McKenna WJ - Search Results

1

The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.

Hedley PL, Kanters JK, Dembic M, Jespersen T, Skibsbye L, Aidt FH, Eschen O, Graff C, Behr ER, Schlamowitz S, Corfield V, McKenna WJ, Christiansen M. Hedley PL, et al. Among authors: mckenna wj. Circ Cardiovasc Genet. 2013 Oct;6(5):452-61. doi: 10.1161/CIRCGENETICS.113.000137. Epub 2013 Sep 10. Circ Cardiovasc Genet. 2013. PMID: 24021552

2

The variation of the sarcolipin gene (SLN) in atrial fibrillation, long QT syndrome and sudden arrhythmic death syndrome.

Nyberg MT, Stoevring B, Behr ER, Ravn LS, McKenna WJ, Christiansen M. Nyberg MT, et al. Among authors: mckenna wj. Clin Chim Acta. 2007 Jan;375(1-2):87-91. doi: 10.1016/j.cca.2006.06.020. Epub 2006 Jun 22. Clin Chim Acta. 2007. PMID: 17010328

3

Functional assessment of compound mutations in the KCNQ1 and KCNH2 genes associated with long QT syndrome.

Grunnet M, Behr ER, Calloe K, Hofman-Bang J, Till J, Christiansen M, McKenna WJ, Olesen SP, Schmitt N. Grunnet M, et al. Among authors: mckenna wj. Heart Rhythm. 2005 Nov;2(11):1238-49. doi: 10.1016/j.hrthm.2005.07.025. Heart Rhythm. 2005. PMID: 16253915

4

High-efficiency multiplex capillary electrophoresis single strand conformation polymorphism (multi-CE-SSCP) mutation screening of SCN5A: a rapid genetic approach to cardiac arrhythmia.

Hofman-Bang J, Behr ER, Hedley P, Tfelt-Hansen J, Kanters JK, Haunsøe S, McKenna WJ, Christiansen M. Hofman-Bang J, et al. Among authors: mckenna wj. Clin Genet. 2006 Jun;69(6):504-11. doi: 10.1111/j.1399-0004.2006.00621.x. Clin Genet. 2006. PMID: 16712702

5

A novel Myosin essential light chain mutation causes hypertrophic cardiomyopathy with late onset and low expressivity.

Andersen PS, Hedley PL, Page SP, Syrris P, Moolman-Smook JC, McKenna WJ, Elliott PM, Christiansen M. Andersen PS, et al. Among authors: mckenna wj. Biochem Res Int. 2012;2012:685108. doi: 10.1155/2012/685108. Epub 2012 Apr 11. Biochem Res Int. 2012. PMID: 22957257 Free PMC article.

6

Genetic risk for acquired arrhythmia.

Behr ER, McKenna WJ. Behr ER, et al. Among authors: mckenna wj. Trends Genet. 2003 Sep;19(9):470-3. doi: 10.1016/S0168-9525(03)00200-2. Trends Genet. 2003. PMID: 12957537 No abstract available.

7

Micro-exons of the cardiac myosin binding protein C gene: flanking introns contain a disproportionately large number of hypertrophic cardiomyopathy mutations.

Frank-Hansen R, Page SP, Syrris P, McKenna WJ, Christiansen M, Andersen PS. Frank-Hansen R, et al. Among authors: mckenna wj. Eur J Hum Genet. 2008 Sep;16(9):1062-9. doi: 10.1038/ejhg.2008.52. Epub 2008 Mar 12. Eur J Hum Genet. 2008. PMID: 18337725

8

Cardiac myosin binding protein-C mutations in families with hypertrophic cardiomyopathy: disease expression in relation to age, gender, and long term outcome.

Page SP, Kounas S, Syrris P, Christiansen M, Frank-Hansen R, Andersen PS, Elliott PM, McKenna WJ. Page SP, et al. Among authors: mckenna wj. Circ Cardiovasc Genet. 2012 Apr 1;5(2):156-66. doi: 10.1161/CIRCGENETICS.111.960831. Epub 2012 Jan 20. Circ Cardiovasc Genet. 2012. PMID: 22267749

9

Hypertrophic Cardiomyopathy.

Behr ER, McKenna WJ. Behr ER, et al. Among authors: mckenna wj. Curr Treat Options Cardiovasc Med. 2002 Dec;4(6):443-453. doi: 10.1007/s11936-002-0039-8. Curr Treat Options Cardiovasc Med. 2002. PMID: 12408787

10

Sudden arrhythmic death syndrome: familial evaluation identifies inheritable heart disease in the majority of families.

Behr ER, Dalageorgou C, Christiansen M, Syrris P, Hughes S, Tome Esteban MT, Rowland E, Jeffery S, McKenna WJ. Behr ER, et al. Among authors: mckenna wj. Eur Heart J. 2008 Jul;29(13):1670-80. doi: 10.1093/eurheartj/ehn219. Epub 2008 May 27. Eur Heart J. 2008. PMID: 18508782

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