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1

No significant association between the XRCC3 Thr241Met polymorphism and lung cancer risk: a meta-analysis

Yun-Hua Xu, Lin-Ping Gu, Ying-Jia Sun, Bai-Jun Cheng, Shun Lu

Journal:

Year:

2013

Language:

english

File:

PDF, 327 KB

english, 2013

2

Immunosuppression and T lymphocytes

Yang, Yi-Qing, Li, Li, Wang, Juan, Zhang, Xian-Ling, Li, Ruo-Gu, Xu, Ying-Jia, Tan, Hong-Wei, Wang, Xin-Hua, Jiang, Jin-Qi, Fang, Wei-Yi, Liu, Xu

Journal:

Year:

1982

Language:

english

File:

PDF, 96 KB

english, 1982

3

Serum levels of cathepsin D, sirtuin1, and endothelial nitric oxide synthase are correlatively reduced in elderly healthy people

Zhong, Yuan, Chen, Alex. F., Zhao, Jian, Gu, Ying-Jia, Fu, Guo-Xiang

Journal:

Aging Clinical and Experimental Research

Year:

2016

Language:

english

File:

PDF, 434 KB

english, 2016

4

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

Wang, Zhi, Song, Hao-Ming, Wang, Fei, Zhao, Cui-Mei, Huang, Ri-Tai, Xue, Song, Li, Ruo-Gu, Qiu, Xing-Biao, Xu, Ying-Jia, Liu, Xing-Yuan, Yang, Yi-Qing

Journal:

International Heart Journal

Year:

2019

File:

PDF, 260 KB

2019

5

GATA6 loss-of-function mutations contribute to familial dilated cardiomyopathy

Xu, Lei, Zhao, Lan, Yuan, Fang, Jiang, Wei-Feng, Liu, Hua, Li, Ruo-Gu, Xu, Ying-Jia, Zhang, Min, Fang, Wei-Yi, Qu, Xin-Kai, Yang, Yi-Qing, Qiu, Xing-Biao

Journal:

International Journal of Molecular Medicine

Year:

2014

Language:

english

File:

PDF, 809 KB

english, 2014

6

PITX2c Loss-of-Function Mutations Responsible for Congenital Atrial Septal Defects

Yuan, Fang, Zhao, Lan, Wang, Juan, Zhang, Wei, Li, Xin, Qiu, Xing-Biao, Li, Ruo-Gu, Xu, Ying-Jia, Xu, Lei, Qu, Xing-Kai, Fang, Wei-Yi, Yang, Yi-Qing

Journal:

International Journal of Medical Sciences

Year:

2013

Language:

english

File:

PDF, 1.03 MB

english, 2013

7

GATA5 loss-of-function mutations associated with congenital bicuspid aortic valve

SHI, LIN-MEI, TAO, JU-WEI, QIU, XING-BIAO, WANG, JUAN, YUAN, FANG, XU, LEI, LIU, HUA, LI, RUO-GU, XU, YING-JIA, WANG, QIAN, ZHENG, HONG-ZHEN, LI, XIN, WANG, XIAO-ZHOU, ZHANG, MIN, QU, XIN-KAI, YANG, Y

Journal:

International Journal of Molecular Medicine

Year:

2014

Language:

english

File:

PDF, 676 KB

english, 2014

8

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation

Li, Ning, Wang, Zhang-Sheng, Wang, Xin-Hua, Xu, Ying-Jia, Qiao, Qi, Li, Xiu-Mei, Di, Ruo-Min, Guo, Xiao-Juan, Li, Ruo-Gu, Zhang, Min, Qiu, Xing-Biao, Yang, Yi-Qing

Journal:

International Journal of Medical Sciences

Year:

2018

Language:

english

File:

PDF, 736 KB

english, 2018

9

Transcatheter coil embolization of multiple coronary artery-to-left ventricle fistulas: report of a rare case

LI, Ruo-gu, FANG, Wei-yi, SHI, Hong-yu, QU, Xin-kai, CHEN, Hui, QIU, Xin-biao, XU, Ying-jia, DONG, Jia-lin, GUAN, Shao-feng, JIANG, Bei, WU, Wei-hua

Journal:

Chinese Medical Journal

Year:

2008

File:

PDF, 381 KB

2008

10

GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot

Wei, Dong, Bao, Han, Liu, Xing-Yuan, Zhou, Ning, Wang, Qian, Li, Ruo-Gu, Xu, Ying-Jia, Yang, Yi-Qing

Journal:

International Journal of Medical Sciences

Year:

2013

Language:

english

File:

PDF, 633 KB

english, 2013

11

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy

Di, Ruo-Min, Yang, Chen-Xi, Zhao, Cui-Mei, Yuan, Fang, Qiao, Qi, Gu, Jia-Ning, Li, Xiu-Mei, Xu, Ying-Jia, Yang, Yi-Qing

Journal:

European Journal of Medical Genetics

Year:

2019

File:

PDF, 727 KB

2019

12

GATA4 Loss-of-Function Mutations Underlie Familial Tetralogy of Fallot

Yang, Yi-Qing, Gharibeh, Lara, Li, Ruo-Gu, Xin, Yuan-Feng, Wang, Juan, Liu, Zhong-Min, Qiu, Xing-Biao, Xu, Ying-Jia, Xu, Lei, Qu, Xin-Kai, Liu, Xu, Fang, Wei-Yi, Huang, Ri-Tai, Xue, Song, Nemer, Georg

Journal:

Year:

2013

Language:

english

File:

PDF, 960 KB

english, 2013

13

A NovelNKX2.6Mutation Associated with Congenital Ventricular Septal Defect

Wang, Juan, Mao, Jian-Hui, Ding, Ke-Ke, Xu, Wei-Jun, Liu, Xing-Yuan, Qiu, Xing-Biao, Li, Ruo-Gu, Qu, Xin-Kai, Xu, Ying-Jia, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

Journal:

Pediatric Cardiology

Year:

2015

Language:

english

File:

PDF, 1.07 MB

english, 2015

14

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

Li, Ruo-Gu, Xu, Ying-Jia, Wang, Juan, Liu, Xing-Yuan, Yuan, Fang, Huang, Ri-Tai, Xue, Song, Li, Li, Liu, Hua, Li, Yan-Jie, Qu, Xin-Kai, Shi, Hong-Yu, Zhang, Min, Qiu, Xing-Biao, Yang, Yi-Qing

Journal:

The American Journal of Cardiology

Year:

2017

Language:

english

File:

PDF, 664 KB

english, 2017

15

A Novel NKX2.5 Loss-of-Function Mutation Associated With Congenital Bicuspid Aortic Valve

Qu, Xin-Kai, Qiu, Xing-Biao, Yuan, Fang, Wang, Juan, Zhao, Cui-Mei, Liu, Xing-Yuan, Zhang, Xian-Ling, Li, Ruo-Gu, Xu, Ying-Jia, Hou, Xu-Min, Fang, Wei-Yi, Liu, Xu, Yang, Yi-Qing

Journal:

The American Journal of Cardiology

Year:

2014

Language:

english

File:

PDF, 211 KB

english, 2014

16

Prevalence and spectrum of GATA5 mutations associated with congenital heart disease

Jiang, Jin-Qi, Li, Ruo-Gu, Wang, Juan, Liu, Xing-Yuan, Xu, Ying-Jia, Fang, Wei-Yi, Chen, Xiao-Zhong, Zhang, Wei, Wang, Xiao-Zhou, Yang, Yi-Qing

Journal:

International Journal of Cardiology

Year:

2013

Language:

english

File:

PDF, 807 KB

english, 2013

17

HAND1 loss-of-function mutation associated with familial dilated cardiomyopathy

Zhou, Yi-Meng, Dai, Xiao-Yong, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Qu, Xin-Kai, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2015

Language:

english

File:

PDF, 719 KB

english, 2015

18

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

Zhao, Lan, Ni, Shi-Hong, Liu, Xing-Yuan, Wei, Dong, Yuan, Fang, Xu, Lei, Xin-Li,, Li, Ruo-Gu, Qu, Xin-Kai, Xu, Ying-Jia, Fang, Wei-Yi, Yang, Yi-Qing, Qiu, Xing-Biao

Journal:

European Journal of Medical Genetics

Year:

2014

Language:

english

File:

PDF, 1.48 MB

english, 2014

19

TBX20 loss-of-function mutation responsible for familial tetralogy of Fallot or sporadic persistent truncus arteriosus

Huang, Ri-Tai, Wang, Juan, Xue, Song, Qiu, Xing-Biao, Shi, Hong-Yu, Li, Ruo-Gu, Qu, Xin-Kai, Yang, Xiao-Xiao, Liu, Hua, Li, Ning, Li, Yan-Jie, Xu, Ying-Jia, Yang, Yi-Qing

Journal:

International Journal of Medical Sciences

Year:

2017

Language:

english

File:

PDF, 1.04 MB

english, 2017

20

Prevalence and Spectrum of NKX2-5 Mutations Associated With Sporadic Adult-Onset Dilated Cardiomyopathy

Xu, Jia-Hong, Gu, Jian-Yun, Guo, Yu-Han, Zhang, Hong, Qiu, Xing-Biao, Li, Ruo-Gu, Shi, Hong-Yu, Liu, Hua, Yang, Xiao-Xiao, Xu, Ying-Jia, Qu, Xin-Kai, Yang, Yi-Qing

Journal:

International Heart Journal

Year:

2017

Language:

english

File:

PDF, 1.52 MB

english, 2017

21

Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block

Xu, Ying-Jia, Qiu, Xing-Biao, Yuan, Fang, Shi, Hong-Yu, Xu, Lei, Hou, Xu-Min, Qu, Xin-Kai, Liu, Xu, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing, Li, Ruo-Gu

Journal:

Molecular Medicine Reports

Year:

2017

Language:

english

File:

PDF, 968 KB

english, 2017

22

ISL1 loss-of-function mutation contributes to congenital heart defects

Ma, Lan, Wang, Juan, Li, Li, Qiao, Qi, Di, Ruo-Min, Li, Xiu-Mei, Xu, Ying-Jia, Zhang, Min, Li, Ruo-Gu, Qiu, Xing-Biao, Li, Xun, Yang, Yi-Qing

Journal:

Heart and Vessels

Year:

2018

Language:

english

File:

PDF, 1.88 MB

english, 2018

23

GATA4 loss-of-function mutation underlies familial dilated cardiomyopathy

Li, Ruo-Gu, Li, Li, Qiu, Xing-Biao, Yuan, Fang, Xu, Lei, Li, Xin, Xu, Ying-Jia, Jiang, Wei-Feng, Jiang, Jin-Qi, Liu, Xu, Fang, Wei-Yi, Zhang, Min, Peng, Lu-Ying, Qu, Xin-Kai, Yang, Yi-Qing

Journal:

Biochemical and Biophysical Research Communications

Year:

2013

Language:

english

File:

PDF, 982 KB

english, 2013

24

ZBTB17 loss-of-function mutation contributes to familial dilated cardiomyopathy

Sun, Yu-Min, Wang, Jun, Xu, Ying-Jia, Wang, Xin-Hua, Yuan, Fang, Liu, Hua, Li, Ruo-Gu, Zhang, Min, Li, Yan-Jie, Shi, Hong-Yu, Zhao, Liang, Qiu, Xing-Biao, Qu, Xin-Kai, Yang, Yi-Qing

Journal:

Heart and Vessels

Year:

2018

Language:

english

File:

PDF, 1.43 MB

english, 2018

25

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

Wang, Zhi, Song, Hao-Ming, Wang, Fei, Zhao, Cui-Mei, Huang, Ri-Tai, Xue, Song, Li, Ruo-Gu, Qiu, Xing-Biao, Xu, Ying-Jia, Liu, Xing-Yuan, Yang, Yi-Qing

Journal:

International Heart Journal

Year:

2019

Language:

english

File:

PDF, 260 KB

english, 2019

26

Prevalence and spectrum of PITX2c mutations associated with familial atrial fibrillation

Yang, Yi-Qing, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Fang, Wei-Yi, Liu, Xu

Journal:

International Journal of Cardiology

Year:

2013

Language:

english

File:

PDF, 628 KB

english, 2013

27

Prevalence and spectrum of LRRC10 mutations associated with idiopathic dilated cardiomyopathy

Qu, Xin-Kai, Yuan, Fang, Li, Ruo-Gu, Xu, Lei, Jing, Wei-Feng, Liu, Hua, Xu, Ying-Jia, Zhang, Min, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Qiu, Xing-Biao

Journal:

Molecular Medicine Reports

Year:

2015

Language:

english

File:

PDF, 718 KB

english, 2015

28

NURSING IN WORKHOUSE INFIRMARIES.

Yang, Yi-Qing, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Fang, Wei-Yi, Liu, Xu

Journal:

Year:

1914

Language:

english

File:

PDF, 364 KB

english, 1914

29

CASZ1 loss-of-function mutation associated with congenital heart disease

Huang, Ri-Tai, Xue, Song, Wang, Juan, Gu, Jian-Yun, Xu, Jia-Hong, Li, Yan-Jie, Li, Ning, Yang, Xiao-Xiao, Liu, Hua, Zhang, Xiao-Dong, Qu, Xin-Kai, Xu, Ying-Jia, Qiu, Xing-Biao, Li, Ruo-Gu, Yang, Yi-Qi

Journal:

Year:

2016

Language:

english

File:

PDF, 948 KB

english, 2016

30

PITX2 loss-of-function mutation contributes to tetralogy of Fallot

Sun, Yu-Min, Wang, Jun, Qiu, Xing-Biao, Yuan, Fang, Xu, Ying-Jia, Li, Ruo-Gu, Qu, Xin-Kai, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

Journal:

Year:

2016

Language:

english

File:

PDF, 840 KB

english, 2016

31

CASZ1 loss-of-function mutation contributes to familial dilated cardiomyopathy

Qiu, Xing-Biao, Qu, Xin-Kai, Li, Ruo-Gu, Liu, Hua, Xu, Ying-Jia, Zhang, Min, Shi, Hong-Yu, Hou, Xu-Min, Liu, Xu, Yuan, Fang, Sun, Yu-Min, Wang, Jun, Huang, Ri-Tai, Xue, Song, Yang, Yi-Qing

Journal:

Clinical Chemistry and Laboratory Medicine

Year:

2017

Language:

english

File:

PDF, 1.02 MB

english, 2017

32

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

Yuan, Fang, Qiu, Xing-Biao, Li, Ruo-Gu, Qu, Xin-Kai, Wang, Juan, Xu, Ying-Jia, Liu, Xu, Fang, Wei-Yi, Yang, Yi-Qing, Liao, De-Ning

Journal:

International Journal of Molecular Medicine

Year:

2014

Language:

english

File:

PDF, 597 KB

english, 2014

33

Prevalence and Spectrum of TBX5 Mutation in Patients with Lone Atrial Fibrillation

Wang, Zhan-Cheng, Ji, Wen-Hui, Ruan, Chang-Wu, Liu, Xing-Yuan, Qiu, Xing-Biao, Yuan, Fang, Li, Ruo-Gu, Xu, Ying-Jia, Liu, Xu, Huang, Ru-Tai, Xue, Song, Yang, Yi-Qing

Journal:

International Journal of Medical Sciences

Year:

2016

Language:

english

File:

PDF, 998 KB

english, 2016

34

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy

Liu, Hua, Xu, Ying-Jia, Li, Ruo-Gu, Wang, Zhang-Sheng, Zhang, Min, Qu, Xin-Kai, Qiao, Qi, Li, Xiu-Mei, Di, Ruo-Min, Qiu, Xing-Biao, Yang, Yi-Qing

Journal:

European Journal of Medical Genetics

Year:

2018

Language:

english

File:

PDF, 767 KB

english, 2018

35

Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy

Xu, Ying-Jia, Wang, Zhang-Sheng, Yang, Chen-Xi, Di, Ruo-Min, Qiao, Qi, Li, Xiu-Mei, Gu, Jia-Ning, Guo, Xiao-Juan, Yang, Yi-Qing

Journal:

Journal of Cardiovascular Translational Research

Year:

2018

Language:

english

File:

PDF, 957 KB

english, 2018

36

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

Qiao, Xiao-Hui, Wang, Qian, Wang, Juan, Liu, Xing-Yuan, Xu, Ying-Jia, Huang, Ri-Tai, Xue, Song, Li, Yan-Jie, Zhang, Min, Qu, Xin-Kai, Li, Ruo-Gu, Qiu, Xing-Biao, Yang, Yi-Qing

Journal:

European Journal of Medical Genetics

Year:

2017

Language:

english

File:

PDF, 605 KB

english, 2017

37

ISL1 loss-of-function variation causes familial atrial fibrillation

Wu, Shao-Hui, Wang, Xing-Hua, Xu, Ying-Jia, Gu, Jia-Ning, Yang, Chen-Xi, Qiao, Qi, Guo, Xiao-Juan, Guo, Yu-Han, Qiu, Xing-Biao, Jiang, Wei-Feng, Yang, Yi-Qing

Journal:

European Journal of Medical Genetics

Year:

2020

File:

PDF, 755 KB

2020

38

GATA6 loss-of-function mutation in atrial fibrillation

Yang, Yi-Qing, Li, Li, Wang, Juan, Zhang, Xian-Ling, Li, Ruo-Gu, Xu, Ying-Jia, Tan, Hong-Wei, Wang, Xin-Hua, Jiang, Jin-Qi, Fang, Wei-Yi, Liu, Xu

Journal:

European Journal of Medical Genetics

Year:

2012

Language:

english

File:

PDF, 653 KB

english, 2012

39

TBX5 loss-of-function mutation contributes to familial dilated cardiomyopathy

Zhang, Xian-Ling, Qiu, Xing-Biao, Yuan, Fang, Wang, Juan, Zhao, Cui-Mei, Li, Ruo-Gu, Xu, Lei, Xu, Ying-Jia, Shi, Hong-Yu, Hou, Xu-Min, Qu, Xin-Kai, Xu, Ya-Wei, Yang, Yi-Qing

Journal:

Biochemical and Biophysical Research Communications

Year:

2015

Language:

english

File:

PDF, 769 KB

english, 2015

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