Olesen SP - Search Results

1

IKs Gain- and Loss-of-Function in Early-Onset Lone Atrial Fibrillation.

Steffensen AB, Refsgaard L, Andersen MN, Vallet C, Mujezinovic A, Haunsø S, Svendsen JH, Olesen SP, Olesen MS, Schmitt N. Steffensen AB, et al. Among authors: olesen sp, olesen ms. J Cardiovasc Electrophysiol. 2015 Jul;26(7):715-23. doi: 10.1111/jce.12666. Epub 2015 May 4. J Cardiovasc Electrophysiol. 2015. PMID: 25786344

2

KCNQ1 mutation Q147R is associated with atrial fibrillation and prolonged QT interval.

Lundby A, Ravn LS, Svendsen JH, Olesen SP, Schmitt N. Lundby A, et al. Among authors: olesen sp. Heart Rhythm. 2007 Dec;4(12):1532-41. doi: 10.1016/j.hrthm.2007.07.022. Epub 2007 Aug 1. Heart Rhythm. 2007. PMID: 17997361

3

KCNE3 mutation V17M identified in a patient with lone atrial fibrillation.

Lundby A, Ravn LS, Svendsen JH, Hauns S, Olesen SP, Schmitt N. Lundby A, et al. Among authors: olesen sp. Cell Physiol Biochem. 2008;21(1-3):47-54. doi: 10.1159/000113746. Epub 2008 Jan 16. Cell Physiol Biochem. 2008. PMID: 18209471

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

High prevalence of long QT syndrome-associated SCN5A variants in patients with early-onset lone atrial fibrillation.

Olesen MS, Yuan L, Liang B, Holst AG, Nielsen N, Nielsen JB, Hedley PL, Christiansen M, Olesen SP, Haunsø S, Schmitt N, Jespersen T, Svendsen JH. Olesen MS, et al. Among authors: olesen sp. Circ Cardiovasc Genet. 2012 Aug 1;5(4):450-9. doi: 10.1161/CIRCGENETICS.111.962597. Epub 2012 Jun 8. Circ Cardiovasc Genet. 2012. PMID: 22685113

6

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation.

Christophersen IE, Olesen MS, Liang B, Andersen MN, Larsen AP, Nielsen JB, Haunsø S, Olesen SP, Tveit A, Svendsen JH, Schmitt N. Christophersen IE, et al. Among authors: olesen sp, olesen ms. Eur Heart J. 2013 May;34(20):1517-25. doi: 10.1093/eurheartj/ehs442. Epub 2012 Dec 21. Eur Heart J. 2013. PMID: 23264583

7

A novel KCND3 gain-of-function mutation associated with early-onset of persistent lone atrial fibrillation.

Olesen MS, Refsgaard L, Holst AG, Larsen AP, Grubb S, Haunsø S, Svendsen JH, Olesen SP, Schmitt N, Calloe K. Olesen MS, et al. Among authors: olesen sp. Cardiovasc Res. 2013 Jun 1;98(3):488-95. doi: 10.1093/cvr/cvt028. Epub 2013 Feb 11. Cardiovasc Res. 2013. PMID: 23400760

8

Very early-onset lone atrial fibrillation patients have a high prevalence of rare variants in genes previously associated with atrial fibrillation.

Olesen MS, Andreasen L, Jabbari J, Refsgaard L, Haunsø S, Olesen SP, Nielsen JB, Schmitt N, Svendsen JH. Olesen MS, et al. Among authors: olesen sp. Heart Rhythm. 2014 Feb;11(2):246-51. doi: 10.1016/j.hrthm.2013.10.034. Epub 2013 Oct 18. Heart Rhythm. 2014. PMID: 24144883

9

Gain-of-function mutations in potassium channel subunit KCNE2 associated with early-onset lone atrial fibrillation.

Nielsen JB, Bentzen BH, Olesen MS, David JP, Olesen SP, Haunsø S, Svendsen JH, Schmitt N. Nielsen JB, et al. Among authors: olesen sp, olesen ms. Biomark Med. 2014;8(4):557-70. doi: 10.2217/bmm.13.137. Biomark Med. 2014. PMID: 24796621

10

Functional consequences of genetic variation in sodium channel modifiers in early onset lone atrial fibrillation.

Denti F, Paludan-Müller C, Olesen SP, Haunsø S, Svendsen JH, Olesen MS, Bentzen BH, Schmitt N. Denti F, et al. Among authors: olesen sp. Per Med. 2018 Mar;15(2):93-102. doi: 10.2217/pme-2017-0076. Epub 2018 Jan 31. Per Med. 2018. PMID: 29714131

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