Haunsø S - Search Results

1

New exome data question the pathogenicity of genetic variants previously associated with catecholaminergic polymorphic ventricular tachycardia.

Jabbari J, Jabbari R, Nielsen MW, Holst AG, Nielsen JB, Haunsø S, Tfelt-Hansen J, Svendsen JH, Olesen MS. Jabbari J, et al. Among authors: haunso s. Circ Cardiovasc Genet. 2013 Oct;6(5):481-9. doi: 10.1161/CIRCGENETICS.113.000118. Epub 2013 Sep 11. Circ Cardiovasc Genet. 2013. PMID: 24025405

2

The pathogenicity of genetic variants previously associated with left ventricular non-compaction.

Abbasi Y, Jabbari J, Jabbari R, Yang RQ, Risgaard B, Køber L, Haunsø S, Tfelt-Hansen J. Abbasi Y, et al. Among authors: haunso s. Mol Genet Genomic Med. 2015 Dec 20;4(2):135-42. doi: 10.1002/mgg3.182. eCollection 2016 Mar. Mol Genet Genomic Med. 2015. PMID: 27066506 Free PMC article.

3

Analysis of 60 706 Exomes Questions the Role of De Novo Variants Previously Implicated in Cardiac Disease.

Paludan-Müller C, Ahlberg G, Ghouse J, Svendsen JH, Haunsø S, Olesen MS. Paludan-Müller C, et al. Among authors: haunso s. Circ Cardiovasc Genet. 2017 Dec;10(6):e001878. doi: 10.1161/CIRCGENETICS.117.001878. Circ Cardiovasc Genet. 2017. PMID: 29237690

4

Sick sinus syndrome, progressive cardiac conduction disease, atrial flutter and ventricular tachycardia caused by a novel SCN5A mutation.

Holst AG, Liang B, Jespersen T, Bundgaard H, Haunso S, Svendsen JH, Tfelt-Hansen J. Holst AG, et al. Among authors: haunso s. Cardiology. 2010;115(4):311-6. doi: 10.1159/000312747. Epub 2010 Apr 15. Cardiology. 2010. PMID: 20395683

5

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

Refsgaard L, Holst AG, Sadjadieh G, Haunsø S, Nielsen JB, Olesen MS. Refsgaard L, et al. Among authors: haunso s. Eur J Hum Genet. 2012 Aug;20(8):905-8. doi: 10.1038/ejhg.2012.23. Epub 2012 Feb 29. Eur J Hum Genet. 2012. PMID: 22378279 Free PMC article.

6

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: haunso s. 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

7

New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants.

Andreasen C, Nielsen JB, Refsgaard L, Holst AG, Christensen AH, Andreasen L, Sajadieh A, Haunsø S, Svendsen JH, Olesen MS. Andreasen C, et al. Among authors: haunso s. Eur J Hum Genet. 2013 Sep;21(9):918-28. doi: 10.1038/ejhg.2012.283. Epub 2013 Jan 9. Eur J Hum Genet. 2013. PMID: 23299917 Free PMC article.

8

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, Refsgaard L, Nielsen JB, Sajadieh A, Winkel BG, Tfelt-Hansen J, Haunsø S, Holst AG, Svendsen JH, Olesen MS. Andreasen C, et al. Among authors: haunso s. Can J Cardiol. 2013 Sep;29(9):1104-9. doi: 10.1016/j.cjca.2012.12.002. Epub 2013 Mar 7. Can J Cardiol. 2013. PMID: 23465283

9

Atrial fibrillation: the role of common and rare genetic variants.

Olesen MS, Nielsen MW, Haunsø S, Svendsen JH. Olesen MS, et al. Among authors: haunso s. Eur J Hum Genet. 2014 Mar;22(3):297-306. doi: 10.1038/ejhg.2013.139. Epub 2013 Jul 10. Eur J Hum Genet. 2014. PMID: 23838598 Free PMC article. Review.

10

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: haunso s. 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

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