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Heart Rhythm|June 9, 2007
A mechanism for sudden infant death syndrome (SIDS): stress-induced leak via ryanodine receptorsDavid J Tester, Miroslav Dura, Elisa Carturan, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 21, 2007
Mutation of an A-kinase-anchoring protein causes long-QT syndromeLei Chen, Michelle L Marquardt, David J Tester, et al.
Circulation. Genomic and Precision Medicine|December 24, 2021
Exome Sequencing Highlights a Potential Role for Concealed Cardiomyopathies in Youthful Sudden Cardiac DeathRaquel Neves, David J Tester, Michael A Simpson, et al.
Mayo Clinic Proceedings|July 4, 2003
Primer on medical genomics. Part VIII: Essentials of medical genetics for the practicing physicianRegina E Ensenauer, Shanda S Reinke, Michael J Ackerman, et al.
Cardiovascular Research|July 19, 2002
A novel SCN5A arrhythmia mutation, M1766L, with expression defect rescued by mexiletineCarmen R Valdivia, Michael J Ackerman, David J Tester, et al.
Circulation. Genomic and Precision Medicine|September 17, 2020
Promise and Potential Peril With Lumacaftor for the Trafficking Defective Type 2 Long-QT Syndrome-Causative Variants, p.G604S, p.N633S, and p.R685P, Using Patient-Specific Re-Engineered CardiomyocytesBailey J O'Hare, C S John Kim, Samantha K Hamrick, et al.
Journal of Cardiovascular Translational Research|June 17, 2025
Evaluation of CACNA1C-Positive Patients Evaluated in a Tertiary Genetic Heart Rhythm ClinicLiwei Yu, Raquel Neves, Martijn M Bos, et al.
Heart Rhythm|February 10, 2022
Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variantKathryn E Tobert, David J Tester, Wei Zhou, et al.
Mayo Clinic Proceedings|November 5, 2016
The Promise and Peril of Precision Medicine: Phenotyping Still Matters MostJaeger P Ackerman, Daniel C Bartos, Jamie D Kapplinger, et al.
Mayo Clinic Proceedings|May 15, 2002
Epinephrine-induced QT interval prolongation: a gene-specific paradoxical response in congenital long QT syndromeMichael J Ackerman, Anant Khositseth, David J Tester, et al.
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