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Catecholaminergic Polymorphic Ventricular Tachycardia: The Cardiac Arrest Where Epinephrine Is Contraindicated

Pediatric critical care medicine, 2019-03, Vol.20 (3), p.262-268

2019

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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

PloS one, 2018-04, Vol.13 (4), p.e0196078-e0196078

2018

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Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations

BMC medical genetics, 2015-05, Vol.16 (1), p.34-34, Article 34

2015

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Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome

Heart rhythm, 2014, Vol.11 (1), p.76-82

2014

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SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

European heart journal, 2018-08, Vol.39 (31), p.2879-2887

2018

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Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation. Arrhythmia and electrophysiology, 2015-10, Vol.8 (5), p.1151-1158

2015

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Update on the Diagnosis and Management of Familial Long QT Syndrome

Heart, lung & circulation, 2016-08, Vol.25 (8), p.769-776

2016

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Risk Stratification in Hypertrophic Cardiomyopathy: Time to Think about the Electrocardiogram

Cardiogenetics, 2019-04, Vol.9 (1), p.7951

Skinner, Jonathan

2019

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Doctors and climate change: First do no harm

Journal of paediatrics and child health, 2021-11, Vol.57 (11), p.1754-1758

Skinner, Jonathan R

2021

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Pre-Test Probability and Genes and Variants of Uncertain Significance in Familial Long QT Syndrome

Heart, lung & circulation, 2020-04, Vol.29 (4), p.512-519

2020

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Routine ECG screening in infancy and early childhood should not be performed

Heart rhythm, 2014-12, Vol.11 (12), p.2322-2327

2014

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Investigation of sudden cardiac arrest: Time to put guidelines into practice

Resuscitation, 2022-10, Vol.179, p.36-37

2022

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Community detection of long QT syndrome with a clinical registry: An alternative to ECG screening programs?

Heart rhythm, 2013-02, Vol.10 (2), p.233-238

2013

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Ventricular extrasystoles and ventricular dysfunction: Too close for comfort?

Heart rhythm, 2016-11, Vol.13 (11), p.2149-2150

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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Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation

Annals of emergency medicine, 2009-07, Vol.54 (1), p.26-32

2009

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High Arrhythmic Burden but Low Mortality during Long-term Follow-up in Arrhythmogenic Right Ventricular Cardiomyopathy

Heart, lung & circulation, 2016-03, Vol.25 (3), p.275-281

2016

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Investigating sudden unexpected death in the young: A chance to prevent further deaths

Resuscitation, 2012-10, Vol.83 (10), p.1185-1186

Skinner, Jonathan R., MB ChB, FRCPCH, FRACP, MD

2012

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Time to act on climate change

Journal of paediatrics and child health, 2022-12

2022

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Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

American journal of physiology. Heart and circulatory physiology, 2020-11, Vol.319 (5), p.H927-H937

2020

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Holter Recordings at Initial Assessment for Long QT Syndrome: Relationship to Genotype Status and Cardiac Events

Journal of cardiovascular development and disease, 2022-05, Vol.9 (5), p.164

2022

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People with long QT syndrome who have attention deficit hyperactivity disorder deserve to be treated properly

Heart rhythm, 2015-08, Vol.12 (8), p.1813-1814

2015

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Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy

BMC cardiovascular disorders, 2019-07, Vol.19 (1), p.174-174, Article 174

2019

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Catecholaminergic Polymorphic Ventricular Tachycardia: The Cardiac Arrest Where Epinephrine Is Contraindicated

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

Assessment of the predictive accuracy of five in silico prediction tools, alone or in combination, and two metaservers to classify long QT syndrome gene mutations

Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year olds

Single nucleotide polymorphisms in arrhythmia genes modify the risk of cardiac events and sudden death in long QT syndrome

SCN5A mutations in 442 neonates and children: genotype–phenotype correlation and identification of higher-risk subgroups

Physical and Psychological Consequences of Left Cardiac Sympathetic Denervation in Long-QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia

Update on the Diagnosis and Management of Familial Long QT Syndrome

Risk Stratification in Hypertrophic Cardiomyopathy: Time to Think about the Electrocardiogram

Doctors and climate change: First do no harm

Pre-Test Probability and Genes and Variants of Uncertain Significance in Familial Long QT Syndrome

Routine ECG screening in infancy and early childhood should not be performed

Investigation of sudden cardiac arrest: Time to put guidelines into practice

Community detection of long QT syndrome with a clinical registry: An alternative to ECG screening programs?

Ventricular extrasystoles and ventricular dysfunction: Too close for comfort?

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

Misdiagnosis of Long QT Syndrome as Epilepsy at First Presentation

High Arrhythmic Burden but Low Mortality during Long-term Follow-up in Arrhythmogenic Right Ventricular Cardiomyopathy

Investigating sudden unexpected death in the young: A chance to prevent further deaths

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

Time to act on climate change

Functional coculture of sympathetic neurons and cardiomyocytes derived from human-induced pluripotent stem cells

Holter Recordings at Initial Assessment for Long QT Syndrome: Relationship to Genotype Status and Cardiac Events

People with long QT syndrome who have attention deficit hyperactivity disorder deserve to be treated properly

Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy

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