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 - Prevalence and clinical importance of titin truncating variants in adults without known congestive heart failure
JP Pirruccello et al, MedRXIV, August 2019 - Hypertrophic cardiomyopathy genetic test reports: A qualitative study of patient understanding of uninformative genetic test results.
Nightingale Brooke M 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 140(7) 595-610 - Utility of genetics for risk stratification in pediatric hypertrophic cardiomyopathy.
Mathew J et al. Clinical genetics 2018 93(2) 310-319 - Development of a Novel Risk Prediction Model for Sudden Cardiac Death in Childhood Hypertrophic Cardiomyopathy (HCM Risk-Kids).
Norrish Gabrielle et al. JAMA cardiology 2019 Aug - Risk Prediction Model in Children With Hypertrophic Cardiomyopathy: A Work in Progress.
Bonow Robert O et al. JAMA cardiology 2019 Aug - Assessing the barriers to cardiac care in carriers of Duchenne and Becker muscular dystrophy.
Eekhoff Lauren et al. Journal of genetic counseling 2019 Aug - A genome-first approach to aggregating rare genetic variants in LMNA for association with electronic health record phenotypes.
Park Joseph et al. Genetics in medicine : official journal of the American College of Medical Genetics 2019 Aug - Using machine learning to predict one-year cardiovascular events in patients with severe dilated cardiomyopathy.
Chen Rui et al. European journal of radiology 2019 Aug 117178-183
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