Molecular autopsy in victims of inherited arrhythmias

Por Semsarian, Christopher, Ingles, Jodie
Publicado no J Arrhythm (2016)

Routinely collected health data to study inherited heart disease: a systematic review (2000–2016)

Por Blanch, Bianca, Sweeting, Joanna, Semsarian, Christopher, Ingles, Jodie
Publicado no Open Heart (2017)

Attitudes, knowledge and consequences of uncertain genetic findings in hypertrophic cardiomyopathy

Por Burns, Charlotte, Yeates, Laura, Spinks, Catherine, Semsarian, Christopher, Ingles, Jodie
Publicado no Eur J Hum Genet (2017)

Physical activity in hypertrophic cardiomyopathy: prevalence of inactivity and perceived barriers

Por Sweeting, Joanna, Ingles, Jodie, Timperio, Anna, Patterson, Jillian, Ball, Kylie, Semsarian, Christopher
Publicado no Open Heart (2016)

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

Por Lam, Lien, Ingles, Jodie, Turner, Christian, Kilborn, Michael, Bagnall, Richard D., Semsarian, Christopher
Publicado no HeartRhythm Case Rep (2015)

LAMP2 shines a light on cardiomyopathy in an athlete

Por Martin, Sophie, Ingles, Jodie, Hunyor, Imre, Bagnall, Richard D., Puranik, Rajesh, Semsarian, Christopher
Publicado no HeartRhythm Case Rep (2017)

Clinical and genetic features of Australian families with long QT syndrome: A registry-based study

Por Burns, Charlotte, Ingles, Jodie, Davis, Andrew M., Connell, Vanessa, Gray, Belinda, Hunt, Lauren, McGaughran, Julie, Semsarian, Christopher
Publicado no J Arrhythm (2016)

A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia

Por Gray, Belinda, Bagnall, Richard D., Lam, Lien, Ingles, Jodie, Turner, Christian, Haan, Eric, Davis, Andrew, Yang, Pei-Chi, Clancy, Colleen E., Sy, Raymond W., Semsarian, Christopher
Publicado no Heart Rhythm (2016)