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Cited by in F6Publishing
For: Qiao Q, Zhao CM, Yang CX, Gu JN, Guo YH, Zhang M, Li RG, Qiu XB, Xu YJ, Yang YQ. Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy. Clin Chem Lab Med 2021;59:955-63. [PMID: 33554560 DOI: 10.1515/cclm-2020-1318] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 0.7] [Reference Citation Analysis]
Number Citing Articles
1 Shi HY, Xie MS, Guo YH, Yang CX, Gu JN, Qiao Q, Di RM, Qiu XB, Xu YJ, Yang YQ. VEZF1 loss-of-function mutation underlying familial dilated cardiomyopathy. Eur J Med Genet 2023;66:104705. [PMID: 36657711 DOI: 10.1016/j.ejmg.2023.104705] [Reference Citation Analysis]
2 Gu JN, Yang CX, Ding YY, Qiao Q, Di RM, Sun YM, Wang J, Yang L, Xu YJ, Yang YQ. Identification of BMP10 as a Novel Gene Contributing to Dilated Cardiomyopathy. Diagnostics (Basel) 2023;13. [PMID: 36673052 DOI: 10.3390/diagnostics13020242] [Reference Citation Analysis]
3 Guo Y, Wang J, Guo X, Gao R, Yang C, Li L, Sun Y, Qiu X, Xu Y, Yang Y. KLF13 Loss‐of‐Function Mutations Underlying Familial Dilated Cardiomyopathy. JAHA 2022. [DOI: 10.1161/jaha.122.027578] [Reference Citation Analysis]
4 She M, Zhang J, Jiang T, Zhang Y, Liu Y, Tang M, Zeng Q. The function of Lmpt in Drosophila heart tissue. Biochemical and Biophysical Research Communications 2022;612:15-21. [DOI: 10.1016/j.bbrc.2022.04.098] [Reference Citation Analysis]
5 Liu B, Ou W, Fang L, Tian C, Xiong Y. Myocyte Enhancer Factor 2A Plays a Central Role in the Regulatory Networks of Cellular Physiopathology. Aging and disease 2022. [DOI: 10.14336/ad.2022.0825] [Reference Citation Analysis]
6 Ke Z, Zhang G, Guo Y, Sun Y, Wang J, Li N, Qiu X, Xu Y, Yang Y. A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus. Genet Mol Biol 2022;45:e20210378. [DOI: 10.1590/1678-4685-gmb-2021-0378] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]