-
1
-
-
84876933197
-
Delisle BP: KCNQ1 mutation causes a high penetrance for familial atrial fibrillation
-
Bartos DC, Anderson JB, Bastiaenen R, Johnson JN, Gollob MH, Tester DJ, Burgess DE, Homfray T, Behr ER, Ackerman MJ, Guicheney P, Delisle BP: KCNQ1 mutation causes a high penetrance for familial atrial fibrillation. J Cardiovasc Electrophysiol 2013; 24: 562-569.
-
(2013)
J Cardiovasc Electrophysiol
, vol.24
, pp. 562-569
-
-
Bartos, D.C.1
Anderson, J.B.2
Bastiaenen, R.3
Johnson, J.N.4
Gollob, M.H.5
Tester, D.J.6
Burgess, D.E.7
Homfray, T.8
Behr, E.R.9
Ackerman, M.J.10
Guicheney, P.11
-
2
-
-
29144494740
-
Genetic testing in the long QT syndrome: Development and validation of an efficient approach to genotyping in clinical practice
-
Napolitano C, Priori SG, Schwartz PJ, Bloise R, Ronchetti E, Nastoli J, Bottelli G, Cerrone M, Leonardi S,: Genetic testing in the long QT syndrome: Development and validation of an efficient approach to genotyping in clinical practice. JAMA 2005; 294: 2975-2980.
-
(2005)
JAMA
, vol.294
, pp. 2975-2980
-
-
Napolitano, C.1
Priori, S.G.2
Schwartz, P.J.3
Bloise, R.4
Ronchetti, E.5
Nastoli, J.6
Bottelli, G.7
Cerrone, M.8
Leonardi, S.9
-
3
-
-
0000297776
-
Familial auricular fibrillation
-
Wolf L,: Familial auricular fibrillation. N Engl J Med 1943; 229396-229398.
-
(1943)
N Engl J Med
, pp. 229396-229398
-
-
Wolf, L.1
-
4
-
-
84865528698
-
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,: Familial aggregation of lone atrial fibrillation in young persons. J Am Coll Cardiol 2012; 60: 917-921.
-
(2012)
J Am Coll Cardiol
, vol.60
, pp. 917-921
-
-
Oyen, N.1
Ranthe, M.F.2
Carstensen, L.3
Boyd, H.A.4
Olesen, M.S.5
Olesen, S.P.6
Wohlfahrt, J.7
Melbye, M.8
-
5
-
-
80052726709
-
The genetics of atrial fibrillation: From the bench to the bedside
-
Xiao J, Liang D, Chen YH,: The genetics of atrial fibrillation: From the bench to the bedside. Annu Rev Genomics Hum Genet 2011; 12:73-96.
-
(2011)
Annu Rev Genomics Hum Genet
, pp. 1273-1296
-
-
Xiao, J.1
Liang, D.2
Chen, Y.H.3
-
6
-
-
84871242129
-
New advances in the genetic basis of atrial fibrillation
-
Mahida S, Ellinor PT,; New advances in the genetic basis of atrial fibrillation. J Cardiovasc Electrophysiol 2012; 23: 1400-1406.
-
(2012)
J Cardiovasc Electrophysiol
, vol.23
, pp. 1400-1406
-
-
Mahida, S.1
Ellinor, P.T.2
-
7
-
-
0037331522
-
Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue
-
Lai LP, Tsai CC, Su MJ, Lin JL, Chen YS, Tseng YZ, Huang SK,: Atrial fibrillation is associated with accumulation of aging-related common type mitochondrial DNA deletion mutation in human atrial tissue. Chest 2003; 123: 539-544.
-
(2003)
Chest
, vol.123
, pp. 539-544
-
-
Lai, L.P.1
Tsai, C.C.2
Su, M.J.3
Lin, J.L.4
Chen, Y.S.5
Tseng, Y.Z.6
Huang, S.K.7
-
8
-
-
34547744975
-
Chronic atrial fibrillation associated with somatic mitochondrial DNA mutations in human atrial tissue
-
Park HW, Ahn Y, Jeong MH, Cho JG, Park JC, Kang JC, Shin MG, Shin JH, Suh SP, Ryang DW, Kim NH, Choi JB, Kim HR,: Chronic atrial fibrillation associated with somatic mitochondrial DNA mutations in human atrial tissue. J Clin Pathol 2007; 60: 948-950.
-
(2007)
J Clin Pathol
, vol.60
, pp. 948-950
-
-
Park, H.W.1
Ahn, Y.2
Jeong, M.H.3
Cho, J.G.4
Park, J.C.5
Kang, J.C.6
Shin, M.G.7
Shin, J.H.8
Suh, S.P.9
Ryang, D.W.10
Kim, N.H.11
Choi, J.B.12
Kim, H.R.13
-
9
-
-
80051710052
-
HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA)
-
Ackerman MJ, Priori SG, Willems S, Berul C, Brugada R, Calkins H, Camm AJ, Ellinor PT, Gollob M, Hamilton R, Hershberger RE, Judge DP, Le Marec H, McKenna WJ, Schulze-Bahr E, Semsarian C, Towbin JA, Watkins H, Wilde A, Wolpert C, Zipes DP,: HRS/EHRA Expert Consensus Statement on the State of Genetic Testing for the Channelopathies and Cardiomyopathies: This document was developed as a partnership between the Heart Rhythm Society (HRS) and the European Heart Rhythm Association (EHRA). Europace 2011; 13: 1077-1109.
-
(2011)
Europace
, vol.13
, pp. 1077-1109
-
-
Ackerman, M.J.1
Priori, S.G.2
Willems, S.3
Berul, C.4
Brugada, R.5
Calkins, H.6
Camm, A.J.7
Ellinor, P.T.8
Gollob, M.9
Hamilton, R.10
Hershberger, R.E.11
Judge, D.P.12
Le Marec, H.13
McKenna, W.J.14
Schulze-Bahr, E.15
Semsarian, C.16
Towbin, J.A.17
Watkins, H.18
Wilde, A.19
Wolpert, C.20
Zipes, D.P.21
more..
-
10
-
-
10344258576
-
Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation
-
Ellinor PT, Moore RK, Patton KK, Ruskin JN, Pollak MR, Macrae CA,: Mutations in the long QT gene, KCNQ1, are an uncommon cause of atrial fibrillation. Heart 2004; 90: 1487-1488.
-
(2004)
Heart
, vol.90
, pp. 1487-1488
-
-
Ellinor, P.T.1
Moore, R.K.2
Patton, K.K.3
Ruskin, J.N.4
Pollak, M.R.5
MacRae, C.A.6
-
11
-
-
39649099974
-
Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation
-
Ravn LS, Aizawa Y, Pollevick GD, Hofman-Bang J, Cordeiro JM, Dixen U, Jensen G, Wu Y, Burashnikov E, Haunso S, Guerchicoff A, Hu D, Svendsen JH, Christiansen M, Antzelevitch C,: Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation. Heart Rhythm 2008; 5: 427-435.
-
(2008)
Heart Rhythm
, vol.5
, pp. 427-435
-
-
Ravn, L.S.1
Aizawa, Y.2
Pollevick, G.D.3
Hofman-Bang, J.4
Cordeiro, J.M.5
Dixen, U.6
Jensen, G.7
Wu, Y.8
Burashnikov, E.9
Haunso, S.10
Guerchicoff, A.11
Hu, D.12
Svendsen, J.H.13
Christiansen, M.14
Antzelevitch, C.15
-
12
-
-
33748367260
-
Potassium channel gene mutations rarely cause atrial fibrillation
-
Ellinor PT, Petrov-Kondratov VI, Zakharova E, Nam EG, MacRae CA,: Potassium channel gene mutations rarely cause atrial fibrillation. BMC Med Genet 2006; 7: 70.
-
(2006)
BMC Med Genet
, vol.7
, pp. 70
-
-
Ellinor, P.T.1
Petrov-Kondratov, V.I.2
Zakharova, E.3
Nam, E.G.4
MacRae, C.A.5
-
13
-
-
42649145054
-
Prevalence of early-onset atrial fibrillation in congenital long QT syndrome
-
Johnson JN, Tester DJ, Perry J, Salisbury BA, Reed CR, Ackerman MJ,: Prevalence of early-onset atrial fibrillation in congenital long QT syndrome. Heart Rhythm 2008; 5: 704-709.
-
(2008)
Heart Rhythm
, vol.5
, pp. 704-709
-
-
Johnson, J.N.1
Tester, D.J.2
Perry, J.3
Salisbury, B.A.4
Reed, C.R.5
Ackerman, M.J.6
-
14
-
-
84863996184
-
ATX-II-induced pulmonary vein arrhythmogenesis related to atrial fibrillation and long QT syndrome
-
Lu YY, Cheng CC, Chen YC, Chen SA, Chen YJ,: ATX-II-induced pulmonary vein arrhythmogenesis related to atrial fibrillation and long QT syndrome. Eur J Clin Invest 2012; 42: 823-831.
-
(2012)
Eur J Clin Invest
, vol.42
, pp. 823-831
-
-
Lu, Y.Y.1
Cheng, C.C.2
Chen, Y.C.3
Chen, S.A.4
Chen, Y.J.5
-
15
-
-
78650106076
-
Knock-in gain-of-function sodium channel mutation prolongs atrial action potentials and alters atrial vulnerability
-
Blana A, Kaese S, Fortmuller L, Laakmann S, Damke D, van Bragt K, Eckstein J, Piccini I, Kirchhefer U, Nattel S, Breithardt G, Carmeliet P, Carmeliet E, Schotten U, Verheule S, Kirchhof P, Fabritz L,: Knock-in gain-of-function sodium channel mutation prolongs atrial action potentials and alters atrial vulnerability. Heart Rhythm 2010; 7: 1862-1869.
-
(2010)
Heart Rhythm
, vol.7
, pp. 1862-1869
-
-
Blana, A.1
Kaese, S.2
Fortmuller, L.3
Laakmann, S.4
Damke, D.5
Van Bragt, K.6
Eckstein, J.7
Piccini, I.8
Kirchhefer, U.9
Nattel, S.10
Breithardt, G.11
Carmeliet, P.12
Carmeliet, E.13
Schotten, U.14
Verheule, S.15
Kirchhof, P.16
Fabritz, L.17
-
16
-
-
84861358469
-
Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel
-
Henrion U, Zumhagen S, Steinke K, Strutz-Seebohm N, Stallmeyer B, Lang F, Schulze-Bahr E, Seebohm G,: Overlapping cardiac phenotype associated with a familial mutation in the voltage sensor of the KCNQ1 channel. Cell Physiol Biochem 2012; 29: 809-818.
-
(2012)
Cell Physiol Biochem
, vol.29
, pp. 809-818
-
-
Henrion, U.1
Zumhagen, S.2
Steinke, K.3
Strutz-Seebohm, N.4
Stallmeyer, B.5
Lang, F.6
Schulze-Bahr, E.7
Seebohm, G.8
-
17
-
-
84858110206
-
Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1
-
Chan PJ, Osteen JD, Xiong D, Bohnen MS, Doshi D, Sampson KJ, Marx SO, Karlin A, Kass RS,: Characterization of KCNQ1 atrial fibrillation mutations reveals distinct dependence on KCNE1. J Gen Physiol 2012; 139: 135-144.
-
(2012)
J Gen Physiol
, vol.139
, pp. 135-144
-
-
Chan, P.J.1
Osteen, J.D.2
Xiong, D.3
Bohnen, M.S.4
Doshi, D.5
Sampson, K.J.6
Marx, S.O.7
Karlin, A.8
Kass, R.S.9
-
18
-
-
73249124602
-
Monitoring of atrial fibrillation burden after surgical ablation: Relevancy of end-point criteria after radiofrequency ablation treatment of patients with lone atrial fibrillation
-
Beukema R, Beukema WP, Sie HT, Misier AR, Delnoy PP, Elvan A,: Monitoring of atrial fibrillation burden after surgical ablation: Relevancy of end-point criteria after radiofrequency ablation treatment of patients with lone atrial fibrillation. Interact Cardiovasc Thorac Surg 2009; 9: 956-959.
-
(2009)
Interact Cardiovasc Thorac Surg
, vol.9
, pp. 956-959
-
-
Beukema, R.1
Beukema, W.P.2
Sie, H.T.3
Misier, A.R.4
Delnoy, P.P.5
Elvan, A.6
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