Fang WY - Search Results

1

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease.

Jiang JQ, Li RG, Wang J, Liu XY, Xu YJ, Fang WY, Chen XZ, Zhang W, Wang XZ, Yang YQ. Jiang JQ, et al. Among authors: fang wy. Int J Cardiol. 2013 May 25;165(3):570-3. doi: 10.1016/j.ijcard.2012.09.039. Epub 2012 Sep 30. Int J Cardiol. 2013. PMID: 23031282 No abstract available.

2

Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation.

Yang YQ, Xu YJ, Li RG, Qu XK, Fang WY, Liu X. Yang YQ, et al. Among authors: fang wy. Int J Cardiol. 2013 Oct 3;168(3):2873-6. doi: 10.1016/j.ijcard.2013.03.141. Epub 2013 Apr 20. Int J Cardiol. 2013. PMID: 23611745 No abstract available.

3

Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.

Yang YQ, Wang J, Wang XH, Wang Q, Tan HW, Zhang M, Shen FF, Jiang JQ, Fang WY, Liu X. Yang YQ, et al. Among authors: fang wy. Int J Cardiol. 2012 May 31;157(2):305-7. doi: 10.1016/j.ijcard.2012.03.132. Epub 2012 Apr 6. Int J Cardiol. 2012. PMID: 22483626 No abstract available.

4

Novel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallot.

Wang J, Luo XJ, Xin YF, Liu Y, Liu ZM, Wang Q, Li RG, Fang WY, Wang XZ, Yang YQ. Wang J, et al. Among authors: fang wy. DNA Cell Biol. 2012 Nov;31(11):1610-7. doi: 10.1089/dna.2012.1814. Epub 2012 Sep 28. DNA Cell Biol. 2012. PMID: 23020118 Free PMC article.

5

A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation.

Wang XH, Huang CX, Wang Q, Li RG, Xu YJ, Liu X, Fang WY, Yang YQ. Wang XH, et al. Among authors: fang wy. Int J Mol Med. 2013 Jan;31(1):43-50. doi: 10.3892/ijmm.2012.1189. Epub 2012 Nov 20. Int J Mol Med. 2013. PMID: 23175127

6

Prevalence and spectrum of GJA5 mutations associated with lone atrial fibrillation.

Shi HF, Yang JF, Wang Q, Li RG, Xu YJ, Qu XK, Fang WY, Liu X, Yang YQ. Shi HF, et al. Among authors: fang wy. Mol Med Rep. 2013 Mar;7(3):767-74. doi: 10.3892/mmr.2012.1252. Epub 2012 Dec 28. Mol Med Rep. 2013. PMID: 23292621

7

PITX2c loss-of-function mutations responsible for congenital atrial septal defects.

Yuan F, Zhao L, Wang J, Zhang W, Li X, Qiu XB, Li RG, Xu YJ, Xu L, Qu XK, Fang WY, Yang YQ. Yuan F, et al. Among authors: fang wy. Int J Med Sci. 2013 Aug 22;10(10):1422-9. doi: 10.7150/ijms.6809. eCollection 2013. Int J Med Sci. 2013. PMID: 23983605 Free PMC article.

8

Prevalence and spectrum of Nkx2.6 mutations in patients with congenital heart disease.

Zhao L, Ni SH, Liu XY, Wei D, Yuan F, Xu L, Xin-Li, Li RG, Qu XK, Xu YJ, Fang WY, Yang YQ, Qiu XB. Zhao L, et al. Among authors: fang wy. Eur J Med Genet. 2014 Oct;57(10):579-86. doi: 10.1016/j.ejmg.2014.08.005. Epub 2014 Sep 3. Eur J Med Genet. 2014. PMID: 25195019

9

A novel NKX2.5 loss-of-function mutation associated with congenital bicuspid aortic valve.

Qu XK, Qiu XB, Yuan F, Wang J, Zhao CM, Liu XY, Zhang XL, Li RG, Xu YJ, Hou XM, Fang WY, Liu X, Yang YQ. Qu XK, et al. Among authors: fang wy. Am J Cardiol. 2014 Dec 15;114(12):1891-5. doi: 10.1016/j.amjcard.2014.09.028. Epub 2014 Sep 28. Am J Cardiol. 2014. PMID: 25438918

10

A novel GATA4 loss-of-function mutation associated with congenital ventricular septal defect.

Yang YQ, Li L, Wang J, Liu XY, Chen XZ, Zhang W, Wang XZ, Jiang JQ, Liu X, Fang WY. Yang YQ, et al. Among authors: fang wy. Pediatr Cardiol. 2012 Apr;33(4):539-46. doi: 10.1007/s00246-011-0146-y. Epub 2011 Nov 20. Pediatr Cardiol. 2012. PMID: 22101736

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