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.
176 related articles for article (PubMed ID: 24498113)
1. Ultra high-resolution gene centric genomic structural analysis of a non-syndromic congenital heart defect, Tetralogy of Fallot. Bittel DC; Zhou XG; Kibiryeva N; Fiedler S; O'Brien JE; Marshall J; Yu S; Liu HY PLoS One; 2014; 9(1):e87472. PubMed ID: 24498113 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications. He GW; Maslen CL; Chen HX; Hou HT; Bai XY; Wang XL; Liu XC; Lu WL; Chen XX; Chen WD; Xing QS; Wu Q; Wang J; Yang Q Clin Genet; 2022 Nov; 102(5):391-403. PubMed ID: 35882632 [TBL] [Abstract][Full Text] [Related]
5. Outlier-based identification of copy number variations using targeted resequencing in a small cohort of patients with Tetralogy of Fallot. Bansal V; Dorn C; Grunert M; Klaassen S; Hetzer R; Berger F; Sperling SR PLoS One; 2014; 9(1):e85375. PubMed ID: 24400131 [TBL] [Abstract][Full Text] [Related]
6. Search for Rare Copy-Number Variants in Congenital Heart Defects Identifies Novel Candidate Genes and a Potential Role for FOXC1 in Patients With Coarctation of the Aorta. Sanchez-Castro M; Eldjouzi H; Charpentier E; Busson PF; Hauet Q; Lindenbaum P; Delasalle-Guyomarch B; Baudry A; Pichon O; Pascal C; Lefort B; Bajolle F; Pezard P; Schott JJ; Dina C; Redon R; Gournay V; Bonnet D; Le Caignec C Circ Cardiovasc Genet; 2016 Feb; 9(1):86-94. PubMed ID: 26643481 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. Application of array-comparative genomic hybridization in tetralogy of Fallot. Liu L; Wang HD; Cui CY; Wu D; Li T; Fan TB; Peng BT; Zhang LZ; Wang CZ Medicine (Baltimore); 2016 Dec; 95(49):e5552. PubMed ID: 27930557 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. 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]
11. New Insights into the Impact of Genome-Wide Copy Number Variations on Complex Congenital Heart Disease in Saudi Arabia. Dasouki MJ; Wakil SM; Al-Harazi O; Alkorashy M; Muiya NP; Andres E; Hagos S; Aldusery H; Dzimiri N; Colak D OMICS; 2020 Jan; 24(1):16-28. PubMed ID: 31855513 [TBL] [Abstract][Full Text] [Related]
12. Gene expression in cardiac tissues from infants with idiopathic conotruncal defects. Bittel DC; Butler MG; Kibiryeva N; Marshall JA; Chen J; Lofland GK; O'Brien JE BMC Med Genomics; 2011 Jan; 4():1. PubMed ID: 21208432 [TBL] [Abstract][Full Text] [Related]
13. Genetic anomalies in fetuses with tetralogy of Fallot by using high-definition chromosomal microarray analysis. Peng R; Zheng J; Xie HN; He M; Lin MF Cardiovasc Ultrasound; 2019 May; 17(1):8. PubMed ID: 31060568 [TBL] [Abstract][Full Text] [Related]
14. Microdeletions and microduplications in patients with congenital heart disease and multiple congenital anomalies. Goldmuntz E; Paluru P; Glessner J; Hakonarson H; Biegel JA; White PS; Gai X; Shaikh TH Congenit Heart Dis; 2011; 6(6):592-602. PubMed ID: 22010865 [TBL] [Abstract][Full Text] [Related]
15. 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]
16. Chromosomal abnormalities among children born with conotruncal cardiac defects. Lammer EJ; Chak JS; Iovannisci DM; Schultz K; Osoegawa K; Yang W; Carmichael SL; Shaw GM Birth Defects Res A Clin Mol Teratol; 2009 Jan; 85(1):30-5. PubMed ID: 19067405 [TBL] [Abstract][Full Text] [Related]
17. Rare copy number variants in a population-based investigation of hypoplastic right heart syndrome. Dimopoulos A; Sicko RJ; Kay DM; Rigler SL; Druschel CM; Caggana M; Browne ML; Fan R; Romitti PA; Brody LC; Mills JL Birth Defects Res; 2017 Jan; 109(1):8-15. PubMed ID: 28009100 [TBL] [Abstract][Full Text] [Related]
18. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans. Haraksingh RR; Abyzov A; Urban AE BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122 [TBL] [Abstract][Full Text] [Related]
19. Transcriptomic analysis of patients with tetralogy of Fallot reveals the effect of chronic hypoxia on myocardial gene expression. Ghorbel MT; Cherif M; Jenkins E; Mokhtari A; Kenny D; Angelini GD; Caputo M J Thorac Cardiovasc Surg; 2010 Aug; 140(2):337-345.e26. PubMed ID: 20416888 [TBL] [Abstract][Full Text] [Related]
20. The study of copy number variations in the regions of PRKAB2 and PPM1K among congenital heart defects patients. Dong HQ; Du YX Rev Assoc Med Bras (1992); 2019 Jul; 65(6):786-790. PubMed ID: 31340305 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]