Li N - Search Results

1

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation.

Li N, Wang ZS, Wang XH, Xu YJ, Qiao Q, Li XM, Di RM, Guo XJ, Li RG, Zhang M, Qiu XB, Yang YQ. Li N, et al. Among authors: li xm, li rg. Int J Med Sci. 2018 Oct 20;15(13):1564-1572. doi: 10.7150/ijms.27424. eCollection 2018. Int J Med Sci. 2018. PMID: 30443179 Free PMC article.

2

CASZ1 loss-of-function mutation associated with congenital heart disease.

Huang RT, Xue S, Wang J, Gu JY, Xu JH, Li YJ, Li N, Yang XX, Liu H, Zhang XD, Qu XK, Xu YJ, Qiu XB, Li RG, Yang YQ. Huang RT, et al. Among authors: li yj, li n, li rg. Gene. 2016 Dec 20;595(1):62-68. doi: 10.1016/j.gene.2016.09.044. Epub 2016 Sep 28. Gene. 2016. PMID: 27693370 Clinical Trial.

3

Impact of prior permanent pacemaker on long-term clinical outcomes of patients undergoing percutaneous coronary intervention.

Li YJ, Zhang WW, Yang XX, Li N, Qiu XB, Qu XK, Fang WY, Yang YQ, Li RG. Li YJ, et al. Among authors: li n, li rg. Clin Cardiol. 2017 Apr;40(4):205-209. doi: 10.1002/clc.22645. Epub 2016 Nov 23. Clin Cardiol. 2017. PMID: 27879000 Free PMC article.

4

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: li yj, li n. Pediatr Cardiol. 2017 Mar;38(3):547-557. doi: 10.1007/s00246-016-1547-8. Epub 2016 Dec 10. Pediatr Cardiol. 2017. PMID: 27942761

5

HAND1 loss-of-function mutation contributes to congenital double outlet right ventricle.

Li L, Wang J, Liu XY, Liu H, Shi HY, Yang XX, Li N, Li YJ, Huang RT, Xue S, Qiu XB, Yang YQ. Li L, et al. Among authors: li yj, li n. Int J Mol Med. 2017 Mar;39(3):711-718. doi: 10.3892/ijmm.2017.2865. Epub 2017 Jan 20. Int J Mol Med. 2017. PMID: 28112363

6

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus.

Huang RT, Wang J, Xue S, Qiu XB, Shi HY, Li RG, Qu XK, Yang XX, Liu H, Li N, Li YJ, Xu YJ, Yang YQ. Huang RT, et al. Among authors: li yj, li n, li rg. Int J Med Sci. 2017 Mar 11;14(4):323-332. doi: 10.7150/ijms.17834. eCollection 2017. Int J Med Sci. 2017. PMID: 28553164 Free PMC article.

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

8

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: li n. 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.

9

Discovery of TBX20 as a Novel Gene Underlying Atrial Fibrillation.

Li N, Li YJ, Guo XJ, Wu SH, Jiang WF, Zhang DL, Wang KW, Li L, Sun YM, Xu YJ, Yang YQ, Qiu XB. Li N, et al. Among authors: li yj, li l. Biology (Basel). 2023 Aug 30;12(9):1186. doi: 10.3390/biology12091186. Biology (Basel). 2023. PMID: 37759586 Free PMC article.

10

Identification and Functional Investigation of SOX4 as a Novel Gene Underpinning Familial Atrial Fibrillation.

Jiang WF, Sun YM, Qiu XB, Wu SH, Ding YY, Li N, Yang CX, Xu YJ, Jiang TB, Yang YQ. Jiang WF, et al. Among authors: li n. Diagnostics (Basel). 2024 Oct 25;14(21):2376. doi: 10.3390/diagnostics14212376. Diagnostics (Basel). 2024. PMID: 39518344 Free PMC article.

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