Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice von Liu, Wangjie, He, Xiaojin, Yang, Shenmin, Zouari, Raoudha, Wang, Jiaxiong, Wu, Huan, Kherraf, Zine-Eddine, Liu, Chunyu, Coutton, Charles, Zhao, Rui, Tang, Dongdong, Tang, Shuyan, Lv, Mingrong, Fang, Youyan, Li, Weiyu, Li, Hong, Zhao, Jianyuan, Wang, Xue, Zhao, Shimin, Zhang, Jingjing, Arnoult, Christophe, Jin, Li, Zhang, Zhiguo, Ray, Pierre F., Cao, Yunxia, Zhang, Feng

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Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice von He, Xiaojin, Liu, Chunyu, Yang, Xiaoyu, Lv, Mingrong, Ni, Xiaoqing, Li, Qiang, Cheng, Huiru, Liu, Wangjie, Tian, Shixiong, Wu, Huan, Gao, Yang, Yang, Chenyu, Tan, Qing, Cong, Jiangshan, Tang, Dongdong, Zhang, Jingjing, Song, Bing, Zhong, Yading, Li, Hang, Zhi, Weiwei, Mao, Xiaohong, Fu, Feifei, Ge, Lei, Shen, Qunshan, Zhang, Manyu, Saiyin, Hexige, Jin, Li, Xu, Yuping, Zhou, Ping, Wei, Zhaolian, Zhang, Feng, Cao, Yunxia

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Editorial: Genetic factors in male infertility von He, Xiaojin, Yang, Shenmin, Lv, Mingrong

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DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath von Wu, Huan, Liu, Yiyuan, Li, Yuqian, Li, Kuokuo, Xu, Chuan, Gao, Yang, Lv, Mingrong, Guo, Rui, Xu, Yuping, Zhou, Ping, Wei, Zhaolian, Hua, Rong, He, Xiaojin, Cao, Yunxia

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Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility von Li, Weiyu, He, Xiaojin, Yang, Shenmin, Liu, Chunyu, Wu, Huan, Liu, Wangjie, Lv, Mingrong, Tang, Dongdong, Tan, Jing, Tang, Shuyan, Chen, Yujie, Wang, Jiajia, Zhang, Zhiguo, Wang, Hongyan, Jin, Li, Zhang, Feng, Cao, Yunxia

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A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia von Ni, Xiaoqing, Wang, Jiajia, Lv, Mingrong, Liu, Chunyu, Zhong, Yading, Tian, Shixiong, Wu, Huan, Cheng, Huiru, Gao, Yang, Tan, Qing, Chen, Beili, Li, Qiang, Song, Bing, Wei, Zhaolian, Zhou, Ping, He, Xiaojin, Zhang, Feng, Cao, Yunxia

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Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF von Xu, Chuan, Tang, Dongdong, Shao, Zhongmei, Geng, Hao, Gao, Yang, Li, Kuokuo, Tan, Qing, Wang, Guanxiong, Wang, Chao, Wu, Huan, Li, Guanjian, Lv, Mingrong, He, Xiaojin, Cao, Yunxia

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Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia von Tang, Dongdong, Li, Kuokuo, Geng, Hao, Xu, Chuan, Lv, Mingrong, Gao, Yang, Wang, Guanxiong, Yu, Hui, Shao, Zhongmei, Shen, Qunshan, Jiang, Hui, Zhang, Xiansheng, He, Xiaojin, Cao, Yunxia

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Sperm DNA integrity status is associated with DNA methylation signatures of imprinted genes and non-imprinted genes von Song, Bing, Wang, Chao, Chen, Yujie, Li, Guanjian, Gao, Yang, Zhu, Fuxi, Wu, Huan, Lv, Mingrong, Zhou, Ping, Wei, Zhaolian, He, Xiaojin, Cao, Yunxia

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Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse von Shen, Qunshan, Martinez, Guillaume, Liu, Hongbin, Beurois, Julie, Wu, Huan, Amiri-Yekta, Amir, Liang, Dan, Kherraf, Zine-Eddine, Bidart, Marie, Cazin, Caroline, Celse, Tristan, Satre, Véronique, Thierry-Mieg, Nicolas, Whitfield, Marjorie, Touré, Aminata, Song, Bing, Lv, Mingrong, Li, Kuokuo, Liu, Chunyu, Tao, Fangbiao, He, Xiaojin, Zhang, Feng, Arnoult, Christophe, Ray, Pierre F., Cao, Yunxia, Coutton, Charles

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Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection von Wu, Huan, Wang, Jiajia, Cheng, Huiru, Gao, Yang, Liu, Wangjie, Zhang, Zhiguo, Jiang, Huanhuan, Li, Weiyu, Zhu, Fuxi, Lv, Mingrong, Liu, Chunyu, Tan, Qing, Zhang, Xiaofeng, Wang, Chao, Ni, Xiaoqing, Chen, Yujie, Song, Bing, Zhou, Ping, Wei, Zhaolian, Zhang, Feng, He, Xiaojin, Cao, Yunxia

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Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia von Tang, Dongdong, Lv, Mingrong, Gao, Yang, Cheng, Huiru, Li, Kuokuo, Xu, Chuan, Geng, Hao, Li, Guanjian, Shen, Qunshan, Wang, Chao, He, Xiaojin, Cao, Yunxia

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Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility von Li, Kuokuo, Wang, Guanxiong, Lv, Mingrong, Wang, Jieyu, Gao, Yang, Tang, Fei, Xu, Chuan, Yang, Wen, Yu, Hui, Shao, Zhongmei, Geng, Hao, Tan, Qing, Shen, Qunshan, Tang, Dongdong, Ni, Xiaoqing, Wang, Tianjuan, Song, Bing, Wu, Huan, Huo, Ran, Zhang, Zhiguo, Xu, Yuping, Zhou, Ping, Tao, Fangbiao, Wei, Zhaolian, He, Xiaojin, Cao, Yunxia

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Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations von Lv, Mingrong, Liu, Chunyu, Ma, Chunjie, Yu, Hui, Shao, Zhongmei, Gao, Yang, Liu, Yiyuan, Wu, Huan, Tang, Dongdong, Tan, Qing, Zhang, Junqiang, Li, Kuokuo, Xu, Chuan, Geng, Hao, Zhang, Jingjing, Li, Hang, Mao, Xiaohong, Ge, Lei, Fu, Feifei, Zhong, Kaixin, Xu, Yuping, Tao, Fangbiao, Zhou, Ping, Wei, Zhaolian, He, Xiaojin, Zhang, Feng, Cao, Yunxia

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A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens von Wu, Huan, Gao, Yang, Ma, Cong, Shen, Qunshan, Wang, Jiajia, Lv, Mingrong, Liu, Chunyu, Cheng, Huiru, Zhu, Fuxi, Tian, Shixiong, Elshewy, Nagwa, Ni, Xiaoqing, Tan, Qing, Xu, Xiaofeng, Zhou, Ping, Wei, Zhaolian, Zhang, Feng, He, Xiaojin, Cao, Yunxia

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Correction: Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia von Tang, Dongdong, Li, Kuokuo, Geng, Hao, Xu, Chuan, Lv, Mingrong, Gao, Yang, Wang, Guanxiong, Yu, Hui, Shao, Zhongmei, Shen, Qunshan, Jiang, Hui, Zhang, Xiansheng, He, Xiaojin, Cao, Yunxia

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Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family von Gao, Yang, Xu, Chuan, Tan, Qing, Shen, Qunshan, Wu, Huan, Lv, Mingrong, Li, Kuokuo, Tang, Dongdong, Song, Bing, Xu, Yuping, Zhou, Ping, Wei, Zhaolian, Tao, Fangbiao, Cao, Yunxia, He, Xiaojin

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Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF von Xu, Chuan, Tang, Dongdong, Shao, Zhongmei, Geng, Hao, Gao, Yang, Li, Kuokuo, Tan, Qing, Wang, Guanxiong, Wang, Chao, Wu, Huan, Li, Guanjian, Lv, Mingrong, He, Xiaojin, Cao, Yunxia

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Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality von Zhang, Manyu, Liu, Chunyu, Chen, Beili, Lv, Mingrong, Zou, Huijuan, Liu, Yajing, Gao, Yang, Wang, Tianjuan, Xing, Qiong, Zhu, Yutong, Wu, Huan, Zhang, Zhiguo, Zhou, Ping, Wei, Zhaolian, He, Xiaojin, Xu, Yuping, Cao, Yunxia

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Association of novel DNAH11 variants with asthenoteratozoospermia lead to male infertility von Guo, Senzhao, Tang, Dongdong, Chen, Yuge, Yu, Hui, Gu, Meng, Geng, Hao, Fang, Jiajun, Wu, Baoyan, Ruan, Lewen, Li, Kuokuo, Xu, Chuan, Gao, Yang, Tan, Qing, Duan, Zongliu, Wu, Huan, Hua, Rong, Guo, Rui, Wei, Zhaolian, Zhou, Ping, Xu, Yuping, Cao, Yunxia, He, Xiaojin, Sha, Yanwei, Lv, Mingrong

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