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Items: 1 to 20 of 174

1.

Rare variants in GJA5 are associated with early-onset lone atrial fibrillation.

Christophersen IE, Holmegard HN, Jabbari J, Sajadieh A, Haunsø S, Tveit A, Svendsen JH, Olesen MS.

Can J Cardiol. 2013 Jan;29(1):111-6. doi: 10.1016/j.cjca.2012.08.002. Epub 2012 Oct 2. Erratum in: Can J Cardiol. 2013 Jan;29(1):129. Sajadieh, Ahmad [added].

PMID:
23040431
2.

A common connexin-40 gene promoter variant affects connexin-40 expression in human atria and is associated with atrial fibrillation.

Wirka RC, Gore S, Van Wagoner DR, Arking DE, Lubitz SA, Lunetta KL, Benjamin EJ, Alonso A, Ellinor PT, Barnard J, Chung MK, Smith JD.

Circ Arrhythm Electrophysiol. 2011 Feb;4(1):87-93. doi: 10.1161/CIRCEP.110.959726. Epub 2010 Nov 13.

3.

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.

Shi HF, Yang JF, Wang Q, Li RG, Xu YJ, Qu XK, Fang WY, Liu X, Yang YQ.

Mol Med Rep. 2013 Mar;7(3):767-74. doi: 10.3892/mmr.2012.1252. Epub 2012 Dec 28.

PMID:
23292621
4.

Low prevalence of connexin-40 gene variants in atrial tissues and blood from atrial fibrillation subjects.

Tchou GD, Wirka RC, Van Wagoner DR, Barnard J, Chung MK, Smith JD.

BMC Med Genet. 2012 Nov 7;13:102. doi: 10.1186/1471-2350-13-102.

5.

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.

Heart Rhythm. 2014 Feb;11(2):246-51. doi: 10.1016/j.hrthm.2013.10.034. Epub 2013 Oct 18.

PMID:
24144883
6.

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.

Europace. 2011 Jul;13(7):963-7. doi: 10.1093/europace/eur007. Epub 2011 Mar 11.

PMID:
21398315
7.

Novel germline GJA5/connexin40 mutations associated with lone atrial fibrillation impair gap junctional intercellular communication.

Sun Y, Yang YQ, Gong XQ, Wang XH, Li RG, Tan HW, Liu X, Fang WY, Bai D.

Hum Mutat. 2013 Apr;34(4):603-9. doi: 10.1002/humu.22278.

PMID:
23348765
8.

Association of rs2200733 at 4q25 with early onset of lone atrial fibrillation in young patients.

Henningsen KM, Olesen MS, Haunsoe S, Svendsen JH.

Scand Cardiovasc J. 2011 Dec;45(6):324-6. doi: 10.3109/14017431.2011.594081. Epub 2011 Jul 27.

PMID:
21793630
9.

Association of human connexin40 gene polymorphisms with atrial vulnerability as a risk factor for idiopathic atrial fibrillation.

Firouzi M, Ramanna H, Kok B, Jongsma HJ, Koeleman BP, Doevendans PA, Groenewegen WA, Hauer RN.

Circ Res. 2004 Aug 20;95(4):e29-33. Epub 2004 Aug 5.

10.

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.

Circ Cardiovasc Genet. 2012 Aug 1;5(4):450-9. doi: 10.1161/CIRCGENETICS.111.962597. Epub 2012 Jun 8.

11.

The association of human connexin 40 genetic polymorphisms with atrial fibrillation.

Juang JM, Chern YR, Tsai CT, Chiang FT, Lin JL, Hwang JJ, Hsu KL, Tseng CD, Tseng YZ, Lai LP.

Int J Cardiol. 2007 Mar 2;116(1):107-12. Epub 2006 Jun 30.

PMID:
16814413
12.

Mutations in the potassium channel subunit KCNE1 are associated with early-onset familial atrial fibrillation.

Olesen MS, Bentzen BH, Nielsen JB, Steffensen AB, David JP, Jabbari J, Jensen HK, Haunsø S, Svendsen JH, Schmitt N.

BMC Med Genet. 2012 Apr 3;13:24. doi: 10.1186/1471-2350-13-24.

13.

The single nucleotide polymorphisms of Kir3.4 gene and their correlation with lone paroxysmal atrial fibrillation in Chinese Han population.

Zhang C, Yuan GH, Cheng ZF, Xu MW, Hou LF, Wei FP.

Heart Lung Circ. 2009 Aug;18(4):257-61. doi: 10.1016/j.hlc.2008.12.002. Epub 2009 Feb 8.

PMID:
19208499
14.

Paradigm of genetic mosaicism and lone atrial fibrillation: physiological characterization of a connexin 43-deletion mutant identified from atrial tissue.

Thibodeau IL, Xu J, Li Q, Liu G, Lam K, Veinot JP, Birnie DH, Jones DL, Krahn AD, Lemery R, Nicholson BJ, Gollob MH.

Circulation. 2010 Jul 20;122(3):236-44. doi: 10.1161/CIRCULATIONAHA.110.961227. Epub 2010 Jul 6.

15.

Genetic modifier of the QTc interval associated with early-onset atrial fibrillation.

Andreasen L, Nielsen JB, Christophersen IE, Holst AG, Sajadieh A, Tveit A, Haunsø S, Svendsen JH, Schmitt N, Olesen MS.

Can J Cardiol. 2013 Oct;29(10):1234-40. doi: 10.1016/j.cjca.2013.06.009.

PMID:
24074973
16.

Atrial fibrillation-linked GJA5/connexin40 mutants impaired gap junctions via different mechanisms.

Bai D.

FEBS Lett. 2014 Apr 17;588(8):1238-43. doi: 10.1016/j.febslet.2014.02.064. Epub 2014 Mar 19. Review.

17.

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation.

Gollob MH, Jones DL, Krahn AD, Danis L, Gong XQ, Shao Q, Liu X, Veinot JP, Tang AS, Stewart AF, Tesson F, Klein GJ, Yee R, Skanes AC, Guiraudon GM, Ebihara L, Bai D.

N Engl J Med. 2006 Jun 22;354(25):2677-88.

18.

Familial aggregation of lone atrial fibrillation in young persons.

Oyen N, Ranthe MF, Carstensen L, Boyd HA, Olesen MS, Olesen SP, Wohlfahrt J, Melbye M.

J Am Coll Cardiol. 2012 Sep 4;60(10):917-21. doi: 10.1016/j.jacc.2012.03.046. Epub 2012 Jun 20.

19.

Genetic loci on chromosomes 4q25, 7p31, and 12p12 are associated with onset of lone atrial fibrillation before the age of 40 years.

Olesen MS, Holst AG, Jabbari J, Nielsen JB, Christophersen IE, Sajadieh A, Haunsø S, Svendsen JH.

Can J Cardiol. 2012 Mar-Apr;28(2):191-5. doi: 10.1016/j.cjca.2011.11.016. Epub 2012 Feb 14.

PMID:
22336519
20.

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.

Cardiovasc Res. 2013 Jun 1;98(3):488-95. doi: 10.1093/cvr/cvt028. Epub 2013 Feb 11.

PMID:
23400760

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