Articles

2024:

• Genetic Testing Yield and Clinical Characteristics of Hypertrophic Cardiomyopathy in Understudied Ethnic Groups Insights From a New Zealand National Registry2022:
• An international multicenter cohort study on implantable cardioverter defibrillators for the treatment of symptomatic children with catecholaminergic polymorphic ventricular tachycardia
• Ebstein’s anomaly- an electrophysiological perspective
• Perspectives and experiences of Māori and Pasifika peoples living with cardiac inherited disease- a qualitative study

2020:

• 2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families
• Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells
• Genetic Cardiovascular Conditions – It’s All About Family
• Genetic testing in Polynesian long QT syndrome probands reveals a lower diagnostic yield and an increased prevalence of rare variants
• Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
• How Patient Perceptions Shape Responses and Outcomes in Inherited Cardiac Conditions
• Normative Heart-Rate Corrected Values for Reploarisation Length From Holter Recordings in Children and Adults
• The trajectory of anxiety and depression in people presenting to a cardiac inherited disease service: a longitudinal study
• Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome

2019:

• Catecholaminergic Polymorphic Ventricular Tachycardia: The Cardiac Arrest Where Epinephrine Is Contraindicated
• Inplantable cardioverter-defibrillators in previously undiagnosed patients with CPVT resuscitated from sudden cardiac arrest

2018:

• Channelopathies That Lead to Sudden Cardiac Death – Clinical and Genetic Aspects
• Clinical Outcomes and Modes of Death in Timothy Syndrome
• Development of a cardiac inherited disease service and clinic registry – A 15-year perspective
• Genomic medicine must reduce, not compound, health inequities the case for hauora-enhancing genomic resources for New Zealand
• Long QT molecular autopsy in sudden unexplained death in the young (1-40 years old) Lessons learnt from an eight year experience in New Zealand
• Penetrance and expressivity of the R858H CACNA1C variant in a five‐generation pedigree segregating an arrhythmogenic channelopathy
• SCN5A mutations in 442 neonates and children genotype phenotype correlation and identification of higher risk subgroups

2017:

• How to measure a QT interval
• Massively Parallel Sequencing of Genes Implicated in Heritable Cardiac Disorders A Strategy for a Small Diagnostic Laboratory
• Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome
• Utility of Post-Mortem Genetic Testing in Cases of Sudden Arrhythmic Death Syndrome

2016:

• A prospective study of sudden cardiac death amoung children and young adults
• Computational cardiology and risk stratification for sudden cardiac death one of the grand challenges for cardiology in the 21st century
• Detection of sudden death syndromes in New Zealand
• Inpatient detection of cardiac-inherited disease the impact of improving family history taking
• Sudden Infant Death QT or Not QT That Is No Longer the Question
• Update on the Diagnosis and Management of Familial LQTS

2015:

• Array comparative genomic hybridization identifies a heterozygous deletion of exon 3 of the RYR2 gene
• Cardiac genetic investigation of sudden cardiac death advances and remaining limitations
• Physical and Psychological consequences of left sympathetic Denervation in Long-QT Syndrome

2014:

• Array Comparative Genomic Hybridization Identifies a Heterozygous Deletion of the Entire kcnj2 gene as a cause of Sudden Cardiac Death
• Expression of a Mutant kcnj2 Gene Transcript in Zebrafish
• Long QT molecular autopsy in sudden infant death syndrome
• Must every child with long QT syndrome take a beta blocker
• Single nucleotide polymorphisms in arrythmia genes modify the risk of cardiac events and sudden death in long QT syndrome

2013:

• Community detection of long QT syndrome with a clinical registry – An alternative to ECG screening programs
• Telltale Hearts

2012:

• Investigation following resuscitated cardiac arrest

2011:

• Symptoms and Signs Associated with Syncope in Young People with Primary Cardiac Arrhythmias

2010:

• The SCN5A gene in Brugada syndrome mutations, variants ,missense and nonsense. What’s a clinician to do?The SCN5A gene in Brugada syndrome mutations, variants, missense and nonsense. What’s a clinician to do?