Last Posted: Aug 24, 2019
- Lessons learned from testing cardiac channelopathy and cardiomyopathy genes in individuals who died suddenly: A two-year prospective study in a large medical examiner's office with an in-house molecular genetics laboratory and genetic counseling services.
Williams Nori et al. Journal of genetic counseling 2019 Aug - Beyond the One Gene-One Disease Paradigm: Complex Genetics and Pleiotropy in Inheritable Cardiac Disorders
Cerrone Marina et al. Circulation 2019 08 (7) 595-610 - Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy.
Mathew J et al. Clinical genetics 2018 93(2) 310-319 - Cardiac Evaluation of Children With a Family History of Sudden Death.
Webster Gregory et al. Journal of the American College of Cardiology 2019 Aug 74(6) 759-770 - Findings of Uncertain Significance and a Family History of Sudden Death: Worth the FUSs?
Ackerman Michael J et al. Journal of the American College of Cardiology 2019 Aug 74(6) 771-773 - Inherited Cardiac Arrhythmias and Channelopathies.
Kline Jessica et al. The Medical clinics of North America 2019 Sep 103(5) 809-820 - Comparable clinical characteristics in Brugada syndrome patients harboring SCN5A or novel SCN10A variants.
Monasky Michelle M 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 2019 Jul - Genetic Counselors' Approach To Postmortem Genetic Testing After Sudden Death: An Exploratory Study.
Liu Gina et al. Academic forensic pathology 2018 Sep 8(3) 738-751 - Cardiovascular genomics and sudden cardiac death in the young.
Isbister Julia et al. Australian journal of general practice 2019 Mar 48(3) 90-95 - European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
F Fellmann et al, EJHG, June 24, 2019
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