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Liu, Wensheng 
ORCID: 0000-0001-7527-5920, Wei, Xiaoli, Liu, Xiaoyan, Chen, Gaowen, Zhang, Xiaoya, Liang, Xiaomei, Isachenko, Vladimir, Sha, Yanwei ORCID: 0000-0002-0321-4915 and Wang, Yifeng
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Biallelic mutations in ARMC12 cause asthenozoospermia and multiple midpiece defects in humans and mice.
J. Med. Genet..
LONDON:
BMJ PUBLISHING GROUP.
ISSN 1468-6244
Sha, Yanwei, Liu, Wensheng, Li, Lin, Serafimovski, Mario, Isachenko, Vladimir, Li, Youzhu, Chen, Jing, Zhao, Bangrong, Wang, Yifeng and Wei, Xiaoli (2021). Pathogenic Variants in ACTRT1 Cause Acephalic Spermatozoa Syndrome. Front. Cell. Dev. Biol., 9. LAUSANNE: FRONTIERS MEDIA SA. ISSN 2296-634X
Wei, Xiaoli, Liu, Wensheng, Zhu, Xingshen, Li, Youzhu, Zhang, Xiaoya, Chen, Jing, Isachenko, Vladimir, Sha, Yanwei and Lu, Zhongxian (2021). Biallelic mutations in KATNAL2 cause male infertility due to oligo-astheno-teratozoospermia. Clin. Genet., 100 (4). S. 376 - 386. HOBOKEN: WILEY. ISSN 1399-0004