Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


Publication year:
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41 - 50 out of 137Page size: 10
  1. 2016
  2. 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

  3. Published

    Genetic Misdiagnoses and the Potential for Health Disparities

    Manrai, A. K., Funke, B. H., Rehm, H. L., Olesen, Morten Steen Salling, Maron, B. A., Szolovits, P., Margulies, D. M., Loscalzo, J. & Kohane, I. S., 18 Aug 2016, In: New England Journal of Medicine. 375, 7, p. 655-65 11 p.

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

  4. Published

    Analyses of more than 60,000 exomes questions the role of numerous genes previously associated with dilated cardiomyopathy

    Nouhravesh, N., Ahlberg, G., Ghouse, J., Andreasen, C., Svendsen, Jesper Hastrup, Haunsø, Stig, Bundgård, Henning, Weeke, P. E. & Olesen, Morten Steen Salling, Nov 2016, In: Molecular Genetics & Genomic Medicine. 4, 6, p. 617-623

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

  5. Published

    The role of common genetic variants in atrial fibrillation

    Paludan-Müller, Christian, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2016, In: Journal of Electrocardiology. 49, 6, p. 864-870

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

  6. 2017
  7. Published

    Numerous Brugada syndrome-associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality

    Ghouse, Jonas, Have, C. T., Skov, M. W., Andreasen, Laura Korsholm, Ahlberg, G., Nielsen, J. B., Skaaby, T., Olesen, Søren-Peter, Grarup, Niels, Linneberg, Allan René, Pedersen, Oluf Borbye, drb459, drb459, Haunsø, Stig, Svendsen, Jesper Hastrup, Hansen, Torben, Kanters, Jørgen K. & Olesen, Morten Steen Salling, May 2017, In: Genetics In Medicine. 19, 5, p. 521-528 8 p.

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

  8. Published

    Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants

    Gregers, E., Ahlberg, G., Christensen, T., Jabbari, J., Larsen, K. O., Herfelt, C. B., Henningsen, K. M., Andreasen, Laura Korsholm, Thiis, J. J., Lund, J., Holme, S., Haunsø, Stig, Bentzen, Bo Hjorth, Schmitt, Nicole, Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, Oct 2017, In: Heart Rhythm. 14, 10, p. 1531-1538

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

  9. Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a KCNA5 p.D322H mutation

    Mora, C., Serzanti, M., Giacomelli, A., Turco, V., Marchina, E., Bertini, V., Piovani, G., Savio, G., Refsgaard, L., Olesen, Morten Steen Salling, Cortellini, V. & Dell'Era, P., Oct 2017, In: Stem Cell Research. 24, p. 29-32 4 p.

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

  10. Generation of induced pluripotent stem cells (iPSC) from an atrial fibrillation patient carrying a PITX2 p.M200V mutation

    Mora, C., Serzanti, M., Giacomelli, A., Beltramone, S., Marchina, E., Bertini, V., Piovani, G., Refsgaard, L., Olesen, Morten Steen Salling, Cortellini, V. & Dell'Era, P., Oct 2017, In: Stem Cell Research. 24, p. 8-11 4 p.

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

  11. Published

    Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease

    Paludan-Müller, Christian, Ahlberg, G., Ghouse, Jonas, Svendsen, Jesper Hastrup, Haunsø, Stig & Olesen, Morten Steen Salling, 2017, In: Circulation. Cardiovascular genetics. 10, 6, 10 p., e001878.

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

  12. 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

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ID: 49763464