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Cited by in F6Publishing

For:	Guo XJ, Qiu XB, Wang J, Guo YH, Yang CX, Li L, Gao RF, Ke ZP, Di RM, Sun YM, Xu YJ, Yang YQ. PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation. J Am Heart Assoc 2021;10:e023517. [PMID: 34845933 DOI: 10.1161/JAHA.121.023517] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]

For:

Guo XJ, Qiu XB, Wang J, Guo YH, Yang CX, Li L, Gao RF, Ke ZP, Di RM, Sun YM, Xu YJ, Yang YQ. PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation. J Am Heart Assoc 2021;10:e023517. [PMID: 34845933 DOI: 10.1161/JAHA.121.023517] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]

Number	Citing Articles
1	Lee DSM, Damrauer SM, Levin MG. Genetics of atrial fibrillation. Curr Opin Cardiol 2023. [PMID: 36789763 DOI: 10.1097/HCO.0000000000001031] [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	Guo Y, Yang Y. Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions. Biology 2022;11:489. [DOI: 10.3390/biology11040489] [Reference Citation Analysis]