478 related articles for article (PubMed ID: 25391453)
1. Next-generation sequencing of nine atrial fibrillation candidate genes identified novel de novo mutations in patients with extreme trait of atrial fibrillation.
Tsai CT; Hsieh CS; Chang SN; Chuang EY; Juang JM; Lin LY; Lai LP; Hwang JJ; Chiang FT; Lin JL
J Med Genet; 2015 Jan; 52(1):28-36. PubMed ID: 25391453
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. Pitx2 impairs calcium handling in a dose-dependent manner by modulating Wnt signalling.
Lozano-Velasco E; Hernández-Torres F; Daimi H; Serra SA; Herraiz A; Hove-Madsen L; Aránega A; Franco D
Cardiovasc Res; 2016 Jan; 109(1):55-66. PubMed ID: 26243430
[TBL] [Abstract][Full Text] [Related]
4. Significant Association Between CAV1 Variant rs3807989 on 7p31 and Atrial Fibrillation in a Chinese Han Population.
Chen S; Wang C; Wang X; Xu C; Wu M; Wang P; Tu X; Wang QK
J Am Heart Assoc; 2015 May; 4(5):. PubMed ID: 25953654
[TBL] [Abstract][Full Text] [Related]
5. Korean Atrial Fibrillation (AF) Network: Genetic Variants for AF Do Not Predict Ablation Success.
Choi EK; Park JH; Lee JY; Nam CM; Hwang MK; Uhm JS; Joung B; Ko YG; Lee MH; Lubitz SA; Ellinor PT; Pak HN
J Am Heart Assoc; 2015 Aug; 4(8):e002046. PubMed ID: 26272656
[TBL] [Abstract][Full Text] [Related]
6. A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.
Zhou YM; Zheng PX; Yang YQ; Ge ZM; Kang WQ
Int J Mol Med; 2013 Oct; 32(4):827-34. PubMed ID: 23913021
[TBL] [Abstract][Full Text] [Related]
7. Incidence of dementia in relation to genetic variants at PITX2, ZFHX3, and ApoE ε4 in atrial fibrillation patients.
Rollo J; Knight S; May HT; Anderson JL; Muhlestein JB; Bunch TJ; Carlquist J
Pacing Clin Electrophysiol; 2015 Feb; 38(2):171-7. PubMed ID: 25494715
[TBL] [Abstract][Full Text] [Related]
8. 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. PubMed ID: 21398315
[TBL] [Abstract][Full Text] [Related]
9. Wolff-Parkinson-White syndrome: De novo variants and evidence for mutational burden in genes associated with atrial fibrillation.
Coban-Akdemir ZH; Charng WL; Azamian M; Paine IS; Punetha J; Grochowski CM; Gambin T; Valdes SO; Cannon B; Zapata G; Hernandez PP; Jhangiani S; Doddapaneni H; Hu J; Boricha F; Muzny DM; Boerwinkle E; Yang Y; Gibbs RA; Posey JE; Wehrens XHT; Belmont JW; Kim JJ; Miyake CY; Lupski JR; Lalani SR
Am J Med Genet A; 2020 Jun; 182(6):1387-1399. PubMed ID: 32233023
[TBL] [Abstract][Full Text] [Related]
10. Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.
Li C; Wang F; Yang Y; Fu F; Xu C; Shi L; Li S; Xia Y; Wu G; Cheng X; Liu H; Wang C; Wang P; Hao J; Ke Y; Zhao Y; Liu M; Zhang R; Gao L; Yu B; Zeng Q; Liao Y; Yang B; Tu X; Wang QK
Hum Genet; 2011 Mar; 129(3):239-46. PubMed ID: 21107608
[TBL] [Abstract][Full Text] [Related]
11. NKX2-6 mutation predisposes to familial atrial fibrillation.
Wang J; Zhang DF; Sun YM; Li RG; Qiu XB; Qu XK; Liu X; Fang WY; Yang YQ
Int J Mol Med; 2014 Dec; 34(6):1581-90. PubMed ID: 25319568
[TBL] [Abstract][Full Text] [Related]
12. A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.
Wang J; Zhang DF; Sun YM; Yang YQ
Eur J Med Genet; 2014 Jan; 57(1):25-31. PubMed ID: 24333117
[TBL] [Abstract][Full Text] [Related]
13. A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.
Huang RT; Xue S; Xu YJ; Zhou M; Yang YQ
Int J Mol Med; 2013 May; 31(5):1119-26. PubMed ID: 23525379
[TBL] [Abstract][Full Text] [Related]
14. Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.
Huang Y; Wang C; Yao Y; Zuo X; Chen S; Xu C; Zhang H; Lu Q; Chang L; Wang F; Wang P; Zhang R; Hu Z; Song Q; Yang X; Li C; Li S; Zhao Y; Yang Q; Yin D; Wang X; Si W; Li X; Xiong X; Wang D; Huang Y; Luo C; Li J; Wang J; Chen J; Wang L; Wang L; Han M; Ye J; Chen F; Liu J; Liu Y; Wu G; Yang B; Cheng X; Liao Y; Wu Y; Ke T; Chen Q; Tu X; Elston R; Rao S; Yang Y; Xia Y; Wang QK
PLoS Genet; 2015 Aug; 11(8):e1005393. PubMed ID: 26267381
[TBL] [Abstract][Full Text] [Related]
15. Genetic Control of Left Atrial Gene Expression Yields Insights into the Genetic Susceptibility for Atrial Fibrillation.
Hsu J; Gore-Panter S; Tchou G; Castel L; Lovano B; Moravec CS; Pettersson GB; Roselli EE; Gillinov AM; McCurry KR; Smedira NG; Barnard J; Van Wagoner DR; Chung MK; Smith JD
Circ Genom Precis Med; 2018 Mar; 11(3):e002107. PubMed ID: 29545482
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Association of atrial fibrillation susceptibility genes, atrial fibrillation phenotypes and response to catheter ablation: a gene-based analysis of GWAS data.
Husser D; Büttner P; Ueberham L; Dinov B; Sommer P; Arya A; Hindricks G; Bollmann A
J Transl Med; 2017 Apr; 15(1):71. PubMed ID: 28381281
[TBL] [Abstract][Full Text] [Related]
18. Targeted deep sequencing reveals no definitive evidence for somatic mosaicism in atrial fibrillation.
Roberts JD; Longoria J; Poon A; Gollob MH; Dewland TA; Kwok PY; Olgin JE; Deo RC; Marcus GM
Circ Cardiovasc Genet; 2015 Feb; 8(1):50-7. PubMed ID: 25406240
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Understanding PITX2-Dependent Atrial Fibrillation Mechanisms through Computational Models.
Bai J; Lu Y; Zhu Y; Wang H; Yin D; Zhang H; Franco D; Zhao J
Int J Mol Sci; 2021 Jul; 22(14):. PubMed ID: 34299303
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]