Morten Steen Salling Olesen
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
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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
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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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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
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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, , 2013, In: Nature Genetics. 45, 9, p. 1044-1049 6 p.Research output: Contribution to journal › Letter › Research › peer-review
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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
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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, , 2013, In: Circulation. Cardiovascular Genetics (Online). 6, 6, p. 615-623 9 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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
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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
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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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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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Risk of atrial fibrillation as a function of the electrocardiographic PR interval: Results from the Copenhagen ECG Study
Nielsen, J. B., Pietersen, A., Graff, C., Lind, B., Struijk, J. J., Olesen, Morten Steen Salling, Haunsø, Stig, Gerds, Thomas Alexander, Ellinor, P. T., Køber, Lars Valeur, Svendsen, Jesper Hastrup & Holst, A. G., 2013, In: Heart rhythm : the official journal of the Heart Rhythm Society. 10, 9, p. 1249-1256 8 p.Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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. 179Research output: Contribution to journal › Journal article › Research › peer-review
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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. 179Research output: Contribution to journal › Journal article › Research › peer-review
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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
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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
ID: 49763464
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Effect of diabetes duration on the relationship between glycaemic control and risk of death in older adults with type 2 diabetes
Research output: Contribution to journal › Journal article › Research › peer-review
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192
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Electrocardiographic Precordial ST‐Segment Deviations and the Risk of Cardiovascular Death: Results From the Copenhagen ECG Study
Research output: Contribution to journal › Journal article › Research › peer-review
Published -
192
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Rare truncating variants in the sarcomeric protein titin associate with familial and early-onset atrial fibrillation
Research output: Contribution to journal › Journal article › Research › peer-review
Published