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G. Ahlberg · SciRah

Researcher profile · Semantic Scholar

G. Ahlberg

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G. Ahlberg — researcher profile on SciRah

h-index: 17
Works: 64
Citations: 1,744

Most-cited papers

Multi-Ethnic Genome-wide Association Study for Atrial Fibrillation
C. Roselli, M. Chaffin, Lu-Chen Weng, S. Aeschbacher +214 more
2018Nature Genetics727 citations Open access
Semantic Scholar
Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
G. Ahlberg, L. Refsgaard, P. Lundegaard, L. Andreasen +14 more
2018Nature Communications125 citations Open access
Semantic Scholar
Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism
J. Ghouse, V. Tragante, G. Ahlberg, S. Rand +32 more
2023Nature Genetics120 citations
Semantic Scholar
DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicine
V. Thambawita, J. Isaksen, Steven Hicks, J. Ghouse +14 more
2021Scientific Reports108 citations Open access
Semantic Scholar
Explaining deep neural networks for knowledge discovery in electrocardiogram analysis
Steven Hicks, J. Isaksen, V. Thambawita, J. Ghouse +13 more
2021Scientific Reports81 citations Open access
Semantic Scholar
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.
J. Ghouse, C. Have, P. Weeke, Jonas Bille Nielsen +13 more
2015European Heart Journal61 citations Open access
Semantic Scholar
Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes
P. Benzoni, G. Campostrini, Sara Landi, Valeria Bertini +25 more
2019Cardiovascular Research59 citations Open access
Semantic Scholar
Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways
William J. Young, N. Lahrouchi, A. Isaacs, T. Duong +162 more
2022Nature Communications53 citations Open access
Semantic Scholar
Early sarcomere and metabolic defects in a zebrafish pitx2c cardiac arrhythmia model
M. M. Collins, G. Ahlberg, C. Hansen, S. Guenther +8 more
2019Proceedings of the National Academy of Sciences of the United States of America46 citations Open access
Semantic Scholar
Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia‐associated variants
C. Paludan-Müller, G. Ahlberg, J. Ghouse, C. Herfelt +4 more
2017Clinical Genetics34 citations
Semantic Scholar
Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy
N. Nouhravesh, G. Ahlberg, J. Ghouse, C. Andreasen +5 more
2016Molecular Genetics & Genomic Medicine30 citations Open access
Semantic Scholar
Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
J. Ghouse, C. Have, M. W. Skov, L. Andreasen +13 more
2016Genetics in Medicine26 citations Open access
Semantic Scholar
Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation
O. Vad, E. Angeli, Martin Liss, G. Ahlberg +11 more
2023JACC: Basic to Translational Science22 citations Open access
Semantic Scholar
Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors.
J. Ghouse, G. Ahlberg, L. Andreasen, K. Banasik +12 more
2021Journal of the American College of Cardiology22 citations Open access
Semantic Scholar
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.
H. Bundgaard, C. Jøns, E. Lodder, J. M. Izarzugaza +14 more
2018New England Journal of Medicine22 citations Open access
Semantic Scholar
Distinguishing pathogenic mutations from background genetic noise in cardiology: The use of large genome databases for genetic interpretation
J. Ghouse, M. W. Skov, R. S. Bigseth, G. Ahlberg +2 more
2018Clinical Genetics22 citations
Semantic Scholar
Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation
O. Vad, C. Paludan-Müller, G. Ahlberg, Silje Madeleine Kalstø +8 more
2020Journal of Clinical Medicine20 citations Open access
Semantic Scholar
Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis
L. Andreasen, L. Bertelsen, J. Ghouse, P. Lundegaard +8 more
2020Scientific Reports17 citations Open access
Semantic Scholar
Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse
K. Hadji-Turdeghal, L. Andreasen, C. Hagen, G. Ahlberg +12 more
2019Cardiovascular Research17 citations Open access
Semantic Scholar
Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.
Emilie Gregers, G. Ahlberg, Thea Christensen, J. Jabbari +12 more
2017Heart Rhythm16 citations
Semantic Scholar
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes
L. Andreasen, G. Ahlberg, Chuyi Tang, C. Andreasen +10 more
2018European Journal of Human Genetics15 citations Open access
Semantic Scholar
A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation
Thea Hansen, Yannan Yan, G. Ahlberg, O. Vad +7 more
2020Scientific Reports13 citations Open access
Semantic Scholar
Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.
J. Ghouse, V. Tragante, Ayesha Muhammad, G. Ahlberg +23 more
2022European Heart Journal12 citations Open access
Semantic Scholar
Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts
C. Paludan-Müller, J. Ghouse, O. Vad, Cecilie B. Herfelt +9 more
2019European Journal of Human Genetics11 citations Open access
Semantic Scholar
Association of Common and Rare Genetic Variation in the 3‐Hydroxy‐3‐Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk
J. Ghouse, G. Ahlberg, A. Skov, H. Bundgaard +1 more
2022Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease9 citations Open access
Semantic Scholar
Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure.
Linea C Trudsø, J. Ghouse, G. Ahlberg, H. Bundgaard +1 more
2022JAMA cardiology8 citations Open access
Semantic Scholar
Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT.
L. Andreasen, G. Ahlberg, Hildur M. Aegisdottir, G. Sveinbjornsson +34 more
2022Circulation Research8 citations Open access
Semantic Scholar
Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease
C. Paludan-Müller, G. Ahlberg, J. Ghouse, J. Svendsen +2 more
2017Circulation: Cardiovascular Genetics6 citations Open access
Semantic Scholar
Atrial Fibrillation Screening According to Genetic Risk: A Secondary Analysis of the Randomized LOOP Study.
O. Vad, S. Diederichsen, L. Y. Xing, C. Paludan-Müller +10 more
2025Journal of the American College of Cardiology5 citations
Semantic Scholar
Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population.
C. Paludan-Müller, Simon Larsen, G. Ahlberg, L. Andreasen +6 more
2022Circulation Genomic and Precision Medicine5 citations Open access
Semantic Scholar
Genome-Wide Association Study of Accessory Atrioventricular Pathways.
Hildur M. Aegisdottir, L. Andreasen, Rosa B. Thorolfsdottir, G. Sveinbjornsson +39 more
2024JAMA cardiology4 citations Open access
Semantic Scholar
Effect of Loss-of-Function Genetic Variants in PCSK9 on Glycemic Traits, Neurocognitive Impairment, and Hepatobiliary Function.
J. Ghouse, G. Ahlberg, H. Bundgaard, M. Olesen
2021Diabetes Care4 citations Open access
Semantic Scholar
DeepFake electrocardiograms: the beginning of the end for privacy issues in medicine
V. Thambawita, J. Isaksen, Steven Hicks, J. Ghouse +14 more
2021medRxiv4 citations Open access
Semantic Scholar
Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest
L. Andreasen, J. Ghouse, M. W. Skov, C. Have +10 more
2018Frontiers in Physiology4 citations Open access
Semantic Scholar
Presence of Atrioventricular Nodal Reentrant Tachycardia Is Associated With Cardiomyopathy, Heart Failure, and Death
C. Paludan-Müller, N. Stampe, L. M. Monfort, L. Andreasen +9 more
2024Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease3 citations Open access
Semantic Scholar
Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation
O. Vad, Yannan Yan, Federico Denti, G. Ahlberg +10 more
2022Frontiers in Genetics3 citations Open access
Semantic Scholar
Rare coding variants in MYH6 are associated with atrial fibrillation: results from 45,596 exomes representing the general population
O. Vad, C. Paludan-Muller, G. Ahlberg, L. Andreasen +5 more
20202 citations
Semantic Scholar
Genetically predicted adipose tissue distribution influences the risk of atherosclerosis.
O. Vad, C. Paludan-Müller, L. M. Monfort, G. Ahlberg +2 more
2023European Journal of Preventive Cardiology1 citations
Semantic Scholar
Loss-of-function variants in founder population highlight atrial myopathy as susceptibility to atrial fibrillation
C. Paludan-Muller, O. Vad, K. Kahnert, G. Ahlberg +9 more
2022European Heart Journal1 citations
Semantic Scholar
Genome-wide multi-trait analysis on cardioembolic stroke identifies 47 novel loci
L. Meseguer Monfort, G. Ahlberg, L. Andreasen, J. Ghouse +4 more
2022European Heart Journal1 citations Open access
Semantic Scholar
Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization
William J. Young, N. Lahrouchi, A. Isaacs, T. Duong +162 more
2021medRxiv1 citations Open access
Semantic Scholar
Integration of Scandinavian genetic data with UK biobank data implicates the RBM20 gene with atrial fibrillation pathogenesis
O. Vad, E. Angeli, Martin Liss, G. Ahlberg +8 more
2021European Heart Journal1 citations
Semantic Scholar
Genome-wide association study of patients with atrioventricular nodal reentry tachycardia
L. Andreasen, G. Ahlberg, J. Hartmann, C. Paludan-Mueller +10 more
2020European Heart Journal1 citations
Semantic Scholar
Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes
L. Andreasen, G. Ahlberg, Chuyi Tang, C. Andreasen +10 more
2018European Journal of Human Genetics1 citations Open access
Semantic Scholar
Interaction between DIO2 polymorphisms and LT4 treatment on psychological well-being outcomes and cardiovascular risk factors: a population-based cross-sectional study in uk biobank
Jensen Christian Zinck, Isaksen Jonas Lynggaard, G. Ahlberg, Olesen Morten Salling +3 more
2023Endocrine Abstracts0 citations
Semantic Scholar
Poster Session 2The morphology of complete and incomplete right bundle branch block in the general population
J. Senftinger, Y. Fakhri, J. Isaksen, G. Ahlberg +4 more
2022Journal of Electrocardiology0 citations
Semantic Scholar
High prevalence of deleterious variants in cardiomyopathy genes in patients with early onset atrial fibrillation
O. Vad, G. Ahlberg, C. Paludan-Muller, L. Refsgaard +5 more
2022European Heart Journal0 citations
Semantic Scholar
Hundreds of new murine genes cause CVD
G. Ahlberg, M. Olesen
2022Nature Cardiovascular Research0 citations
Semantic Scholar
Genome-wide association study on cerebral white-matter hyperintensities in 36,577 individuals
J. Jespersen, G. Ahlberg, L. Andreasen, J. Ghouse +6 more
2022European Heart Journal0 citations
Semantic Scholar
Poster Session 1Baseline filtering alleviates generalization issues for neural networks for electrocardiogram analysis
J. Isaksen, Steven Hicks, V. Thambawita, S. Mæland +10 more
2022Journal of Electrocardiology0 citations
Semantic Scholar

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