Search research articles
Contact Us
Filters
Showing results (21-30 of 45) with videos related to
Page
of 5
Sort By:
Frontiers in Genetics
|
February 14, 2022
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation
Oliver Bundgaard Vad, Yannan Yan, Federico Denti, et al.
Frontiers in Physiology
|
July 26, 2018
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest
Laura Andreasen, Jonas Ghouse, Morten W Skov, et al.
Journal of the American College of Cardiology
|
October 29, 2025
Atrial Fibrillation Screening According to Genetic Risk: A Secondary Analysis of the Randomized LOOP Study
Oliver B Vad, Søren Z Diederichsen, Lucas Y Xing, et al.
Journal of the American College of Cardiology
|
August 13, 2021
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Jonas Ghouse, Gustav Ahlberg, Laura Andreasen, et al.
Journal of the American Heart Association
|
April 30, 2024
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death
Christian Paludan-Müller, Niels K Stampe, Laia M Monfort, et al.
JACC. Basic to Translational Science
|
March 21, 2024
Loss of Cardiac Splicing Regulator <i>RBM20</i> Is Associated With Early-Onset Atrial Fibrillation
Oliver B Vad, Elisavet Angeli, Martin Liss, et al.
Heart Rhythm
|
May 28, 2017
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants
Emilie Gregers, Gustav Ahlberg, Thea Christensen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2016
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
Jonas Ghouse, Christian T Have, Morten W Skov, et al.
Scientific Reports
|
May 27, 2021
Explaining deep neural networks for knowledge discovery in electrocardiogram analysis
Steven A Hicks, Jonas L Isaksen, Vajira Thambawita, et al.
Cardiovascular Research
|
May 4, 2019
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse
Katra Hadji-Turdeghal, Laura Andreasen, Christian M Hagen, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 45) with videos related to
Sort By:
Page
of 5
Frontiers in Genetics
|
February 14, 2022
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation
Oliver Bundgaard Vad, Yannan Yan, Federico Denti, et al.
Frontiers in Physiology
|
July 26, 2018
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest
Laura Andreasen, Jonas Ghouse, Morten W Skov, et al.
Journal of the American College of Cardiology
|
October 29, 2025
Atrial Fibrillation Screening According to Genetic Risk: A Secondary Analysis of the Randomized LOOP Study
Oliver B Vad, Søren Z Diederichsen, Lucas Y Xing, et al.
Journal of the American College of Cardiology
|
August 13, 2021
Association of Variants Near the Bradykinin Receptor B<sub>2</sub> Gene With Angioedema in Patients Taking ACE Inhibitors
Jonas Ghouse, Gustav Ahlberg, Laura Andreasen, et al.
Journal of the American Heart Association
|
April 30, 2024
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death
Christian Paludan-Müller, Niels K Stampe, Laia M Monfort, et al.
JACC. Basic to Translational Science
|
March 21, 2024
Loss of Cardiac Splicing Regulator <i>RBM20</i> Is Associated With Early-Onset Atrial Fibrillation
Oliver B Vad, Elisavet Angeli, Martin Liss, et al.
Heart Rhythm
|
May 28, 2017
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants
Emilie Gregers, Gustav Ahlberg, Thea Christensen, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
October 7, 2016
Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
Jonas Ghouse, Christian T Have, Morten W Skov, et al.
Scientific Reports
|
May 27, 2021
Explaining deep neural networks for knowledge discovery in electrocardiogram analysis
Steven A Hicks, Jonas L Isaksen, Vajira Thambawita, et al.
Cardiovascular Research
|
May 4, 2019
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse
Katra Hadji-Turdeghal, Laura Andreasen, Christian M Hagen, et al.
Page
of 5