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Circulation. Arrhythmia and Electrophysiology|July 9, 2021
Management of Congenital Long-QT Syndrome: Commentary From the ExpertsElizabeth S Kaufman, Lee L Eckhardt, Michael J Ackerman, et al.American Journal of Human Genetics|January 13, 2022
The genetic architecture of pediatric cardiomyopathyStephanie M Ware, Surbhi Bhatnagar, Phillip J Dexheimer, et al.American Heart Journal|June 14, 2023
Cardiac imaging and biomarkers for assessing myocardial fibrosis in children with hypertrophic cardiomyopathySonya Kirmani, Pamela K Woodard, Ling Shi, et al.Journal of Medical Genetics|September 25, 2008
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficitsS R Lalani, J V Thakuria, G F Cox, et al.Journal of the American Heart Association|April 28, 2021
Genetic Causes of Cardiomyopathy in Children: First Results From the Pediatric Cardiomyopathy Genes StudyStephanie M Ware, James D Wilkinson, Muhammad Tariq, et al.Heart Rhythm|May 13, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathyJeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.Heart Rhythm|November 3, 2019
2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summaryJeffrey A Towbin, William J McKenna, Dominic J Abrams, et al.Nature Genetics|December 7, 2010
CCDC39 is required for assembly of inner dynein arms and the dynein regulatory complex and for normal ciliary motility in humans and dogsAnne-Christine Merveille, Erica E Davis, Anita Becker-Heck, et al.Human Molecular Genetics|March 12, 2016
A genome-wide association study of congenital cardiovascular left-sided lesions shows association with a locus on chromosome 20Neil A Hanchard, Shanker Swaminathan, Kristine Bucasas, et al.JAMA|July 12, 2013
The state of US health, 1990-2010: burden of diseases, injuries, and risk factorsChristopher J L Murray, Charles Atkinson, Kavi Bhalla, et al.Pageof 44