1. A novel FBN2 mutation cosegregates with congenital contractural arachnodactyly in a five‐generation Chinese family. Issue 8 (3rd July 2018) Authors: Zhou, Shiyuan; Wang, Fengyu; Dou, Yongheng; Zhou, Jiping; Hao, Gefang; Xu, Chengqi; Wang, Qing K.; Wang, Haili; Wang, Pengyun Journal: Clinical case reports Issue: Volume 6:Issue 8(2018) Page Start: 1612 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Genetic association analysis between IL9 and coronary artery disease in a Chinese Han population. (February 2022) Authors: Zha, Lingfeng; Dong, Jiangtao; Chen, Qianwen; Liao, Yuhua; Zhang, Hongsong; Xie, Tian; Tang, Tingting; Xia, Ni; Zhang, Min; Jiao, Jiao; Zhou, Yingchao; Wu, Jianfei; Yang, Xiangping; Xu, Chengqi; Wang, Qing K.; Tu, Xin; Cheng, Xiang; Nie, Shaofang Journal: Cytokine Issue: Volume 150(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Genome-Wide Analysis of DNA Methylation and Acute Coronary Syndrome. Issue 11 (26th May 2017) Authors: Li, Jun; Zhu, Xiaoyan; Yu, Kuai; Jiang, Haijing; Zhang, Yizhi; Deng, Siyun; Cheng, Longxian; Liu, Xuezhen; Zhong, Jia; Zhang, Xiaomin; He, Meian; Chen, Weihong; Yuan, Jing; Gao, Ming; Bai, Yansen; Han, Xu; Liu, Bing; Luo, Xiaoting; Mei, Wenhua; He, Xiaosheng Journal: Circulation research Issue: Volume 120:Issue 11(2017) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance. (27th July 2022) Authors: Fang, Chen; Wang, Pengxia; Yu, Dong; Zhang, Xiaoyu; Gou, Dongzhi; Liang, Lina; Bai, Xuemei; Xie, Wen; Li, Hui; Pu, Jielin; Yao, Yufeng; Wang, Binbin; Ren, Xiang; Ke, Tie; Tu, Xin; Xu, Chengqi; Wang, Qing K. Journal: Circulation Issue: Volume 15:Number 5(2022) Page Start: e003603 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction. (March 2016) Authors: Chen, Shanshan; Wang, Xiaojing; Wang, Junhan; Zhao, Yuanyuan; Wang, Dan; Tan, Chengcheng; Fa, Jingjing; Zhang, Rongfeng; Wang, Fan; Xu, Chaoping; Huang, Yufeng; Li, Sisi; Yin, Dan; Xiong, Xin; Li, Xiuchun; Chen, Qiuyun; Tu, Xin; Yang, Yanzong; Xia, Yunlong; Xu, Chengqi Journal: Atherosclerosis Issue: Volume 246(2016) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Genomic variant in CAV1 increases susceptibility to coronary artery disease and myocardial infarction. (March 2016) Authors: Chen, Shanshan; Wang, Xiaojing; Wang, Junhan; Zhao, Yuanyuan; Wang, Dan; Tan, Chengcheng; Fa, Jingjing; Zhang, Rongfeng; Wang, Fan; Xu, Chaoping; Huang, Yufeng; Li, Sisi; Yin, Dan; Xiong, Xin; Li, Xiuchun; Chen, Qiuyun; Tu, Xin; Yang, Yanzong; Xia, Yunlong; Xu, Chengqi Journal: Atherosclerosis Issue: Volume 246(2016) Page Start: 148 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Identification and characterization of a special type of subnuclear structure: AGGF1‐coated paraspeckles. Issue 6 (24th May 2022) Authors: Zhao, Jinyan; Xie, Wen; Yang, Zhongcheng; Zhao, Miao; Ke, Tie; Xu, Chengqi; Li, Hui; Chen, Qiuyun; Wang, Qing K. Journal: FASEB journal Issue: Volume 36:Issue 6(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Identification and functional analysis of two new de novo KCNMA1 variants associated with Liang–Wang syndrome. (23rd February 2022) Authors: Liang, Lina; Liu, Huihui; Bartholdi, Deborah; van Haeringen, Arie; Fernandez‐Jaén, Alberto; Peeters, Els E. A.; Xiong, Hongbo; Bai, Xuemei; Xu, Chengqi; Ke, Tie; Wang, Qing K. Journal: Acta physiologica Issue: Volume 235:Number 1(2022) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Identification of a p.Trp403* nonsense variant in PHEX causing X‐linked hypophosphatemia by inhibiting p38 MAPK signaling. Issue 7 (28th March 2019) Authors: Li, Wei; Tan, Lingfang; Li, Xin; Zhang, Xiaoyu; Wu, Xiaoyan; Chen, Hongbo; Hu, Lihua; Wang, Xiaobei; Luo, Xiaoping; Wang, Fan; Xu, Chengqi; Chen, Qiuyun; Jin, Runming; Wang, Qing K. Journal: Human mutation Issue: Volume 40:Issue 7(2019) Page Start: 879 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Losartan protects against myocardial ischemia and reperfusion injury via vascular integrity preservation. Issue 7 (16th April 2019) Authors: Li, Yong; Yao, Yufeng; Li, Jia; Chen, Qiuyun; Zhang, Lu; Wang, Qing K. Journal: FASEB journal Issue: Volume 33:Issue 7(2019) Page Start: 8555 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗