Author

Carla M. Haglund-Turnquist

Observed name: Carla Haglund-Turnquist

Institution: Mayo Clinic

Observed institution: Mayo Clinic

ORCID: 0000-0002-5082-226X

Observed ORCID: 0000-0002-5082-226X

OpenAlex ID: A5062403048

Vigorous Exercise in Patients With Congenital Long QT Syndrome: Results of the Prospective, Observational, Multinational LIVE-LQTS Study

2024 · Rachel Lampert, Sharlene Day, et al. · Circulation · 28

Identification of a Novel Homozygous Multi-Exon Duplication in RYR2 Among Children With Exertion-Related Unexplained Sudden Deaths in the Amish Community

2020 · David J. Tester, Hannah M. Bombei, et al. · JAMA Cardiology · 28

Molecular characterization of the calcium release channel deficiency syndrome

2020 · David J. Tester, CS John Kim, et al. · JCI Insight · 21

Genome sequencing in a genetically elusive multigenerational long QT syndrome pedigree identifies a novel LQT2-causative deeply intronic KCNH2 variant

2022 · Kathryn E. Tobert, David J. Tester, et al. · Heart Rhythm · 13

Elucidation of ALG10B as a Novel Long-QT Syndrome–Susceptibility Gene

2023 · Wei Zhou, Dan Ye, et al. · Circulation Genomic and Precision Medicine · 4

Ventricular conduction is a marker for arrhythmic risk in SCN5A- E1784K overlap sodium channel disease

2026 · Michael W T Tanck, Yanushi D Wijeyeratne, et al. · EP Europace

Lb-469807-01 Impact of Vigorous Exercise in the Long Qt Syndrome by Genotype, Age, and Sex: Data From the Lifestyle and Exercise in Long Qt Syndrome Registry (live-lqts)

2024 · Rachel Lampert, Sharlene Day, et al. · Heart Rhythm

Mp-470543-001 Genome Sequencing in Multiple Autosomal Dominant Pedigrees of Congenital Long Qt Syndrome and a Negative Clinical Genetic Test Yield Pathogenic Deep Intronic Variants in Kcnq1 and Kcnh2

2024 · David Tester, Carla Haglund-Turnquist, et al. · Heart Rhythm

En-452414-5 Ventricular Conduction Is a Marker for Arrhythmic Risk in Overlap Sodium Channel Disease

2023 · Yanushi D. Wijeyeratne, Michael Tanck, et al. · Heart Rhythm

Po-630-04 Elucidation of Alg10b as a Novel Long Qt Syndrome Susceptibility Gene

2022 · Wei Zhou, Dan Ye, et al. · Heart Rhythm

Abstract 14385: Genome Sequencing and Re-Engineered Heart Cell-Disease Modeling Identifies a Novel Deep Intronic Variant in a Multi-Generational Long QT Syndrome Pedigree

2021 · Kathryn E Tobert, David J Tester, et al. · Circulation

B-po05-027 Genome Sequencing in a Genetically Elusive Multi-generational Long Qt Syndrome Pedigree Identifies a Novel Pathogenic Cause

2021 · Kathryn E. Tobert, David Tester, et al. · Heart Rhythm

Abstract 12295: Characterization of a Novel Homozygous Multi-exon Ryr2 Duplication Associated With Exertion-related Sudden Unexplained Death in the Young in the Amish Community Using Patient-specific Hipsc-cardiomyocytes

2019 · David J. Tester, CS John Kim, et al. · Circulation

Abstract 12260: Whole Exome Molecular Autopsy With Copy Number Variant Analysis of Multiple Autopsy Negative Sudden Unexplained Deaths Among Amish Siblings Yields the Discovery of a Novel Homozygous Multi-exon Duplication in the Ryr2-Encoded Ryanodine Receptor

2019 · David J. Tester, Hannah Bombei, et al. · Circulation

Works count: 14

Citation count: 94

H-index: 4

I10-index: 4