BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

181 related articles for article (PubMed ID: 25539802)

  • 1. Chromosome 16q22 variants in a region associated with cardiovascular phenotypes correlate with ZFHX3 expression in a transcript-specific manner.
    Martin RI; Owens WA; Cunnington MS; Mayosi BM; Koref MS; Keavney BD
    BMC Genet; 2014 Dec; 15():136. PubMed ID: 25539802
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Maintenance of low inflammation level by the ZFHX3 SNP rs2106261 minor allele contributes to reduced atrial fibrillation recurrence after pulmonary vein isolation.
    Tomomori S; Nakano Y; Ochi H; Onohara Y; Sairaku A; Tokuyama T; Motoda C; Matsumura H; Amioka M; Hironobe N; Ookubo Y; Okamura S; Kawazoe H; Chayama K; Kihara Y
    PLoS One; 2018; 13(9):e0203281. PubMed ID: 30180182
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke.
    Gudbjartsson DF; Holm H; Gretarsdottir S; Thorleifsson G; Walters GB; Thorgeirsson G; Gulcher J; Mathiesen EB; Njølstad I; Nyrnes A; Wilsgaard T; Hald EM; Hveem K; Stoltenberg C; Kucera G; Stubblefield T; Carter S; Roden D; Ng MC; Baum L; So WY; Wong KS; Chan JC; Gieger C; Wichmann HE; Gschwendtner A; Dichgans M; Kuhlenbäumer G; Berger K; Ringelstein EB; Bevan S; Markus HS; Kostulas K; Hillert J; Sveinbjörnsdóttir S; Valdimarsson EM; Løchen ML; Ma RC; Darbar D; Kong A; Arnar DO; Thorsteinsdottir U; Stefansson K
    Nat Genet; 2009 Aug; 41(8):876-8. PubMed ID: 19597491
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. 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]  

  • 7. A genome-wide association study identifies novel and functionally related susceptibility Loci for Kawasaki disease.
    Burgner D; Davila S; Breunis WB; Ng SB; Li Y; Bonnard C; Ling L; Wright VJ; Thalamuthu A; Odam M; Shimizu C; Burns JC; Levin M; Kuijpers TW; Hibberd ML;
    PLoS Genet; 2009 Jan; 5(1):e1000319. PubMed ID: 19132087
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Variants in ZFHX3 are associated with atrial fibrillation in individuals of European ancestry.
    Benjamin EJ; Rice KM; Arking DE; Pfeufer A; van Noord C; Smith AV; Schnabel RB; Bis JC; Boerwinkle E; Sinner MF; Dehghan A; Lubitz SA; D'Agostino RB; Lumley T; Ehret GB; Heeringa J; Aspelund T; Newton-Cheh C; Larson MG; Marciante KD; Soliman EZ; Rivadeneira F; Wang TJ; Eiríksdottir G; Levy D; Psaty BM; Li M; Chamberlain AM; Hofman A; Vasan RS; Harris TB; Rotter JI; Kao WH; Agarwal SK; Stricker BH; Wang K; Launer LJ; Smith NL; Chakravarti A; Uitterlinden AG; Wolf PA; Sotoodehnia N; Köttgen A; van Duijn CM; Meitinger T; Mueller M; Perz S; Steinbeck G; Wichmann HE; Lunetta KL; Heckbert SR; Gudnason V; Alonso A; Kääb S; Ellinor PT; Witteman JC
    Nat Genet; 2009 Aug; 41(8):879-81. PubMed ID: 19597492
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic polymorphisms confer risk of atrial fibrillation in patients with heart failure: a population-based study.
    Smith JG; Melander O; Sjögren M; Hedblad B; Engström G; Newton-Cheh C; Platonov PG
    Eur J Heart Fail; 2013 Mar; 15(3):250-7. PubMed ID: 23132824
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Common genetic variants and response to atrial fibrillation ablation.
    Shoemaker MB; Bollmann A; Lubitz SA; Ueberham L; Saini H; Montgomery J; Edwards T; Yoneda Z; Sinner MF; Arya A; Sommer P; Delaney J; Goyal SK; Saavedra P; Kanagasundram A; Whalen SP; Roden DM; Hindricks G; Ellis CR; Ellinor PT; Darbar D; Husser D
    Circ Arrhythm Electrophysiol; 2015 Apr; 8(2):296-302. PubMed ID: 25684755
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons.
    Zhai C; Cong H; Liu Y; Zhang Y; Liu X; Zhang H; Ren Z
    BMC Cardiovasc Disord; 2015 Jun; 15():58. PubMed ID: 26112950
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Loss of the Atrial Fibrillation-Related Gene,
    Jameson HS; Hanley A; Hill MC; Xiao L; Ye J; Bapat A; Ronzier E; Hall AW; Hucker WJ; Clauss S; Barazza M; Silber E; Mina JA; Tucker NR; Mills RW; Dong JT; Milan DJ; Ellinor PT
    Circ Res; 2023 Aug; 133(4):313-329. PubMed ID: 37449401
    [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. 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]  

  • 17. Association of ZFHX3 gene variation with atrial fibrillation, cerebral infarction, and lung thromboembolism: An autopsy study.
    Zaw KTT; Sato N; Ikeda S; Thu KS; Mieno MN; Arai T; Mori S; Furukawa T; Sasano T; Sawabe M; Tanaka M; Muramatsu M
    J Cardiol; 2017 Aug; 70(2):180-184. PubMed ID: 28007413
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Population-specific genome-wide mapping of expression quantitative trait loci in the colon of Han Chinese.
    Guo CC; Wei N; Liang SH; Wang BL; Sha SM; Wu KC
    J Dig Dis; 2016 Sep; 17(9):600-609. PubMed ID: 27534592
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Extensive Ethnic Variation and Linkage Disequilibrium at the
    Nagelkerke SQ; Tacke CE; Breunis WB; Tanck MWT; Geissler J; Png E; Hoang LT; van der Heijden J; Naim ANM; Yeung RSM; Levin ML; Wright VJ; Burgner DP; Ponsonby AL; Ellis JA; Cimaz R; Shimizu C; Burns JC; Fijnvandraat K; van der Schoot CE; van den Berg TK; de Boer M; Davila S; Hibberd ML; Kuijpers TW;
    Front Immunol; 2019; 10():185. PubMed ID: 30949161
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular Characterization of the Lipid Genome-Wide Association Study Signal on Chromosome 18q11.2 Implicates HNF4A-Mediated Regulation of the TMEM241 Gene.
    Rodríguez A; Gonzalez L; Ko A; Alvarez M; Miao Z; Bhagat Y; Nikkola E; Cruz-Bautista I; Arellano-Campos O; Muñoz-Hernández LL; Ordóñez-Sánchez ML; Rodriguez-Guillen R; Mohlke KL; Laakso M; Tusie-Luna T; Aguilar-Salinas CA; Pajukanta P
    Arterioscler Thromb Vasc Biol; 2016 Jul; 36(7):1350-5. PubMed ID: 27199446
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.