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Hugh D Allen

Showing results (31-40 of 48) with videos related to

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International Journal of Cardiology|July 9, 2016
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window currentAndrew P Landstrom, Nicole J Boczek, Dan Ye, et al.
The Journal of Pediatrics|September 3, 2018
Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart SyndromeAndrew L Dailey-Schwartz, Hanna J Tadros, Mahshid Sababi Azamian, et al.
Heart Rhythm|March 5, 2018
Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noiseAndrew P Landstrom, Ernesto Fernandez, Jill A Rosenfeld, et al.
Journal of Cardiac Surgery|February 19, 2021
Smaller right pulmonary artery is associated with longer survival time without scimitar vein repairCarlos Bonilla-Ramirez, Katherine B Salciccioli, Athar M Qureshi, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophyRita Wen Kaspar, Hugh D Allen, Will C Ray, et al.
Journal of Personalized Medicine|May 28, 2022
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric CardiomyopathyLeonie M Kurzlechner, Edward G Jones, Amy M Berkman, et al.
Scientific Reports|June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathyEdward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Circulation. Arrhythmia and Electrophysiology|April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test ReferralsAndrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac deathAlexandra M Markunas, Perathu K R Manivannan, Jordan E Ezekian, et al.
Journal of Molecular and Cellular Cardiology|April 13, 2020
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomesHanna J Tadros, Chelsea S Life, Gustavo Garcia, et al.
Pageof 5

Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
International Journal of Cardiology|July 9, 2016
Novel long QT syndrome-associated missense mutation, L762F, in CACNA1C-encoded L-type calcium channel imparts a slower inactivation tau and increased sustained and window currentAndrew P Landstrom, Nicole J Boczek, Dan Ye, et al.
The Journal of Pediatrics|September 3, 2018
Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart SyndromeAndrew L Dailey-Schwartz, Hanna J Tadros, Mahshid Sababi Azamian, et al.
Heart Rhythm|March 5, 2018
Amino acid-level signal-to-noise analysis of incidentally identified variants in genes associated with long QT syndrome during pediatric whole exome sequencing reflects background genetic noiseAndrew P Landstrom, Ernesto Fernandez, Jill A Rosenfeld, et al.
Journal of Cardiac Surgery|February 19, 2021
Smaller right pulmonary artery is associated with longer survival time without scimitar vein repairCarlos Bonilla-Ramirez, Katherine B Salciccioli, Athar M Qureshi, et al.
Circulation. Cardiovascular Genetics|December 25, 2009
Analysis of dystrophin deletion mutations predicts age of cardiomyopathy onset in becker muscular dystrophyRita Wen Kaspar, Hugh D Allen, Will C Ray, et al.
Journal of Personalized Medicine|May 28, 2022
Signal-to-Noise Analysis Can Inform the Likelihood That Incidentally Identified Variants in Sarcomeric Genes Are Associated with Pediatric CardiomyopathyLeonie M Kurzlechner, Edward G Jones, Amy M Berkman, et al.
Scientific Reports|June 23, 2019
Analysis of enriched rare variants in JPH2-encoded junctophilin-2 among Greater Middle Eastern individuals reveals a novel homozygous variant associated with neonatal dilated cardiomyopathyEdward G Jones, Neda Mazaheri, Reza Maroofian, et al.
Circulation. Arrhythmia and Electrophysiology|April 14, 2017
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test ReferralsAndrew P Landstrom, Andrew L Dailey-Schwartz, Jill A Rosenfeld, et al.
American Journal of Medical Genetics. Part A|December 28, 2020
TBX5-encoded T-box transcription factor 5 variant T223M is associated with long QT syndrome and pediatric sudden cardiac deathAlexandra M Markunas, Perathu K R Manivannan, Jordan E Ezekian, et al.
Journal of Molecular and Cellular Cardiology|April 13, 2020
Meta-analysis of cardiomyopathy-associated variants in troponin genes identifies loci and intragenic hot spots that are associated with worse clinical outcomesHanna J Tadros, Chelsea S Life, Gustavo Garcia, et al.
Pageof 5