2018:
- Channelopathies That Lead to Sudden Cardiac Death – Clinical and Genetic Aspects
- Clinical Outcomes and Modes of Death in Timothy Syndrome
- 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:
2011:
2010:
- Improving the safety of oxygen therapy in hospitals summary of a safety report from the National Patient Safety Agency
- 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?