Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


Publication year:
All
71 - 80 out of 135Page size: 10
  1. 2019
  2. Published

    Visit-to-Visit Variability of Hemoglobin A1c in People Without Diabetes and Risk of Major Adverse Cardiovascular Events and All-Cause Mortality

    Ghouse, Jonas, Skov, M. W., Kanters, Jørgen K., Lind, B., Isaksen, Jonas L., Blanche, Paul Frédéric, Haunsø, Stig, Køber, Lars Valeur, Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling, Holst, A. G., Gerds, Thomas Alexander & Nielsen, J. B., 2019, In: Diabetes Care. 42, 1, p. 134-141 8 p.

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

  3. Published

    Reappraisal of variants previously linked with sudden infant death syndrome: results from three population-based cohorts

    Paludan-Müller, Christian, Ghouse, Jonas, Vad, O. B., Herfelt, C. B., Lundegaard, Pia Rengtved, Ahlberg, G., Schmitt, Nicole, Svendsen, Jesper Hastrup, Haunsø, Stig, Bundgård, Henning, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2019, In: European Journal of Human Genetics. 27, 9, p. 1427-1435

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

  4. Published

    Clinical implications of electrocardiographic bundle branch block in primary care

    Rasmussen, P. V., Skov, M. W., Ghouse, J., Pietersen, A., Hansen, S. M., Torp-Pedersen, C., Køber, Lars Valeur, Haunsø, Stig, Olesen, Morten Steen Salling, Svendsen, Jesper Hastrup, Melgaard, J., Graff, C., Holst, A. G. & Nielsen, J. B., 2019, In: Heart. 105, 15, p. 1160-1167

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

  5. Published

    Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation

    Seifert, M. B., Olesen, Morten Steen Salling, Christophersen, I. E., Nielsen, J. B., Carlson, J., Holmqvist, F., Tveit, A., Haunsø, Stig, Svendsen, Jesper Hastrup & Platonov, P. G., 2019, In: Annals of Noninvasive Electrocardiology (Online). 24, 6, 9 p., e12661.

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

  6. Published

    Reevaluation of genetic variants previously associated with arrhythmogenic right ventricular cardiomyopathy integrating population-based cohorts and proteomics data

    Ye, J. Z., Delmar, M., Lundby, Alicia & Olesen, Morten Steen Salling, 2019, In: Clinical Genetics. 96, 6, p. 506-514

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

  7. 2018
  8. Published

    Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation

    Ahlberg, G., Refsgaard, L., Lundegaard, Pia Rengtved, Andreasen, Laura Korsholm, Ranthe, M. F., Linscheid, N., Nielsen, J. B., Melbye, M., Haunsø, Stig, Sajadieh, Ahmad, Camp, L., Olesen, Søren-Peter, Rasmussen, Simon, Lundby, Alicia, Ellinor, P. T., Holst, A. G., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2018, In: Nature Communications. 9, 1, 11 p., 4316.

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

  9. Published

    Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

    Andreasen, Laura Korsholm, Ghouse, J., Skov, M. W., Have, C. T., Ahlberg, G., Rasmussen, P. V., Linneberg, Allan René, Pedersen, Oluf Borbye, Platonov, P. G., Haunsø, Stig, Svendsen, Jesper Hastrup, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, 2018, In: Frontiers in Physiology. 9, p. 1-9 894.

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

  10. Published

    Next-generation sequencing of AV nodal reentrant tachycardia patients identifies broad spectrum of variants in ion channel genes

    Andreasen, Laura Korsholm, Ahlberg, G., Tang, C., Andreasen, C., Hartmann, J. P., Tfelt-Hansen, Jacob, Behr, E. R., Pehrson, S., Haunsø, Stig, LuCamp, Weeke, P. E., Jespersen, Thomas, Olesen, Morten Steen Salling & Svendsen, Jesper Hastrup, 2018, In: European Journal of Human Genetics. 26, p. 660–668

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

  11. Published

    A Novel Familial Cardiac Arrhythmia Syndrome with Widespread ST-Segment Depression

    Bundgård, Henning, Jøns, C., Lodder, E. M., Izarzugaza, J. M. G., Romero Herrera, J. A., Pehrson, S., Tfelt-Hansen, Jacob, Ahlberg, G., Olesen, Morten Steen Salling, Holst, A. G., Wellens, H., de Villiers, C., Hastings, R., Stuart, G., Brunak, Søren, Wilde, A. A. M., Watkins, H. & Christensen, A. H., 2018, In: The New England Journal of Medicine. 379, 18, p. 1780-1781 2 p.

    Research output: Contribution to journal › Comment/debate › Research

  12. 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

Previous 1...4 5 6 7 8 9 10 11 ...14 Next

ID: 49763464