Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


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  1. Published

    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, Bastiaenen, R., Tfelt-Hansen, J., Olesen, Morten Steen Salling, Kääb, S., Beckmann, B. M., Weeke, P., Watanabe, H., Endo, N., Minamino, T., Horie, M., Ohno, S., Hasegawa, K., Makita, N., Nogami, A., Shimizu, W., Aiba, T., Froguel, P., Balkau, B., Lantieri, O., Torchio, M., Wiese, C., Weber, D., Wolswinkel, R., Coronel, R., Boukens, B. J., Bézieau, S., Charpentier, E., Chatel, S., Despres, A., Gros, F., Kyndt, F., Lecointe, S., Lindenbaum, P., Portero, V., Violleau, J., Gessler, M., Tan, H. L., Roden, D. M., Christoffels, V. M., Le Marec, H., Wilde, A. A., Probst, V., Schott, J., Dina, C. & Redon, R., 2013, In: Nature Genetics. 45, 9, p. 1044-1049 6 p.

    Research output: Contribution to journal › Letter › Research › peer-review

  2. Published

    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

  3. Published

    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, Christensen, Alex Hørby, Kimonis, V. & Milting, H., 2013, In: Circulation. Cardiovascular Genetics (Online). 6, 6, p. 615-623 9 p.

    Research output: Contribution to journal › Journal article › Research › peer-review

  4. 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

  5. Published

    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

  6. Published

    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

  7. Published

    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

  8. Published

    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. 2617-2619

    Research output: Contribution to journal › Letter › Research › peer-review

  9. Published

    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

  10. Published

    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

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ID: 49763464