Ri-Tai Huang - Search Results

Year	Number of Results
2010	1
2012	2
2013	4
2014	2
2015	3
2016	6
2017	10
2018	4
2019	2
2022	4
2023	2
2024	2

1

SMAD1 Loss-of-Function Variant Responsible for Congenital Heart Disease.

Wang Z, Qiao XH, Xu YJ, Liu XY, Huang RT, Xue S, Qiu HY, Yang YQ. Wang Z, et al. Among authors: huang rt. Biomed Res Int. 2022 Mar 3;2022:9916325. doi: 10.1155/2022/9916325. eCollection 2022. Biomed Res Int. 2022. PMID: 35281600 Free PMC article.

2

SMAD4 loss-of-function mutation predisposes to congenital heart disease.

Wang Y, Xu YJ, Yang CX, Huang RT, Xue S, Yuan F, Yang YQ. Wang Y, et al. Among authors: huang rt. Eur J Med Genet. 2023 Jan;66(1):104677. doi: 10.1016/j.ejmg.2022.104677. Epub 2022 Dec 7. Eur J Med Genet. 2023. PMID: 36496093

3

Somatic GATA4 mutation contributes to tetralogy of Fallot.

Abhinav P, Li YJ, Huang RT, Liu XY, Gu JN, Yang CX, Xu YJ, Wang J, Yang YQ. Abhinav P, et al. Among authors: huang rt. Exp Ther Med. 2024 Jan 8;27(2):91. doi: 10.3892/etm.2024.12379. eCollection 2024 Feb. Exp Ther Med. 2024. PMID: 38274337 Free PMC article.

4

Meta-analysis of clinical studies comparing coronary artery bypass grafting with percutaneous coronary intervention in patients with end-stage renal disease.

Zheng H, Xue S, Lian F, Huang RT, Hu ZL, Wang YY. Zheng H, et al. Among authors: huang rt. Eur J Cardiothorac Surg. 2013 Mar;43(3):459-67. doi: 10.1093/ejcts/ezs360. Epub 2012 Jul 9. Eur J Cardiothorac Surg. 2013. PMID: 22778175 Review.

5

Identification of SOX18 as a New Gene Predisposing to Congenital Heart Disease.

Shi HY, Xie MS, Yang CX, Huang RT, Xue S, Liu XY, Xu YJ, Yang YQ. Shi HY, et al. Among authors: huang rt. Diagnostics (Basel). 2022 Aug 8;12(8):1917. doi: 10.3390/diagnostics12081917. Diagnostics (Basel). 2022. PMID: 36010266 Free PMC article.

6

SOX7 loss-of-function variation as a cause of familial congenital heart disease.

Huang RT, Guo YH, Yang CX, Gu JN, Qiu XB, Shi HY, Xu YJ, Xue S, Yang YQ. Huang RT, et al. Am J Transl Res. 2022 Mar 15;14(3):1672-1684. eCollection 2022. Am J Transl Res. 2022. PMID: 35422912 Free PMC article.

7

TBX1 loss-of-function mutation contributes to congenital conotruncal defects.

Zhang M, Li FX, Liu XY, Hou JY, Ni SH, Wang J, Zhao CM, Zhang W, Kong Y, Huang RT, Xue S, Yang YQ. Zhang M, et al. Among authors: huang rt. Exp Ther Med. 2018 Jan;15(1):447-453. doi: 10.3892/etm.2017.5362. Epub 2017 Oct 24. Exp Ther Med. 2018. PMID: 29250159 Free PMC article.

8

Discovery of GJC1 (Cx45) as a New Gene Underlying Congenital Heart Disease and Arrhythmias.

Li YJ, Wang J, Ye WG, Liu XY, Li L, Qiu XB, Chen H, Xu YJ, Yang YQ, Bai D, Huang RT. Li YJ, et al. Among authors: huang rt. Biology (Basel). 2023 Feb 21;12(3):346. doi: 10.3390/biology12030346. Biology (Basel). 2023. PMID: 36979038 Free PMC article.

9

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. Among authors: huang rt. Gene. 2016 Feb 15;577(2):258-64. doi: 10.1016/j.gene.2015.12.001. Epub 2015 Dec 2. Gene. 2016. PMID: 26657035

10

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. Among authors: huang rt. 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.

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