Similar articles for PMID: 20937753

Year	Number of Results
1996	2
1997	1
2000	1
2001	1
2002	1
2003	2
2004	1
2005	1
2006	3
2007	4
2008	2
2009	6
2010	5
2011	7
2012	12
2013	9
2014	8
2015	10
2016	4
2017	4
2018	8
2019	10
2020	4
2021	7
2022	5
2023	3
2024	0

1

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. Griffin HR, et al. Heart. 2010 Oct;96(20):1651-5. doi: 10.1136/hrt.2010.200121. Heart. 2010. PMID: 20937753 Free PMC article.

2

Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot.

Rauch R, Hofbeck M, Zweier C, Koch A, Zink S, Trautmann U, Hoyer J, Kaulitz R, Singer H, Rauch A. Rauch R, et al. J Med Genet. 2010 May;47(5):321-31. doi: 10.1136/jmg.2009.070391. Epub 2009 Nov 30. J Med Genet. 2010. PMID: 19948535 Free article.

3

TBX1 gene mutation screening in patients with non-syndromic Fallot tetralogy.

Cabuk F, Karabulut HG, Tuncali T, Karademir S, Bozdayi M, Tükün A. Cabuk F, et al. Turk J Pediatr. 2007 Jan-Mar;49(1):61-8. Turk J Pediatr. 2007. PMID: 17479646 Clinical Trial.

4

Single nucleotide polymorphism discovery in TBX1 in individuals with and without 22q11.2 deletion syndrome.

Heike CL, Starr JR, Rieder MJ, Cunningham ML, Edwards KL, Stanaway IB, Crawford DC. Heike CL, et al. Birth Defects Res A Clin Mol Teratol. 2010 Jan;88(1):54-63. doi: 10.1002/bdra.20604. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 19645056 Free PMC article.

5

Detecting 22q11.2 deletion in Chinese children with conotruncal heart defects and single nucleotide polymorphisms in the haploid TBX1 locus.

Xu YJ, Wang J, Xu R, Zhao PJ, Wang XK, Sun HJ, Bao LM, Shen J, Fu QH, Li F, Sun K. Xu YJ, et al. BMC Med Genet. 2011 Dec 21;12:169. doi: 10.1186/1471-2350-12-169. BMC Med Genet. 2011. PMID: 22185286 Free PMC article.

6

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. Gioli-Pereira L, et al. Int J Cardiol. 2008 Jun 6;126(3):374-8. doi: 10.1016/j.ijcard.2007.04.043. Epub 2007 Jun 29. Int J Cardiol. 2008. PMID: 17604138

7

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.

8

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. Aguayo-Gómez A, et al. Pediatr Cardiol. 2015 Dec;36(8):1642-6. doi: 10.1007/s00246-015-1210-9. Epub 2015 Jun 3. Pediatr Cardiol. 2015. PMID: 26036351

9

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. Töpf A, et al. PLoS One. 2014 Aug 5;9(8):e95453. doi: 10.1371/journal.pone.0095453. eCollection 2014. PLoS One. 2014. PMID: 25093829 Free PMC article.

10

Identification of novel significant variants of ZFPM2/FOG2 in non-syndromic Tetralogy of Fallot and double outlet right ventricle in a Chinese Han population.

Huang X, Niu W, Zhang Z, Zhou C, Xu Z, Liu J, Su Z, Ding W, Zhang H. Huang X, et al. Mol Biol Rep. 2014;41(4):2671-7. doi: 10.1007/s11033-014-3126-5. Epub 2014 Jan 28. Mol Biol Rep. 2014. PMID: 24469719

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

103 results

Results by year