Morten Steen Salling Olesen
Professor MSO
Molecular Cardiology and Membrane Proteins
Blegdamsvej 3
2200 København N.
- 2014
- Published
Nationwide (Denmark) Study of Symptoms Preceding Sudden Death due to Arrhythmogenic Right Ventricular Cardiomyopathy
Sadjadieh, G., Jabbari, R., Risgaard, B., Olesen, Morten Steen Salling, Haunsø, Stig, Tfelt-Hansen, J. & Winkel, B. G., 1 Apr 2014, In: American Journal of Cardiology. 113, 7, p. 1250-1254 5 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Integrating genetic, transcriptional, and functional analyses to identify 5 novel genes for atrial fibrillation
Sinner, M. F., Tucker, N. R., Lunetta, K. L., Ozaki, K., Smith, J. G., Trompet, S., Bis, J. C., Lin, H., Chung, M. K., Nielsen, J. B., Lubitz, S. A., Krijthe, B. P., Magnani, J. W., Ye, J., Gollob, M. H., Tsunoda, T., Müller-Nurasyid, M., Lichtner, P., Peters, A., Dolmatova, E. & 31 others, , 2014, In: Circulation. 130, 15, p. 1225-1235 11 p.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
New population-based exome data question the pathogenicity of some genetic variants previously associated with Marfan syndrome
Yang, R., Jabbari, J., Cheng, X., Jabbari, R., Nielsen, J. B., Risgaard, B., Chen, X., Sajadieh, Ahmad, Haunsø, Stig, Svendsen, Jesper Hastrup, Olesen, Morten Steen Salling & Tfelt-Hansen, J., 2014, In: B M C Genetics. 15, p. 1-8 8 p., 74.Research output: Contribution to journal › Journal article › Research › peer-review
- Published
Investigations of the Navβ1b sodium channel subunit in human ventricle; functional characterization of the H162P Brugada Syndrome mutant
Yuan, L., Koivumaki, J., Liang, B., Lorentzen, L. G., Tang, C., Andersen, M. N., Svendsen, Jesper Hastrup, Tfelt-Hansen, J., Maleckar, M., Schmitt, Nicole, Olesen, Morten Steen Salling & Jespersen, Thomas, 21 Feb 2014, In: American Journal of Physiology: Heart and Circulatory Physiology. 306, 8, p. H1204-12Research output: Contribution to journal › Journal article › Research › peer-review
- 2013
- 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
- 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
- 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
- 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, , 2013, In: Nature Genetics. 45, 9, p. 1044-1049 6 p.Research output: Contribution to journal › Letter › Research › peer-review
- 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
- 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, , 2013, In: Circulation. Cardiovascular Genetics (Online). 6, 6, p. 615-623 9 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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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 -
190
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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