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Daniel J. Clemens

Observed names: Daniel Clemens, Daniel J Clemens
ORCID: 0000-0003-2102-5306
Observed ORCID: 0000-0003-2102-5306
OpenAlex ID: A5011992882
International Triadin Knockout Syndrome Registry
2019 · Daniel J. Clemens, David J. Tester, et al. · Circulation Genomic and Precision Medicine · 49
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Human Induced Pluripotent Stem Cell-Derived Non-Cardiomyocytes Modulate Cardiac Electrophysiological Maturation Through Connexin 43-Mediated Cell-Cell Interactions
2019 · Sherri M. Biendarra-Tiegs, Daniel J. Clemens, et al. · Stem Cells and Development · 29
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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 benign
2017 · Daniel J. Clemens, Anne R. Lentino, et al. · Heart Rhythm · 20
SARS-CoV-2 spike protein-mediated cardiomyocyte fusion may contribute to increased arrhythmic risk in COVID-19
2023 · Daniel J. Clemens, Dan Ye, et al. · PLoS ONE · 18
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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 transcript
2020 · Daniel J. Clemens, David J. Tester, et al. · Heart Rhythm · 14
Analysis of TTN Truncating Variants in >74 000 Cases Reveals New Clinically Relevant Gene Regions
2025 · Matteo Vatta, Ellen Regalado, et al. · Circulation Genomic and Precision Medicine · 13
Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes
2023 · Daniel J. Clemens, Dan Ye, et al. · Stem Cell Reports · 13
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SARS-CoV-2 direct cardiac damage through spike-mediated cardiomyocyte fusion
2020 · Jay Schneider, David Pease, et al. · Research Square · 9
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Prevalence and Phenotypic Correlations of Calmodulinopathy-Causative CALM1-3 Variants Detected in a Multicenter Molecular Autopsy Cohort of Sudden Unexplained Death Victims
2020 · Daniel J. Clemens, Belinda Gray, et al. · Circulation Genomic and Precision Medicine · 7
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Triadin Knockout Syndrome Is Absent in a Multi-Center Molecular Autopsy Cohort of Sudden Infant Death Syndrome and Sudden Unexplained Death in the Young and Is Extremely Rare in the General Population
2020 · Daniel J. Clemens, Belinda Gray, et al. · Circulation Genomic and Precision Medicine · 6
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Utilization of the genome aggregation database, in silico tools, and heterologous expression patch-clamp studies to identify and demote previously published type 2 long QT syndrome: Causative variants from pathogenic to likely benign
2019 · Connor L. Mattivi, Dan Ye, et al. · Heart Rhythm · 5
B-ab18-03 Sars-cov-2 Direct Cardiac Damage Through Spike-mediated Cardiomyocyte Fusion May Contribute to Increased Arrhythmic Risk in Covid-19
2021 · Daniel J. Clemens, Dan Ye, et al. · Heart Rhythm · 3
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P222: TTN truncating variants are enriched in cardiomyopathy/arrhythmia and neuromuscular cases and M-band exon 358 contributes to primary cardiomyopathy/arrhythmia
2024 · Ellen Regalado, Dan Swartzlander, et al. · Genetics in Medicine Open · 1
B-yia2-02 Cellular and Electrophysiological Characterization of Triadin Knockout Syndrome Using Human Induced Pluripotent Stem Cell-derived Cardiomyocytes
2021 · Daniel J. Clemens, Dan Ye, et al. · Heart Rhythm
B-po04-001 Characterization of Extreme N-terminal Ryr2 Variants Found Outside Cpvt1 Variant Cluster Regions Show Ca2+ Handling Abnormalities Consistent With Classical Cpvt
2021 · Marissa Joy Stutzman, Changsung John Kim, et al. · Heart Rhythm
Abstract 16901: Utilizing In Silico Pathogenicity Prediction Tools and Heterologous Expression Patch Clamp Studies to Identify Bona Fide Pathogenic KCNH2 Variants Among Publically Available Exomes Derived From Subjects Without Evidence for Either Type 2 Long QT Syndrome or Type 1 Short QT Syndrome
2018 · Connor L Mattivi, Dan Ye, et al. · Circulation
Abstract 16606: Utilization of the Genome Aggregation Database, In Silico Tools, and Heterologous Expression Patch Clamp Studies to Identify and Demote Previously Published Type 2 Long QT Syndrome-Causative Variants From Pathogenic to Likely Benign
2018 · Connor L Mattivi, Dan Ye, et al. · Circulation
Abstract 19352: Utilizing the Genome Aggregation Database, in silico Tools, and Patch Clamp Heterologous Expression Studies to Demote Previously Published Type 1 Long QT Syndrome Mutations From Pathogenic to Benign
2017 · Daniel J. Clemens, Anne Lentino, et al. · Circulation
Works count: 18
Citation count: 187
H-index: 8
I10-index: 7
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