1. A genome‐wide association study identifies novel association between genetic variants in GGT7 and LINC00944 and hypertension. Issue 5 (21st May 2021) Authors: Tan, Chengcheng; Zhang, Hongfu; Yu, Dong; Hu, Yao; Wang, Pengxia; Wang, Dan; Fa, Jingjing; Ran, Han; Zhang, Xiaoyu; Chen, Yanming; Qin, Weixi; Fang, Chen; Ke, Tie; Dong, Nianguo; Cai, Jianping; He, Qing; Huo, Shaofeng; Wang, Junhan; Ren, Xiang; Tu, Xin Journal: Clinical and translational medicine Issue: Volume 11:Issue 5(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Alpha-actin-2 mutations in Chinese patients with a non-syndromatic thoracic aortic aneurysm. Issue 1 (December 2016) Authors: Ke, Tie; Han, Meng; Zhao, Miao; Wang, Qing; Zhang, Huazhi; Zhao, Yuanyuan; Ruan, Xinlong; Li, Hui; Xu, Chengqi; Sun, Tucheng Journal: BMC medical genetics Issue: Volume 17:Issue 1(2016) Page Start: 1 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Angiogenic factor AGGF1 acts as a tumor suppressor by modulating p53 post-transcriptional modifications and stability via MDM2. (28th January 2021) Authors: Si, Wenxia; Zhou, Bisheng; Xie, Wen; Li, Hui; Li, Ke; Li, Sisi; Deng, Wenbing; Shi, Pengcheng; Yuan, Chao; Ke, Tie; Ren, Xiang; Tu, Xin; Zeng, Xiaomei; Weigelt, Britta; Rubin, Brian P.; Chen, Qiuyun; Xu, Chengqi; Wang, Qing Kenneth Journal: Cancer letters Issue: Volume 497(2021) Page Start: 28 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. 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) ↗
6. 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) ↗
7. Lamin A mutation impairs interaction with nucleoporin NUP155 and disrupts nucleocytoplasmic transport in atrial fibrillation. Issue 3 (8th December 2018) Authors: Han, Meng; Zhao, Miao; Cheng, Chen; Huang, Yuan; Han, Shengna; Li, Wenjuan; Tu, Xin; Luo, Xuan; Yu, Xiaoling; Liu, Yinan; Chen, Qiuyun; Ren, Xiang; Wang, Qing Kenneth; Ke, Tie Journal: Human mutation Issue: Volume 40:Issue 3(2019) Page Start: 310 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mog1 knockout causes cardiac hypertrophy and heart failure by downregulating tbx5‐cryab‐hspb2 signalling in zebrafish. (22nd October 2020) Authors: Gou, Dongzhi; Zhou, Juan; Song, Qixue; Wang, Zhijie; Bai, Xuemei; Zhang, Yidan; Zuo, Mengxia; Wang, Fan; Chen, Ailan; Yousaf, Muhammad; Yang, Zhongcheng; Peng, Huixing; Li, Ke; Xie, Wen; Tang, Jingluo; Yao, Yufeng; Han, Meng; Ke, Tie; Chen, Qiuyun; Xu, Chengqi Journal: Acta physiologica Issue: Volume 231:Number 3(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. NINJ2 deficiency inhibits preadipocyte differentiation and promotes insulin resistance through regulating insulin signaling. Issue 1 (11th December 2022) Authors: Peng, Huixin; Yu, Yubing; Wang, Pengyun; Yao, Yufeng; Wu, Xinna; Zheng, Qian; Wang, Jing; Tian, Beijia; Wang, Yifan; Ke, Tie; Liu, Mugen; Tu, Xin; Liu, Huiying; Wang, Qing K.; Xu, Chengqi Journal: Obesity Issue: Volume 31:Issue 1(2023) Page Start: 123 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Significant association of rare variant p.Gly8Ser in cardiac sodium channel β4‐subunit SCN4B with atrial fibrillation. (1st March 2019) Authors: Xiong, Hongbo; Yang, Qin; Zhang, Xiaoping; Wang, Pengxia; Chen, Feifei; Liu, Ying; Wang, Pengyun; Zhao, Yuanyuan; Li, Sisi; Huang, Yufeng; Chen, Shanshan; Wang, Xiaojing; Zhang, Hongfu; Yu, Dong; Tan, Chencheng; Fang, Cheng; Huang, Yuan; Wu, Gang; Wu, Yanxia; Cheng, Xiang Journal: Annals of human genetics Issue: Volume 83:Number 4(2019:Jul.) Page Start: 239 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗