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James R Priest

Showing results (31-40 of 64) with videos related to

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Developmental Cell|November 15, 2016
Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac CellsGuang Li, Adele Xu, Sopheak Sim, et al.
The Journal of Pediatrics|December 20, 2017
First Trimester Plasma Glucose Values in Women without Diabetes are Associated with Risk for Congenital Heart Disease in OffspringEmmi I T Helle, Preston Biegley, Joshua W Knowles, et al.
Genetic Epidemiology|December 5, 2018
Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohortsEmmi Helle, Aldo Córdova-Palomera, Tiina Ojala, et al.
Pediatric Cardiology|October 29, 2021
Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic ConditionsDana B Gal, Ana Morales, Susan Rojahn, et al.
Heart Rhythm|June 29, 2014
Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencingJames R Priest, Scott R Ceresnak, Frederick E Dewey, et al.
Circulation. Genomic and Precision Medicine|April 5, 2023
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic CardiomyopathyMengyao Yu, Andrew R Harper, Matthew Aguirre, et al.
Circulation|March 1, 2019
Substantial Cardiovascular Morbidity in Adults With Lower-Complexity Congenital Heart DiseasePriyanka Saha, Praneetha Potiny, Joseph Rigdon, et al.
Nature Communications|July 17, 2019
Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequencesJason A Fries, Paroma Varma, Vincent S Chen, et al.
HGG Advances|May 7, 2025
The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humansMinna Ampuja, Sabina Ericsson, Ilkka Paatero, et al.
American Heart Journal|November 24, 2007
Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary diseaseMark A Hlatky, Thomas Quertermous, Derek B Boothroyd, et al.
Pageof 7

Showing results (31-40 of 64) with videos related to

Sort By:
Pageof 7
Developmental Cell|November 15, 2016
Transcriptomic Profiling Maps Anatomically Patterned Subpopulations among Single Embryonic Cardiac CellsGuang Li, Adele Xu, Sopheak Sim, et al.
The Journal of Pediatrics|December 20, 2017
First Trimester Plasma Glucose Values in Women without Diabetes are Associated with Risk for Congenital Heart Disease in OffspringEmmi I T Helle, Preston Biegley, Joshua W Knowles, et al.
Genetic Epidemiology|December 5, 2018
Loss of function, missense, and intronic variants in NOTCH1 confer different risks for left ventricular outflow tract obstructive heart defects in two European cohortsEmmi Helle, Aldo Córdova-Palomera, Tiina Ojala, et al.
Pediatric Cardiology|October 29, 2021
Comprehensive Genetic Testing for Pediatric Hypertrophic Cardiomyopathy Reveals Clinical Management Opportunities and Syndromic ConditionsDana B Gal, Ana Morales, Susan Rojahn, et al.
Heart Rhythm|June 29, 2014
Molecular diagnosis of long QT syndrome at 10 days of life by rapid whole genome sequencingJames R Priest, Scott R Ceresnak, Frederick E Dewey, et al.
Circulation. Genomic and Precision Medicine|April 5, 2023
Genetic Determinants of the Interventricular Septum Are Linked to Ventricular Septal Defects and Hypertrophic CardiomyopathyMengyao Yu, Andrew R Harper, Matthew Aguirre, et al.
Circulation|March 1, 2019
Substantial Cardiovascular Morbidity in Adults With Lower-Complexity Congenital Heart DiseasePriyanka Saha, Praneetha Potiny, Joseph Rigdon, et al.
Nature Communications|July 17, 2019
Weakly supervised classification of aortic valve malformations using unlabeled cardiac MRI sequencesJason A Fries, Paroma Varma, Vincent S Chen, et al.
HGG Advances|May 7, 2025
The ERBB2 c.1795C>T, p.Arg599Cys variant is associated with left ventricular outflow tract obstruction defects in humansMinna Ampuja, Sabina Ericsson, Ilkka Paatero, et al.
American Heart Journal|November 24, 2007
Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary diseaseMark A Hlatky, Thomas Quertermous, Derek B Boothroyd, et al.
Pageof 7