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For: Joziasse IC, van de Smagt JJ, Smith K, Bakkers J, Sieswerda GJ, Mulder BJ, Doevendans PA. Genes in congenital heart disease: atrioventricular valve formation. Basic Res Cardiol 2008;103:216-27. [PMID: 18392768 DOI: 10.1007/s00395-008-0713-4] [Cited by in Crossref: 35] [Cited by in F6Publishing: 33] [Article Influence: 2.5] [Reference Citation Analysis]
Number Citing Articles
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14 Chen Z, Zhu JY, Fu Y, Richman A, Han Z. Wnt4 is required for ostia development in the Drosophila heart. Dev Biol 2016;413:188-98. [PMID: 26994311 DOI: 10.1016/j.ydbio.2016.03.008] [Cited by in Crossref: 7] [Cited by in F6Publishing: 5] [Article Influence: 1.2] [Reference Citation Analysis]
15 Ouyang P, Saarel E, Bai Y, Luo C, Lv Q, Xu Y, Wang F, Fan C, Younoszai A, Chen Q, Tu X, Wang QK. A de novo mutation in NKX2.5 associated with atrial septal defects, ventricular noncompaction, syncope and sudden death. Clin Chim Acta 2011;412:170-5. [PMID: 20932824 DOI: 10.1016/j.cca.2010.09.035] [Cited by in Crossref: 53] [Cited by in F6Publishing: 43] [Article Influence: 4.4] [Reference Citation Analysis]
16 Sun X, Meng Y, You T, Li P, Wu H, Yu M, Xie X. Association of growth/differentiation factor 1 gene polymorphisms with the risk of congenital heart disease in the Chinese Han population. Mol Biol Rep 2013;40:1291-9. [PMID: 23076529 DOI: 10.1007/s11033-012-2172-0] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 0.9] [Reference Citation Analysis]
17 Parker HG, Kilroy-Glynn P. Myxomatous mitral valve disease in dogs: does size matter? J Vet Cardiol 2012;14:19-29. [PMID: 22356836 DOI: 10.1016/j.jvc.2012.01.006] [Cited by in Crossref: 35] [Cited by in F6Publishing: 23] [Article Influence: 3.5] [Reference Citation Analysis]
18 van der Bom T, Zomer AC, Zwinderman AH, Meijboom FJ, Bouma BJ, Mulder BJ. The changing epidemiology of congenital heart disease. Nat Rev Cardiol. 2011;8:50-60. [PMID: 21045784 DOI: 10.1038/nrcardio.2010.166] [Cited by in Crossref: 334] [Cited by in F6Publishing: 297] [Article Influence: 27.8] [Reference Citation Analysis]
19 Gunawan F, Gentile A, Fukuda R, Tsedeke AT, Jiménez-Amilburu V, Ramadass R, Iida A, Sehara-Fujisawa A, Stainier DYR. Focal adhesions are essential to drive zebrafish heart valve morphogenesis. J Cell Biol 2019;218:1039-54. [PMID: 30635353 DOI: 10.1083/jcb.201807175] [Cited by in Crossref: 25] [Cited by in F6Publishing: 21] [Article Influence: 8.3] [Reference Citation Analysis]
20 Pavone LM, Norris RA. Distinct signaling pathways activated by "extracellular" and "intracellular" serotonin in heart valve development and disease. Cell Biochem Biophys 2013;67:819-28. [PMID: 23605455 DOI: 10.1007/s12013-013-9606-8] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 1.1] [Reference Citation Analysis]
21 Zhou Y, Bai K, Wang Y, Meng Z, Zhou S, Jiang S, Wang H, Wang J, Yang M, Wang Q, Sun K, Chen S. Identification of Rare Variants in Right Ventricular Outflow Tract Obstruction Congenital Heart Disease by Whole-Exome Sequencing. Front Cardiovasc Med 2022;8:811156. [DOI: 10.3389/fcvm.2021.811156] [Reference Citation Analysis]
22 Joziasse IC, van der Smagt JJ, Poot M, Hochstenbach R, Nelen MR, van Gijn M, Dooijes D, Mulder BJ, Doevendans PA. A duplication including GATA4 does not co-segregate with congenital heart defects. Am J Med Genet A 2009;149A:1062-6. [PMID: 19353638 DOI: 10.1002/ajmg.a.32769] [Cited by in Crossref: 7] [Cited by in F6Publishing: 9] [Article Influence: 0.5] [Reference Citation Analysis]
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30 Luna-Zurita L, Prados B, Grego-Bessa J, Luxán G, del Monte G, Benguría A, Adams RH, Pérez-Pomares JM, de la Pompa JL. Integration of a Notch-dependent mesenchymal gene program and Bmp2-driven cell invasiveness regulates murine cardiac valve formation. J Clin Invest 2010;120:3493-507. [PMID: 20890042 DOI: 10.1172/JCI42666] [Cited by in Crossref: 164] [Cited by in F6Publishing: 99] [Article Influence: 13.7] [Reference Citation Analysis]
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32 Deng X, Pan H, Wang J, Wang B, Cheng Z, Cheng L, Zhao L, Li H, Ma X. Functional Analysis of Two Novel Mutations in TWIST1 Protein Motifs Found in Ventricular Septal Defect Patients. Pediatr Cardiol 2015;36:1602-9. [DOI: 10.1007/s00246-015-1202-9] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 0.6] [Reference Citation Analysis]
33 Bens S, Haake A, Tönnies H, Vater I, Stephani U, Holterhus PM, Siebert R, Caliebe A. A de novo 1.1Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation. Eur J Med Genet 2011;54:e501-4. [PMID: 21700002 DOI: 10.1016/j.ejmg.2011.05.004] [Cited by in Crossref: 13] [Cited by in F6Publishing: 10] [Article Influence: 1.2] [Reference Citation Analysis]
34 Chowdhury S, Erickson SW, MacLeod SL, Cleves MA, Hu P, Karim MA, Hobbs CA. Maternal genome-wide DNA methylation patterns and congenital heart defects. PLoS One 2011;6:e16506. [PMID: 21297937 DOI: 10.1371/journal.pone.0016506] [Cited by in Crossref: 52] [Cited by in F6Publishing: 45] [Article Influence: 4.7] [Reference Citation Analysis]
35 Chen YM, Li X, Song GX, Liu M, Fan Y, Wu LJ, Li H, Zhang QJ, Liu YQ, Qian LM. Effect of LYRM1 knockdown on proliferation, apoptosis, differentiation and mitochondrial function in the P19 cell model of cardiac differentiation in vitro. J Bioenerg Biomembr 2016;48:33-41. [PMID: 26759027 DOI: 10.1007/s10863-015-9638-4] [Cited by in Crossref: 3] [Cited by in F6Publishing: 3] [Article Influence: 0.5] [Reference Citation Analysis]