302 related articles for article (PubMed ID: 27624063)
1. The role of common genetic variants in atrial fibrillation.
Paludan-Müller C; Svendsen JH; Olesen MS
J Electrocardiol; 2016; 49(6):864-870. PubMed ID: 27624063
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. [Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].
Sinner MF; Pfeufer A; Kääb S
Herzschrittmacherther Elektrophysiol; 2006 Jun; 17(2):95-105. PubMed ID: 16786468
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Atrial fibrillation: the role of common and rare genetic variants.
Olesen MS; Nielsen MW; Haunsø S; Svendsen JH
Eur J Hum Genet; 2014 Mar; 22(3):297-306. PubMed ID: 23838598
[TBL] [Abstract][Full Text] [Related]
6. Novel association of polymorphic genetic variants with predictors of outcome of catheter ablation in atrial fibrillation: new directions from a prospective study (DECAF).
Mohanty S; Hall AW; Mohanty P; Prakash S; Trivedi C; Di Biase L; Santangeli P; Bai R; Burkhardt JD; Gallinghouse GJ; Horton R; Sanchez JE; Hranitzky PM; Al-Ahmad A; Iyer VR; Natale A
J Interv Card Electrophysiol; 2016 Jan; 45(1):7-17. PubMed ID: 26497660
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. New advances in the genetic basis of atrial fibrillation.
Mahida S; Ellinor PT
J Cardiovasc Electrophysiol; 2012 Dec; 23(12):1400-6. PubMed ID: 23066792
[TBL] [Abstract][Full Text] [Related]
9. Genomics of Atrial Fibrillation.
Gutierrez A; Chung MK
Curr Cardiol Rep; 2016 Jun; 18(6):55. PubMed ID: 27139902
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. GWAS contribution to atrial fibrillation and atrial fibrillation-related stroke: pathophysiological implications.
Cruz D; Pinto R; Freitas-Silva M; Nunes JP; Medeiros R
Pharmacogenomics; 2019 Jul; 20(10):765-780. PubMed ID: 31368859
[TBL] [Abstract][Full Text] [Related]
12. Common and rare variants in SCN10A modulate the risk of atrial fibrillation.
Jabbari J; Olesen MS; Yuan L; Nielsen JB; Liang B; Macri V; Christophersen IE; Nielsen N; Sajadieh A; Ellinor PT; Grunnet M; Haunsø S; Holst AG; Svendsen JH; Jespersen T
Circ Cardiovasc Genet; 2015 Feb; 8(1):64-73. PubMed ID: 25691686
[TBL] [Abstract][Full Text] [Related]
13. The rs3807989 G/A polymorphism in CAV1 is associated with the risk of atrial fibrillation in Chinese Han populations.
Liu Y; Ni B; Lin Y; Chen XG; Chen M; Hu Z; Zhang F
Pacing Clin Electrophysiol; 2015 Feb; 38(2):164-70. PubMed ID: 25196315
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. [Atrial fibrillation and genetic abnormalities].
Shimizu W
Nihon Rinsho; 2013 Jan; 71(1):161-6. PubMed ID: 23631189
[TBL] [Abstract][Full Text] [Related]
18. Polymorphisms but not mutations of the KCNQ1 gene are associated with lone atrial fibrillation in the Chinese Han population.
Chu HM; Feng MJ; Li YG; Zhang YX; Ma JF; He B; Yu YB; Liu J; Chen XM
ScientificWorldJournal; 2013; 2013():373454. PubMed ID: 23710137
[TBL] [Abstract][Full Text] [Related]
19. The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG).
Sinner MF; Pfeufer A; Akyol M; Beckmann BM; Hinterseer M; Wacker A; Perz S; Sauter W; Illig T; Näbauer M; Schmitt C; Wichmann HE; Schömig A; Steinbeck G; Meitinger T; Kääb S
Eur Heart J; 2008 Apr; 29(7):907-14. PubMed ID: 18222980
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
