Yang CX - Search Results

1

KLF13 Loss-of-Function Mutations Underlying Familial Dilated Cardiomyopathy.

Guo YH, Wang J, Guo XJ, Gao RF, Yang CX, Li L, Sun YM, Qiu XB, Xu YJ, Yang YQ. Guo YH, et al. Among authors: yang cx, yang yq. J Am Heart Assoc. 2022 Nov 15;11(22):e027578. doi: 10.1161/JAHA.122.027578. Epub 2022 Nov 8. J Am Heart Assoc. 2022. PMID: 36346048 Free PMC article.

2

Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy.

Xu YJ, Wang ZS, Yang CX, Di RM, Qiao Q, Li XM, Gu JN, Guo XJ, Yang YQ. Xu YJ, et al. Among authors: yang cx, yang yq. J Cardiovasc Transl Res. 2019 Jun;12(3):257-267. doi: 10.1007/s12265-018-9851-8. Epub 2018 Dec 10. J Cardiovasc Transl Res. 2019. PMID: 30536204

3

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.

Di RM, Yang CX, Zhao CM, Yuan F, Qiao Q, Gu JN, Li XM, Xu YJ, Yang YQ. Di RM, et al. Among authors: yang cx, yang yq. Eur J Med Genet. 2020 Apr;63(4):103827. doi: 10.1016/j.ejmg.2019.103827. Epub 2019 Dec 16. Eur J Med Genet. 2020. PMID: 31857253

4

A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.

Zhang Y, Sun YM, Xu YJ, Zhao CM, Yuan F, Guo XJ, Guo YH, Yang CX, Gu JN, Qiao Q, Wang J, Yang YQ. Zhang Y, et al. Among authors: yang cx, yang yq. Int Heart J. 2020 Jul 30;61(4):761-768. doi: 10.1536/ihj.19-650. Epub 2020 Jul 8. Int Heart J. 2020. PMID: 32641638 Free article.

5

ISL1 loss-of-function variation causes familial atrial fibrillation.

Wu SH, Wang XH, Xu YJ, Gu JN, Yang CX, Qiao Q, Guo XJ, Guo YH, Qiu XB, Jiang WF, Yang YQ. Wu SH, et al. Among authors: yang cx, yang yq. Eur J Med Genet. 2020 Nov;63(11):104029. doi: 10.1016/j.ejmg.2020.104029. Epub 2020 Aug 6. Eur J Med Genet. 2020. PMID: 32771629

6

Detection and functional characterization of a novel MEF2A variation responsible for familial dilated cardiomyopathy.

Qiao Q, Zhao CM, Yang CX, Gu JN, Guo YH, Zhang M, Li RG, Qiu XB, Xu YJ, Yang YQ. Qiao Q, et al. Among authors: yang cx, yang yq. Clin Chem Lab Med. 2020 Dec 3;59(5):955-963. doi: 10.1515/cclm-2020-1318. Print 2021 Apr 27. Clin Chem Lab Med. 2020. PMID: 33554560

7

Atrial Arrhythmias in Patients with Severe COVID-19.

Han KY, Qiao Q, Zhu YQ, Chen XG, Kang XX, Zhang GF, Cai XC, Du Y, Jin J, Di RM, Yang CX, Zhang FX, Xu YJ. Han KY, et al. Among authors: yang cx. Cardiol Res Pract. 2021 Mar 12;2021:8874450. doi: 10.1155/2021/8874450. eCollection 2021. Cardiol Res Pract. 2021. PMID: 33777449 Free PMC article.

8

SOX17 loss-of-function variation underlying familial congenital heart disease.

Zhao L, Jiang WF, Yang CX, Qiao Q, Xu YJ, Shi HY, Qiu XB, Wu SH, Yang YQ. Zhao L, et al. Among authors: yang cx, yang yq. Eur J Med Genet. 2021 May;64(5):104211. doi: 10.1016/j.ejmg.2021.104211. Epub 2021 Mar 29. Eur J Med Genet. 2021. PMID: 33794346

9

KLF15 Loss-of-Function Mutation Underlying Atrial Fibrillation as well as Ventricular Arrhythmias and Cardiomyopathy.

Li N, Xu YJ, Shi HY, Yang CX, Guo YH, Li RG, Qiu XB, Yang YQ, Zhang M. Li N, et al. Among authors: yang cx, yang yq. Genes (Basel). 2021 Mar 12;12(3):408. doi: 10.3390/genes12030408. Genes (Basel). 2021. PMID: 33809104 Free PMC article.

10

SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension.

Wang TM, Wang SS, Xu YJ, Zhao CM, Qiao XH, Yang CX, Liu XY, Yang YQ. Wang TM, et al. Among authors: yang cx, yang yq. Int Heart J. 2021 May 29;62(3):566-574. doi: 10.1536/ihj.20-711. Epub 2021 May 1. Int Heart J. 2021. PMID: 33952808 Free article.

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