Sun YM - Search Results

1

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: sun ym. 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.

2

Coronary arteriovenous fistula with giant aneurysm formation treated with percutaneous intervention.

Sun YM, Wang J, Yang G, Zhou Y, Zhang Y, Xu ZQ. Sun YM, et al. Chin Med J (Engl). 2010 Jan 5;123(1):114-6. Chin Med J (Engl). 2010. PMID: 20137588 No abstract available.

3

Mutation spectrum of the GATA4 gene in patients with idiopathic atrial fibrillation.

Wang J, Sun YM, Yang YQ. Wang J, et al. Among authors: sun ym. Mol Biol Rep. 2012 Aug;39(8):8127-35. doi: 10.1007/s11033-012-1660-6. Epub 2012 May 3. Mol Biol Rep. 2012. PMID: 22552926

4

Successful catheter aspiration and local low-dose thrombolysis in an acute renal artery embolism.

Wang J, Zhang Y, Sun YM, Zhou Y. Wang J, et al. Among authors: sun ym. Cardiovasc Revasc Med. 2013 Sep-Oct;14(5):302-4. doi: 10.1016/j.carrev.2013.03.002. Epub 2013 Apr 24. Cardiovasc Revasc Med. 2013. PMID: 24034863

5

A novel PITX2c loss-of-function mutation associated with familial atrial fibrillation.

Wang J, Zhang DF, Sun YM, Yang YQ. Wang J, et al. Among authors: sun ym. Eur J Med Genet. 2014 Jan;57(1):25-31. doi: 10.1016/j.ejmg.2013.11.004. Epub 2013 Dec 10. Eur J Med Genet. 2014. PMID: 24333117

6

NKX2-6 mutation predisposes to familial atrial fibrillation.

Wang J, Zhang DF, Sun YM, Li RG, Qiu XB, Qu XK, Liu X, Fang WY, Yang YQ. Wang J, et al. Among authors: sun ym. Int J Mol Med. 2014 Dec;34(6):1581-90. doi: 10.3892/ijmm.2014.1971. Epub 2014 Oct 16. Int J Mol Med. 2014. PMID: 25319568

7

PITX2 loss-of-function mutation contributes to tetralogy of Fallot.

Sun YM, Wang J, Qiu XB, Yuan F, Xu YJ, Li RG, Qu XK, Huang RT, Xue S, Yang YQ. Sun YM, et al. Gene. 2016 Feb 15;577(2):258-64. doi: 10.1016/j.gene.2015.12.001. Epub 2015 Dec 2. Gene. 2016. PMID: 26657035

8

A HAND2 Loss-of-Function Mutation Causes Familial Ventricular Septal Defect and Pulmonary Stenosis.

Sun YM, Wang J, Qiu XB, Yuan F, Li RG, Xu YJ, Qu XK, Shi HY, Hou XM, Huang RT, Xue S, Yang YQ. Sun YM, et al. G3 (Bethesda). 2016 Apr 7;6(4):987-92. doi: 10.1534/g3.115.026518. G3 (Bethesda). 2016. PMID: 26865696 Free PMC article.

9

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy.

Qiu XB, Qu XK, Li RG, Liu H, Xu YJ, Zhang M, Shi HY, Hou XM, Liu X, Yuan F, Sun YM, Wang J, Huang RT, Xue S, Yang YQ. Qiu XB, et al. Among authors: sun ym. Clin Chem Lab Med. 2017 Aug 28;55(9):1417-1425. doi: 10.1515/cclm-2016-0612. Clin Chem Lab Med. 2017. PMID: 28099117

10

MEF2C loss-of-function mutation associated with familial dilated cardiomyopathy.

Yuan F, Qiu ZH, Wang XH, Sun YM, Wang J, Li RG, Liu H, Zhang M, Shi HY, Zhao L, Jiang WF, Liu X, Qiu XB, Qu XK, Yang YQ. Yuan F, et al. Among authors: sun ym. Clin Chem Lab Med. 2018 Feb 23;56(3):502-511. doi: 10.1515/cclm-2017-0461. Clin Chem Lab Med. 2018. PMID: 28902616

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