Xing-Yuan Liu - Search Results

Year	Number of Results
2003	1
2004	1
2008	1
2009	2
2010	4
2011	5
2012	7
2013	4
2014	5
2015	6
2016	2
2017	6
2018	8
2019	1
2021	1
2022	4
2023	2
2024	3

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: liu xy. 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

SOX17 Loss-of-Function Mutation Underlying Familial Pulmonary Arterial Hypertension.

Wang TM, Wang SS, Xu YJ, Zhao CM, Qiao XH, Yang CX, Liu XY, Yang YQ. Wang TM, et al. Among authors: liu xy. Int Heart J. 2021 May 29;62(3):566-574. doi: 10.1536/ihj.20-711. Epub 2021 May 1. Int Heart J. 2021. PMID: 33952808 Free article.

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: liu xy. 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

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: liu xy. Diagnostics (Basel). 2022 Aug 8;12(8):1917. doi: 10.3390/diagnostics12081917. Diagnostics (Basel). 2022. PMID: 36010266 Free PMC article.

5

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: liu xy. 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.

6

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: liu xy. Biology (Basel). 2023 Feb 21;12(3):346. doi: 10.3390/biology12030346. Biology (Basel). 2023. PMID: 36979038 Free PMC article.

7

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: liu xy. 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.

8

Short-term effects of air pollution on respiratory diseases among young children in Wuhan city, China.

Huang ZH, Liu XY, Zhao T, Jiao KZ, Ma XX, Ren Z, Qiu YF, Liao JL, Ma L. Huang ZH, et al. Among authors: liu xy. World J Pediatr. 2022 May;18(5):333-342. doi: 10.1007/s12519-022-00533-5. Epub 2022 Mar 25. World J Pediatr. 2022. PMID: 35334045 Free PMC article.

9

GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.

Xu YJ, Di RM, Qiao Q, Li XM, Huang RT, Xue S, Liu XY, Wang J, Yang YQ. Xu YJ, et al. Among authors: liu xy. Gene. 2018 Jul 15;663:115-120. doi: 10.1016/j.gene.2018.04.018. Epub 2018 Apr 10. Gene. 2018. PMID: 29653232

10

GATA4 Loss-of-Function Mutation and the Congenitally Bicuspid Aortic Valve.

Li RG, Xu YJ, Wang J, Liu XY, Yuan F, Huang RT, Xue S, Li L, Liu H, Li YJ, Qu XK, Shi HY, Zhang M, Qiu XB, Yang YQ. Li RG, et al. Among authors: liu xy. Am J Cardiol. 2018 Feb 15;121(4):469-474. doi: 10.1016/j.amjcard.2017.11.012. Epub 2017 Nov 23. Am J Cardiol. 2018. PMID: 29325903

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

52 results

Results by year

Search Page

Filters

My NCBI Filters

Results by year

Text availability

Article attribute

Article type

Publication date

Search Results

52 results

Results by year