Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


  1. Published

    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 journalJournal articleResearchpeer-review

  2. Published

    Atrial fibrillation: the role of common and rare genetic variants

    Olesen, Morten Steen Salling, Nielsen, M. W., Haunsø, Stig & Svendsen, Jesper Hastrup, Mar 2014, In: European Journal of Human Genetics. 22, 3, p. 297-306 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  3. Published

    Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation

    Olesen, Morten Steen Salling, Andreasen, Laura Korsholm, Jabbari, J., Refsgaard, L., Haunsø, Stig, Olesen, Søren-Peter, Nielsen, J. B., Schmitt, Nicole & Svendsen, Jesper Hastrup, Feb 2014, In: Heart Rhythm. 11, 2, p. 246-251 6 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  4. Published

    Fascicular heart blocks and risk of adverse cardiovascular outcomes: Results from a large primary care population

    Nyholm, B. C., Ghouse, J., Lee, C. J. Y., Rasmussen, P. V., Pietersen, A., Hansen, S. M., Torp-Pedersen, Christian, Køber, Lars Valeur, Haunsø, Stig, Olesen, Morten Steen Salling, Svendsen, Jesper Hastrup, Graff, C., Holst, A. G., Nielsen, J. B. & Skov, M. W., 2022, In: Heart Rhythm. 19, 2, p. 252-259 8 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. Published

    Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction

    Ntalla, I., Weng, L. C., Cartwright, J. H., Hall, A. W., Sveinbjornsson, G., Tucker, N. R., Choi, S. H., Chaffin, M. D., Roselli, C., Barnes, M. R., Mifsud, B., Warren, H. R., Hayward, C., Marten, J., Cranley, J. J., Concas, M. P., Gasparini, P., Boutin, T., Kolcic, I., Polasek, O. & 167 others, Rudan, I., Araujo, N. M., Lima-Costa, M. F., Ribeiro, A. L. P., Souza, R. P., Tarazona-Santos, E., Giedraitis, V., Ingelsson, E., Mahajan, A., Morris, A. P., Del Greco M, F., Foco, L., Gögele, M., Hicks, A. A., Cook, J. P., Lind, L., Lindgren, C. M., Sundström, J., Nelson, C. P., Riaz, M. B., Samani, N. J., Sinagra, G., Ulivi, S., Kähönen, M., Mishra, P. P., Mononen, N., Nikus, K., Caulfield, M. J., Dominiczak, A., Padmanabhan, S., Montasser, M. E., O’Connell, J. R., Ryan, K., Shuldiner, A. R., Aeschbacher, S., Conen, D., Risch, L., Thériault, S., Hutri-Kähönen, N., Lehtimäki, T., Lyytikäinen, L. P., Raitakari, O. T., Barnes, C. L. K., Campbell, H., Joshi, P. K., Wilson, J. F., Isaacs, A., Kors, J. A., van Duijn, C. M., Huang, P. L., Gudnason, V., Harris, T. B., Launer, L. J., Smith, A. V., Bottinger, E. P., Loos, Ruth, Nadkarni, G. N., Preuss, M. H., Correa, A., Mei, H., Wilson, J., Meitinger, T., Müller-Nurasyid, M., Peters, A., Waldenberger, M., Mangino, M., Spector, T. D., Rienstra, M., van de Vegte, Y. J., van der Harst, P., Verweij, N., Kääb, S., Schramm, K., Sinner, M. F., Strauch, K., Cutler, M. J., Fatkin, D., London, B., Olesen, Morten Steen Salling, Roden, D. M., Benjamin Shoemaker, M., Gustav Smith, J., Biggs, M. L., Bis, J. C., Brody, J. A., Psaty, B. M., Rice, K., Sotoodehnia, N., De Grandi, A., Fuchsberger, C., Pattaro, C., Pramstaller, P. P., Ford, I., Wouter Jukema, J., Macfarlane, P. W., Trompet, S., Dörr, M., Felix, S. B., Völker, U., Weiss, S., Havulinna, A. S., Jula, A., Sääksjärvi, K., Salomaa, V., Guo, X., Heckbert, S. R., Lin, H. J., Rotter, J. I., Taylor, K. D., Yao, J., de Mutsert, R., Maan, A. C., Mook-Kanamori, D. O., Noordam, R., Cucca, F., Ding, J., Lakatta, E. G., Qian, Y., Tarasov, K. V., Levy, D., Lin, H., Newton-Cheh, C. H., Lunetta, K. L., Murray, A. D., Porteous, D. J., Smith, B. H., Stricker, B. H., Uitterlinden, A., van den Berg, M. E., Haessler, J., Jackson, R. D., Kooperberg, C., Peters, U., Reiner, A. P., Whitsel, E. A., Alonso, A., Arking, D. E., Boerwinkle, E., Ehret, G. B., Soliman, E. Z., Avery, C. L., Gogarten, S. M., Kerr, K. F., Laurie, C. C., Seyerle, A. A., Stilp, A., Assa, S., Abdullah Said, M., Yldau van der Ende, M., Lambiase, P. D., Orini, M., Ramirez, J., Van Duijvenboden, S., Arnar, D. O., Gudbjartsson, D. F., Holm, H., Sulem, P., Thorleifsson, G., Thorolfsdottir, R. B., Thorsteinsdottir, U., Benjamin, E. J., Tinker, A., Stefansson, K., Ellinor, P. T., Jamshidi, Y., Lubitz, S. A. & Munroe, P. B., 1 Dec 2020, In: Nature Communications. 11, 1, 2542.

    Research output: Contribution to journalJournal articleResearchpeer-review

  6. Published

    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. 617-623

    Research output: Contribution to journalJournal articleResearchpeer-review

  7. Published

    Screening of the Ito regulatory subunit Klf15 in patients with early-onset lone atrial fibrillation

    Nielsen, M. W., Olesen, Morten Steen Salling, Refsgaard, L., Haunsø, Stig & Svendsen, Jesper Hastrup, 2013, In: Frontiers in Genetics. 4, p. 1-2 2 p., 88.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    The genetic component of Brugada syndrome

    Nielsen, M. W., Holst, A. G., Olesen, Søren-Peter & Olesen, Morten Steen Salling, 2013, In: Frontiers in Physiology. 4, p. 179

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. Published

    The genetic component of Brugada syndrome

    Nielsen, M. W., Holst, A. G., Olesen, Søren-Peter & Olesen, Morten Steen Salling, 2013, In: Frontiers in Physiology. 4, p. 179

    Research output: Contribution to journalJournal articleResearchpeer-review

  10. Published

    Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation

    Nielsen, J. B., Bentzen, Bo Hjorth, Olesen, Morten Steen Salling, David, J., Olesen, Søren-Peter, Haunsø, Stig, Svendsen, Jesper Hastrup & Schmitt, Nicole, Apr 2014, In: Biomarkers in Medicine. 8, 4, p. 557-570 14 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

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ID: 49763464