Morten Steen Salling Olesen

Morten Steen Salling Olesen

Professor MSO


Publication year:
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1 - 10 out of 17Page size: 10
  1. 2013
  2. 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

  3. 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

  4. 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

  5. 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

  6. 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

  7. 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

  8. Published

    Rare Variants in GJA5 Are Associated With Early-Onset Lone Atrial Fibrillation

    Christophersen, I. E., Holmegard, H. N., Jabbari, J., Sajadieh, Ahmad, Haunsø, Stig, Tveit, A., Svendsen, Jesper Hastrup & Olesen, Morten Steen Salling, 2013, In: Canadian Journal of Cardiology. 29, 1, p. 111-6 6 p.

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

  9. 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

  10. 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

  11. 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

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