Molecular autopsy in victims of inherited arrhythmias

por Semsarian, Christopher, Ingles, Jodie
Publicado 2016

What do we do and how do we do it? Assessing genetic counselling in the modern era

por Yeates, Laura, McEwen, Alison, Ingles, Jodie
Publicado 2020

Sex Differences in Hypertrophic Cardiomyopathy: Interaction With Genetics and Environment

por Butters, Alexandra, Lakdawala, Neal K., Ingles, Jodie
Publicado 2021

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

por Blanch, Bianca, Sweeting, Joanna, Semsarian, Christopher, Ingles, Jodie
Publicado 2017

Evaluating a custom-designed aid to improve communication of genetic results in families with hypertrophic cardiomyopathy: study protocol for a randomised controlled trial

por Burns, Charlotte, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie
Publicado 2019

Sudden Cardiac Arrest in the Paediatric Population

por Franciosi, Sonia, Abrams, Dominic J., Ingles, Jodie, Sanatani, Shubhayan
Publicado 2022

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

por Smagarinsky, Yana, Burns, Charlotte, Spinks, Catherine, Semsarian, Christopher, Ingles, Jodie
Publicado 2017

Needs analysis of parents following sudden cardiac death in the young

por McDonald, Kristie, Sharpe, Louise, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie
Publicado 2020

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 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 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 2017

Rare desmin variant causing penetrant life-threatening arrhythmic cardiomyopathy

por Oomen, Ad W.G.J., Jones, Katherine, Yeates, Laura, Semsarian, Christopher, Ingles, Jodie, Sy, Raymond W.
Publicado 2018

Doctor-patient care relationship in genetic cardiomyopathies: An exploratory study on clinical consultations

por Fioretti, Chiara, Magni, Elisa, Barlocco, Fausto, Tomberli, Alessia, Baldini, Katia, Ingles, Jodie, Smorti, Andrea, Olivotto, Iacopo
Publicado 2020

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 2016

Using codesign focus groups to develop an online COmmunity suPporting familiEs after Sudden Cardiac Death (COPE-SCD) in the young

por Yeates, Laura, Gardner, Karen, Do, Judy, van den Heuvel, Lieke, Fleming, Gabrielle, Semsarian, Christopher, McEwen, Alison, Adlard, Leesa, Ingles, Jodie
Publicado 2022

The Australian Genetic Heart Disease Registry: Protocol for a Data Linkage Study

por Butters, Alexandra, Blanch, Bianca, Kemp-Casey, Anna, Do, Judy, Yeates, Laura, Leslie, Felicity, Semsarian, Christopher, Nedkoff, Lee, Briffa, Tom, Ingles, Jodie, Sweeting, Joanna
Publicado 2023

Patients With Genetic Heart Disease and COVID-19: A Cardiac Society of Australia and New Zealand (CSANZ) Consensus Statement

por Gray, Belinda, Semsarian, Christopher, Fatkin, Diane, Ingles, Jodie, Atherton, John J., Davis, Andrew M., Sanders, Prashanthan, Pachter, Nicholas, Skinner, Jonathan R., Stiles, Martin K.
Publicado 2020

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

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

Genetic architecture of left ventricular noncompaction in adults

por Ross, Samantha Barratt, Singer, Emma S., Driscoll, Elizabeth, Nowak, Natalie, Yeates, Laura, Puranik, Rajesh, Sy, Raymond W., Rajagopalan, Sulekha, Barratt, Alexandra, Ingles, Jodie, Bagnall, Richard D., Semsarian, Christopher
Publicado 2020

A prospective longitudinal study of health-related quality of life and psychological wellbeing after an implantable cardioverter-defibrillator in patients with genetic heart diseas...

por van den Heuvel, Lieke M., Sarina, Tanya, Sweeting, Joanna, Yeates, Laura, Bates, Kezia, Spinks, Catherine, O’Donnell, Catherine, Sears, Samuel F., McGeechan, Kevin, Semsarian, Christopher, Ingles, Jodie
Publicado 2022