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Dan M Roden

Showing results (201-210 of 593) with videos related to

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Nature|January 25, 2002
A calcium sensor in the sodium channel modulates cardiac excitabilityHanno L Tan, Sabina Kupershmidt, Rong Zhang, et al.
European Heart Journal|August 9, 2021
Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance studyJoe-Elie Salem, Lee S Nguyen, Javid J Moslehi, et al.
Pediatric Research|March 7, 2003
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndromeWalter H Johnson, Ping Yang, Tao Yang, et al.
Plos One|March 3, 2012
Characterization of genome-wide association-identified variants for atrial fibrillation in African AmericansJessica T Delaney, Janina M Jeff, Nancy J Brown, et al.
Scientific Reports|November 19, 2016
Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS dataDaniela Husser, Laura Ueberham, Borislav Dinov, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
A clinical algorithm to identify people with the glucose-6-phosphate dehydrogenase p.Val68Met variant at risk for diabetes undertreatmentYash Pershad, Joseph H Breeyear, Robert W Corty, et al.
Nature Communications|September 27, 2024
ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variantsMatthew J O'Neill, Tao Yang, Julie Laudeman, et al.
Nature Reviews. Drug Discovery|November 1, 2007
Identifying genetic risk factors for serious adverse drug reactions: current progress and challengesRussell A Wilke, Debbie W Lin, Dan M Roden, et al.
Annals of Emergency Medicine|August 24, 2010
A clinical prediction model to estimate risk for 30-day adverse events in emergency department patients with symptomatic atrial fibrillationTyler W Barrett, Amy R Martin, Alan B Storrow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Dominant negative effects of SCN5A missense variantsMatthew J O'Neill, Ayesha Muhammad, Bian Li, et al.
Pageof 60

Showing results (201-210 of 593) with videos related to

Sort By:
Pageof 60
Nature|January 25, 2002
A calcium sensor in the sodium channel modulates cardiac excitabilityHanno L Tan, Sabina Kupershmidt, Rong Zhang, et al.
European Heart Journal|August 9, 2021
Anticancer drug-induced life-threatening ventricular arrhythmias: a World Health Organization pharmacovigilance studyJoe-Elie Salem, Lee S Nguyen, Javid J Moslehi, et al.
Pediatric Research|March 7, 2003
Clinical, genetic, and biophysical characterization of a homozygous HERG mutation causing severe neonatal long QT syndromeWalter H Johnson, Ping Yang, Tao Yang, et al.
Plos One|March 3, 2012
Characterization of genome-wide association-identified variants for atrial fibrillation in African AmericansJessica T Delaney, Janina M Jeff, Nancy J Brown, et al.
Scientific Reports|November 19, 2016
Genomic contributors to atrial electroanatomical remodeling and atrial fibrillation progression: Pathway enrichment analysis of GWAS dataDaniela Husser, Laura Ueberham, Borislav Dinov, et al.
Medrxiv : the Preprint Server for Health Sciences|January 27, 2025
A clinical algorithm to identify people with the glucose-6-phosphate dehydrogenase p.Val68Met variant at risk for diabetes undertreatmentYash Pershad, Joseph H Breeyear, Robert W Corty, et al.
Nature Communications|September 27, 2024
ParSE-seq: a calibrated multiplexed assay to facilitate the clinical classification of putative splice-altering variantsMatthew J O'Neill, Tao Yang, Julie Laudeman, et al.
Nature Reviews. Drug Discovery|November 1, 2007
Identifying genetic risk factors for serious adverse drug reactions: current progress and challengesRussell A Wilke, Debbie W Lin, Dan M Roden, et al.
Annals of Emergency Medicine|August 24, 2010
A clinical prediction model to estimate risk for 30-day adverse events in emergency department patients with symptomatic atrial fibrillationTyler W Barrett, Amy R Martin, Alan B Storrow, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 20, 2022
Dominant negative effects of SCN5A missense variantsMatthew J O'Neill, Ayesha Muhammad, Bian Li, et al.
Pageof 60