Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


Publication year:
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11 - 17 out of 17Page size: 10
  1. 2013
  2. 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 journal › Journal article › Research › peer-review

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

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

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

  6. 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

  7. 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

  8. 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

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