176 related articles for article (PubMed ID: 22503907)
1. A common variant in the PTPN11 gene contributes to the risk of tetralogy of Fallot.
Goodship JA; Hall D; Topf A; Mamasoula C; Griffin H; Rahman TJ; Glen E; Tan H; Palomino Doza J; Relton CL; Bentham J; Bhattacharya S; Cosgrove C; Brook D; Granados-Riveron J; Bu'Lock FA; O'Sullivan J; Stuart AG; Parsons J; Cordell HJ; Keavney B
Circ Cardiovasc Genet; 2012 Jun; 5(3):287-92. PubMed ID: 22503907
[TBL] [Abstract][Full Text] [Related]
2. Functional polymorphisms of the neuropilin 1 gene are associated with the risk of tetralogy of Fallot in a Chinese Han population.
Fan SH; Shen ZY; Xiao YM
Gene; 2018 May; 653():72-79. PubMed ID: 29432830
[TBL] [Abstract][Full Text] [Related]
3. VEGF Gene Polymorphisms are Associated with Risk of Tetralogy of Fallot.
Li X; Liu CL; Li XX; Li QC; Ma LM; Liu GL
Med Sci Monit; 2015 Nov; 21():3474-82. PubMed ID: 26558525
[TBL] [Abstract][Full Text] [Related]
4. Whole Exome Sequencing Reveals the Major Genetic Contributors to Nonsyndromic Tetralogy of Fallot.
Page DJ; Miossec MJ; Williams SG; Monaghan RM; Fotiou E; Cordell HJ; Sutcliffe L; Topf A; Bourgey M; Bourque G; Eveleigh R; Dunwoodie SL; Winlaw DS; Bhattacharya S; Breckpot J; Devriendt K; Gewillig M; Brook JD; Setchfield KJ; Bu'Lock FA; O'Sullivan J; Stuart G; Bezzina CR; Mulder BJM; Postma AV; Bentham JR; Baron M; Bhaskar SS; Black GC; Newman WG; Hentges KE; Lathrop GM; Santibanez-Koref M; Keavney BD
Circ Res; 2019 Feb; 124(4):553-563. PubMed ID: 30582441
[TBL] [Abstract][Full Text] [Related]
5. Low-frequency intermediate penetrance variants in the ROCK1 gene predispose to Tetralogy of Fallot.
Palomino Doza J; Topf A; Bentham J; Bhattacharya S; Cosgrove C; Brook JD; Granados-Riveron J; Bu'Lock FA; O'Sullivan J; Stuart AG; Parsons J; Relton C; Goodship J; Henderson DJ; Keavney B
BMC Genet; 2013 Jun; 14():57. PubMed ID: 23782575
[TBL] [Abstract][Full Text] [Related]
6. Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the
Guo T; Repetto GM; McDonald McGinn DM; Chung JH; Nomaru H; Campbell CL; Blonska A; Bassett AS; Chow EWC; Mlynarski EE; Swillen A; Vermeesch J; Devriendt K; Gothelf D; Carmel M; Michaelovsky E; Schneider M; Eliez S; Antonarakis SE; Coleman K; Tomita-Mitchell A; Mitchell ME; Digilio MC; Dallapiccola B; Marino B; Philip N; Busa T; Kushan-Wells L; Bearden CE; Piotrowicz M; Hawuła W; Roberts AE; Tassone F; Simon TJ; van Duin EDA; van Amelsvoort TA; Kates WR; Zackai E; Johnston HR; Cutler DJ; Agopian AJ; Goldmuntz E; Mitchell LE; Wang T; Emanuel BS; Morrow BE;
Circ Cardiovasc Genet; 2017 Oct; 10(5):e001690. PubMed ID: 29025761
[TBL] [Abstract][Full Text] [Related]
7. The Functional Polymorphism R129W in the
Shi Y; Li Y; Wang Y; Zhuang J; Wang H; Hu M; Mo X; Yue S; Chen Y; Fan X; Chen J; Cai W; Zhu X; Wan Y; Zhong Y; Ye X; Li F; Zhou Z; Dai G; Luo R; Ocorr K; Jiang Z; Li X; Zhu P; Wu X; Yuan W
Genet Test Mol Biomarkers; 2019 Sep; 23(9):601-609. PubMed ID: 31386585
[No Abstract] [Full Text] [Related]
8. Rare copy number variations in adults with tetralogy of Fallot implicate novel risk gene pathways.
Silversides CK; Lionel AC; Costain G; Merico D; Migita O; Liu B; Yuen T; Rickaby J; Thiruvahindrapuram B; Marshall CR; Scherer SW; Bassett AS
PLoS Genet; 2012; 8(8):e1002843. PubMed ID: 22912587
[TBL] [Abstract][Full Text] [Related]
9. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot.
Cordell HJ; Töpf A; Mamasoula C; Postma AV; Bentham J; Zelenika D; Heath S; Blue G; Cosgrove C; Granados Riveron J; Darlay R; Soemedi R; Wilson IJ; Ayers KL; Rahman TJ; Hall D; Mulder BJ; Zwinderman AH; van Engelen K; Brook JD; Setchfield K; Bu'Lock FA; Thornborough C; O'Sullivan J; Stuart AG; Parsons J; Bhattacharya S; Winlaw D; Mital S; Gewillig M; Breckpot J; Devriendt K; Moorman AF; Rauch A; Lathrop GM; Keavney BD; Goodship JA
Hum Mol Genet; 2013 Apr; 22(7):1473-81. PubMed ID: 23297363
[TBL] [Abstract][Full Text] [Related]
10. Molecular and clinical studies in 107 Noonan syndrome affected individuals with PTPN11 mutations.
Athota JP; Bhat M; Nampoothiri S; Gowrishankar K; Narayanachar SG; Puttamallesh V; Farooque MO; Shetty S
BMC Med Genet; 2020 Mar; 21(1):50. PubMed ID: 32164556
[TBL] [Abstract][Full Text] [Related]
11. Genetic variations of VEGF gene were associated with tetralogy of fallot risk in a Chinese Han population.
Yan L; Ge Q; Xi C; Zhang X; Guo Y
Genet Test Mol Biomarkers; 2015 May; 19(5):264-71. PubMed ID: 25894981
[TBL] [Abstract][Full Text] [Related]
12. De novo copy number variants identify new genes and loci in isolated sporadic tetralogy of Fallot.
Greenway SC; Pereira AC; Lin JC; DePalma SR; Israel SJ; Mesquita SM; Ergul E; Conta JH; Korn JM; McCarroll SA; Gorham JM; Gabriel S; Altshuler DM; Quintanilla-Dieck Mde L; Artunduaga MA; Eavey RD; Plenge RM; Shadick NA; Weinblatt ME; De Jager PL; Hafler DA; Breitbart RE; Seidman JG; Seidman CE
Nat Genet; 2009 Aug; 41(8):931-5. PubMed ID: 19597493
[TBL] [Abstract][Full Text] [Related]
13. Molecular and clinical profile of patients referred as Noonan or Noonan-like syndrome in Greece: a cohort of 86 patients.
Papadopoulos G; Papadopoulou A; Kosma K; Papadimitriou A; Papaevangelou V; Kanaka-Gantenbein C; Bountouvi E; Kitsiou-Tzeli S
Eur J Pediatr; 2022 Oct; 181(10):3691-3700. PubMed ID: 35904599
[TBL] [Abstract][Full Text] [Related]
14. Genetic variants at 10p11 confer risk of Tetralogy of Fallot in Chinese of Nanjing.
Xu J; Lin Y; Si L; Jin G; Dai J; Wang C; Chen J; Da M; Hu Y; Yi C; Hu Z; Shen H; Mo X; Chen Y; Wang X
PLoS One; 2014; 9(3):e89636. PubMed ID: 24594544
[TBL] [Abstract][Full Text] [Related]
15. GATA5 loss-of-function mutations underlie tetralogy of fallot.
Wei D; Bao H; Liu XY; Zhou N; Wang Q; Li RG; Xu YJ; Yang YQ
Int J Med Sci; 2013; 10(1):34-42. PubMed ID: 23289003
[TBL] [Abstract][Full Text] [Related]
16. Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants.
Griffin HR; Töpf A; Glen E; Zweier C; Stuart AG; Parsons J; Peart I; Deanfield J; O'Sullivan J; Rauch A; Scambler P; Burn J; Cordell HJ; Keavney B; Goodship JA
Heart; 2010 Oct; 96(20):1651-5. PubMed ID: 20937753
[TBL] [Abstract][Full Text] [Related]
17. Gene-environment regulatory circuits of right ventricular pathology in tetralogy of fallot.
Zhao Y; Kang X; Gao F; Guzman A; Lau RP; Biniwale R; Wadehra M; Reemtsen B; Garg M; Halnon N; Quintero-Rivera F; Van Arsdell G; Coppola G; Nelson SF; Touma M;
J Mol Med (Berl); 2019 Dec; 97(12):1711-1722. PubMed ID: 31834445
[TBL] [Abstract][Full Text] [Related]
18. GATA4 loss-of-function mutations underlie familial tetralogy of fallot.
Yang YQ; Gharibeh L; Li RG; Xin YF; Wang J; Liu ZM; Qiu XB; Xu YJ; Xu L; Qu XK; Liu X; Fang WY; Huang RT; Xue S; Nemer G
Hum Mutat; 2013 Dec; 34(12):1662-71. PubMed ID: 24000169
[TBL] [Abstract][Full Text] [Related]
19. Clinical and mutation profile of pediatric patients with RASopathy-associated hypertrophic cardiomyopathy: results from a Chinese cohort.
Chen H; Li X; Liu X; Wang J; Zhang Z; Wu J; Huang M; Guo Y; Li F; Wang X; Fu L
Orphanet J Rare Dis; 2019 Feb; 14(1):29. PubMed ID: 30732632
[TBL] [Abstract][Full Text] [Related]
20. Mitogen-activated protein kinase signal pathways play an important role in right ventricular hypertrophy of tetralogy of Fallot.
Zhang HS; Wu QY; Xu M; Zhou YX; Shui CX
Chin Med J (Engl); 2012 Jul; 125(13):2243-9. PubMed ID: 22882842
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
