Genetic Basis of Sudden Unexpected Death in Epilepsy

by Richard D. Bagnall, Richard D. Bagnall, Douglas E. Crompton, Douglas E. Crompton, Christopher Semsarian, Christopher Semsarian, Christopher Semsarian
Published 2017-07-01

Characterization of the first induced pluripotent stem cell line generated from a patient with autosomal dominant catecholaminergic polymorphic ventricular tachycardia due to a het...

by Samantha Ross, Mira Holliday, Seakcheng Lim, Christopher Semsarian
Published 2019-05-01

Generation of an induced pluripotent stem cell line from a hypertrophic cardiomyopathy patient with a pathogenic myosin binding protein C (MYBPC3) p.Arg502Trp mutation

by Mira Holliday, Samantha Barratt Ross, Seakcheng Lim, Christopher Semsarian
Published 2018-12-01

Generation of induced pluripotent stem cells (iPSCs) from a hypertrophic cardiomyopathy patient with the pathogenic variant p.Val698Ala in beta-myosin heavy chain (MYH7) gene

by Samantha Barratt Ross, Stuart T. Fraser, Natalie Nowak, Christopher Semsarian
Published 2017-04-01

Development of a communication aid for explaining hypertrophic cardiomyopathy genetic test results

by Yana Smagarinsky, Charlotte Burns, Catherine Spinks, Christopher Semsarian, Jodie Ingles
Published 2017-11-01

Peripheral blood derived induced pluripotent stem cells (iPSCs) from a female with familial hypertrophic cardiomyopathy

by Samantha Barratt Ross, Stuart T. Fraser, Richard D. Bagnall, Christopher Semsarian
Published 2017-04-01

Needs analysis of parents following sudden cardiac death in the young

by Christopher Semsarian, Laura Yeates, Jodie Ingles, Kristie McDonald, Louise Sharpe
Published 2020-12-01

Left Ventricular Non-Compaction: Review of the Current Diagnostic Challenges and Consequences in Athletes

by Giuseppe Femia, Christopher Semsarian, Samantha B. Ross, David Celermajer, Rajesh Puranik
Published 2020-12-01

Long term CMR follow up of patients with right ventricular abnormality and clinically suspected arrhythmogenic right ventricular cardiomyopathy (ARVC)

by Giuseppe Femia, Christopher Semsarian, Mark McGuire, Raymond W. Sy, Rajesh Puranik
Published 2019-12-01

Global microRNA profiling of the mouse ventricles during development of severe hypertrophic cardiomyopathy and heart failure.

by Richard D Bagnall, Tatiana Tsoutsman, Rhian E Shephard, William Ritchie, Christopher Semsarian
Published 2012-01-01

Are Variants Causing Cardiac Arrhythmia Risk Factors in Sudden Unexpected Death in Epilepsy?

by Lauren E. Bleakley, Ming S. Soh, Richard D. Bagnall, Richard D. Bagnall, Lynette G. Sadleir, Samuel Gooley, Christopher Semsarian, Christopher Semsarian, Ingrid E. Scheffer, Ingrid E. Scheffer, Ingrid E. Scheffer, Samuel F. Berkovic, Christopher A. Reid
Published 2020-09-01

Molecular autopsy in victims of inherited arrhythmias

by Christopher Semsarian, MBBS, PhD, MPH, Jodie Ingles, BBiomedSci, GradDipGenCouns, PhD, MPH
Published 2016-10-01

Development of induced pluripotent stem cells from a patient with hypertrophic cardiomyopathy who carries the pathogenic myosin heavy chain 7 mutation p.Arg403Gln

by Mira Holliday, Samantha Barratt Ross, Seakcheng Lim, Melissa Mangala, Adam Hill, Henrietta Cserne Szappanos, Livia Hool, Christopher Semsarian
Published 2018-12-01

Relations between right ventricular morphology and clinical, electrical and genetic parameters in Brugada Syndrome.

by Belinda Gray, Ganesh Kumar Gnanappa, Richard D Bagnall, Giuseppe Femia, Laura Yeates, Jodie Ingles, Charlotte Burns, Rajesh Puranik, Stuart M Grieve, Christopher Semsarian, Raymond W Sy
Published 2018-01-01

Electrophysiological and Structural Remodeling of the Atria in a Mouse Model of Troponin-I Mutation Linked Hypertrophic Cardiomyopathy: Implications for Atrial Fibrillation

by Wei-Wen Lim, Melissa Neo, Shivshankar Thanigaimani, Pawel Kuklik, Anand N. Ganesan, Dennis H. Lau, Tatiana Tsoutsman, Jonathan M. Kalman, Christopher Semsarian, David A. Saint, Prashanthan Sanders
Published 2021-06-01

LAMP2 shines a light on cardiomyopathy in an athlete

by Sophie Martin, MBBS, Jodie Ingles, BBiomedSci, PhD, MPH, Imre Hunyor, MBBS, DPhil, Richard D. Bagnall, BSc, PhD, Rajesh Puranik, MBBS, PhD, Christopher Semsarian, MBBS, PhD, MPH, FHRS
Published 2017-03-01

Holt-Oram syndrome in two families diagnosed with left ventricular noncompaction and conduction disease

by Samantha Barratt Ross, BMedSci, Richard D. Bagnall, BS, PhD, Laura Yeates, BS, GradDipGenCouns, Raymond W. Sy, MBBS, PhD, FHRS, Christopher Semsarian, MBBS, PhD, MPH, FHRS
Published 2018-04-01

Exome sequencing identifies a novel mutation in the MYH6 gene in a family with early-onset sinus node dysfunction, ventricular arrhythmias, and cardiac arrest

by Lien Lam, BSc, PhD, Jodie Ingles, BBiomed Sci, PhD, MPH, Christian Turner, MBBS, Michael Kilborn, MBBS, PhD, Richard D. Bagnall, BSc, PhD, Christopher Semsarian, MBBS, PhD, MPH, FHRS
Published 2015-05-01

Genetic variants associated with inherited cardiovascular disorders among 13,131 asymptomatic older adults of European descent

by Paul Lacaze, Robert Sebra, Moeen Riaz, Jodie Ingles, Jane Tiller, Bryony A. Thompson, Paul A. James, Diane Fatkin, Christopher Semsarian, Christopher M. Reid, Andrew M. Tonkin, Ingrid Winship, Eric Schadt, John J. McNeil
Published 2021-06-01

Loss‐of‐function variants in Kv11.1 cardiac channels as a biomarker for SUDEP

by Ming S. Soh, Richard D. Bagnall, Mark F. Bennett, Lauren E. Bleakley, Erlina S. Mohamed Syazwan, A. Marie Phillips, Mathew D. F. Chiam, Chaseley E. McKenzie, Michael Hildebrand, Douglas Crompton, Melanie Bahlo, Christopher Semsarian, Ingrid E. Scheffer, Samuel F. Berkovic, Christopher A. Reid
Published 2021-07-01