Similar articles for PMID: 15235040

Year	Number of Results
1965	1
1972	1
1974	2
1977	1
1995	3
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1997	2
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1999	1
2000	1
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2008	6
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2011	3
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2013	2
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2015	2
2016	5
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2018	2
2020	1
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1

A novel GATA4 mutation completely segregated with atrial septal defect in a large Japanese family.

Okubo A, Miyoshi O, Baba K, Takagi M, Tsukamoto K, Kinoshita A, Yoshiura K, Kishino T, Ohta T, Niikawa N, Matsumoto N. Okubo A, et al. J Med Genet. 2004 Jul;41(7):e97. doi: 10.1136/jmg.2004.018895. J Med Genet. 2004. PMID: 15235040 Free PMC article. No abstract available.

2

A novel mutation of GATA4 (K319E) is responsible for familial atrial septal defect and pulmonary valve stenosis.

Xiang R, Fan LL, Huang H, Cao BB, Li XP, Peng DQ, Xia K. Xiang R, et al. Gene. 2014 Jan 25;534(2):320-3. Gene. 2014. PMID: 24498650

3

GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5.

Garg V, Kathiriya IS, Barnes R, Schluterman MK, King IN, Butler CA, Rothrock CR, Eapen RS, Hirayama-Yamada K, Joo K, Matsuoka R, Cohen JC, Srivastava D. Garg V, et al. Nature. 2003 Jul 24;424(6947):443-7. doi: 10.1038/nature01827. Epub 2003 Jul 6. Nature. 2003. PMID: 12845333

4

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

5

Noncompaction of the left ventricular myocardium in a boy with a novel chromosome 8p23.1 deletion.

Blinder JJ, Martinez HR, Craigen WJ, Belmont J, Pignatelli RH, Jefferies JL. Blinder JJ, et al. Am J Med Genet A. 2011 Sep;155A(9):2215-20. doi: 10.1002/ajmg.a.34129. Epub 2011 Aug 10. Am J Med Genet A. 2011. PMID: 21834050

6

A new syndrome with noncompaction cardiomyopathy, bradycardia, pulmonary stenosis, atrial septal defect and heterotaxy with suggestive linkage to chromosome 6p.

Wessels MW, De Graaf BM, Cohen-Overbeek TE, Spitaels SE, de Groot-de Laat LE, Ten Cate FJ, Frohn-Mulder IF, de Krijger R, Bartelings MM, Essed N, Wladimiroff JW, Niermeijer MF, Heutink P, Oostra BA, Dooijes D, Bertoli-Avella AM, Willems PJ. Wessels MW, et al. Hum Genet. 2008 Jan;122(6):595-603. doi: 10.1007/s00439-007-0436-x. Epub 2007 Oct 16. Hum Genet. 2008. PMID: 17938964

7

Genetic screening of 104 patients with congenitally malformed hearts revealed a fresh mutation of GATA4 in those with atrial septal defects.

Hamanoue H, Rahayuningsih SE, Hirahara Y, Itoh J, Yokoyama U, Mizuguchi T, Saitsu H, Miyake N, Hirahara F, Matsumoto N. Hamanoue H, et al. Cardiol Young. 2009 Sep;19(5):482-5. doi: 10.1017/S1047951109990813. Epub 2009 Aug 13. Cardiol Young. 2009. PMID: 19678963

8

Interaction makes the heart grow stronger.

Packham EA, David Brook J. Packham EA, et al. Trends Mol Med. 2003 Oct;9(10):407-9. doi: 10.1016/j.molmed.2003.08.009. Trends Mol Med. 2003. PMID: 14557051 Review.

9

Spectrum of atrial septal defects associated with mutations of NKX2.5 and GATA4 transcription factors.

Sarkozy A, Conti E, Neri C, D'Agostino R, Digilio MC, Esposito G, Toscano A, Marino B, Pizzuti A, Dallapiccola B. Sarkozy A, et al. J Med Genet. 2005 Feb;42(2):e16. doi: 10.1136/jmg.2004.026740. J Med Genet. 2005. PMID: 15689439 Free PMC article. No abstract available.

10

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.

Sun YM, Wang J, Qiu XB, Yuan F, Li RG, Xu YJ, Qu XK, Shi HY, Hou XM, Huang RT, Xue S, Yang YQ. Sun YM, et al. G3 (Bethesda). 2016 Apr 7;6(4):987-92. doi: 10.1534/g3.115.026518. G3 (Bethesda). 2016. PMID: 26865696 Free PMC article.

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