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International Journal of Legal Medicine|February 8, 2014
Association of common variants in NOS1AP gene with sudden unexplained nocturnal death syndrome in the southern Chinese Han populationLei Huang, Yangeng Yu, Yili Chen, et al.
Mayo Clinic Proceedings|December 10, 2003
Ethnic differences in cardiac potassium channel variants: implications for genetic susceptibility to sudden cardiac death and genetic testing for congenital long QT syndromeMichael J Ackerman, David J Tester, Gregg S Jones, et al.
Heart Rhythm|February 6, 2007
Novel mechanism for sudden infant death syndrome: persistent late sodium current secondary to mutations in caveolin-3Lisa B Cronk, Bin Ye, Toshihiko Kaku, et al.
Heart Rhythm|July 5, 2006
Genotypic heterogeneity and phenotypic mimicry among unrelated patients referred for catecholaminergic polymorphic ventricular tachycardia genetic testingDavid J Tester, Puneeta Arya, Melissa Will, et al.
Heart Rhythm|December 4, 2017
Using the genome aggregation database, computational pathogenicity prediction tools, and patch clamp heterologous expression studies to demote previously published long QT syndrome type 1 mutations from pathogenic to benignDaniel J Clemens, Anne R Lentino, Jamie D Kapplinger, et al.
Circulation. Genomic and Precision Medicine|May 18, 2021
Development of a Patient-Specific p.D85N-Potassium Voltage-Gated Channel Subfamily E Member 1-Induced Pluripotent Stem Cell-Derived Cardiomyocyte Model for Drug-Induced Long QT SyndromeMaengjo Kim, Dan Ye, C S John Kim, et al.
Forensic Science International|February 18, 2014
Is sudden unexplained nocturnal death syndrome in Southern China a cardiac sodium channel dysfunction disorder?Chao Liu, David J Tester, Yiding Hou, et al.
Circulation Research|September 23, 2003
A ubiquitous splice variant and a common polymorphism affect heterologous expression of recombinant human SCN5A heart sodium channelsJonathan C Makielski, Bin Ye, Carmen R Valdivia, et al.
European Heart Journal. Case Reports|May 9, 2022
Red herring pathogenic variants: a case report of premature ventricular contraction-triggered ventricular fibrillation with an incidental pathogenic LMNA variantRamin Garmany, Raquel Neves, Fatima Ali Ahmed, et al.
JACC. Clinical Electrophysiology|January 26, 2019
Plakophilin-2 Truncation Variants in Patients Clinically Diagnosed With Catecholaminergic Polymorphic Ventricular Tachycardia and Decedents With Exercise-Associated Autopsy Negative Sudden Unexplained Death in the YoungDavid J Tester, Jaeger P Ackerman, John R Giudicessi, et al.
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