1. A novel deep intronic COL2A1 mutation in a family with early‐onset high myopia/ocular‐only Stickler syndrome. (20th March 2020) Authors: Sun, Wenmin; Xiao, Xueshan; Li, Shiqiang; Jia, Xiaoyun; Zhang, Qingjiong Journal: Ophthalmic and physiological optics Issue: Volume 40:Number 3(2020:May) Page Start: 281 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel missense mutation of GJA8 causes congenital cataract in a large Mauritanian family. Issue 6 (November 2019) Authors: Hadrami, Mouna; Bonnet, Crystel; Veten, Fatimetou; Zeitz, Christina; Condroyer, Christel; Wang, Panfeng; Biya, Mohamed; Sidi Ahmed, Med Ahmed; Zhang, Qingjiong; Cheikh, Sidi; Audo, Isabelle; Petit, Christine; Houmeida, Ahmed Journal: European journal of ophthalmology Issue: Volume 29:Issue 6(2019) Page Start: 621 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel variant in IDH3A identified in a case with Leber congenital amaurosis accompanied by macular pseudocoloboma. (3rd September 2018) Authors: Sun, Wenmin; Zhang, Qingjiong Journal: Ophthalmic genetics Issue: Volume 39:Number 5(2018) Page Start: 662 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. An overview of myopia genetics. (November 2019) Authors: Cai, Xue-Bi; Shen, Shou-Ren; Chen, De-Fu; Zhang, Qingjiong; Jin, Zi-Bing Journal: Experimental eye research Issue: Volume 188(2019) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Biallelic mutations in USP45, encoding a deubiquitinating enzyme, are associated with Leber congenital amaurosis. Issue 5 (20th December 2018) Authors: Yi, Zhen; Ouyang, Jiamin; Sun, Wenmin; Xiao, Xueshan; Li, Shiqiang; Jia, Xiaoyun; Wang, Panfeng; Zhang, Qingjiong Journal: Journal of medical genetics Issue: Volume 56:Issue 5(2019) Page Start: 325 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Biallelic variants in CPAMD8 are associated with primary open-angle glaucoma and primary angle-closure glaucoma. Issue 12 (21st June 2021) Authors: Li, Xueqing; Sun, Wenmin; Xiao, Xueshan; Fang, Lei; Li, Shiqiang; Liu, Xing; Zhang, Qingjiong Journal: British journal of ophthalmology Issue: Volume 106:Issue 12(2022) Page Start: 1710 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Blockage of Notch Signaling Inhibits the Migration and Proliferation of Retinal Pigment Epithelial Cells. (25th December 2013) Authors: Liu, Weiwei; Jin, Guorong; Long, Chongde; Zhou, Xin; Tang, Yan; Huang, Shan; Kuang, Xielan; Wu, Lizi; Zhang, Qingjiong; Shen, Huangxuan Other Names: Mansour A. M. Academic Editor.; Mizota A. Academic Editor. Journal: TheScientificWorldjournal Issue: Volume 2013(2013) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Clinical and genetic features of retinoschisis in 120 families with RS1 mutations. Issue 3 (13th October 2021) Authors: Xiao, Sainan; Sun, Wenmin; Xiao, Xueshan; Li, Shiqiang; Luo, Hualei; Jia, Xiaoyun; Ouyang, Jiamin; Li, Xueqing; Wang, Yingwei; Jiang, Yi; Wang, Panfeng; Zhang, Qingjiong Journal: British journal of ophthalmology Issue: Volume 107:Issue 3(2023) Page Start: 367 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Correspondence to Rossetti et al.'s review of the phenotypic spectrum associated with haploinsufficiency of MYRF. Issue 11 (11th August 2019) Authors: Sun, Wenmin; Xiao, Xueshan; Zhang, Qingjiong Journal: American journal of medical genetics Issue: Volume 179:Issue 11(2019) Page Start: 2315 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. CPSF1 mutations are associated with early-onset high myopia and involved in retinal ganglion cell axon projection. (26th January 2019) Authors: Ouyang, Jiamin; Sun, Wenmin; Xiao, Xueshan; Li, Shiqiang; Jia, Xiaoyun; Zhou, Lin; Wang, Panfeng; Zhang, Qingjiong Journal: Human molecular genetics Issue: Volume 28:Number 12(2019) Page Start: 1959 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗