Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


  1. Published

    Discovery of the first genome-wide significant risk loci for syncope and collapse: [Meeting Abstract]

    Ahlberg, G., lvs502, lvs502, Andreasen, L., Hagen, C. M., Ghouse, Jonas, Baekvad-Hansen, M., Bybjerg-Grauholm, J., Hougaard, D. M., Hedley, P., Haunsø, Stig, Svendsen, Jesper Hastrup, Jepps, Thomas Andrew Qvistgaard, Skov, M. W., Christiansen, M. & Olesen, Morten Steen Salling, 2019, In: European Heart Journal. 40, S1, p. 2539-2539 4259 .

    Research output: Contribution to journalConference abstract in journalResearch

  2. Published

    Genome wide association study based on cardiac magnetic resonance imaging in 23,634 individuals identifies five new loci associated with left atrial enlargement

    Ahlberg, G., Andreasen, Laura Korsholm, Ghouse, Jonas, Haunsø, Stig, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2020, In: European Journal of Human Genetics. 28, SUPPL 1, p. 63-64

    Research output: Contribution to journalConference abstract in journalResearchpeer-review

  3. Published

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

    Ahlberg, G., Refsgaard, L., Lundegaard, Pia Rengtved, Andreasen, Laura Korsholm, Ranthe, M. F., Linscheid, N., Nielsen, J. B., Melbye, M., Haunsø, Stig, Sajadieh, Ahmad, Camp, L., Olesen, Søren-Peter, Rasmussen, Simon, Lundby, Alicia, Ellinor, P. T., Holst, A. G., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2018, In: Nature Communications. 9, 1, 11 p., 4316.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

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

    Ahlberg, G., Andreasen, L., Ghouse, Jonas, Bertelsen, L., Bundgård, Henning, Haunsø, Stig, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2021, In: European Heart Journal. 42, 44, p. 4523–4534

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Atrial fibrillation - a complex polygenetic disease

    Andersen, J. H., Andreasen, Laura Korsholm & Olesen, Morten Steen Salling, 2021, In: European Journal of Human Genetics. 29, p. 1051-1060 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    Mutations in Genes Encoding Cardiac Ion Channels Previously Associated With Sudden Infant Death Syndrome (SIDS) Are Present With High Frequency in New Exome Data

    Andreasen, C. H., Refsgaard, L., Nielsen, J. B., Sajadieh, Ahmad, Winkel, B. G., Tfelt-Hansen, J., Haunsø, Stig, Holst, A. G., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2013, In: Canadian Journal of Cardiology. 29, 9, p. 1104-1109 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants

    Andreasen, C. H., Nielsen, J. B., Refsgaard, L., Holst, A. G., Christensen, Alex Hørby, Andreasen, Laura Korsholm, Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2013, In: European Journal of Human Genetics. 21, 9, p. 918-928 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

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

    Andreasen, Laura Korsholm, Bertelsen, L., Ghouse, Jonas, Lundegaard, Pia Rengtved, Ahlberg, G., Refsgaard, L., Rasmussen, T. B., Eiskjær, H., Haunsø, Stig, Vejlstrup, N., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2020, In: Scientific Reports. 10, 1, 8 p., 10039.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    Brugada syndrome risk loci seem protective against atrial fibrillation

    Andreasen, Laura Korsholm, Nielsen, J. B., Darkner, S., Christophersen, I. E., Jabbari, J., Refsgaard, L., Thiis, J. J., Sajadieh, Ahmad, Tveit, A., Haunsø, Stig, Svendsen, Jesper Hastrup, Schmitt, Nicole & Olesen, Morten Steen Salling, 26 Mar 2014, In: European Journal of Human Genetics. 22, p. 1357-1361 5 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Genetic aspects of lone atrial fibrillation: what do we know?

    Andreasen, Laura Korsholm, Nielsen, J. B. & Olesen, Morten Steen Salling, 2015, In: Current Pharmaceutical Design. 21, 5, p. 667-78 12 p.

    Research output: Contribution to journalReviewResearchpeer-review

  11. Published

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

    Andreasen, Laura Korsholm, Ghouse, J., Skov, M. W., Have, C. T., Ahlberg, G., Rasmussen, P. V., Linneberg, Allan René, Pedersen, Oluf Borbye, Platonov, P. G., Haunsø, Stig, Svendsen, Jesper Hastrup, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2018, In: Frontiers in Physiology. 9, p. 1-9 894.

    Research output: Contribution to journalJournal articleResearchpeer-review

  12. Published

    Genetic Variants Close to TTN, NKX2-5, and MYH6 Associate With AVNRT

    Andreasen, L., Ahlberg, G., Ægisdóttir, H. M., Sveinbjörnsson, G., Lundegaard, P. R., Hartmann, J. P., Paludan-Müller, C., Hadji-Turdeghal, K., Ghouse, J., Pehrson, S., Jensen, H. K., Riahi, S., Hansen, J., Sandgaard, N., Sørensen, E., Banasik, K., Sækmose, S. G., Bruun, M. T., Hjalgrim, H., Erikstrup, C. & 18 others, Pedersen, Ole Birger Vesterager, Wittig, M., Haunsø, Stig, Ostrowski, Sisse Rye, Genomic Consortium, D., Franke, A., Brunak, Søren, Kanters, Jørgen K., Ellervik, Christina, Bundgård, Henning, Ullum, H., Gudbjartsson, D. F., Thorsteinsdottir, U., Holm, H., Arnar, D. O., Stefansson, K., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2022, In: Circulation Research. 131, 10, p. 862-865

    Research output: Contribution to journalLetterResearchpeer-review

  13. Published

    Genetic Modifier of the QTc Interval Associated With Early-Onset Atrial Fibrillation

    Andreasen, Laura Korsholm, Nielsen, J. B., Christophersen, I. E., Holst, A. G., Sajadieh, Ahmad, Tveit, A., Haunsø, Stig, Svendsen, Jesper Hastrup, Schmitt, Nicole & Olesen, Morten Steen Salling, Oct 2013, In: Canadian Journal of Cardiology. 29, 10, p. 1234-40 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  14. Published

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

    Andreasen, Laura Korsholm, Ahlberg, G., Tang, C., Andreasen, C., Hartmann, J. P., Tfelt-Hansen, Jacob, Behr, E. R., Pehrson, S., Haunsø, Stig, LuCamp, Weeke, P. E., Jespersen, Thomas, Olesen, Morten Steen Salling & Svendsen, Jesper Hastrup, 2018, In: European Journal of Human Genetics. 26, p. 660–668

    Research output: Contribution to journalJournal articleResearchpeer-review

  15. Published

    Electrocardiographic Tpeak-Tend interval and risk of cardiovascular morbidity and mortality: Results from the Copenhagen ECG study

    Bachmann, T. N., Skov, M. W., Rasmussen, P., Graff, C., Pietersen, A., Lind, B., Struijk, J. J., Olesen, Morten Steen Salling, Haunsø, Stig, Køber, Lars Valeur, Svendsen, Jesper Hastrup, Holst, A. G. & Nielsen, J. B., Apr 2016, In: Heart rhythm : the official journal of the Heart Rhythm Society. 13, 4, p. 915-924 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  16. Published

    Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

    Behr, E. R., Savio-Galimberti, E., Barc, J., Holst, A. G., Petropoulou, E., Prins, B. P., Jabbari, J., Torchio, M., Berthet, M., Mizusawa, Y., Yang, T., Nannenberg, E. A., Dagradi, F., Weeke, P., Bastiaenan, R., Ackerman, M. J., Haunso, S., Leenhardt, A., Kääb, S., Probst, V. & 13 others, Redon, R., Sharma, S., Wilde, A., Tfelt-Hansen, J., Schwartz, P., Roden, D. M., Bezzina, C. R., Olesen, Morten Steen Salling, Darbar, D., Guicheney, P., Crotti, L., UK10K Consortium, U. C. & Jamshidi, Y., 1 Jun 2015, In: Cardiovascular Research. 106, 3, p. 520-529 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  17. Published

    Left Atrial Remodeling and Cerebrovascular Disease Assessed by Magnetic Resonance Imaging in Continuously Monitored Patients

    Bertelsen, L., Diederichsen, S. Z., Frederiksen, K. S., Haugan, K. J., Brandes, A., Graff, C., Krieger, D., Højberg, S., Olesen, Morten Steen Salling, Biering-Sørensen, Tor, Køber, Lars Valeur, Vejlstrup, N., Hasselbalch, Steen & Svendsen, Jesper Hastrup, 2022, In: Cerebrovascular Diseases. 51, 3, p. 403–412

    Research output: Contribution to journalJournal articleResearchpeer-review

  18. Published

    Left Atrial Late Gadolinium Enhancement is Associated With Incident Atrial Fibrillation as Detected by Continuous Monitoring With Implantable Loop Recorders

    Bertelsen, L., Diederichsen, S. Z., Haugan, K. J., Brandes, A., Graff, C., Krieger, D., Kronborg, C., Køber, Lars Valeur, Peters, D. C., Olesen, Morten Steen Salling, Højberg, S., Vejlstrup, N. & Svendsen, Jesper Hastrup, 2020, In: JACC. Cardiovascular imaging. 13, 8, p. 1690-1700 11 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  19. Published

    Verification of threshold for image intensity ratio analyses of late gadolinium enhancement magnetic resonance imaging of left atrial fibrosis in 1.5T scans

    Bertelsen, L., Alarcón, F., Andreasen, Laura Korsholm, Benito, E., Olesen, Morten Steen Salling, Vejlstrup, N., Mont, L. & Svendsen, Jesper Hastrup, 2020, In: International Journal of Cardiovascular Imaging. 36, p. 513–520 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  20. Published

    Cardiac magnetic resonance systematically overestimates mitral regurgitations by the indirect method

    Bertelsen, L., Vejlstrup, N., Andreasen, Laura Korsholm, Olesen, Morten Steen Salling & Svendsen, Jesper Hastrup, 2020, In: Open Heart. 7, 2, 9 p., e001323.

    Research output: Contribution to journalJournal articleResearchpeer-review

  21. 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 journalLetterResearchpeer-review

  22. 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 journalComment/debateResearchpeer-review

  23. 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 journalJournal articleResearchpeer-review

  24. 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 journalComment/debateResearch

  25. 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 journalJournal articleResearchpeer-review

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ID: 49763464