Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


  1. 2013
  2. 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

  3. 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

  4. Published

    Genetic variation in the two-pore domain potassium channel, TASK-1, may contribute to an atrial substrate for arrhythmogenesis

    Liang, B., Soka, M., Christensen, Alex Hørby, Olesen, Morten Steen Salling, Larsen, A. P., Knop, Filip Krag, Wang, F., Nielsen, J. B., Andersen, M. N., Humphreys, D., Mann, S. A., Huttner, I. G., Vandenberg, J. I., Svendsen, Jesper Hastrup, Haunsø, Stig, Preiss, T., Seebohm, G., Olesen, Søren-Peter, Schmitt, Nicole & Fatkin, D., 27 Dec 2013, In: Journal of Molecular and Cellular Cardiology. 67, p. 69-76 7 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  5. 2014
  6. 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 journalJournal articleResearchpeer-review

  7. Published

    New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome

    Yang, R., Jabbari, J., Cheng, X., Jabbari, R., Nielsen, J. B., Risgaard, B., Chen, X., Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling & Tfelt-Hansen, J., 2014, In: B M C Genetics. 15, p. 1-8 8 p., 74.

    Research output: Contribution to journalJournal articleResearchpeer-review

  8. Published

    Risk prediction of cardiovascular death based on the QTc interval: evaluating age and gender differences in a large primary care population

    Nielsen, J. B., Graff, C., Rasmussen, P. V., Pietersen, A., Lind, B., Olesen, Morten Steen Salling, Struijk, J. J., Haunsø, Stig, Svendsen, Jesper Hastrup, Køber, Lars Valeur, Gerds, Thomas Alexander & Holst, A. G., 2014, In: European Heart Journal. 35, 20, p. 1335-44 10 p.

    Research output: Contribution to journalJournal articleResearchpeer-review

  9. 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

  10. 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 journalJournal articleResearchpeer-review

  11. 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

  12. 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

Previous 1 2 3 4 5 6 7 8 ...14 Next

ID: 49763464