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For: Qiao XH, Wang Q, Wang J, Liu XY, Xu YJ, Huang RT, Xue S, Li YJ, Zhang M, Qu XK, Li RG, Qiu XB, Yang YQ. A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect. Eur J Med Genet 2018;61:197-203. [PMID: 29222010 DOI: 10.1016/j.ejmg.2017.12.003] [Cited by in Crossref: 21] [Cited by in F6Publishing: 21] [Article Influence: 4.2] [Reference Citation Analysis]
Number Citing Articles
1 Ishii S, Koibuchi N. COUP-TFII in Kidneys, from Embryos to Sick Adults. Diagnostics 2022;12:1181. [DOI: 10.3390/diagnostics12051181] [Reference Citation Analysis]
2 Yu Z, Pek NMQ, Gu M. Delving into the Molecular World of Single Ventricle Congenital Heart Disease. Curr Cardiol Rep 2022. [PMID: 35218503 DOI: 10.1007/s11886-022-01667-8] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
3 Martin KE, Ravisankar P, Beerens MEM, Macrae CA, Waxman JS. Nr2f1a maintains atrial nkx2.5 expression to repress pacemaker identity within venous atrial cardiomyocytes.. [DOI: 10.1101/2022.02.24.481762] [Reference Citation Analysis]
4 Ono M, Tanaka M, Hiroshima S, Sawano K, Ogawa Y, Nagasaki K, Saitoh A. Diagnosis of Chromosome 15q-Terminal Deletion Syndrome through Elevated Fasting Serum Growth Hormone Levels. Endocrines 2022;3:92-9. [DOI: 10.3390/endocrines3010008] [Reference Citation Analysis]
5 Martin KE, Waxman JS. Atrial and Sinoatrial Node Development in the Zebrafish Heart. J Cardiovasc Dev Dis 2021;8:15. [PMID: 33572147 DOI: 10.3390/jcdd8020015] [Cited by in Crossref: 6] [Cited by in F6Publishing: 6] [Article Influence: 6.0] [Reference Citation Analysis]
6 Yao Y, Marra AN, Yelon D. Pathways Regulating Establishment and Maintenance of Cardiac Chamber Identity in Zebrafish. J Cardiovasc Dev Dis 2021;8:13. [PMID: 33572830 DOI: 10.3390/jcdd8020013] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
7 Kartha CC. Sequelae of Genetic Defects in Cardiomyocytes. Cardiomyocytes in Health and Disease 2021. [DOI: 10.1007/978-3-030-85536-9_10] [Reference Citation Analysis]
8 Jiang WF, Xu YJ, Zhao CM, Wang XH, Qiu XB, Liu X, Wu SH, Yang YQ. A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve. Genet Mol Biol 2020;43:e20200142. [PMID: 33306779 DOI: 10.1590/1678-4685-GMB-2020-0142] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
9 Wu SH, Wang XH, Xu YJ, Gu JN, Yang CX, Qiao Q, Guo XJ, Guo YH, Qiu XB, Jiang WF, Yang YQ. ISL1 loss-of-function variation causes familial atrial fibrillation. Eur J Med Genet 2020;63:104029. [PMID: 32771629 DOI: 10.1016/j.ejmg.2020.104029] [Cited by in Crossref: 9] [Cited by in F6Publishing: 7] [Article Influence: 4.5] [Reference Citation Analysis]
10 Di R, Yang C, Zhao C, Yuan F, Qiao Q, Gu J, Li X, Xu Y, Yang Y. Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy. European Journal of Medical Genetics 2020;63:103827. [DOI: 10.1016/j.ejmg.2019.103827] [Cited by in Crossref: 9] [Cited by in F6Publishing: 8] [Article Influence: 4.5] [Reference Citation Analysis]
11 Suluba E, Shuwei L, Xia Q, Mwanga A. Congenital heart diseases: genetics, non-inherited risk factors, and signaling pathways. Egypt J Med Hum Genet 2020;21. [DOI: 10.1186/s43042-020-0050-1] [Cited by in Crossref: 9] [Cited by in F6Publishing: 10] [Article Influence: 4.5] [Reference Citation Analysis]
12 Polvani S, Pepe S, Milani S, Galli A. COUP-TFII in Health and Disease. Cells 2019;9:E101. [PMID: 31906104 DOI: 10.3390/cells9010101] [Cited by in Crossref: 22] [Cited by in F6Publishing: 23] [Article Influence: 7.3] [Reference Citation Analysis]
13 Nees SN, Chung WK. The genetics of isolated congenital heart disease. Am J Med Genet C Semin Med Genet 2020;184:97-106. [PMID: 31876989 DOI: 10.1002/ajmg.c.31763] [Cited by in Crossref: 18] [Cited by in F6Publishing: 18] [Article Influence: 6.0] [Reference Citation Analysis]
14 Williams K, Carson J, Lo C. Genetics of Congenital Heart Disease. Biomolecules 2019;9:E879. [PMID: 31888141 DOI: 10.3390/biom9120879] [Cited by in Crossref: 48] [Cited by in F6Publishing: 52] [Article Influence: 16.0] [Reference Citation Analysis]
15 Wang E, Nie Y, Fan X, Zheng Z, Hu S. Intronic Polymorphisms in Gene of Second Heart Field as Risk Factors for Human Congenital Heart Disease in a Chinese Population. DNA Cell Biol 2019;38:521-31. [PMID: 31013439 DOI: 10.1089/dna.2018.4254] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 1.3] [Reference Citation Analysis]
16 Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ. ISL1 loss-of-function mutation contributes to congenital heart defects. Heart Vessels 2019;34:658-68. [PMID: 30390123 DOI: 10.1007/s00380-018-1289-z] [Cited by in Crossref: 17] [Cited by in F6Publishing: 13] [Article Influence: 4.3] [Reference Citation Analysis]
17 Lu CX, Wang W, Wang Q, Liu XY, Yang YQ. A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle. Pediatr Cardiol 2018;39:794-804. [PMID: 29468350 DOI: 10.1007/s00246-018-1822-y] [Cited by in Crossref: 17] [Cited by in F6Publishing: 19] [Article Influence: 4.3] [Reference Citation Analysis]