Similar articles for PMID: 20659440

Year	Number of Results
1999	1
2000	2
2002	1
2003	3
2004	1
2005	2
2006	3
2007	4
2008	6
2009	11
2010	14
2011	18
2012	12
2013	7
2014	13
2015	12
2016	13
2017	7
2018	9
2019	7
2020	2
2021	8
2022	12
2023	1
2024	0

1

A novel mutation of GATA4 in a familial atrial septal defect.

Chen Y, Mao J, Sun Y, Zhang Q, Cheng HB, Yan WH, Choy KW, Li H. Chen Y, et al. Clin Chim Acta. 2010 Nov 11;411(21-22):1741-5. doi: 10.1016/j.cca.2010.07.021. Epub 2010 Jul 24. Clin Chim Acta. 2010. PMID: 20659440

2

A novel mutation in GATA4 gene associated with dominant inherited familial atrial septal defect.

Chen Y, Han ZQ, Yan WD, Tang CZ, Xie JY, Chen H, Hu DY. Chen Y, et al. J Thorac Cardiovasc Surg. 2010 Sep;140(3):684-7. doi: 10.1016/j.jtcvs.2010.01.013. Epub 2010 Mar 26. J Thorac Cardiovasc Surg. 2010. PMID: 20347099 Free article.

3

Genetic variations of NKX2-5 in sporadic atrial septal defect and ventricular septal defect in Chinese Yunnan population.

Cao Y, Wang J, Wei C, Hou Z, Li Y, Zou H, Meng M, Wang W, Jiang L. Cao Y, et al. Gene. 2016 Jan 1;575(1):29-33. doi: 10.1016/j.gene.2015.08.033. Epub 2015 Aug 20. Gene. 2016. PMID: 26297999 Clinical Trial.

4

The M310T mutation in the GATA4 gene is a novel pathogenic target of the familial atrial septal defect.

Bu H, Sun G, Zhu Y, Yang Y, Tan Z, Zhao T, Hu S. Bu H, et al. BMC Cardiovasc Disord. 2021 Jan 6;21(1):12. doi: 10.1186/s12872-020-01822-5. BMC Cardiovasc Disord. 2021. PMID: 33413087 Free PMC article.

5

Phenotypes with GATA4 or NKX2.5 mutations in familial atrial septal defect.

Hirayama-Yamada K, Kamisago M, Akimoto K, Aotsuka H, Nakamura Y, Tomita H, Furutani M, Imamura S, Takao A, Nakazawa M, Matsuoka R. Hirayama-Yamada K, et al. Am J Med Genet A. 2005 May 15;135(1):47-52. doi: 10.1002/ajmg.a.30684. Am J Med Genet A. 2005. PMID: 15810002

6

Association of NKX2-5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children.

Behiry EG, Al-Azzouny MA, Sabry D, Behairy OG, Salem NE. Behiry EG, et al. Mol Genet Genomic Med. 2019 May;7(5):e612. doi: 10.1002/mgg3.612. Epub 2019 Mar 4. Mol Genet Genomic Med. 2019. PMID: 30834692 Free PMC article.

7

A novel mutation of GATA4 (K300T) associated with familial atrial septal defect.

Chen J, Qi B, Zhao J, Liu W, Duan R, Zhang M. Chen J, et al. Gene. 2016 Jan 10;575(2 Pt 2):473-477. doi: 10.1016/j.gene.2015.09.021. Epub 2015 Sep 12. Gene. 2016. PMID: 26376067

8

Germline mutations in NKX2-5, GATA4, and CRELD1 are rare in a Mexican sample of Down syndrome patients with endocardial cushion and septal heart defects.

Alcántara-Ortigoza MA, De Rubens-Figueroa J, Reyna-Fabian ME, Estandía-Ortega B, González-del Angel A, Molina-Álvarez B, Velázquez-Aragón JA, Villagómez-Martínez S, Pereira-López GI, Martínez-Cruz V, Álvarez-Gómez RM, Díaz-García L. Alcántara-Ortigoza MA, et al. Pediatr Cardiol. 2015 Apr;36(4):802-8. doi: 10.1007/s00246-014-1091-3. Epub 2014 Dec 19. Pediatr Cardiol. 2015. PMID: 25524324

9

Congenital heart diseases and their association with the variant distribution features on susceptibility genes.

Su W, Zhu P, Wang R, Wu Q, Wang M, Zhang X, Mei L, Tang J, Kumar M, Wang X, Su L, Dong N. Su W, et al. Clin Genet. 2017 Mar;91(3):349-354. doi: 10.1111/cge.12835. Epub 2016 Sep 5. Clin Genet. 2017. PMID: 27426723 Review.

10

GATA4 and NKX2.5 gene analysis in Chinese Uygur patients with congenital heart disease.

Zhang WM, Li XF, Ma ZY, Zhang J, Zhou SH, Li T, Shi L, Li ZZ. Zhang WM, et al. Chin Med J (Engl). 2009 Feb 20;122(4):416-9. Chin Med J (Engl). 2009. PMID: 19302747

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