Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


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  1. Published

    Implantable loop recorder detection of atrial fibrillation to prevent stroke (The LOOP Study): a randomised controlled trial

    Svendsen, Jesper Hastrup, Diederichsen, S. Z., Højberg, S., Krieger, D. W., Graff, C., Kronborg, C., Olesen, Morten Steen Salling, Nielsen, J. B., Holst, A. G., Brandes, A., Haugan, K. J. & Køber, Lars Valeur, 2021, In: The Lancet. 398, 10310, p. 1507-1516 10 p.

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

  2. Published

    Insights into the genome-wide association studies of the electrocardiographic early repolarization pattern

    Risgaard, B., Olesen, Morten Steen Salling & Tfelt-Hansen, J., Oct 2012, In: Heart Rhythm. 9, 10, p. 1635-6 2 p.

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

  3. Published

    Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation

    Sinner, M. F., Tucker, N. R., Lunetta, K. L., Ozaki, K., Smith, J. G., Trompet, S., Bis, J. C., Lin, H., Chung, M. K., Nielsen, J. B., Lubitz, S. A., Krijthe, B. P., Magnani, J. W., Ye, J., Gollob, M. H., Tsunoda, T., Müller-Nurasyid, M., Lichtner, P., Peters, A., Dolmatova, E. & 31 others, Kubo, M., Smith, J. D., Psaty, B. M., Smith, N. L., Jukema, J. W., Chasman, D. I., Albert, C. M., Ebana, Y., Furukawa, T., Macfarlane, P. W., Harris, T. B., Darbar, D., Dörr, M., Holst, A. G., Svendsen, Jesper Hastrup, Hofman, A., Uitterlinden, A. G., Gudnason, V., Isobe, M., Malik, R., Dichgans, M., Rosand, J., Van Wagoner, D. R., Benjamin, E. J., Milan, D. J., Melander, O., Heckbert, S. R., Ford, I., Liu, Y., Olesen, Morten Steen Salling & METASTROKE Consortium, M. C., 2014, In: Circulation. 130, 15, p. 1225-1235 11 p.

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

  4. Published

    Integration of 60,000 exomes and ACMG guidelines question the role of Catecholaminergic Polymorphic Ventricular Tachycardia-associated variants

    Paludan-Müller, Christian, Ahlberg, Gustav, Ghouse, Jonas, Herfelt, C., Svendsen, Jesper Hastrup, Haunsø, Stig, Kanters, Jørgen K. & Olesen, Morten Steen Salling, Jan 2017, In: Clinical Genetics. 91, 1, p. 63–72

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

  5. Published

    Integration of Scandinavian genetic data with UK biobank data implicates the RBM20 gene with atrial fibrillation pathogenesis

    Vad, O. B., Angeli, Elisavet, Liss, M., Ahlberg, G., Andreasen, L., Christophersen, I. E., Tveit, A., Haunsø, Stig, Svendsen, Jesper Hastrup, Lundegaard, Pia Rengtved, Gotthardt, M. & Olesen, Morten Steen Salling, 2021, In: European Heart Journal. 42, p. 3319-3319 1 p.

    Research output: Contribution to journal › Conference abstract in journal › Research

  6. Published

    Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis

    Ghouse, J., Sveinbjörnsson, G., Vujkovic, M., Seidelin, A-S., Gellert-Kristensen, H., Ahlberg, G., Tragante, V., Rand, S. A., Brancale, J., Vilarinho, S., Lundegaard, P. R., Sørensen, E., Erikstrup, C., Bruun, M. T., Jensen, B. A., Brunak, S., Banasik, K., Ullum, H., Verweij, N., Lotta, L. & 31 others, Baras, A., Mirshahi, T., Carey, D. J., Kaplan, D. E., Lynch, J., Morgan, T., Schwantes-An, T., Dochtermann, D. R., Pyarajan, S., Tsao, P. S., Laisk, T., Mägi, R., Kozlitina, J., Tybjærg-Hansen, Anne, Jones, D., Knowlton, K. U., Nadauld, L., Ferkingstad, E., Björnsson, E. S., Ulfarsson, M. O., Sturluson, Á., Sulem, P., Pedersen, Ole Birger Vesterager, Ostrowski, Sisse Rye, Gudbjartsson, D. F., Stefansson, K., Olesen, Morten Steen Salling, Chang, K., Bundgård, Henning, Stender, Stefan & DBDS Genomic Consortium, D. G. C., 2024, In: Nature Genetics. 56, p. 827–837 18 p.

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

  7. Published

    Investigating gene-microRNA networks in atrial fibrillation patients with mitral valve regurgitation

    Santos, J. L., Rodríguez, I., Olesen, Morten Steen Salling, Bentzen, Bo Hjorth & Schmitt, Nicole, 2020, In: PLoS ONE. 15, 5, 21 p., e0232719.

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

  8. Published

    Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada Syndrome mutant

    Yuan, L., Koivumaki, J., Liang, B., Lorentzen, L. G., Tang, C., Andersen, M. N., Svendsen, Jesper Hastrup, Tfelt-Hansen, J., Maleckar, M., Schmitt, Nicole, Olesen, Morten Steen Salling & Jespersen, Thomas, 21 Feb 2014, In: American Journal of Physiology: Heart and Circulatory Physiology. 306, 8, p. H1204-12

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

  9. Published

    J-shaped association between QTc interval duration and the risk of atrial fibrillation: Results From the Copenhagen ECG Study

    Nielsen, J. B., Graff, C., Pietersen, A., Lind, B., Struijk, J. J., Olesen, Morten Steen Salling, Haunsø, Stig, Gerds, Thomas Alexander, Svendsen, Jesper Hastrup, Køber, Lars Valeur & Holst, A. G., 2013, In: Journal of the American College of Cardiology. 61, 25, p. 2557-2564 8 p.

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

  10. Published

    KCNE1 G38S polymorphism is not the cause of long QT syndrome

    Kanters, Jørgen K., Olesen, Morten Steen Salling & Christiansen, M., 20 Jan 2016, In: Journal of Electrocardiology. 49, 2, p. 249-50 2 p.

    Research output: Contribution to journal › Comment/debate › Research › peer-review

  11. 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 journal › Journal article › Research › peer-review

  12. 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 journal › Journal article › Research › peer-review

  13. Published

    Loss of Cardiac Splicing Regulator RBM20 Is Associated With Early-Onset Atrial Fibrillation

    Vad, Oliver Tim Bundgaard, Angeli, Elisavet, Liss, M., Ahlberg, Gustav, Andreasen, Laura Korsholm, Christophersen, I. E., Hansen, Camilla Collin, Møller, S., Hellsten, Ylva, Haunsø, Stig, Tveit, A., Svendsen, Jesper Hastrup, Gotthardt, M., Lundegaard, Pia Rengtved & Olesen, Morten Steen Salling, 2024, In: JACC: Basic to Translational Science. 9, 2, p. 163-180

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

  14. Published

    Loss-of-Function Variants in Cytoskeletal Genes Are Associated with Early-Onset Atrial Fibrillation

    Vad, O. B., Paludan-Müller, Christian, Ahlberg, G., Kalsto, S. M., Ghouse, Jonas, Andreasen, Laura Korsholm, Haunsø, Stig, Tveit, A., Sajadieh, Ahmad, Christophersen, I. E., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2020, In: Journal of Clinical Medicine. 9, 2, 12 p., 372.

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

  15. Published

    Loss-of-Function Variants in the SYNPO2L Gene Are Associated With Atrial Fibrillation

    Clausen, A. G., Vad, O. B., Andersen, J. H. & Olesen, Morten Steen Salling, 2021, In: Frontiers in Cardiovascular Medicine. 8, 9 p., 650667.

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

  16. Published

    Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease

    Nielsen, J. B., Rom, O., Surakka, I., Graham, S. E., Zhou, W., Roychowdhury, T., Fritsche, L. G., Taliun, S. A. G., Sidore, C., Liu, Y., Gabrielsen, M. E., Skogholt, A. H., Wolford, B., Overton, W., Zhao, Y., Chen, J., Zhang, H., Hornsby, W. E., Acheampong, A., Grooms, A. & 30 others, Schaefer, A., Zajac, G. J. M., Villacorta, L., Zhang, J., Brumpton, B., Loset, M., Rai, V., Lundegaard, Pia Rengtved, Olesen, Morten Steen Salling, Taylor, K. D., Palmer, N. D., Chen, Y., Choi, S. H., Lubitz, S. A., Ellinor, P. T., Barnes, K. C., Daya, M., Rafaels, N., Weiss, S. T., Lasky-Su, J., Tracy, R. P., Vasan, R. S., Cupples, L. A., Mathias, R. A., Yanek, L. R., Becker, L. C., Peyser, P. A., Bielak, L. F., Smith, J. A. & Aslibekyan, S., 2020, In: Nature Communications. 11, 1, 12 p., 6417.

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

  17. 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 journal › Journal article › Research › peer-review

  18. Published

    Multi-ethnic genome-wide association study for atrial fibrillation

    Roselli, C., Chaffin, M. D., Weng, L-C., Aeschbacher, S., Ahlberg, G., Albert, C. M., Almgren, P., Alonso, A., Anderson, C. D., Aragam, K. G., Arking, D. E., Barnard, J., Bartz, T. M., Benjamin, E. J., Bihlmeyer, N. A., Bis, J. C., Bloom, H. L., Boerwinkle, E., Bottinger, E. B., Brody, J. A. & 34 others, Calkins, H., Campbell, A., Cappola, T. P., Carlquist, J., Chasman, D. I., Chen, L. Y., Chen, Y. I., Choi, E., Choi, S. H., Christophersen, I. E., Chung, M. K., Cole, J. W., Conen, D., Cook, J., Crijns, H. J., Cutler, M. J., Damrauer, S. M., Daniels, B. R., Darbar, D., Delgado, G., Denny, J. C., Dichgans, M., Doerr, M., Dudink, E. A., Lind, L., Loos, Ruth, Olesen, Morten Steen Salling, Refsgaard, L., Svendsen, Jesper Hastrup, Weeke, P. E., et al., E. A., Lubitz, S. A., Lunetta, K. L. & Ellinor, P. T., Sep 2018, In: Nature Genetics. 50, 9, p. 1225-1233

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

  19. Published

    Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications

    Sterenborg, R. B. T. M., Steinbrenner, I., Li, Y., Bujnis, M. N., Naito, T., Marouli, E., Galesloot, T. E., Babajide, O., Andreasen, L., Astrup, A., Åsvold, B. O., Bandinelli, S., Beekman, M., Beilby, J. P., Bork-Jensen, J., Boutin, T., Brody, J. A., Brown, S. J., Brumpton, B., Campbell, P. J. & 121 others, Cappola, A. R., Ceresini, G., Chaker, L., Chasman, D. I., Concas, M. P., Coutinho de Almeida, R., Cross, S. M., Cucca, F., Deary, I. J., Kjaergaard, A. D., Echouffo Tcheugui, J. B., Ellervik, Christina, Eriksson, J. G., Ferrucci, L., Freudenberg, J., Fuchsberger, C., Gieger, C., Giulianini, F., Gögele, M., Graham, S. E., Grarup, Niels, Gunjača, I., Hansen, Torben, Harding, B. N., Harris, S. E., Haunsø, Stig, Hayward, C., Hui, J., Ittermann, T., Jukema, J. W., Kajantie, E., Kanters, Jørgen K., Kårhus, L. L., Kiemeney, L. A. L. M., Kloppenburg, M., Kühnel, B., Lahti, J., Langenberg, C., Lapauw, B., Leese, G., Li, S., Liewald, D. C. M., Linneberg, Allan René, Lominchar, J. V. T., Luan, J., Martin, N. G., Matana, A., Meima, M. E., Meitinger, T., Meulenbelt, I., Mitchell, B. D., Møllehave, L. T., Mora, S., Naitza, S., Nauck, M., Netea-Maier, R. T., Noordam, R., Nursyifa, Casia, Okada, Y., Onano, S., Papadopoulou, A., Palmer, C. N. A., Pattaro, C., Pedersen, Oluf Borbye, Peters, A., Pietzner, M., Polašek, O., Pramstaller, P. P., Psaty, B. M., Punda, A., Ray, D., Redmond, P., Richards, J. B., Ridker, P. M., Russ, T. C., Ryan, K. A., Olesen, Morten Steen Salling, Schultheiss, U. T., Selvin, E., Siddiqui, M. K., Sidore, C., Slagboom, P. E., Sørensen, Thorkild I.A., Soto-Pedre, E., Spector, T. D., Spedicati, B., Srinivasan, S., Starr, J. M., Stott, D. J., Tanaka, T., Torlak, V., Trompet, S., Tuhkanen, J., Uitterlinden, A. G., van den Akker, E. B., van den Eynde, T., van der Klauw, M. M., van Heemst, D., Verroken, C., Visser, W. E., Vojinovic, D., Völzke, H., Waldenberger, M., Walsh, J. P., Wareham, N. J., Weiss, S., Willer, C. J., Wilson, S. G., Wolffenbuttel, B. H. R., Wouters, H. J. C. M., Wright, M. J., Yang, Q., Zemunik, T., Zhou, W., Zhu, G., Zöllner, S., Smit, J. W. A., Peeters, R. P., Köttgen, A., Teumer, A. & Medici, M., 2024, In: Nature Communications. 15, 1, 18 p., 888.

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

  20. 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

  21. Published

    Mutation analysis of the candidate genes -, , and in patients with arrhythmogenic right ventricular cardiomyopathy

    Refsgaard, L., Olesen, Morten Steen Salling, Møller, D. V., Christiansen, M., Haunsø, Stig, Svendsen, Jesper Hastrup & Christensen, Alex Hørby, 1 Dec 2012, In: Applied and Translational Genomics. 1, p. 44-46

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

  22. 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 journal › Journal article › Research › peer-review

  23. Published

    Nationwide (Denmark) Study of Symptoms Preceding Sudden Death due to Arrhythmogenic Right Ventricular Cardiomyopathy

    Sadjadieh, G., Jabbari, R., Risgaard, B., Olesen, Morten Steen Salling, Haunsø, Stig, Tfelt-Hansen, J. & Winkel, B. G., 1 Apr 2014, In: American Journal of Cardiology. 113, 7, p. 1250-1254 5 p.

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

  24. 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

  25. Published

    New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia

    Jabbari, J., Jabbari, R., Nielsen, M. W., Holst, A. G., Nielsen, J. B., Haunsø, Stig, Tfelt-Hansen, J., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2013, In: Circulation. Cardiovascular Genetics (Online). 6, 5, p. 481-489 9 p.

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

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ID: 49763464