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Cited by in F6Publishing
For: Xu Y, Wang Z, Yang C, Di R, Qiao Q, Li X, Gu J, Guo X, Yang Y. Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy. J of Cardiovasc Trans Res 2019;12:257-67. [DOI: 10.1007/s12265-018-9851-8] [Cited by in Crossref: 11] [Cited by in F6Publishing: 12] [Article Influence: 2.2] [Reference Citation Analysis]
Number Citing Articles
1 Man Y, Yi C, Fan M, Yang T, Liu P, Liu S, Wang G. Identification of a novel missense mutation in the TPM1 gene via exome sequencing in a Chinese family with dilated cardiomyopathy: A case report and literature review. Medicine (Baltimore) 2022;101:e28551. [PMID: 35029218 DOI: 10.1097/MD.0000000000028551] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
2 Ataklte F, Vasan RS. Heart failure risk estimation based on novel biomarkers. Expert Rev Mol Diagn 2021;21:655-72. [PMID: 34014781 DOI: 10.1080/14737159.2021.1933446] [Reference Citation Analysis]
3 Zhao L, Jiang WF, Yang CX, Qiao Q, Xu YJ, Shi HY, Qiu XB, Wu SH, Yang YQ. SOX17 loss-of-function variation underlying familial congenital heart disease. Eur J Med Genet 2021;64:104211. [PMID: 33794346 DOI: 10.1016/j.ejmg.2021.104211] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
4 Hua TR, Zhang SY. Cardiomyopathies in China: A 2018-2019 state-of-the-art review. Chronic Dis Transl Med 2020;6:224-38. [PMID: 33336168 DOI: 10.1016/j.cdtm.2020.05.006] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
5 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]
6 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: 1.7] [Reference Citation Analysis]
7 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: 3.0] [Reference Citation Analysis]
8 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: 3.0] [Reference Citation Analysis]
9 Almomani R, Herkert JC, Posafalvi A, Post JG, Boven LG, van der Zwaag PA, Willems PHGM, van Veen-Hof IH, Verhagen JMA, Wessels MW, Nikkels PGJ, Wintjes LT, van den Berg MP, Sinke RJ, Rodenburg RJ, Niezen-Koning KE, van Tintelen JP, Jongbloed JDH. Homozygous damaging SOD2 variant causes lethal neonatal dilated cardiomyopathy. J Med Genet 2020;57:23-30. [PMID: 31494578 DOI: 10.1136/jmedgenet-2019-106330] [Cited by in Crossref: 8] [Cited by in F6Publishing: 9] [Article Influence: 2.0] [Reference Citation Analysis]
10 Brodehl A, Ebbinghaus H, Deutsch MA, Gummert J, Gärtner A, Ratnavadivel S, Milting H. Human Induced Pluripotent Stem-Cell-Derived Cardiomyocytes as Models for Genetic Cardiomyopathies. Int J Mol Sci 2019;20:E4381. [PMID: 31489928 DOI: 10.3390/ijms20184381] [Cited by in Crossref: 33] [Cited by in F6Publishing: 34] [Article Influence: 8.3] [Reference Citation Analysis]
11 Lamounier Júnior A, Ferrari F, Max R, Ritt LEF, Stein R. Importance of Genetic Testing in Dilated Cardiomyopathy: Applications and Challenges in Clinical Practice. Arq Bras Cardiol 2019;113:274-81. [PMID: 31483024 DOI: 10.5935/abc.20190144] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]