Similar articles for PMID: 22912587

Year	Number of Results
1996	1
2000	1
2001	1
2002	1
2003	1
2005	1
2007	1
2008	7
2009	6
2010	9
2011	10
2012	15
2013	18
2014	19
2015	5
2016	11
2017	11
2018	5
2019	16
2020	10
2021	8
2022	13
2023	4
2024	0

1

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. Silversides CK, et al. PLoS Genet. 2012;8(8):e1002843. doi: 10.1371/journal.pgen.1002843. Epub 2012 Aug 9. PLoS Genet. 2012. PMID: 22912587 Free PMC article.

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. Costain G, et al. Int J Cardiol. 2016 Feb 1;204:115-21. doi: 10.1016/j.ijcard.2015.11.127. Epub 2015 Nov 22. Int J Cardiol. 2016. PMID: 26655555

3

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. Greenway SC, et al. Nat Genet. 2009 Aug;41(8):931-5. doi: 10.1038/ng.415. Epub 2009 Jul 13. Nat Genet. 2009. PMID: 19597493 Free PMC article.

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. He GW, et al. Clin Genet. 2022 Nov;102(5):391-403. doi: 10.1111/cge.14201. Epub 2022 Aug 2. Clin Genet. 2022. PMID: 35882632

5

Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3.

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; International 22q11.2 Consortium/Brain and Behavior Consortium*. Guo T, et al. Circ Cardiovasc Genet. 2017 Oct;10(5):e001690. doi: 10.1161/CIRCGENETICS.116.001690. Circ Cardiovasc Genet. 2017. PMID: 29025761 Free PMC article.

6

Rare de novo copy number variants in patients with congenital pulmonary atresia.

Xie L, Chen JL, Zhang WZ, Wang SZ, Zhao TL, Huang C, Wang J, Yang JF, Yang YF, Tan ZP. Xie L, et al. PLoS One. 2014 May 14;9(5):e96471. doi: 10.1371/journal.pone.0096471. eCollection 2014. PLoS One. 2014. PMID: 24826987 Free PMC article.

7

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 Jr, Marshall J, Yu S, Liu HY. Bittel DC, et al. PLoS One. 2014 Jan 31;9(1):e87472. doi: 10.1371/journal.pone.0087472. eCollection 2014. PLoS One. 2014. PMID: 24498113 Free PMC article. Clinical Trial.

8

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. Bansal V, et al. PLoS One. 2014 Jan 6;9(1):e85375. doi: 10.1371/journal.pone.0085375. eCollection 2014. PLoS One. 2014. PMID: 24400131 Free PMC article.

9

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. Dasouki MJ, et al. OMICS. 2020 Jan;24(1):16-28. doi: 10.1089/omi.2019.0165. Epub 2019 Dec 19. OMICS. 2020. PMID: 31855513

10

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. Peng R, et al. Cardiovasc Ultrasound. 2019 May 6;17(1):8. doi: 10.1186/s12947-019-0159-x. Cardiovasc Ultrasound. 2019. PMID: 31060568 Free PMC article.

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