G. Ahlberg

发表

Explaining deep neural networks for knowledge discovery in electrocardiogram analysis

Vajira Lasantha Thambawita, N. Grarup, M. Maleckar, 2021, Scientific Reports.

Human iPSC modelling of a familial form of atrial fibrillation reveals a gain of function of If and ICaL in patient-derived cardiomyocytes

M. Memo, A. Consiglio, Á. Raya, 2019, Cardiovascular research.

Association of Variants Near the Bradykinin Receptor B2 Gene With Angioedema in Patients Taking ACE Inhibitors.

H. Ullum, S. Brunak, N. Eriksson, 2021, Journal of the American College of Cardiology.

Next-generation sequencing of AV Nodal Reentrant 1 Tachycardia patients identifies broad spectrum of 2 variants in ion channel genes 3

J. Svendsen, E. Behr, P. Weeke, 2017 .

Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts

Jørgen K. Kanters, T. Hansen, J. Svendsen, 2019, European Journal of Human Genetics.

Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

J. Svendsen, H. Bundgaard, P. Weeke, 2016, Molecular genetics & genomic medicine.

Effect of Loss-of-Function Genetic Variants in PCSK9 on Glycemic Traits, Neurocognitive Impairment, and Hepatobiliary Function.

H. Bundgaard, M. Olesen, J. Ghouse, 2021, Diabetes care.

Association of Common and Rare Genetic Variation in the 3‐Hydroxy‐3‐Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk

H. Bundgaard, M. Olesen, J. Ghouse, 2022, Journal of the American Heart Association.

Polygenic risk score for ACE-inhibitor-associated cough based on the discovery of new genetic loci.

D. Gudbjartsson, H. Ullum, U. Thorsteinsdóttir, 2022, European heart journal.

A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation

J. Svendsen, M. Olesen, L. Refsgaard, 2020, Scientific Reports.

Genetic analyses of the electrocardiographic QT interval and its components identify additional loci and pathways

M. P. Concas, May E. Montasser, Henry J. Lin, 2022, Nature Communications.

Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia‐associated variants

J. Svendsen, M. Olesen, S. Haunsø, 2017, Clinical genetics.

Hundreds of new murine genes cause CVD

M. Olesen, G. Ahlberg, 2022, Nature Cardiovascular Research.

Association of PCSK9 Loss-of-Function Variants With Risk of Heart Failure.

H. Bundgaard, M. Olesen, J. Ghouse, 2022, JAMA cardiology.

Multi-ethnic genome-wide association study for atrial fibrillation

Jay A. Montgomery, Nathan A. Bihlmeyer, Henry J. Lin, 2018, Nature Genetics.

Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality

Jørgen K. Kanters, T. Hansen, O. Pedersen, 2016, Genetics in Medicine.

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, 2018, Clinical genetics.

Genome-wide meta-analysis identifies 93 risk loci and enables risk prediction equivalent to monogenic forms of venous thromboembolism

D. Gudbjartsson, U. Thorsteinsdóttir, K. Stefánsson, 2023, Nature Genetics.

Genome-wide association study identifies 18 novel loci associated with left atrial volume and function

J. Svendsen, H. Bundgaard, M. Olesen, 2021, European heart journal.

Common variants near the bradykinin receptor B2 gene are associated with angioedema induced by angiotensin-converting-enzyme inhibitor treatment - a genome wide association study

H. Ullum, S. Brunak, N. Eriksson, 2020, medRxiv.

Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease

J. Svendsen, M. Olesen, S. Haunsø, 2017, Circulation. Cardiovascular genetics.

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

J. Svendsen, M. Olesen, S. Haunsø, 2017, Heart rhythm.

Early sarcomere and metabolic defects in a zebrafish pitx2c cardiac arrhythmia model

Y. Hellsten, D. Stainier, R. Marín-Juez, 2019, Proceedings of the National Academy of Sciences.

Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation

S. Rasmussen, J. Svendsen, P. Ellinor, 2018, Nature Communications.

Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation

J. Svendsen, M. Olesen, S. Haunsø, 2022, Frontiers in Genetics.

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.

Jørgen K. Kanters, T. Hansen, O. Pedersen, 2015, European heart journal.

Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

Jørgen K. Kanters, T. Hansen, O. Pedersen, 2018, Front. Physiol..

Genome-wide association study identifies locus at chromosome 2q32.1 associated with syncope and collapse

Jørgen K. Kanters, J. Svendsen, D. Hougaard, 2019, Cardiovascular research.

A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression.

S. Brunak, A. Wilde, H. Wellens, 2018, The New England journal of medicine.

Genetic analyses of the QT interval and its components in over 250K individuals identifies new loci and pathways affecting ventricular depolarization and repolarization

Jørgen K. Kanters, M. P. Concas, May E. Montasser, 2021, medRxiv.

Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation

J. Svendsen, A. Tveit, A. Sajadieh, 2020, Journal of clinical medicine.

Early-onset atrial fibrillation patients show reduced left ventricular ejection fraction and increased atrial fibrosis

J. Svendsen, T. B. Rasmussen, M. Olesen, 2020, Scientific Reports.

DeepFake electrocardiograms using generative adversarial networks are the beginning of the end for privacy issues in medicine

Jørgen K. Kanters, T. Hansen, N. Grarup, 2021, Scientific Reports.

Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes

J. Svendsen, E. Behr, P. Weeke, 2018, European Journal of Human Genetics.

Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts

J. Svendsen, M. Olesen, P. Lundegaard, 2019, European Journal of Human Genetics.

DeepFake electrocardiograms the key for open science for artificial intelligence in medicine

Jørgen K. Kanters, T. Hansen, N. Grarup, 2021 .

Apr 30, 2019 Rare truncating variants in the sarcomeric protein titin associate with familial and

J. Svendsen, P. Ellinor, M. Melbye, 2018 .

Multi-ethnic genome-wide association study for atrial fibrillation

Jay A. Montgomery, Brian R. Daniels, Blair H. Smith, 2018, Nature Genetics.

DeepFake electrocardiograms: the beginning of the end for privacy issues in medicine

Vajira Lasantha Thambawita, N. Grarup, M. Maleckar, 2021, medRxiv.

Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.

J. Svendsen, M. Olesen, S. Haunsø, 2017, Heart rhythm.

Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval.

Jørgen K. Kanters, O. Pedersen, N. Grarup, 2015, European heart journal.

Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation

A. Tveit, Y. Hellsten, P. Lundegaard, 2023, JACC. Basic to translational science.