297 related articles for article (PubMed ID: 24120998)
1. Candidate gene approach to identifying rare genetic variants associated with lone atrial fibrillation.
Weeke P; Parvez B; Blair M; Short L; Ingram C; Kucera G; Stubblefield T; Roden DM; Darbar D
Heart Rhythm; 2014 Jan; 11(1):46-52. PubMed ID: 24120998
[TBL] [Abstract][Full Text] [Related]
2. 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. PubMed ID: 24144883
[TBL] [Abstract][Full Text] [Related]
3. Functional Characterization of Rare Variants Implicated in Susceptibility to Lone Atrial Fibrillation.
Hayashi K; Konno T; Tada H; Tani S; Liu L; Fujino N; Nohara A; Hodatsu A; Tsuda T; Tanaka Y; Kawashiri MA; Ino H; Makita N; Yamagishi M
Circ Arrhythm Electrophysiol; 2015 Oct; 8(5):1095-104. PubMed ID: 26129877
[TBL] [Abstract][Full Text] [Related]
4. Examining rare and low-frequency genetic variants previously associated with lone or familial forms of atrial fibrillation in an electronic medical record system: a cautionary note.
Weeke P; Denny JC; Basterache L; Shaffer C; Bowton E; Ingram C; Darbar D; Roden DM
Circ Cardiovasc Genet; 2015 Feb; 8(1):58-63. PubMed ID: 25410959
[TBL] [Abstract][Full Text] [Related]
5. A genotype-dependent intermediate ECG phenotype in patients with persistent lone atrial fibrillation genotype ECG-phenotype correlation in atrial fibrillation.
Husser D; Stridh M; Sörnmo L; Roden DM; Darbar D; Bollmann A
Circ Arrhythm Electrophysiol; 2009 Feb; 2(1):24-8. PubMed ID: 19305639
[TBL] [Abstract][Full Text] [Related]
6. Association of Rare Genetic Variants and Early-Onset Atrial Fibrillation in Ethnic Minority Individuals.
Chalazan B; Mol D; Darbar FA; Ornelas-Loredo A; Al-Azzam B; Chen Y; Tofovic D; Sridhar A; Alzahrani Z; Ellinor P; Darbar D
JAMA Cardiol; 2021 Jul; 6(7):811-819. PubMed ID: 33950154
[TBL] [Abstract][Full Text] [Related]
7. 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; 13():102. PubMed ID: 23134779
[TBL] [Abstract][Full Text] [Related]
8. The genetics of atrial fibrillation.
Hayashi K; Tada H; Yamagishi M
Curr Opin Cardiol; 2017 Jan; 32(1):10-16. PubMed ID: 27861186
[TBL] [Abstract][Full Text] [Related]
9. Whole-exome sequencing in familial atrial fibrillation.
Weeke P; Muhammad R; Delaney JT; Shaffer C; Mosley JD; Blair M; Short L; Stubblefield T; Roden DM; Darbar D;
Eur Heart J; 2014 Sep; 35(36):2477-83. PubMed ID: 24727801
[TBL] [Abstract][Full Text] [Related]
10. 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. PubMed ID: 23040431
[TBL] [Abstract][Full Text] [Related]
11. 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; 5(4):450-9. PubMed ID: 22685113
[TBL] [Abstract][Full Text] [Related]
12. Whole Exome Sequencing in Atrial Fibrillation.
Lubitz SA; Brody JA; Bihlmeyer NA; Roselli C; Weng LC; Christophersen IE; Alonso A; Boerwinkle E; Gibbs RA; Bis JC; ; Cupples LA; Mohler PJ; Nickerson DA; Muzny D; Perez MV; Psaty BM; Soliman EZ; Sotoodehnia N; Lunetta KL; Benjamin EJ; Heckbert SR; Arking DE; Ellinor PT; Lin H
PLoS Genet; 2016 Sep; 12(9):e1006284. PubMed ID: 27589061
[TBL] [Abstract][Full Text] [Related]
13. Assessment of interleukin-1 gene cluster polymorphisms in lone atrial fibrillation: new insight into the role of inflammation in atrial fibrillation.
Gungor B; Ekmekci A; Arman A; Ozcan KS; Ucer E; Alper AT; Calik N; Yilmaz H; Tezel T; Coker A; Bolca O
Pacing Clin Electrophysiol; 2013 Oct; 36(10):1220-7. PubMed ID: 23713812
[TBL] [Abstract][Full Text] [Related]
14. Genetic aspects of lone atrial fibrillation: what do we know?
Andreasen L; Nielsen JB; Olesen MS
Curr Pharm Des; 2015; 21(5):667-78. PubMed ID: 25175087
[TBL] [Abstract][Full Text] [Related]
15. SCN10A/Nav1.8 modulation of peak and late sodium currents in patients with early onset atrial fibrillation.
Savio-Galimberti E; Weeke P; Muhammad R; Blair M; Ansari S; Short L; Atack TC; Kor K; Vanoye CG; Olesen MS; LuCamp ; Yang T; George AL; Roden DM; Darbar D
Cardiovasc Res; 2014 Nov; 104(2):355-63. PubMed ID: 25053638
[TBL] [Abstract][Full Text] [Related]
16. Deep sequencing of atrial fibrillation patients with mitral valve regurgitation shows no evidence of mosaicism but reveals novel rare germline variants.
Gregers E; Ahlberg G; Christensen T; Jabbari J; Larsen KO; Herfelt CB; Henningsen KM; Andreasen L; Thiis JJ; Lund J; Holme S; Haunsø S; Bentzen BH; Schmitt N; Svendsen JH; Olesen MS
Heart Rhythm; 2017 Oct; 14(10):1531-1538. PubMed ID: 28549997
[TBL] [Abstract][Full Text] [Related]
17. Targeted sequencing in candidate genes for atrial fibrillation: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Targeted Sequencing Study.
Lin H; Sinner MF; Brody JA; Arking DE; Lunetta KL; Rienstra M; Lubitz SA; Magnani JW; Sotoodehnia N; McKnight B; McManus DD; Boerwinkle E; Psaty BM; Rotter JI; Bis JC; Gibbs RA; Muzny D; Kovar CL; Morrison AC; Gupta M; Folsom AR; Kääb S; Heckbert SR; Alonso A; Ellinor PT; Benjamin EJ;
Heart Rhythm; 2014 Mar; 11(3):452-7. PubMed ID: 24239840
[TBL] [Abstract][Full Text] [Related]
18. Genetic variants associated with risk of atrial fibrillation regulate expression of PITX2, CAV1, MYOZ1, C9orf3 and FANCC.
Martin RI; Babaei MS; Choy MK; Owens WA; Chico TJ; Keenan D; Yonan N; Koref MS; Keavney BD
J Mol Cell Cardiol; 2015 Aug; 85():207-14. PubMed ID: 26073630
[TBL] [Abstract][Full Text] [Related]
19. Genetic variants on chromosomes 7p31 and 12p12 are associated with abnormal atrial electrical activation in patients with early-onset lone atrial fibrillation.
Seifert MB; Olesen MS; Christophersen IE; Nielsen JB; Carlson J; Holmqvist F; Tveit A; Haunsø S; Svendsen JH; Platonov PG
Ann Noninvasive Electrocardiol; 2019 Nov; 24(6):e12661. PubMed ID: 31152482
[TBL] [Abstract][Full Text] [Related]
20. Chromosome 4q25 variants are genetic modifiers of rare ion channel mutations associated with familial atrial fibrillation.
Ritchie MD; Rowan S; Kucera G; Stubblefield T; Blair M; Carter S; Roden DM; Darbar D
J Am Coll Cardiol; 2012 Sep; 60(13):1173-81. PubMed ID: 22818067
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
