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Mayo Clinic Proceedings|February 3, 2024
Temporal Association Between Vaping and Risk of Cardiac EventsSahej Bains, Ramin Garmany, Raquel Neves, et al.
Heart Rhythm|April 7, 2018
Long QT syndrome type 5-Lite: Defining the clinical phenotype associated with the potentially proarrhythmic p.Asp85Asn-KCNE1 common genetic variantConor M Lane, John R Giudicessi, Dan Ye, et al.
Heart Rhythm|May 27, 2025
Molecular and functional characterization of DENND3 as a novel regulator of ion channel traffickingShan Gao, Dan Ye, Raquel Neves, et al.
Heart Rhythm|July 28, 2009
Unique mixed phenotype and unexpected functional effect revealed by novel compound heterozygosity mutations involving SCN5AArgelia Medeiros-Domingo, Bi-Hua Tan, Pedro Iturralde-Torres, et al.
Circulation. Cardiovascular Genetics|September 6, 2012
Phylogenetic and physicochemical analyses enhance the classification of rare nonsynonymous single nucleotide variants in type 1 and 2 long-QT syndromeJohn R Giudicessi, Jamie D Kapplinger, David J Tester, et al.
Circulation|June 20, 2018
Importance of Variant Interpretation in Whole-Exome Molecular Autopsy: Population-Based Case SeriesGarrett W Shanks, David J Tester, Jaeger P Ackerman, et al.
American Journal of Physiology. Heart and Circulatory Physiology|February 21, 2004
Molecular and functional characterization of common polymorphisms in HERG (KCNH2) potassium channelsBlake D Anson, Michael J Ackerman, David J Tester, et al.
Heart Rhythm|March 8, 2007
KCNJ2 mutations in arrhythmia patients referred for LQT testing: a mutation T305A with novel effect on rectification propertiesLee L Eckhardt, Amanda L Farley, Esther Rodriguez, 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 5, 2026
Calcium release channel deficiency syndrome in patients diagnosed with idiopathic ventricular fibrillation and decedents classified as sudden unexplained death in the youngLucilla Giammarino, Raquel Neves, David J Tester, et al.
Congenital Heart Disease|May 25, 2016
Molecular and Functional Characterization of Rare CACNA1C Variants in Sudden Unexplained Death in the YoungBrittan S Sutphin, Nicole J Boczek, Héctor Barajas-Martínez, et al.
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