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Methods in Molecular Medicine|October 31, 2006
Mutation detection in congenital long QT syndrome: cardiac channel gene screen using PCR, dHPLC, and direct DNA sequencingDavid J Tester, Melissa L Will, Michael J AckermanHerzschrittmachertherapie & Elektrophysiologie|September 21, 2012
The molecular autopsy: an indispensable step following sudden cardiac death in the young?Nicole J Boczek, David J Tester, Michael J AckermanHeart Rhythm|May 3, 2008
Overrepresentation of the proarrhythmic, sudden death predisposing sodium channel polymorphism S1103Y in a population-based cohort of African-American sudden infant death syndromeDavid W Van Norstrand, David J Tester, Michael J AckermanInternational Journal of Cardiology|May 11, 2020
Discovery and characterization of a monogenetic insult, caveolin-3-V37L, that precipitated oligo-proteomic perturbations governing repolarization reserveDan Ye, Wei Zhou, David J Tester, et al.Heart Rhythm|May 14, 2020
Phenotype-guided whole genome analysis in a patient with genetically elusive long QT syndrome yields a novel TRDN-encoded triadin pathogenetic substrate for triadin knockout syndrome and reveals a novel primate-specific cardiac TRDN transcriptDaniel J Clemens, David J Tester, Isabelle Marty, et al.Mayo Clinic Proceedings|October 4, 2011
Unexplained drownings and the cardiac channelopathies: a molecular autopsy seriesDavid J Tester, Argelia Medeiros-Domingo, Melissa L Will, et al.Journal of Child Neurology|April 17, 2010
Cardiac channel molecular autopsy for sudden unexpected death in epilepsyJonathan N Johnson, David J Tester, Nancy E Bass, et al.Heart Rhythm|September 29, 2005
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testingDavid J Tester, Laura J Kopplin, Melissa L Will, et al.Journal of the American College of Cardiology|February 21, 2006
Effect of clinical phenotype on yield of long QT syndrome genetic testingDavid J Tester, Melissa L Will, Carla M Haglund, et al.Circulation. Arrhythmia and Electrophysiology|October 22, 2009
Protein kinase A-dependent biophysical phenotype for V227F-KCNJ2 mutation in catecholaminergic polymorphic ventricular tachycardiaAmanda L Vega, David J Tester, Michael J Ackerman, et al.Pageof 69