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Jonathan R Skinner

Showing results (101-110 of 128) with videos related to

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Molecular Genetics & Genomic Medicine|October 23, 2018
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathyR J McKinlay Gardner, Ian G Crozier, Alex L Binfield, et al.
Heart Rhythm|November 13, 2010
Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year oldsJonathan R Skinner, Jackie Crawford, Warren Smith, et al.
BMC Cardiovascular Disorders|July 25, 2019
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsyHariharan Raju, James S Ware, Jonathan R Skinner, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 27, 2018
Arrhythmias in congenital heart disease: a position paper of the European Heart Rhythm Association (EHRA), Association for European Paediatric and Congenital Cardiology (AEPC), and the European Society of Cardiology (ESC) Working Group on Grown-up Congenital heart disease, endorsed by HRS, PACES, APHRS, and SOLAECEAntonio Hernández-Madrid, Thomas Paul, Dominic Abrams, et al.
JACC. Clinical Electrophysiology|December 21, 2024
International Multicenter Cohort Study on Beta-Blocker-Free Treatment Strategies for Catecholaminergic Polymorphic Ventricular Tachycardia PatientsRaquel Neves, Sahej Bains, J Martijn Bos, et al.
European Heart Journal|April 4, 2026
DMPK 3' untranslated repeat expansions in unexplained sudden cardiac death in the youngZoe Ward, Jackson O'Neill, Rachael Stiles, et al.
The New Zealand Medical Journal|August 18, 2018
Genomic medicine must reduce, not compound, health inequities: the case for hauora-enhancing genomic resources for New ZealandStephen P Robertson, Jennie Harre Hindmarsh, Sarah Berry, et al.
Heart, Lung & Circulation|May 27, 2020
Position Statement on the Management of Cardiac Electrophysiology and Cardiac Implantable Electronic Devices in Australia During the COVID-19 Pandemic: A Living DocumentSaurabh Kumar, Haris Haqqani, Gareth Wynn, et al.
The New England Journal of Medicine|June 23, 2016
A Prospective Study of Sudden Cardiac Death among Children and Young AdultsRichard D Bagnall, Robert G Weintraub, Jodie Ingles, et al.
European Heart Journal|March 5, 2025
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data setsAlexandra Butters, Kate Thomson, Franki Harrington, et al.
Pageof 13

Showing results (101-110 of 128) with videos related to

Sort By:
Pageof 13
Molecular Genetics & Genomic Medicine|October 23, 2018
Penetrance and expressivity of the R858H CACNA1C variant in a five-generation pedigree segregating an arrhythmogenic channelopathyR J McKinlay Gardner, Ian G Crozier, Alex L Binfield, et al.
Heart Rhythm|November 13, 2010
Prospective, population-based long QT molecular autopsy study of postmortem negative sudden death in 1 to 40 year oldsJonathan R Skinner, Jackie Crawford, Warren Smith, et al.
BMC Cardiovascular Disorders|July 25, 2019
Next-generation sequencing using microfluidic PCR enrichment for molecular autopsyHariharan Raju, James S Ware, Jonathan R Skinner, et al.
Europace : European Pacing, Arrhythmias, and Cardiac Electrophysiology : Journal of the Working Groups on Cardiac Pacing, Arrhythmias, and Cardiac Cellular Electrophysiology of the European Society of Cardiology|March 27, 2018
Arrhythmias in congenital heart disease: a position paper of the European Heart Rhythm Association (EHRA), Association for European Paediatric and Congenital Cardiology (AEPC), and the European Society of Cardiology (ESC) Working Group on Grown-up Congenital heart disease, endorsed by HRS, PACES, APHRS, and SOLAECEAntonio Hernández-Madrid, Thomas Paul, Dominic Abrams, et al.
JACC. Clinical Electrophysiology|December 21, 2024
International Multicenter Cohort Study on Beta-Blocker-Free Treatment Strategies for Catecholaminergic Polymorphic Ventricular Tachycardia PatientsRaquel Neves, Sahej Bains, J Martijn Bos, et al.
European Heart Journal|April 4, 2026
DMPK 3' untranslated repeat expansions in unexplained sudden cardiac death in the youngZoe Ward, Jackson O'Neill, Rachael Stiles, et al.
The New Zealand Medical Journal|August 18, 2018
Genomic medicine must reduce, not compound, health inequities: the case for hauora-enhancing genomic resources for New ZealandStephen P Robertson, Jennie Harre Hindmarsh, Sarah Berry, et al.
Heart, Lung & Circulation|May 27, 2020
Position Statement on the Management of Cardiac Electrophysiology and Cardiac Implantable Electronic Devices in Australia During the COVID-19 Pandemic: A Living DocumentSaurabh Kumar, Haris Haqqani, Gareth Wynn, et al.
The New England Journal of Medicine|June 23, 2016
A Prospective Study of Sudden Cardiac Death among Children and Young AdultsRichard D Bagnall, Robert G Weintraub, Jodie Ingles, et al.
European Heart Journal|March 5, 2025
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data setsAlexandra Butters, Kate Thomson, Franki Harrington, et al.
Pageof 13