These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
148 related articles for article (PubMed ID: 24563425)
1. Reproductive fitness and genetic transmission of tetralogy of Fallot in the molecular age. Chin-Yee NJ; Costain G; Swaby JA; Silversides CK; Bassett AS Circ Cardiovasc Genet; 2014 Apr; 7(2):102-9. PubMed ID: 24563425 [TBL] [Abstract][Full Text] [Related]
2. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries. Costain G; Lionel AC; Ogura L; Marshall CR; Scherer SW; Silversides CK; Bassett AS Int J Cardiol; 2016 Feb; 204():115-21. PubMed ID: 26655555 [TBL] [Abstract][Full Text] [Related]
3. Tetralogy of Fallot in men: quality of life, family, education, and employment. Bygstad E; Pedersen LC; Pedersen TA; Hjortdal VE Cardiol Young; 2012 Aug; 22(4):417-23. PubMed ID: 22166680 [TBL] [Abstract][Full Text] [Related]
4. 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]
5. Influence of genes and the environment in familial congenital heart defects. Wang X; Li P; Chen S; Xi L; Guo Y; Guo A; Sun K Mol Med Rep; 2014 Feb; 9(2):695-700. PubMed ID: 24337398 [TBL] [Abstract][Full Text] [Related]
6. The inheritance of conotruncal malformations: a review and report of two siblings with tetralogy of Fallot with pulmonary atresia. Wulfsberg EA; Zintz EJ; Moore JW Clin Genet; 1991 Jul; 40(1):12-6. PubMed ID: 1884513 [TBL] [Abstract][Full Text] [Related]
7. PITX2 loss-of-function mutation contributes to tetralogy of Fallot. Sun YM; Wang J; Qiu XB; Yuan F; Xu YJ; Li RG; Qu XK; Huang RT; Xue S; Yang YQ Gene; 2016 Feb; 577(2):258-64. PubMed ID: 26657035 [TBL] [Abstract][Full Text] [Related]
8. 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]
9. Poorer right ventricular systolic function and exercise capacity in women after repair of tetralogy of fallot: a sex comparison of standard deviation scores based on sex-specific reference values in healthy control subjects. Sarikouch S; Boethig D; Peters B; Kropf S; Dubowy KO; Lange P; Kuehne T; Haverich A; Beerbaum P; Circ Cardiovasc Imaging; 2013 Nov; 6(6):924-33. PubMed ID: 24132714 [TBL] [Abstract][Full Text] [Related]
10. The effects of pregnancy on right ventricular remodeling in women with repaired tetralogy of Fallot. Egidy Assenza G; Cassater D; Landzberg M; Geva T; Schreier J; Graham D; Volpe M; Barker N; Economy K; Valente AM Int J Cardiol; 2013 Oct; 168(3):1847-52. PubMed ID: 23369674 [TBL] [Abstract][Full Text] [Related]
11. Identification of Copy Number Variations in Isolated Tetralogy of Fallot. Aguayo-Gómez A; Arteaga-Vázquez J; Svyryd Y; Calderón-Colmenero J; Zamora-González C; Vargas-Alarcón G; Mutchinick OM Pediatr Cardiol; 2015 Dec; 36(8):1642-6. PubMed ID: 26036351 [TBL] [Abstract][Full Text] [Related]
12. Frequency of 22q11.2 microdeletion in sporadic non-syndromic tetralogy of Fallot cases. Gioli-Pereira L; Pereira AC; Bergara D; Mesquita S; Lopes AA; Krieger JE Int J Cardiol; 2008 Jun; 126(3):374-8. PubMed ID: 17604138 [TBL] [Abstract][Full Text] [Related]
13. DNA microarray and quantitative analysis reveal enhanced myocardial VEGF expression with stunted angiogenesis in human tetralogy of Fallot. Peters TH; Sharma V; Yilmaz E; Mooi WJ; Bogers AJ; Sharma HS Cell Biochem Biophys; 2013 Nov; 67(2):305-16. PubMed ID: 23897578 [TBL] [Abstract][Full Text] [Related]
14. 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]
15. Effect of Concomitant Birth Defects and Genetic Anomalies on Infant Mortality in Tetralogy of Fallot. Jernigan EG; Strassle PD; Stebbins RC; Meyer RE; Nelson JS Birth Defects Res; 2017 Aug; 109(14):1154-1165. PubMed ID: 28627098 [TBL] [Abstract][Full Text] [Related]
16. Geographic distribution of live births with tetralogy of Fallot in North Carolina 2003 to 2012. Nelson JS; Stebbins RC; Strassle PD; Meyer RE Birth Defects Res A Clin Mol Teratol; 2016 Nov; 106(11):881-887. PubMed ID: 27891781 [TBL] [Abstract][Full Text] [Related]
17. Late risk of outcomes for adults with repaired tetralogy of Fallot from an inception cohort spanning four decades. Hickey EJ; Veldtman G; Bradley TJ; Gengsakul A; Manlhiot C; Williams WG; Webb GD; McCrindle BW Eur J Cardiothorac Surg; 2009 Jan; 35(1):156-64; discussion 164. PubMed ID: 18848456 [TBL] [Abstract][Full Text] [Related]
18. A novel HAND2 loss-of-function mutation responsible for tetralogy of Fallot. Lu CX; Gong HR; Liu XY; Wang J; Zhao CM; Huang RT; Xue S; Yang YQ Int J Mol Med; 2016 Feb; 37(2):445-51. PubMed ID: 26676105 [TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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] [Next] [New Search]