122 related articles for article (PubMed ID: 36071769)
21. Whole-Exome Sequencing Reveals a Novel Mutation of FLNA Gene in an Iranian Family with Nonsyndromic Tetralogy of Fallot.
Kalayinia S; Maleki M; Mahdavi M; Mahdieh N
Lab Med; 2021 Nov; 52(6):614-618. PubMed ID: 33942857
[TBL] [Abstract][Full Text] [Related]
22. The identification of novel gene mutations for degenerative lumbar spinal stenosis using whole-exome sequencing in a Chinese cohort.
Jiang X; Chen D
BMC Med Genomics; 2021 May; 14(1):134. PubMed ID: 34020649
[TBL] [Abstract][Full Text] [Related]
23. Functionally significant, rare transcription factor variants in tetralogy of Fallot.
Töpf A; Griffin HR; Glen E; Soemedi R; Brown DL; Hall D; Rahman TJ; Eloranta JJ; Jüngst C; Stuart AG; O'Sullivan J; Keavney BD; Goodship JA
PLoS One; 2014; 9(8):e95453. PubMed ID: 25093829
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Haploinsufficiency of vascular endothelial growth factor related signaling genes is associated with tetralogy of Fallot.
Reuter MS; Jobling R; Chaturvedi RR; Manshaei R; Costain G; Heung T; Curtis M; Hosseini SM; Liston E; Lowther C; Oechslin E; Sticht H; Thiruvahindrapuram B; Mil SV; Wald RM; Walker S; Marshall CR; Silversides CK; Scherer SW; Kim RH; Bassett AS
Genet Med; 2019 Apr; 21(4):1001-1007. PubMed ID: 30232381
[TBL] [Abstract][Full Text] [Related]
26. Somatic mutations in the GATA6 gene underlie sporadic tetralogy of Fallot.
Huang RT; Xue S; Xu YJ; Yang YQ
Int J Mol Med; 2013 Jan; 31(1):51-8. PubMed ID: 23175051
[TBL] [Abstract][Full Text] [Related]
27. Sequencing of a Chinese tetralogy of Fallot cohort reveals clustering mutations in myogenic heart progenitors.
Tang CSM; Mononen M; Lam WY; Jin SC; Zhuang X; Garcia-Barcelo MM; Lin Q; Yang Y; Sahara M; Eroglu E; Chien KR; Hong H; Tam PKH; Gruber PJ
JCI Insight; 2022 Jan; 7(2):. PubMed ID: 34905512
[TBL] [Abstract][Full Text] [Related]
28. Whole-exome sequencing identifies cancer-associated variants of the endo-lysosomal ion transport channels in the Saudi population.
Binobaid L; As Sobeai HM; Alhazzani K; AlAbdi L; Alwazae MM; Alotaibi M; Parrington J; Alhoshani A
Saudi Pharm J; 2024 Mar; 32(3):101961. PubMed ID: 38313820
[TBL] [Abstract][Full Text] [Related]
29. Rare and private variations in neural crest, apoptosis and sarcomere genes define the polygenic background of isolated Tetralogy of Fallot.
Grunert M; Dorn C; Schueler M; Dunkel I; Schlesinger J; Mebus S; Alexi-Meskishvili V; Perrot A; Wassilew K; Timmermann B; Hetzer R; Berger F; Sperling SR
Hum Mol Genet; 2014 Jun; 23(12):3115-28. PubMed ID: 24459294
[TBL] [Abstract][Full Text] [Related]
30. Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing.
Zhou Y; Bai K; Wang Y; Meng Z; Zhou S; Jiang S; Wang H; Wang J; Yang M; Wang Q; Sun K; Chen S
Front Cardiovasc Med; 2021; 8():811156. PubMed ID: 35141295
[TBL] [Abstract][Full Text] [Related]
31. New mutations in ZFPM2/FOG2 gene in tetralogy of Fallot and double outlet right ventricle.
De Luca A; Sarkozy A; Ferese R; Consoli F; Lepri F; Dentici ML; Vergara P; De Zorzi A; Versacci P; Digilio MC; Marino B; Dallapiccola B
Clin Genet; 2011 Aug; 80(2):184-90. PubMed ID: 20807224
[TBL] [Abstract][Full Text] [Related]
32. Identification of TBX5 mutations in a series of 94 patients with Tetralogy of Fallot.
Baban A; Postma AV; Marini M; Trocchio G; Santilli A; Pelegrini M; Sirleto P; Lerone M; Albanese SB; Barnett P; Boogerd CJ; Dallapiccola B; Digilio MC; Ravazzolo R; Pongiglione G
Am J Med Genet A; 2014 Dec; 164A(12):3100-7. PubMed ID: 25263169
[TBL] [Abstract][Full Text] [Related]
33. Somatic
Abhinav P; Li YJ; Huang RT; Liu XY; Gu JN; Yang CX; Xu YJ; Wang J; Yang YQ
Exp Ther Med; 2024 Feb; 27(2):91. PubMed ID: 38274337
[TBL] [Abstract][Full Text] [Related]
34. A New Family with a Novel
Börklü E; Altunoğlu U; Eraslan S; Kayserili H
Mol Syndromol; 2022 May; 13(3):206-211. PubMed ID: 35707595
[No Abstract] [Full Text] [Related]
35. Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing.
Xing J; Wang H; Xie Y; Fan T; Cui C; Li Y; Wang S; Gu W; Wang C; Tang H; Liu L
Open Life Sci; 2023; 18(1):20220593. PubMed ID: 37215497
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. 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]
38. GATA4 molecular screening and assessment of environmental risk factors in a Moroccan cohort with tetralogy of Fallot.
El Bouchikhi I; Belhassan K; Moufid FZ; Houssaini MI; Bouguenouch L; Samri I; Bouhrim M; Ouldim K; Atmani S
Afr Health Sci; 2018 Dec; 18(4):922-930. PubMed ID: 30766556
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]
