A novel desmocollin-2 mutation reveals insights into the molecular link between desmosomes and gap junctions

by Gehmlich, Katja, Lambiase, Pier D., Asimaki, Angeliki, Ciaccio, Edward J., Ehler, Elisabeth, Syrris, Petros, Saffitz, Jeffrey E., McKenna, William J.
Published 2011

Arrhythmogenic right ventricular cardiomyopathy/dysplasia on the basis of the revised diagnostic criteria in affected families with desmosomal mutations

by Protonotarios, Nikos, Anastasakis, Aris, Antoniades, Loizos, Chlouverakis, Gregory, Syrris, Petros, Basso, Cristina, Asimaki, Angeliki, Theopistou, Artemisia, Stefanadis, Christodoulos, Thiene, Gaetano, McKenna, William J., Tsatsopoulou, Adalena
Published 2011

A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity

by Andersen, Paal Skytt, Hedley, Paula Louise, Page, Stephen P., Syrris, Petros, Moolman-Smook, Johanna Catharina, McKenna, William John, Elliott, Perry Mark, Christiansen, Michael
Published 2012

Genetic complexity in hypertrophic cardiomyopathy revealed by high-throughput sequencing

by Lopes, Luis R, Zekavati, Anna, Syrris, Petros, Hubank, Mike, Giambartolomei, Claudia, Dalageorgou, Chrysoula, Jenkins, Sharon, McKenna, William, Plagnol, Vincent, Elliott, Perry M
Published 2013

It's not just the mitral valve - abnormal motion of the whole aorto-mitral apparatus occurs in both overt and subclinical hypertrophic cardiomyopathy

by Obianyo, Chinwe, Captur, Gaby, Syrris, Petros, Lopes, Luis, Patel, Vimal, Reant, Patricia, Mirabel, Mariana, Manisty, Charlotte, Bassett, Paul, Sado, Daniel, Talmud, Phillippa, Elliott, Perry M, Moon, James C
Published 2016

Mechanistic insights into arrhythmogenic right ventricular cardiomyopathy caused by desmocollin-2 mutations

by Gehmlich, Katja, Syrris, Petros, Peskett, Emma, Evans, Alison, Ehler, Elisabeth, Asimaki, Angeliki, Anastasakis, Aris, Tsatsopoulou, Adalena, Vouliotis, Apostolos-Ilias, Stefanadis, Christodoulos, Saffitz, Jeffrey E., Protonotarios, Nikos, McKenna, William J.
Published 2011

Electrophysiological abnormalities precede overt structural changes in arrhythmogenic right ventricular cardiomyopathy due to mutations in desmoplakin-A combined murine and human s...

by Gomes, John, Finlay, Malcolm, Ahmed, Akbar K., Ciaccio, Edward J., Asimaki, Angeliki, Saffitz, Jeffrey E., Quarta, Giovanni, Nobles, Muriel, Syrris, Petros, Chaubey, Sanjay, McKenna, William J., Tinker, Andrew, Lambiase, Pier D.
Published 2012

Abnormal septal convexity into the left ventricle occurs in subclinical hypertrophic cardiomyopathy

by Reant, Patricia, Captur, Gabriella, Mirabel, Mariana, Nasis, Arthur, M. Sado, Daniel, Maestrini, Viviana, Castelletti, Silvia, Manisty, Charlotte, Herrey, Anna S., Syrris, Petros, Tome-Esteban, Maite, Jenkins, Sharon, Elliott, Perry M., McKenna, William J., Moon, James C.
Published 2015

Novel genotype–phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy

by Lopes, Luis R, Syrris, Petros, Guttmann, Oliver P, O'Mahony, Constantinos, Tang, Hak Chiaw, Dalageorgou, Chrysoula, Jenkins, Sharon, Hubank, Mike, Monserrat, Lorenzo, McKenna, William J, Plagnol, Vincent, Elliott, Perry M
Published 2015

Dynamic Conduction and Repolarisation Changes in Early Arrhythmogenic Right Ventricular Cardiomyopathy versus Benign Outflow Tract Ectopy Demonstrated by High Density Mapping & Pac...

by Finlay, Malcolm C., Ahmed, Akbar K., Sugrue, Alan, Bhar-Amato, Justine, Quarta, Giovanni, Pantazis, Antonis, Ciaccio, Edward J., Syrris, Petros, Sen-Chowdhry, Srijita, Ben-Simon, Ron, Chow, Anthony W., Lowe, Martin D., Segal, Oliver R., McKenna, William J., Lambiase, Pier D.
Published 2014