Similar articles for PMID: 29222010

Year	Number of Results
1988	2
1994	1
1998	1
2000	1
2002	2
2007	2
2008	1
2009	2
2010	7
2011	11
2012	19
2013	15
2014	14
2015	14
2016	17
2017	17
2018	17
2019	8
2020	11
2021	13
2022	10
2023	4
2024	0

1

A novel NR2F2 loss-of-function mutation predisposes to congenital heart defect.

Qiao XH, Wang Q, Wang J, Liu XY, Xu YJ, Huang RT, Xue S, Li YJ, Zhang M, Qu XK, Li RG, Qiu XB, Yang YQ. Qiao XH, et al. Eur J Med Genet. 2018 Apr;61(4):197-203. doi: 10.1016/j.ejmg.2017.12.003. Epub 2017 Dec 6. Eur J Med Genet. 2018. PMID: 29222010

2

A Novel MEF2C Loss-of-Function Mutation Associated with Congenital Double Outlet Right Ventricle.

Lu CX, Wang W, Wang Q, Liu XY, Yang YQ. Lu CX, et al. Pediatr Cardiol. 2018 Apr;39(4):794-804. doi: 10.1007/s00246-018-1822-y. Epub 2018 Feb 21. Pediatr Cardiol. 2018. PMID: 29468350

3

MEF2C loss-of-function mutation contributes to congenital heart defects.

Qiao XH, Wang F, Zhang XL, Huang RT, Xue S, Wang J, Qiu XB, Liu XY, Yang YQ. Qiao XH, et al. Int J Med Sci. 2017 Sep 8;14(11):1143-1153. doi: 10.7150/ijms.21353. eCollection 2017. Int J Med Sci. 2017. PMID: 29104469 Free PMC article.

4

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. 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.

5

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.

6

A Novel TBX1 Loss-of-Function Mutation Associated with Congenital Heart Disease.

Pan Y, Wang ZG, Liu XY, Zhao H, Zhou N, Zheng GF, Qiu XB, Li RG, Yuan F, Shi HY, Hou XM, Yang YQ. Pan Y, et al. Pediatr Cardiol. 2015 Oct;36(7):1400-10. doi: 10.1007/s00246-015-1173-x. Epub 2015 Apr 10. Pediatr Cardiol. 2015. PMID: 25860641

7

MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.

Zhang M, Li FX, Liu XY, Huang RT, Xue S, Yang XX, Li YJ, Liu H, Shi HY, Pan X, Qiu XB, Yang YQ. Zhang M, et al. Mol Med Rep. 2017 Sep;16(3):2747-2754. doi: 10.3892/mmr.2017.6875. Epub 2017 Jun 29. Mol Med Rep. 2017. PMID: 28677747

8

TBX20 loss-of-function mutation contributes to double outlet right ventricle.

Pan Y, Geng R, Zhou N, Zheng GF, Zhao H, Wang J, Zhao CM, Qiu XB, Yang YQ, Liu XY. Pan Y, et al. Int J Mol Med. 2015 Apr;35(4):1058-66. doi: 10.3892/ijmm.2015.2077. Epub 2015 Jan 22. Int J Mol Med. 2015. PMID: 25625280

9

A New ISL1 Loss-of-Function Mutation Predisposes to Congenital Double Outlet Right Ventricle.

Wang Z, Song HM, Wang F, Zhao CM, Huang RT, Xue S, Li RG, Qiu XB, Xu YJ, Liu XY, Yang YQ. Wang Z, et al. Int Heart J. 2019 Sep 27;60(5):1113-1122. doi: 10.1536/ihj.18-685. Epub 2019 Sep 4. Int Heart J. 2019. PMID: 31484864 Free article.

10

PITX2 Loss-of-Function Mutation Contributes to Congenital Endocardial Cushion Defect and Axenfeld-Rieger Syndrome.

Zhao CM, Peng LY, Li L, Liu XY, Wang J, Zhang XL, Yuan F, Li RG, Qiu XB, Yang YQ. Zhao CM, et al. PLoS One. 2015 Apr 20;10(4):e0124409. doi: 10.1371/journal.pone.0124409. eCollection 2015. PLoS One. 2015. PMID: 25893250 Free PMC article.

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