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Gustav Ahlberg

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European Heart Journal|July 11, 2015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT intervalJonas Ghouse, Christian Theil Have, Peter Weeke, 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.
Scientific Reports|November 10, 2021
DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicineVajira Thambawita, Jonas L Isaksen, Steven A Hicks, et al.
The New England Journal of Medicine|November 1, 2018
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment DepressionHenning Bundgaard, Christian Jøns, Elisabeth M Lodder, et al.
European Heart Journal|April 10, 2025
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndromeAlex Hørby Christensen, Gang Pan, Rasmus L Marvig, et al.
Cardiovascular Research|September 11, 2019
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytesPatrizia Benzoni, Giulia Campostrini, Sara Landi, et al.
European Heart Journal|June 25, 2022
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic lociJonas Ghouse, Vinicius Tragante, Ayesha Muhammad, et al.
Nature Genetics|November 14, 2025
Genome-wide association study and polygenic risk prediction of hypothyroidismSøren A Rand, Gustav Ahlberg, Vinicius Tragante, et al.
Nature Genetics|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Circulation Research|October 7, 2022
Genetic Variants Close to <i>TTN</i>, <i>NKX2-5</i>, and <i>MYH6</i> Associate With AVNRTLaura Andreasen, Gustav Ahlberg, Hildur M Ægisdottir, et al.
Pageof 5

Showing results (31-40 of 45) with videos related to

Sort By:
Pageof 5
European Heart Journal|July 11, 2015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT intervalJonas Ghouse, Christian Theil Have, Peter Weeke, 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.
Scientific Reports|November 10, 2021
DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicineVajira Thambawita, Jonas L Isaksen, Steven A Hicks, et al.
The New England Journal of Medicine|November 1, 2018
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment DepressionHenning Bundgaard, Christian Jøns, Elisabeth M Lodder, et al.
European Heart Journal|April 10, 2025
Gain-of-function enhancer variant near KCNB1 causes familial ST-depression syndromeAlex Hørby Christensen, Gang Pan, Rasmus L Marvig, et al.
Cardiovascular Research|September 11, 2019
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytesPatrizia Benzoni, Giulia Campostrini, Sara Landi, et al.
European Heart Journal|June 25, 2022
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic lociJonas Ghouse, Vinicius Tragante, Ayesha Muhammad, et al.
Nature Genetics|November 14, 2025
Genome-wide association study and polygenic risk prediction of hypothyroidismSøren A Rand, Gustav Ahlberg, Vinicius Tragante, et al.
Nature Genetics|January 19, 2023
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolismJonas Ghouse, Vinicius Tragante, Gustav Ahlberg, et al.
Circulation Research|October 7, 2022
Genetic Variants Close to <i>TTN</i>, <i>NKX2-5</i>, and <i>MYH6</i> Associate With AVNRTLaura Andreasen, Gustav Ahlberg, Hildur M Ægisdottir, et al.
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