovic, N.; Jakovljevic, D. G.; Bosnic, Z.
Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy
2020-01-01 Mazzarotto, F.; Olivotto, I.; Walsh, R.
Arrhythmogenic potential of myocardial disarray in hypertrophic cardiomyopathy: genetic basis, functional consequences and relation to sudden cardiac death
2021-01-01 Finocchiaro, G.; Sheikh, N.; Leone, O.; Westaby, J.; Mazzarotto, F.; Pantazis, A.; Ferrantini, C.; Sacconi, L.; Papadakis, M.; Sharma, S.; Sheppard, M. N.; Olivotto, I.
Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency
2022-01-01 Pioner, J. M.; Santini, L.; Palandri, C.; Langione, M.; Grandinetti, B.; Querceto, S.; Martella, D.; Mazzantini, C.; Scellini, B.; Giammarino, L.; Lupi, F.; Mazzarotto, F.; Gowran, A.; Rovina, D.; Santoro, R.; Pompilio, G.; Tesi, C.; Parmeggiani, C.; Regnier, M.; Cerbai, E.; Mack, D. L.; Poggesi, C.; Ferrantini, C.; Coppini, R.
CLINICAL AND GENETIC CHARACTERISTICS OF FAMILIAL DILATED CARDIOMYOPATHY IN A LARGE UK PROSPECTIVE COHORT
2016-01-01 Tayal, U; Buchan, Rj; Whiffin, N; Newsome, S; Mazzarotto, F; Walsh, R; Ware, Js; Cook, S; Prasad, S
Comparison of long-term clinical course and outcome of MYBPC3-versus MYH7-related hypertrophic cardiomyopathy
2019-01-01 Fumagalli, C; Fedele, E; Beltrami, M; Maurizi, N; Passantino, S; Targetti, M; Arretini, A; Baldini, K; Tomberli, A; Mazzarotto, F; Coppini, R; Ferrantini, C; Cecchi, F; Poggesi, C; Olivotto, I
Comparison of long-term outcome in anthracycline-related versus idiopathic dilated cardiomyopathy: a single centre experience
2018-01-01 Fornaro, A; Olivotto, I; Rigacci, L; Ciaccheri, M; Tomberli, B; Ferrantini, C; Coppini, R; Girolami, F; Mazzarotto, F; Chiostri, M; Milli, M; Marchionni, N; Castelli, G
Comprehensive Assessment of Rare Genetic Variation in Dilated Cardiomyopathy Genes in Patients and Controls (vol 101, pg A41, 2015)
2015-01-01 Tayal, U; Mazzarotto, F; Buchan, R; Walsh, R; Barton, P; Ware, J; Cook, S
Comprehensive sequencing of dilated cardiomyopathy genes reveals additive effects of multiple genes on disease risk and severity
2015-01-01 Mazzarotto, F; Walsh, R; Buchan, Rj; John, S; Edwards, Ec; Tayal, U; Prasad, Sk; Barton, Pjr; Ware, Js; Cook, Sa
Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation
2021-01-01 Thompson, A. D.; Helms, A. S.; Kannan, A.; Yob, J.; Lakdawala, N. K.; Wittekind, S. G.; Pereira, A. C.; Jacoby, D. L.; Colan, S. D.; Ashley, E. A.; Saberi, S.; Ware, J. S.; Ingles, J.; Semsarian, C.; Michels, M.; Mazzarotto, F.; Olivotto, I.; Ho, C. Y.; Day, S. M.
Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing?
2020-01-01 Mazzarotto, F.; Olivotto, I.; Boschi, B.; Girolami, F.; Poggesi, C.; Barton, P. J. R.; Walsh, R.
Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center
2019-01-01 Mazzarotto, F; Girolami, F; Boschi, B; Barlocco, F; Tomberli, A; Baldini, K; Coppini, R; Tanini, I; Bardi, S; Contini, E; Cecchi, F; Pelo, E; Cook, Sa; Cerbai, E; Poggesi, C; Torricelli, F; Walsh, R; Olivotto, I
Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning
2022-01-01 Piculin, M.; Smole, T.; Zunkovic, B.; Kokalj, E.; Robnik-Sikonja, M.; Kukar, M.; Fotiadis, D. I.; Pezoulas, V. C.; Tachos, N. S.; Barlocco, F.; Mazzarotto, F.; Popovic, D.; Maier, L. S.; Velicki, L.; Olivotto, I.; Macgowan, G. A.; Jakovljevic, D. G.; Filipovic, N.; Bosnic, Z.
Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions
2021-01-01 Zhang, X.; Walsh, R.; Whiffin, N.; Buchan, R.; Midwinter, W.; Wilk, A.; Govind, R.; Li, N.; Ahmad, M.; Mazzarotto, F.; Roberts, A.; Theotokis, P. I.; Mazaika, E.; Allouba, M.; de Marvao, A.; Pua, C. J.; Day, S. M.; Ashley, E.; Colan, S. D.; Michels, M.; Pereira, A. C.; Jacoby, D.; Ho, C. Y.; Olivotto, I.; Gunnarsson, G. T.; Jefferies, J. L.; Semsarian, C.; Ingles, J.; O'Regan, D. P.; Aguib, Y.; Yacoub, M. H.; Cook, S. A.; Barton, P. J. R.; Bottolo, L.; Ware, J. S.
EFFECTS OF TRUNCATING VARIANTS IN TITIN ON CARDIAC PHENOTYPE AND LEFT VENTRICULAR REMODELLING IN DILATED CARDIOMYOPATHY
2016-01-01 Tayal, U; Buchan, Rj; Whiffin, N; Newsome, S; Mazzarotto, F; Walsh, R; Ware, Js; Prasad, S; Cook, S
Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls
2021-01-01 Walsh, R.; Lahrouchi, N.; Tadros, R.; Kyndt, F.; Glinge, C.; Postema, P. G.; Amin, A. S.; Nannenberg, E. A.; Ware, J. S.; Whiffin, N.; Mazzarotto, F.; Skoric-Milosavljevic, D.; Krijger, C.; Arbelo, E.; Babuty, D.; Barajas-Martinez, H.; Beckmann, B. M.; Bezieau, S.; Bos, J. M.; Breckpot, J.; Campuzano, O.; Castelletti, S.; Celen, C.; Clauss, S.; Corveleyn, A.; Crotti, L.; Dagradi, F.; de Asmundis, C.; Denjoy, I.; Dittmann, S.; Ellinor, P. T.; Ortuno, C. G.; Giustetto, C.; Gourraud, J. -B.; Hazeki, D.; Horie, M.; Ishikawa, T.; Itoh, H.; Kaneko, Y.; Kanters, J. K.; Kimoto, H.; Kotta, M. -C.; Krapels, I. P. C.; Kurabayashi, M.; Lazarte, J.; Leenhardt, A.; Loeys, B. L.; Lundin, C.; Makiyama, T.; Mansourati, J.; Martins, R. P.; Mazzanti, A.; Morner, S.; Napolitano, C.; Ohkubo, K.; Papadakis, M.; Rudic, B.; Molina, M. S.; Sacher, F.; Sahin, H.; Sarquella-Brugada, G.; Sebastiano, R.; Sharma, S.; Sheppard, M. N.; Shimamoto, K.; Shoemaker, M. B.; Stallmeyer, B.; Steinfurt, J.; Tanaka, Y.; Tester, D. J.; Usuda, K.; van der Zwaag, P. A.; Van Dooren, S.; Van Laer, L.; Winbo, A.; Winkel, B. G.; Yamagata, K.; Zumhagen, S.; Volders, P. G. A.; Lubitz, S. A.; Antzelevitch, C.; Platonov, P. G.; Odening, K. E.; Roden, D. M.; Roberts, J. D.; Skinner, J. R.; Tfelt-Hansen, J.; van den Berg, M. P.; Olesen, M. S.; Lambiase, P. D.; Borggrefe, M.; Hayashi, K.; Rydberg, A.; Nakajima, T.; Yoshinaga, M.; Saenen, J. B.; Kaab, S.; Brugada, P.; Robyns, T.; Giachino, D. F.; Ackerman, M. J.; Brugada, R.; Brugada, J.; Gimeno, J. R.; Hasdemir, C.; Guicheney, P.; Priori, S. G.; Schulze-Bahr, E.; Makita, N.; Schwartz, P. J.; Shimizu, W.; Aiba, T.; Schott, J. -J.; Redon, R.; Ohno, S.; Probst, V.; Arnaout, A. A.; Amelot, M.; Anselme, F.; Billon, O.; Defaye, P.; Dupuis, J. -M.; Jesel, L.; Laurent, G.; Maury, P.; Pasquie, J. -L.; Wiart, F.; Behr, E. R.; Barc, J.; Bezzina, C. R.
Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death
2021-01-01 Walsh, Roddy; Adler, Arnon; Amin, Ahmad S; Abiusi, Emanuela; Care, Melanie; Bikker, Hennie; Amenta, Simona; Feilotter, Harriet; Nannenberg, Eline A; Mazzarotto, Francesco; Trevisan, Valentina; Garcia, John; Hershberger, Ray E; Perez, Marco V; Sturm, Amy C; Ware, James S; Zareba, Wojciech; Novelli, Valeria; Wilde, Arthur A M; Gollob, Michael H
Evidence-Based Assessment of Genes in Dilated Cardiomyopathy
2021-01-01 Jordan, E.; Peterson, L.; Ai, T.; Asatryan, B.; Bronicki, L.; Brown, E.; Celeghin, R.; Edwards, M.; Fan, J.; Ingles, J.; James, C. A.; Jarinova, O.; Johnson, R.; Judge, D. P.; Lahrouchi, N.; Lekanne Deprez, R. H.; Lumbers, R. T.; Mazzarotto, F.; Medeiros Domingo, A.; Miller, R. L.; Morales, A.; Murray, B.; Peters, S.; Pilichou, K.; Protonotarios, A.; Semsarian, C.; Shah, P.; Syrris, P.; Thaxton, C.; Van Tintelen, J. P.; Walsh, R.; Wang, J.; Ware, J.; Hershberger, R. E.
Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies
2023-01-01 Lipov, A.; Jurgens, S. J.; Mazzarotto, F.; Allouba, M.; Pirruccello, J. P.; Aguib, Y.; Gennarelli, M.; Yacoub, M. H.; Ellinor, P. T.; Bezzina, C. R.; Walsh, R.
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathy | 1-gen-2019 | Horvat, C; Johnson, R; Lam, L; Munro, J; Mazzarotto, F; Roberts, Am; Herman, Ds; Parfenov, M; Haghighi, A; Mcdonough, B; Depalma, Sr; Keogh, Am; Macdonald, Ps; Hayward, Cs; Roberts, A; Barton, Pjr; Felkin, Le; Giannoulatou, E; Cook, Sa; Seidman, Jg; Seidman, Ce; Fatkin, D | |
| A machine learning-based risk stratification model for ventricular tachycardia and heart failure in hypertrophic cardiomyopathy | 1-gen-2021 | Smole, T.; Zunkovic, B.; Piculin, M.; Kokalj, E.; Robnik-Sikonja, M.; Kukar, M.; Fotiadis, D. I.; Pezoulas, V. C.; Tachos, N. S.; Barlocco, F.; Mazzarotto, F.; Popovic, D.; Maier, L.; Velicki, L.; Macgowan, G. A.; Olivotto, I.; Filipovic, N.; Jakovljevic, D. G.; Bosnic, Z. | |
| Advantages and Perils of Clinical Whole-Exome and Whole-Genome Sequencing in Cardiomyopathy | 1-gen-2020 | Mazzarotto, F.; Olivotto, I.; Walsh, R. | |
| Arrhythmogenic potential of myocardial disarray in hypertrophic cardiomyopathy: genetic basis, functional consequences and relation to sudden cardiac death | 1-gen-2021 | Finocchiaro, G.; Sheikh, N.; Leone, O.; Westaby, J.; Mazzarotto, F.; Pantazis, A.; Ferrantini, C.; Sacconi, L.; Papadakis, M.; Sharma, S.; Sheppard, M. N.; Olivotto, I. | |
| Calcium handling maturation and adaptation to increased substrate stiffness in human iPSC-derived cardiomyocytes: The impact of full-length dystrophin deficiency | 1-gen-2022 | Pioner, J. M.; Santini, L.; Palandri, C.; Langione, M.; Grandinetti, B.; Querceto, S.; Martella, D.; Mazzantini, C.; Scellini, B.; Giammarino, L.; Lupi, F.; Mazzarotto, F.; Gowran, A.; Rovina, D.; Santoro, R.; Pompilio, G.; Tesi, C.; Parmeggiani, C.; Regnier, M.; Cerbai, E.; Mack, D. L.; Poggesi, C.; Ferrantini, C.; Coppini, R. | |
| CLINICAL AND GENETIC CHARACTERISTICS OF FAMILIAL DILATED CARDIOMYOPATHY IN A LARGE UK PROSPECTIVE COHORT | 1-gen-2016 | Tayal, U; Buchan, Rj; Whiffin, N; Newsome, S; Mazzarotto, F; Walsh, R; Ware, Js; Cook, S; Prasad, S | |
| Comparison of long-term clinical course and outcome of MYBPC3-versus MYH7-related hypertrophic cardiomyopathy | 1-gen-2019 | Fumagalli, C; Fedele, E; Beltrami, M; Maurizi, N; Passantino, S; Targetti, M; Arretini, A; Baldini, K; Tomberli, A; Mazzarotto, F; Coppini, R; Ferrantini, C; Cecchi, F; Poggesi, C; Olivotto, I | |
| Comparison of long-term outcome in anthracycline-related versus idiopathic dilated cardiomyopathy: a single centre experience | 1-gen-2018 | Fornaro, A; Olivotto, I; Rigacci, L; Ciaccheri, M; Tomberli, B; Ferrantini, C; Coppini, R; Girolami, F; Mazzarotto, F; Chiostri, M; Milli, M; Marchionni, N; Castelli, G | |
| Comprehensive Assessment of Rare Genetic Variation in Dilated Cardiomyopathy Genes in Patients and Controls (vol 101, pg A41, 2015) | 1-gen-2015 | Tayal, U; Mazzarotto, F; Buchan, R; Walsh, R; Barton, P; Ware, J; Cook, S | |
| Comprehensive sequencing of dilated cardiomyopathy genes reveals additive effects of multiple genes on disease risk and severity | 1-gen-2015 | Mazzarotto, F; Walsh, R; Buchan, Rj; John, S; Edwards, Ec; Tayal, U; Prasad, Sk; Barton, Pjr; Ware, Js; Cook, Sa | |
| Computational prediction of protein subdomain stability in MYBPC3 enables clinical risk stratification in hypertrophic cardiomyopathy and enhances variant interpretation | 1-gen-2021 | Thompson, A. D.; Helms, A. S.; Kannan, A.; Yob, J.; Lakdawala, N. K.; Wittekind, S. G.; Pereira, A. C.; Jacoby, D. L.; Colan, S. D.; Ashley, E. A.; Saberi, S.; Ware, J. S.; Ingles, J.; Semsarian, C.; Michels, M.; Mazzarotto, F.; Olivotto, I.; Ho, C. Y.; Day, S. M. | |
| Contemporary Insights Into the Genetics of Hypertrophic Cardiomyopathy: Toward a New Era in Clinical Testing? | 1-gen-2020 | Mazzarotto, F.; Olivotto, I.; Boschi, B.; Girolami, F.; Poggesi, C.; Barton, P. J. R.; Walsh, R. | |
| Defining the diagnostic effectiveness of genes for inclusion in panels: the experience of two decades of genetic testing for hypertrophic cardiomyopathy at a single center | 1-gen-2019 | Mazzarotto, F; Girolami, F; Boschi, B; Barlocco, F; Tomberli, A; Baldini, K; Coppini, R; Tanini, I; Bardi, S; Contini, E; Cecchi, F; Pelo, E; Cook, Sa; Cerbai, E; Poggesi, C; Torricelli, F; Walsh, R; Olivotto, I | |
| Disease Progression of Hypertrophic Cardiomyopathy: Modeling Using Machine Learning | 1-gen-2022 | Piculin, M.; Smole, T.; Zunkovic, B.; Kokalj, E.; Robnik-Sikonja, M.; Kukar, M.; Fotiadis, D. I.; Pezoulas, V. C.; Tachos, N. S.; Barlocco, F.; Mazzarotto, F.; Popovic, D.; Maier, L. S.; Velicki, L.; Olivotto, I.; Macgowan, G. A.; Jakovljevic, D. G.; Filipovic, N.; Bosnic, Z. | |
| Disease-specific variant pathogenicity prediction significantly improves variant interpretation in inherited cardiac conditions | 1-gen-2021 | Zhang, X.; Walsh, R.; Whiffin, N.; Buchan, R.; Midwinter, W.; Wilk, A.; Govind, R.; Li, N.; Ahmad, M.; Mazzarotto, F.; Roberts, A.; Theotokis, P. I.; Mazaika, E.; Allouba, M.; de Marvao, A.; Pua, C. J.; Day, S. M.; Ashley, E.; Colan, S. D.; Michels, M.; Pereira, A. C.; Jacoby, D.; Ho, C. Y.; Olivotto, I.; Gunnarsson, G. T.; Jefferies, J. L.; Semsarian, C.; Ingles, J.; O'Regan, D. P.; Aguib, Y.; Yacoub, M. H.; Cook, S. A.; Barton, P. J. R.; Bottolo, L.; Ware, J. S. | |
| EFFECTS OF TRUNCATING VARIANTS IN TITIN ON CARDIAC PHENOTYPE AND LEFT VENTRICULAR REMODELLING IN DILATED CARDIOMYOPATHY | 1-gen-2016 | Tayal, U; Buchan, Rj; Whiffin, N; Newsome, S; Mazzarotto, F; Walsh, R; Ware, Js; Prasad, S; Cook, S | |
| Enhancing rare variant interpretation in inherited arrhythmias through quantitative analysis of consortium disease cohorts and population controls | 1-gen-2021 | Walsh, R.; Lahrouchi, N.; Tadros, R.; Kyndt, F.; Glinge, C.; Postema, P. G.; Amin, A. S.; Nannenberg, E. A.; Ware, J. S.; Whiffin, N.; Mazzarotto, F.; Skoric-Milosavljevic, D.; Krijger, C.; Arbelo, E.; Babuty, D.; Barajas-Martinez, H.; Beckmann, B. M.; Bezieau, S.; Bos, J. M.; Breckpot, J.; Campuzano, O.; Castelletti, S.; Celen, C.; Clauss, S.; Corveleyn, A.; Crotti, L.; Dagradi, F.; de Asmundis, C.; Denjoy, I.; Dittmann, S.; Ellinor, P. T.; Ortuno, C. G.; Giustetto, C.; Gourraud, J. -B.; Hazeki, D.; Horie, M.; Ishikawa, T.; Itoh, H.; Kaneko, Y.; Kanters, J. K.; Kimoto, H.; Kotta, M. -C.; Krapels, I. P. C.; Kurabayashi, M.; Lazarte, J.; Leenhardt, A.; Loeys, B. L.; Lundin, C.; Makiyama, T.; Mansourati, J.; Martins, R. P.; Mazzanti, A.; Morner, S.; Napolitano, C.; Ohkubo, K.; Papadakis, M.; Rudic, B.; Molina, M. S.; Sacher, F.; Sahin, H.; Sarquella-Brugada, G.; Sebastiano, R.; Sharma, S.; Sheppard, M. N.; Shimamoto, K.; Shoemaker, M. B.; Stallmeyer, B.; Steinfurt, J.; Tanaka, Y.; Tester, D. J.; Usuda, K.; van der Zwaag, P. A.; Van Dooren, S.; Van Laer, L.; Winbo, A.; Winkel, B. G.; Yamagata, K.; Zumhagen, S.; Volders, P. G. A.; Lubitz, S. A.; Antzelevitch, C.; Platonov, P. G.; Odening, K. E.; Roden, D. M.; Roberts, J. D.; Skinner, J. R.; Tfelt-Hansen, J.; van den Berg, M. P.; Olesen, M. S.; Lambiase, P. D.; Borggrefe, M.; Hayashi, K.; Rydberg, A.; Nakajima, T.; Yoshinaga, M.; Saenen, J. B.; Kaab, S.; Brugada, P.; Robyns, T.; Giachino, D. F.; Ackerman, M. J.; Brugada, R.; Brugada, J.; Gimeno, J. R.; Hasdemir, C.; Guicheney, P.; Priori, S. G.; Schulze-Bahr, E.; Makita, N.; Schwartz, P. J.; Shimizu, W.; Aiba, T.; Schott, J. -J.; Redon, R.; Ohno, S.; Probst, V.; Arnaout, A. A.; Amelot, M.; Anselme, F.; Billon, O.; Defaye, P.; Dupuis, J. -M.; Jesel, L.; Laurent, G.; Maury, P.; Pasquie, J. -L.; Wiart, F.; Behr, E. R.; Barc, J.; Bezzina, C. R. | |
| Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death | 1-gen-2021 | Walsh, Roddy; Adler, Arnon; Amin, Ahmad S; Abiusi, Emanuela; Care, Melanie; Bikker, Hennie; Amenta, Simona; Feilotter, Harriet; Nannenberg, Eline A; Mazzarotto, Francesco; Trevisan, Valentina; Garcia, John; Hershberger, Ray E; Perez, Marco V; Sturm, Amy C; Ware, James S; Zareba, Wojciech; Novelli, Valeria; Wilde, Arthur A M; Gollob, Michael H | |
| Evidence-Based Assessment of Genes in Dilated Cardiomyopathy | 1-gen-2021 | Jordan, E.; Peterson, L.; Ai, T.; Asatryan, B.; Bronicki, L.; Brown, E.; Celeghin, R.; Edwards, M.; Fan, J.; Ingles, J.; James, C. A.; Jarinova, O.; Johnson, R.; Judge, D. P.; Lahrouchi, N.; Lekanne Deprez, R. H.; Lumbers, R. T.; Mazzarotto, F.; Medeiros Domingo, A.; Miller, R. L.; Morales, A.; Murray, B.; Peters, S.; Pilichou, K.; Protonotarios, A.; Semsarian, C.; Shah, P.; Syrris, P.; Thaxton, C.; Van Tintelen, J. P.; Walsh, R.; Wang, J.; Ware, J.; Hershberger, R. E. | |
| Exploring the complex spectrum of dominance and recessiveness in genetic cardiomyopathies | 1-gen-2023 | Lipov, A.; Jurgens, S. J.; Mazzarotto, F.; Allouba, M.; Pirruccello, J. P.; Aguib, Y.; Gennarelli, M.; Yacoub, M. H.; Ellinor, P. T.; Bezzina, C. R.; Walsh, R. |