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For: 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]
Number Citing Articles
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6 Khatami M, Ghorbani S, Adriani MR, Bahaloo S, Naeini MA, Heidari MM, Hadadzadeh M. Novel Point Mutations in 3'-Untranslated Region of GATA4 Gene Are Associated with Sporadic Non-syndromic Atrial and Ventricular Septal Defects. Curr Med Sci 2021. [PMID: 34652630 DOI: 10.1007/s11596-021-2428-9] [Reference Citation Analysis]
7 Manivannan S, Mansfield C, Zhang X, Kodigepalli KM, Majumdar U, Garg V, Basu M. Single-cell Transcriptomic Profiling Unveils Cardiac Cell-type Specific Response to Maternal Hyperglycemia Underlying the Risk of Congenital Heart Defects.. [DOI: 10.1101/2021.05.28.446177] [Reference Citation Analysis]
8 Padula SL, Velayutham N, Yutzey KE. Transcriptional Regulation of Postnatal Cardiomyocyte Maturation and Regeneration. Int J Mol Sci 2021;22:3288. [PMID: 33807107 DOI: 10.3390/ijms22063288] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 5.0] [Reference Citation Analysis]
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11 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]
12 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]
13 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]
14 Loid P, Mustila T, Mäkitie RE, Viljakainen H, Kämpe A, Tossavainen P, Lipsanen-Nyman M, Pekkinen M, Mäkitie O. Rare Variants in Genes Linked to Appetite Control and Hypothalamic Development in Early-Onset Severe Obesity. Front Endocrinol (Lausanne) 2020;11:81. [PMID: 32153512 DOI: 10.3389/fendo.2020.00081] [Cited by in Crossref: 11] [Cited by in F6Publishing: 11] [Article Influence: 5.5] [Reference Citation Analysis]
15 Ding Z, Yang W, Yi K, Ding Y, Zhou D, Xie X, You T. Correlations between ISL1 rs1017 polymorphism and congenital heart disease risk: A PRISMA-compliant meta-analysis. Medicine (Baltimore) 2020;99:e18715. [PMID: 31914083 DOI: 10.1097/MD.0000000000018715] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]