Olesen MS - Search Results

1

High prevalence of genetic variants previously associated with Brugada syndrome in new exome data.

Risgaard B, Jabbari R, Refsgaard L, Holst AG, Haunsø S, Sadjadieh A, Winkel BG, Olesen MS, Tfelt-Hansen J. Risgaard B, et al. Among authors: olesen ms. Clin Genet. 2013 Nov;84(5):489-95. doi: 10.1111/cge.12126. Epub 2013 Mar 11. Clin Genet. 2013. PMID: 23414114

2

Single nucleotide polymorphisms in inflammatory genes and the risk of early onset of lone atrial fibrillation.

Henningsen KM, Olesen MS, Pedersen M, Nielsen L, Haunsø S, Bruunsgaard H, Svendsen JH. Henningsen KM, et al. Among authors: olesen ms. Inflamm Res. 2010 Nov;59(11):965-9. doi: 10.1007/s00011-010-0210-8. Epub 2010 May 20. Inflamm Res. 2010. PMID: 20490891

3

[Catecholaminergic polymorphic ventricular tachycardia is a rare inherited heart disease].

Holst AG, Tfelt-Hansen J, Olesen MS, Theilade J, Winkel BG, Christensen AH, Bundgaard H, Haunsø S, Svendsen JH. Holst AG, et al. Among authors: olesen ms. Ugeskr Laeger. 2010 Aug 2;172(31):2140-4. Ugeskr Laeger. 2010. PMID: 20670590 Review. Danish.

4

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation.

Olesen MS, Jespersen T, Nielsen JB, Liang B, Møller DV, Hedley P, Christiansen M, Varró A, Olesen SP, Haunsø S, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: olesen sp. Cardiovasc Res. 2011 Mar 1;89(4):786-93. doi: 10.1093/cvr/cvq348. Epub 2010 Nov 4. Cardiovasc Res. 2011. PMID: 21051419

5

Incomplete right bundle branch block: a novel electrocardiographic marker for lone atrial fibrillation.

Nielsen JB, Olesen MS, Tangø M, Haunsø S, Holst AG, Svendsen JH. Nielsen JB, et al. Among authors: olesen ms. Europace. 2011 Feb;13(2):182-7. doi: 10.1093/europace/euq436. Epub 2010 Dec 7. Europace. 2011. PMID: 21138928

6

Whole-genome amplified DNA from stored dried blood spots is reliable in high resolution melting curve and sequencing analysis.

Winkel BG, Hollegaard MV, Olesen MS, Svendsen JH, Haunsø S, Hougaard DM, Tfelt-Hansen J. Winkel BG, et al. Among authors: olesen ms. BMC Med Genet. 2011 Feb 9;12:22. doi: 10.1186/1471-2350-12-22. BMC Med Genet. 2011. PMID: 21306642 Free PMC article.

7

Screening of KCNN3 in patients with early-onset lone atrial fibrillation.

Olesen MS, Jabbari J, Holst AG, Nielsen JB, Steinbrüchel DA, Jespersen T, Haunsø S, Svendsen JH. Olesen MS, et al. Europace. 2011 Jul;13(7):963-7. doi: 10.1093/europace/eur007. Epub 2011 Mar 11. Europace. 2011. PMID: 21398315

8

Common polymorphisms in KCNJ5 [corrected] are associated with early-onset lone atrial fibrillation in Caucasians.

Jabbari J, Olesen MS, Holst AG, Nielsen JB, Haunso S, Svendsen JH. Jabbari J, et al. Among authors: olesen ms. Cardiology. 2011;118(2):116-20. doi: 10.1159/000323840. Epub 2011 May 9. Cardiology. 2011. PMID: 21555883

9

A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias.

Olesen MS, Jensen NF, Holst AG, Nielsen JB, Tfelt-Hansen J, Jespersen T, Sajadieh A, Haunsø S, Lund JT, Calloe K, Schmitt N, Svendsen JH. Olesen MS, et al. Can J Cardiol. 2011 Jul-Aug;27(4):523.e17-23. doi: 10.1016/j.cjca.2011.01.003. Epub 2011 May 28. Can J Cardiol. 2011. PMID: 21621375 English, French.

10

Letter by Olesen et al regarding article, "MOG1: a new susceptibility gene for Brugada syndrome".

Olesen MS, Holst AG, Schmitt N. Olesen MS, et al. Circ Cardiovasc Genet. 2011 Oct;4(5):e22; author reply e23. doi: 10.1161/CIRCGENETICS.111.960799. Circ Cardiovasc Genet. 2011. PMID: 22010171 No abstract available.

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