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Laura Andreasen

Showing results (21-30 of 37) with videos related to

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European Journal of Human Genetics : EJHG|February 4, 2018
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genesLaura Andreasen, Gustav Ahlberg, Chuyi Tang, 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 InhibitorsJonas Ghouse, Gustav Ahlberg, Laura Andreasen, 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 ArrestLaura 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 StudyOliver B Vad, Søren Z Diederichsen, Lucas Y Xing, et al.
Journal of the American Heart Association|April 30, 2024
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and DeathChristian 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 FibrillationOliver 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 variantsEmilie 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 mortalityJonas Ghouse, Christian T Have, Morten W Skov, et al.
Cardiovascular Research|May 4, 2019
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapseKatra Hadji-Turdeghal, Laura Andreasen, Christian M Hagen, et al.
Nature Communications|October 19, 2018
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillationGustav Ahlberg, Lena Refsgaard, Pia R Lundegaard, et al.
Pageof 4

Showing results (21-30 of 37) with videos related to

Sort By:
Pageof 4
European Journal of Human Genetics : EJHG|February 4, 2018
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genesLaura Andreasen, Gustav Ahlberg, Chuyi Tang, 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 InhibitorsJonas Ghouse, Gustav Ahlberg, Laura Andreasen, 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 ArrestLaura 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 StudyOliver B Vad, Søren Z Diederichsen, Lucas Y Xing, et al.
Journal of the American Heart Association|April 30, 2024
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and DeathChristian 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 FibrillationOliver 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 variantsEmilie 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 mortalityJonas Ghouse, Christian T Have, Morten W Skov, et al.
Cardiovascular Research|May 4, 2019
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapseKatra Hadji-Turdeghal, Laura Andreasen, Christian M Hagen, et al.
Nature Communications|October 19, 2018
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillationGustav Ahlberg, Lena Refsgaard, Pia R Lundegaard, et al.
Pageof 4