Morten Steen Salling Olesen
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
- Published
A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression
Bundgård, Henning, Jøns, C., Lodder, E. M., Izarzugaza, J. M. G., Romero Herrera, J. A., Pehrson, S., Tfelt-Hansen, Jacob, Ahlberg, G., Olesen, Morten Steen Salling, Holst, A. G., Wellens, H., de Villiers, C., Hastings, R., Stuart, G., Brunak, Søren, Wilde, A. A. M., Watkins, H. & Christensen, A. H., 2018, In: The New England Journal of Medicine. 379, 18, p. 1780-1781 2 p.Research output: Contribution to journal › Comment/debate › Research
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A Novel Loss-of-Function Variant in the Chloride Ion Channel Gene Clcn2 Associates with Atrial Fibrillation
Hansen, T. H., Yan, Y., Ahlberg, G., Vad, O. B., Refsgaard, L., Dos Santos, J. L., Mutsaers, N., Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, 29 Jan 2020, In: Scientific Reports. 10, 1, 10 p., 1453.Research output: Contribution to journal › Journal article › Research › peer-review
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A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation
Olesen, Morten Steen Salling, Refsgaard, L., Holst, A. G., Larsen, A. P., Grubb, Søren, Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Søren-Peter, Schmitt, Nicole & Callø, Kirstine, 2013, In: Cardiovascular Research. 98, 3, p. 488-495 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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A phase 1 trial of AP30663, a KCa2 channel inhibitor in development for conversion of atrial fibrillation
Yfanti, C., Vestbjerg, B., van't Westende, J., Edvardsson, N., Monfort, L. M., Olesen, Morten Steen Salling, Bentzen, Bo Hjorth, Grunnet, Morten, Eveleens Maarse, B. C., Diness, Jonas Goldin, Kemme, M. J. B., Sørensen, U., Moerland, M., van Esdonk, M. J., Klaassen, E. S., Gal, P. & Holst, A. G., 2024, In: British Journal of Clinical Pharmacology. 90, 4, p. 1027-1035Research output: Contribution to journal › Journal article › Research › peer-review
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A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation
Henningsen, Kristoffer Mads Aaris, Olesen, Morten Steen Salling, Sajadieh, G., Haunsø, Stig & Svendsen, Jesper Hastrup, 2013, In: Journal of Negative Results in BioMedicine. 12, 2 p., 1.Research output: Contribution to journal › Journal article › Research › peer-review
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Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy
Nouhravesh, N., Ahlberg, G., Ghouse, J., Andreasen, C., Svendsen, Jesper Hastrup, Haunsø, Stig, Bundgård, Henning, Weeke, P. E. & Olesen, Morten Steen Salling, Nov 2016, In: Molecular Genetics & Genomic Medicine. 4, 6, p. 617-623Research output: Contribution to journal › Journal article › Research › peer-review
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Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease
Paludan-Müller, Christian, Ahlberg, G., Ghouse, Jonas, Svendsen, Jesper Hastrup, Haunsø, Stig & Olesen, Morten Steen Salling, 2017, In: Circulation. Cardiovascular genetics. 10, 6, 10 p., e001878.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Association between primary care electrocardiogram markers and Alzheimer's disease
Isaksen, Jonas L., Ghouse, Jonas, Skov, M. W., Olesen, Morten Steen Salling, Holst, A. G., Pietersen, A., Nielsen, J. B., Maier, A., Graff, C., Gerds, Thomas Alexander, Frikke-Schmidt, Ruth & Kanters, Jørgen K., 2023, In: Journal of the Neurological Sciences. 447, 6 p., 120581.Research output: Contribution to journal › Journal article › Research › peer-review
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Association of DIO2 and MCT10 Polymorphisms With Persistent Symptoms in LT4-Treated Patients in the UK Biobank
Jensen, Christian Zinck, Isaksen, Jonas L., Ahlberg, Gustav, Olesen, Morten Steen Salling, Nygaard, Birte, Ellervik, Christina & Kanters, Jørgen K., 2024, In: The Journal of clinical endocrinology and metabolism. 109, 2, p. e613-e622 10 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Association of Common and Rare Genetic Variation in the 3-Hydroxy-3-Methylglutaryl Coenzyme A Reductase Gene and Cataract Risk
Ghouse, Jonas, Ahlberg, Gustav, Skov, A. G., Bundgård, Henning & Olesen, Morten Steen Salling, 2022, In: Journal of the American Heart Association. 11, 12, p. 1-39 e025361.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 49763464
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225
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Effect of diabetes duration on the relationship between glycaemic control and risk of death in older adults with type 2 diabetes
Research output: Contribution to journal › Journal article › Research › peer-review
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193
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Electrocardiographic Precordial ST‐Segment Deviations and the Risk of Cardiovascular Death: Results From the Copenhagen ECG Study
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
192
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Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
Research output: Contribution to journal › Journal article › Research › peer-review
Published