Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


Publication year:
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101 - 125 out of 137Page size: 25
  1. 2015
  2. Published

    The role of the sodium current complex in a nonreferred nationwide cohort of sudden infant death syndrome

    Winkel, B. G., Yuan, L., Olesen, Morten Steen Salling, Sadjadieh, G., Wang, Y., Risgaard, B., Jabbari, R., Haunsø, Stig, Holst, A. G., Hollegaard, M. V., Tfelt-Hansen, J. & Jespersen, Thomas, Jun 2015, In: Heart rhythm : the official journal of the Heart Rhythm Society. 12, 6, p. 1241-1249 9 p.

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

  3. Published

    Common and rare variants in SCN10A modulate the risk of atrial fibrillation.

    Jabbari, J., Olesen, Morten Steen Salling, Yuan, L., Nielsen, J. B., Liang, B., Macri, V., Christophersen, I. E., Nielsen, N., Sajadieh, Ahmad, Ellinor, P. T., Grunnet, Morten, Haunsø, Stig, Holst, A. G., Svendsen, Jesper Hastrup & Jespersen, Thomas, 2015, In: Circulation: Cardiovascular Genetics. 8, 1, p. 64-73 10 p.

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

  4. 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 journal › Review › Research › peer-review

  5. Published

    IKs Gain- and Loss-of-Function In Early-Onset Lone Atrial Fibrillation

    Steffensen, Annette Buur, Refsgaard, L., Andersen, M. N., Vallet, C., Mujezinovic, A., Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Søren-Peter, Olesen, Morten Steen Salling & Schmitt, Nicole, 2015, In: Journal of Cardiovascular Electrophysiology. 26, 7, p. 715-23 9 p.

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

  6. 2014
  7. Published

    Electrocardiographic Precordial ST‐Segment Deviations and the Risk of Cardiovascular Death: Results From the Copenhagen ECG Study

    Rasmussen, P. V., Nielsen, J. B., Pietersen, A., Graff, C., Lind, B., Struijk, J. J., Olesen, Morten Steen Salling, Haunsø, Stig, Køber, Lars Valeur, Svendsen, Jesper Hastrup & Holst, A. G., Jun 2014, In: American Heart Association. Journal. Cardiovascular and Cerebrovascular Disease. 3, 3, p. 1-16 16 p., e000549.

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

  8. 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

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

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

  12. 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

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

  14. 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

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

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

  17. 2013
  18. 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 journal › Journal article › Research › peer-review

  19. 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

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

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

  22. Published

    A polymorphism associated with increased levels of YKL-40 and the risk of early onset of lone atrial fibrillation

    Henningsen, Kristoffer Mads Aaris, Olesen, Morten Steen Salling, Sajadieh, G., Haunsø, Stig & Svendsen, Jesper Hastrup, 2013, In: Journal of Negative Results in BioMedicine. 12, 2 p., 1.

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

  23. 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

  24. Published

    Familial atrial fibrillation predicts increased risk of mortality: A study in Danish twins

    Christophersen, I. E., Budtz-Joergensen, Esben, Olesen, Morten Steen Salling, Haunsø, Stig, Christensen, K. & Svendsen, Jesper Hastrup, 2013, In: Circulation: Arrhythmia and Electrophysiology. 6, 1, p. 10-15 6 p.

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

  25. 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

  26. 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

  27. 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

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

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ID: 49763464