Similar articles for PMID: 23525379

Year	Number of Results
1996	1
1998	1
1999	3
2000	1
2001	3
2002	2
2003	1
2004	3
2005	5
2006	7
2007	2
2008	6
2009	7
2010	13
2011	11
2012	18
2013	21
2014	19
2015	21
2016	18
2017	14
2018	14
2019	11
2020	7
2021	6
2022	9
2023	2
2024	0

1

A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation.

Huang RT, Xue S, Xu YJ, Zhou M, Yang YQ. Huang RT, et al. Int J Mol Med. 2013 May;31(5):1119-26. doi: 10.3892/ijmm.2013.1316. Epub 2013 Mar 22. Int J Mol Med. 2013. PMID: 23525379

2

Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillation.

Yu H, Xu JH, Song HM, Zhao L, Xu WJ, Wang J, Li RG, Xu L, Jiang WF, Qiu XB, Jiang JQ, Qu XK, Liu X, Fang WY, Jiang JF, Yang YQ. Yu H, et al. Int J Med Sci. 2014 Apr 7;11(6):554-63. doi: 10.7150/ijms.8407. eCollection 2014. Int J Med Sci. 2014. PMID: 24782644 Free PMC article.

3

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. 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

4

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

Wang J, Zhang DF, Sun YM, Yang YQ. Wang J, et al. 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

5

A novel PITX2c loss‑of‑function mutation underlies lone atrial fibrillation.

Zhou YM, Zheng PX, Yang YQ, Ge ZM, Kang WQ. Zhou YM, et al. Int J Mol Med. 2013 Oct;32(4):827-34. doi: 10.3892/ijmm.2013.1463. Epub 2013 Aug 2. Int J Mol Med. 2013. PMID: 23913021

6

Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.

Xie WH, Chang C, Xu YJ, Li RG, Qu XK, Fang WY, Liu X, Yang YQ. Xie WH, et al. Clinics (Sao Paulo). 2013 Jun;68(6):777-84. doi: 10.6061/clinics/2013(06)09. Clinics (Sao Paulo). 2013. PMID: 23778487 Free PMC article.

7

A novel NKX2-5 loss-of-function mutation predisposes to familial dilated cardiomyopathy and arrhythmias.

Yuan F, Qiu XB, Li RG, Qu XK, Wang J, Xu YJ, Liu X, Fang WY, Yang YQ, Liao DN. Yuan F, et al. Int J Mol Med. 2015 Feb;35(2):478-86. doi: 10.3892/ijmm.2014.2029. Epub 2014 Dec 9. Int J Mol Med. 2015. PMID: 25503402 Clinical Trial.

8

GATA6 loss-of-function mutation in atrial fibrillation.

Yang YQ, Li L, Wang J, Zhang XL, Li RG, Xu YJ, Tan HW, Wang XH, Jiang JQ, Fang WY, Liu X. Yang YQ, et al. Eur J Med Genet. 2012 Oct;55(10):520-6. doi: 10.1016/j.ejmg.2012.06.007. Epub 2012 Jun 26. Eur J Med Genet. 2012. PMID: 22750565

9

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. 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.

10

Mutations of the SCN4B-encoded sodium channel β4 subunit in familial atrial fibrillation.

Li RG, Wang Q, Xu YJ, Zhang M, Qu XK, Liu X, Fang WY, Yang YQ. Li RG, et al. Int J Mol Med. 2013 Jul;32(1):144-50. doi: 10.3892/ijmm.2013.1355. Epub 2013 Apr 22. Int J Mol Med. 2013. PMID: 23604097

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