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Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives

European heart journal, 2015-06, Vol.36 (21), p.1290-1296

2015

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Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

Journal of medical genetics, 2005-10, Vol.42 (10), p.e59-e59

2005

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New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

Journal of the American College of Cardiology, 2015-03, Vol.65 (12), p.1249-1254

2015

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Initial Findings and Reflections of the Australian Genomics Cardiovascular Disorders Flagship

Heart, lung & circulation, 2024-07, Vol.33, p.S110-S111

2024

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Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen–Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT)

International journal of cardiology, 2015-12, Vol.201, p.473-475

2015

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Sudden cardiac death in the young: a clinical genetic approach

Internal medicine journal, 2007-01, Vol.37 (1), p.32-37

2007

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Improving the diagnosis of LV non-compaction with cardiac magnetic resonance imaging

International journal of cardiology, 2015-02, Vol.181, p.430-436

2015

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Clinical audit of a cardiac screening policy in elite Australian cricketers

Journal of science and medicine in sport, 2018-11, Vol.21, p.S61-S61

2018

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The role of diastolic filling in preserving left ventricular stroke volume — An MRI study

International journal of cardiology, 2013-09, Vol.168 (2), p.1596-1598

2013

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A Novel Therapy to Prevent Cardiac Hypertrophy in a Troponin I Mutant Mouse Model

Heart, lung & circulation, 2016-08, Vol.25, p.S73-S73

2016

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A Prospective Study of Sudden Cardiac Death among Children and Young Adults

The New England journal of medicine, 2016-06, Vol.374 (25), p.2441-2452

2016

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The AliveCor handheld heart monitor: Turning your iPhone into a single-lead electrocardiogram (ECG)

Journal of science and medicine in sport, 2013-12, Vol.16, p.e61-e61

2013

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

Heart, lung & circulation, 2015, Vol.24, p.S389-S389

2015

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Assessment of Physical Activity in Hypertrophic Cardiomyopathy

Heart, lung & circulation, 2016-08, Vol.25, p.S4-S4

2016

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Prolonged ECG monitoring unmasks a high prevalence of spontaneous type 1 changes in “drug-induced” Brugada syndrome

Heart, lung & circulation, 2015, Vol.24, p.S405-S405

2015

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Analysis of temporal and spatial variability of spontaneous type 1 brugada ECG: correlation with symptoms and sudden cardiac death events

Heart, lung & circulation, 2015, Vol.24, p.S399-S400

2015

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Sudden cardiac death from genetic heart disease: psychological impact to the surviving at-risk family members

Heart, lung & circulation, 2015, Vol.24, p.S406-S406

2015

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Access, uptake and communication of genetic test results in Australian families with long QT syndrome (LQTS)

Heart, lung & circulation, 2014, Vol.23, p.e7-e7

2014

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Illumina TruSight Cardiomyopathy Sequencing Panel: Application to hypertrophic cardiomyopathy

Heart, lung & circulation, 2014, Vol.23, p.e5-e5

2014

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Clinical and genetic characteristics of hypertrophic cardiomyopathy patients with end-stage disease: A registry-based study

Heart, lung & circulation, 2014, Vol.23, p.e8-e9

2014

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Cost-Effectiveness of the ‘Molecular Autopsy’ in Sudden Unexplained Death in the Young

Heart, lung & circulation, 2012, Vol.21, p.S266-S266

2012

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Athletic Activity for Patients With Hypertrophic Cardiomyopathy and Other Inherited Cardiovascular Diseases: JACC Focus Seminar 3/4

Journal of the American College of Cardiology, 2022-09, Vol.80 (13), p.1268-1283

2022

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Comparison of Apical and Non-Apical HCM: Clinical, Imaging, and Genetic Analysis

Heart, lung & circulation, 2024-07, Vol.33, p.S113-S113

2024

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Manual vs AI Evaluation of LV Mass in HCM Patients in CMR

Heart, lung & circulation, 2024-08, Vol.33, p.S204-S204

2024

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Bioinformatic Re-analysis of Data From the Australian Genomics Cardiovascular Genetic Disorders Flagship

Heart, lung & circulation, 2022, Vol.31, p.S6-S6

2022

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Sudden cardiac death in the young: the molecular autopsy and a practical approach to surviving relatives

Compound and double mutations in patients with hypertrophic cardiomyopathy: implications for genetic testing and counselling

New Perspectives on the Prevalence of Hypertrophic Cardiomyopathy

Initial Findings and Reflections of the Australian Genomics Cardiovascular Disorders Flagship

Rarity and phenotypic heterogeneity provide challenges in the diagnosis of Andersen–Tawil syndrome: Two cases presenting with ECGs mimicking catecholaminergic polymorphic ventricular tachycardia (CPVT)

Sudden cardiac death in the young: a clinical genetic approach

Improving the diagnosis of LV non-compaction with cardiac magnetic resonance imaging

Clinical audit of a cardiac screening policy in elite Australian cricketers

The role of diastolic filling in preserving left ventricular stroke volume — An MRI study

A Novel Therapy to Prevent Cardiac Hypertrophy in a Troponin I Mutant Mouse Model

A Prospective Study of Sudden Cardiac Death among Children and Young Adults

The AliveCor handheld heart monitor: Turning your iPhone into a single-lead electrocardiogram (ECG)

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

Assessment of Physical Activity in Hypertrophic Cardiomyopathy

Prolonged ECG monitoring unmasks a high prevalence of spontaneous type 1 changes in “drug-induced” Brugada syndrome

Analysis of temporal and spatial variability of spontaneous type 1 brugada ECG: correlation with symptoms and sudden cardiac death events

Sudden cardiac death from genetic heart disease: psychological impact to the surviving at-risk family members

Access, uptake and communication of genetic test results in Australian families with long QT syndrome (LQTS)

Illumina TruSight Cardiomyopathy Sequencing Panel: Application to hypertrophic cardiomyopathy

Clinical and genetic characteristics of hypertrophic cardiomyopathy patients with end-stage disease: A registry-based study

Cost-Effectiveness of the ‘Molecular Autopsy’ in Sudden Unexplained Death in the Young

Athletic Activity for Patients With Hypertrophic Cardiomyopathy and Other Inherited Cardiovascular Diseases: JACC Focus Seminar 3/4

Comparison of Apical and Non-Apical HCM: Clinical, Imaging, and Genetic Analysis

Manual vs AI Evaluation of LV Mass in HCM Patients in CMR

Bioinformatic Re-analysis of Data From the Australian Genomics Cardiovascular Genetic Disorders Flagship

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