Morten Salling Olesen

Professor

Denmark

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Professor Morten Salling Olesen is a faculty member at the University of Copenhagen in Denmark. His research primarily focuses on atrial fibrillation, genetic determinants of cardiovascular diseases, and the effects of screening and risk factor control on cardiac health. His recent publications include studies on genome-wide associations, polygenic risk prediction, and the epidemiology of atrial fibrillation.

Articles (16)

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2025

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2024

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2024

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2024

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2024

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2024

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2024

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2024

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2023

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2023

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2022

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2022

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2022

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2022

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2021

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2020

Collaborators (14)

Jesper Hastrup Svendsen

Professor

University of Copenhagen

DENMARK

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Elsayed Soliman

Director/Professor

Wake Forest School of Medicine

UNITED STATES

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Søren Zöga Diederichsen

DENMARK

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Nicholas Marston

Harvard University

UNITED STATES

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Pia Lundegaard

Københavns Universitet

DENMARK

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Axel Brandes

Professor

University of Southern Denmark

DENMARK

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Lars Kober

Professor

Rigshospitalet

DENMARK

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Kazuo Miyazawa

Broad Institute of MIT and Harvard

UNITED STATES

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Eleonora MARCHINA

MD, Assistant Professor of Medical Genetics

University of Brescia

ITALY

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Thomas Jespersen

Københavns Universitet

DENMARK

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Diane Fatkin

Victor Chang Cardiac Research Institute

AUSTRALIA

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Jonas Isaksen

Københavns Universitet

DENMARK

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Bjarni Jóhann Vilhjálmsson

Professor

Aarhus University

DENMARK

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Christina Ellervik

Affiliate Professor

DENMARK

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Morten Salling Olesen

Research Interests

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About

Articles (16)

Meta-analysis of genome-wide associations and polygenic risk prediction for atrial fibrillation in more than 180,000 cases.

Association of DIO2 and MCT10 Polymorphisms With Persistent Symptoms in LT4-Treated Patients in the UK Biobank

Heart Failure Events After Long-term Continuous Screening for Atrial Fibrillation: Results From the Randomized LOOP Study

Potential Influence of Risk Factor Control on the Association Between Lipoprotein(a) and Atherosclerotic Cardiovascular Disease

Genetic Determinants of Left Atrial Function Are Associated With Stroke

Novel Genes Associated With Atrial Fibrillation and the Predictive Models for AF Incorporating Polygenic Risk Scores and PheWAS-Derived Risk Factors

The ABC‐Stroke Risk Score and Effects of Atrial Fibrillation Screening on Stroke Prevention: Results From the Randomized LOOP Study

Tackling a growing healthcare challenge: atrial fibrillation epidemiology, prevention, and underlying causes

Effects of Atrial Fibrillation Screening According to N-Terminal Pro-B-Type Natriuretic Peptide: A Secondary Analysis of the Randomized LOOP Study

Genetic Atrial Cardiomyopathies: Common Features, Specific Differences, and Broader Relevance to Understanding Atrial Cardiomyopathy

Systolic Blood Pressure and Effects of Screening for Atrial Fibrillation With Long-Term Continuous Monitoring (a LOOP Substudy)

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

Hundreds of new murine genes cause CVD

Clinical Implications of SCN10A Loss-of-Function Variants in 169 610 Exomes Representing the General Population

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

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

Collaborators (14)

Jesper Hastrup Svendsen

Elsayed Soliman

Søren Zöga Diederichsen

Nicholas Marston

Pia Lundegaard

Axel Brandes

Lars Kober

Kazuo Miyazawa

Eleonora MARCHINA

Thomas Jespersen

Diane Fatkin

Jonas Isaksen

Bjarni Jóhann Vilhjálmsson

Christina Ellervik

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