Guo YH - Search Results

1

Atrial Fibrillation: Focus on Myocardial Connexins and Gap Junctions.

Guo YH, Yang YQ. Guo YH, et al. Biology (Basel). 2022 Mar 23;11(4):489. doi: 10.3390/biology11040489. Biology (Basel). 2022. PMID: 35453689 Free PMC article. Review.

2

HAND1 Loss-of-Function Mutation Causes Tetralogy of Fallot.

Wang J, Hu XQ, Guo YH, Gu JY, Xu JH, Li YJ, Li N, Yang XX, Yang YQ. Wang J, et al. Among authors: guo yh. Pediatr Cardiol. 2017 Mar;38(3):547-557. doi: 10.1007/s00246-016-1547-8. Epub 2016 Dec 10. Pediatr Cardiol. 2017. PMID: 27942761

3

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy.

Xu JH, Gu JY, Guo YH, Zhang H, Qiu XB, Li RG, Shi HY, Liu H, Yang XX, Xu YJ, Qu XK, Yang YQ. Xu JH, et al. Among authors: guo yh. Int Heart J. 2017 Aug 3;58(4):521-529. doi: 10.1536/ihj.16-440. Epub 2017 Jul 10. Int Heart J. 2017. PMID: 28690296 Free article.

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: guo xj, guo yh. 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: guo xj, guo yh. 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: guo yh. 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

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: guo yh. Genes (Basel). 2021 Mar 12;12(3):408. doi: 10.3390/genes12030408. Genes (Basel). 2021. PMID: 33809104 Free PMC article.

8

PRRX1 Loss-of-Function Mutations Underlying Familial Atrial Fibrillation.

Guo XJ, Qiu XB, Wang J, Guo YH, Yang CX, Li L, Gao RF, Ke ZP, Di RM, Sun YM, Xu YJ, Yang YQ. Guo XJ, et al. Among authors: guo yh. J Am Heart Assoc. 2021 Dec 7;10(23):e023517. doi: 10.1161/JAHA.121.023517. Epub 2021 Nov 30. J Am Heart Assoc. 2021. PMID: 34845933 Free PMC article.

9

A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus.

Ke ZP, Zhang GF, Guo YH, Sun YM, Wang J, Li N, Qiu XB, Xu YJ, Yang YQ. Ke ZP, et al. Among authors: guo yh. Genet Mol Biol. 2022 Mar 30;45(2):e20210378. doi: 10.1590/1678-4685-GMB-2021-0378. eCollection 2022. Genet Mol Biol. 2022. PMID: 35377386 Free PMC article.

10

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

Huang RT, Guo YH, Yang CX, Gu JN, Qiu XB, Shi HY, Xu YJ, Xue S, Yang YQ. Huang RT, et al. Among authors: guo yh. Am J Transl Res. 2022 Mar 15;14(3):1672-1684. eCollection 2022. Am J Transl Res. 2022. PMID: 35422912 Free PMC article.

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