1. Biallelic mutations in Sperm flagellum 2 cause human multiple morphological abnormalities of the sperm flagella (MMAF) phenotype. Issue 5 (23rd July 2019) Authors: Sha, Yanwei; Liu, Wensheng; Wei, Xiaoli; Zhu, Xingshen; Luo, Xiangmin; Liang, Lei; Guo, Tonghang Journal: Clinical genetics Issue: Volume 96:Issue 5(2019) Page Start: 385 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Loss‐of‐function mutations in centrosomal protein 112 is associated with human acephalic spermatozoa phenotype. Issue 2 (24th November 2019) Authors: Sha, Yanwei; Wang, Xiong; Yuan, JinTing; Zhu, Xingshen; Su, Zhiying; Zhang, Xuequan; Xu, Xiaohui; Wei, Xiaoli Journal: Clinical genetics Issue: Volume 97:Issue 2(2020) Page Start: 321 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Loss‐of‐function mutation in TSGA10 causes acephalic spermatozoa phenotype in human. Issue 7 (15th May 2020) Authors: Ye, Yuanyuan; Wei, Xiaoli; Sha, Yanwei; Li, Na; Yan, Xiaohong; Cheng, Ling; Qiao, Duanrui; Zhou, Weidong; Wu, Rongfeng; Liu, Qiaobin; Li, Youzhu Journal: Molecular genetics & genomic medicine Issue: Volume 8:Issue 7(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Pedigree analysis of two brothers with severe oligozoospermia caused by maternal inv(X) (p22.3, q22) chromosome abnormality. (30th April 2020) Authors: Ge, Yunsheng; Sha, Yanwei; Cai, Meijiao; Chen, Xiaolu; Sha, Yankun; Xu, Xiaohui Journal: Andrologia Issue: Volume 52:Number 6(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Biallelic mutations in KATNAL2 cause male infertility due to oligo‐astheno‐teratozoospermia. Issue 4 (11th June 2021) Authors: Wei, Xiaoli; Liu, Wensheng; Zhu, Xingshen; Li, Youzhu; Zhang, Xiaoya; Chen, Jing; Isachenko, Vladimir; Sha, Yanwei; Lu, Zhongxian Journal: Clinical genetics Issue: Volume 100:Issue 4(2021) Page Start: 376 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Bi-allelic mutations in DNAH7 cause asthenozoospermia by impairing the integrality of axoneme structure. (3rd September 2021) Authors: Wei, Xiaoli; Sha, Yanwei; Wei, Zijie; Zhu, Xingshen; He, Fengming; Zhang, Xiaoya; Liu, Wensheng; Wang, Yifeng; Lu, Zhongxian Journal: Acta biochimica et biophysica Sinica Issue: Volume 53:Number 10(2021) Page Start: 1300 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. CCDC9 is identified as a novel candidate gene of severe asthenozoospermia. (2nd November 2019) Authors: Sha, Yanwei; Xu, Yankai; Wei, Xiaoli; Liu, Wensheng; Mei, Libin; Lin, Shaobin; Ji, Zhiyong; Wang, Xu; Su, Zhiying; Qiu, Pingping; Chen, Jing; Wang, Xiong Journal: Systems biology in reproductive medicine Issue: Volume 65:Number 6(2019:Dec.) Page Start: 465 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Biallelic mutations of CFAP58 are associated with multiple morphological abnormalities of the sperm flagella. Issue 3 (18th December 2020) Authors: Sha, Yankun; Sha, Yanwei; Liu, Wensheng; Zhu, Xingshen; Weng, Mingxiang; Zhang, Xinzong; Wang, Yifeng; Zhou, Huiliang Journal: Clinical genetics Issue: Volume 99:Issue 3(2021) Page Start: 443 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. DNAH17 is associated with asthenozoospermia and multiple morphological abnormalities of sperm flagella. (16th December 2019) Authors: Sha, Yanwei; Wei, Xiaoli; Ding, Lu; Mei, Libin; Huang, Xianjing; Lin, Shaobin; Su, Zhiying; Kong, Lingyuan; Zhang, Yi; Ji, Zhiyong Journal: Annals of human genetics Issue: Volume 84:Number 3(2020:May) Page Start: 271 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. A familial analysis of two brothers with azoospermia caused by maternal 46, Y, t(X; 1) (q28; q21) chromosomal abnormality. (3rd November 2020) Authors: Li, Youzhu; Sha, Yanwei; Wei, Zijie; Liu, Wensheng; Mei, Libin; hong, Yun; Jiang, Lizhi; Ge, Yunsheng; Xie, Yuanzhi Other Names: Agarwal Ashok guestEditor.; Baskaran Saradha guestEditor.; Durairajanayagam Damayanthi guestEditor.; Ramasamy Ranjith guestEditor.; Ko Edmund guestEditor. Journal: Andrologia Issue: Volume 53:Number 1(2021) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗