Morten Steen Salling Olesen
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
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Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death
Bezzina, C., Barc, J., Mizusawa, Y., Remme, C. A., Gourraud, J-B., Simonet, F., Verkerk, A. O., Schwartz, P. J., Crotti, L., Dagradi, F., Guicheney, P., Fressart, V., Leenhardt, A., Antzelevitch, C., Bartkowiak, S., Borggrefe, M., Schimpf, R., Schulze-Bahr, E., Zumhagen, S., Behr, E. R. & 45 others, , 2013, In: Nature Genetics. 45, 9, p. 1044-1049 6 p.Research output: Contribution to journal › Letter › Research › peer-review
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Erratum: Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death (Nature Genetics (2013) 45 (1044-1049))
Brugada GWAS Genetics, B. G. G., 1 Nov 2013, In: Nature Genetics. 45, 11, 1 p.Research output: Contribution to journal › Comment/debate › Research › peer-review
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The Novel Desmin Mutant p.A120D Impairs Filament Formation, Prevents Intercalated Disk Localization, and Causes Sudden Cardiac Death
Brodehl, A., Dieding, M., Klauke, B., Dec, E., Madaan, S., Huang, T., Gargus, J., Fatima, A., Saric, T., Cakar, H., Walhorn, V., Tönsing, K., Skrzipczyk, T., Cebulla, R., Gerdes, D., Schulz, U., Gummert, J., Svendsen, J. H., Olesen, M. S. S., Anselmetti, D. & 3 others, , 2013, In: Circulation. Cardiovascular Genetics (Online). 6, 6, p. 615-623 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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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Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Nav1.5 gain-of-function mutation (G213D)
Callø, Kirstine, Broendberg, A. K., Christensen, A. H., Pedersen, L. N., Olesen, Morten Steen Salling, de Los Angeles Tejada, M., Friis, S., Thomsen, Morten Bækgaard, Bundgård, Henning & Jensen, H. K., 15 Apr 2018, In: International Journal of Cardiology. 257, p. 160-167 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Dyslipidemia, inflammation, calcification, and adiposity in aortic stenosis: a genome-wide study
Wells, Q. S., Söderberg, S., Stefánsson, K., Schott, J., Rader, D. J., Clarke, R., Engert, J. C., Thanassoulis, G. & Therapeutic targets for AoRtic stenosis using GEneTics (TARGET) Consortium, T. T. F. A. S. U. G. (. C., 2023, In: European Heart Journal. 44, 21, p. 1927-1939 13 p.Research output: Contribution to journal › Journal article › Research › peer-review
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The two-pore domain potassium channel, TWIK-1, has a role in the regulation of heart rate and atrial size
Christensen, A. H., Chatelain, F. C., Huttner, I. G., Olesen, Morten Steen Salling, Soka, M., Feliciangeli, S., Horvat, C., Santiago, C. F., Vandenberg, J. I., Schmitt, Nicole, Olesen, Søren-Peter, Lesage, F. & Fatkin, D., Aug 2016, In: Journal of Molecular and Cellular Cardiology. 97, p. 24-35 12 p.Research output: Contribution to journal › Journal article › Research › peer-review
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Natural History and Clinical Characteristics of the First 10 Danish Families With Familial ST-Depression Syndrome
Christensen, A. H., Nyholm, B. C., Vissing, C. R., Pietersen, A., Tfelt-Hansen, Jacob, Olesen, Morten Steen Salling, Pehrson, S., Iversen, Kasper, Jensen, H. K. & Bundgård, Henning, 2021, In: Journal of the American College of Cardiology. 77, 20, p. 2617-2619Research output: Contribution to journal › Letter › Research › peer-review
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Electrocardiographic Findings, Arrhythmias, and Left Ventricular Involvement in Familial ST-Depression Syndrome
Christensen, Alex Hørby, Vissing, C. R., Pietersen, A., Tfelt-Hansen, Jacob, Jensen, Thomas Hartvig Lindkær, Pehrson, S., Henriksen, F. L., Sandgaard, N. C. F., Iversen, Kasper, Jensen, H. K., Olesen, Morten Steen Salling & Bundgård, Henning, 2022, In: Circulation. Arrhythmia and electrophysiology. 15, 4, p. 231-240 e010688.Research output: Contribution to journal › Journal article › Research › peer-review
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Rare Variants in GJA5 Are Associated With Early-Onset Lone Atrial Fibrillation
Christophersen, I. E., Holmegard, H. N., Jabbari, J., Sajadieh, Ahmad, Haunsø, Stig, Tveit, A., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2013, In: Canadian Journal of Cardiology. 29, 1, p. 111-6 6 p.Research output: Contribution to journal › Journal article › Research › peer-review
ID: 49763464
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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