A hemizygous loss‐of‐function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia von Luo, Chen, Chen, Zixu, Meng, Lanlan, Tan, Chen, He, Wenbin, Tu, Chaofeng, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Tan, Yue‐Qiu, Hu, Tong‐Yao

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Biallelic mutations in MOS cause female infertility characterized by human early embryonic arrest and fragmentation von Zhang, Yin‐Li, Zheng, Wei, Ren, Peipei, Hu, Huiling, Tong, Xiaomei, Zhang, Shuo‐Ping, Li, Xiang, Wang, Haichao, Jiang, Jun‐Chao, Jin, Jiamin, Yang, Weijie, Cao, Lanrui, He, Yuanlin, Ma, Yerong, Zhang, Yingyi, Gu, Yifan, Hu, Liang, Luo, Keli, Gong, Fei, Lu, Guang‐Xiu, Lin, Ge, Fan, Heng‐Yu, Zhang, Songying

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XRCC2 mutation causes premature ovarian insufficiency as well as non‐obstructive azoospermia in humans von Zhang, Ya‐Xin, Li, Hai‐Yu, He, Wen‐Bin, Tu, Chaofeng, Du, Juan, Li, Wen, Lu, Guang‐Xiu, Lin, Ge, Yang, Yongjia, Tan, Yue‐Qiu

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Sperm flagellar 2 (SPEF2) is essential for sperm flagellar assembly in humans von Li, Dong-Yan, Yang, Xiao-Xuan, Tu, Chao-Feng, Wang, Wei-Li, Meng, Lan-Lan, Lu, Guang-Xiu, Tan, Yue-Qiu, Zhang, Qian-Jun, Du, Juan

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Mutant ZP1 in Familial Infertility von Huang, Hua-Lin, Lv, Chao, Zhao, Ying-Chun, Li, Wen, He, Xue-Mei, Li, Ping, Sha, Ai-Guo, Tian, Xiao, Papasian, Christopher J, Deng, Hong-Wen, Lu, Guang-Xiu, Xiao, Hong-Mei

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Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility von Hu, Tong‐Yao, Zhang, Huan, Meng, Lan‐Lan, Yuan, Shi‐Min, Tu, Chao‐Feng, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Nie, Hong‐Chuan, Tan, Yue‐Qiu

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Defects in phospholipase C zeta cause polyspermy and low fertilization after conventional IVF: not just ICSI failure von Che, Jian-Fang, Wu, Hui-Xia, Zeng, Si-Cong, Wu, Yue-Ren, Dai, Jing, Cheng, De-Hua, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Dai, Can

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Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia von Wang, Yurong, Liu, Ling, Tan, Chen, Meng, Guiquan, Meng, Lanlan, Nie, Hongchuan, Du, Juan, Lu, Guang-Xiu, Lin, Ge, He, Wen-Bin, Tan, Yue-Qiu

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In-Frame Variants in STAG3 Gene Cause Premature Ovarian Insufficiency von Xiao, Wen-Juan, He, Wen-Bin, Zhang, Ya-Xin, Meng, Lan-Lan, Lu, Guang-Xiu, Lin, Ge, Tan, Yue-Qiu, Du, Juan

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Inner cell mass incarceration in 8-shaped blastocysts does not increase monozygotic twinning in preimplantation genetic diagnosis and screening patients von Gu, Yi-Fan, Zhou, Qin-Wei, Zhang, Shuo-Ping, Lu, Chang-Fu, Gong, Fei, Tan, Yue-Qiu, Lu, Guang-Xiu, Lin, Ge

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Clinical and neonatal outcomes of patients of different ages following transfer of thawed cleavage embryos and blastocysts cultured from thawed cleavage-stage embryos von Zhou, Qin-Wei, Jing, Shuang, Xu, Li, Guo, Hui, Lu, Chang-Fu, Gong, Fei, Lu, Guang-Xiu, Lin, Ge, Gu, Yi-Fan

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X‐chromosome inactivation pattern of amniocytes predicts the risk of dystrophinopathy in fetal carriers of DMD mutations von He, Wen‐Bin, Du, Juan, Xie, Ping‐Yuan, Zhou, Shuang, Zhang, Ya‐Xin, Lu, Guang‐Xiu, Lin, Ge, Li, Wen, Tan, Yue‐Qiu

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A newly discovered mutation in PICK1 in a human with globozoospermia von Liu, Gang, Shi, Qiu-Wen, Lu, Guang-Xiu

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Histological endometrial dating: a reliable tool for personalized frozen-thawed embryo transfer in patients with repeated implantation failure in natural cycles von Li, Yuan, Wen, Quan, Hu, Jing, Liao, Jingnan, Fan, Xiangxiu, Chen, Huijun, Zhao, Qi, Lu, Guang-Xiu, Lin, Ge, Gong, Fei

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The clinical and neonatal outcomes after stimulation of immotile spermatozoa using SperMagic medium von Gu, Yi‐Fan, Zhou, Qin‐Wei, Zhang, Shuo‐Ping, Lu, Chang‐Fu, Gong, Fei, Shi, Yun, Lu, Guang‐Xiu, Lin, Ge

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Trophectoderm Biopsy Differentially Influences the Level of Serum β-Human Chorionic Gonadotropin With Different Embryonic Trophectoderm Scores in Early Pregnancy From 7847 Single-B... von Li, Yuan, Wen, Quan, Liao, Jingnan, Ma, Shujuan, Zhang, Shuoping, Gu, Yifan, Tang, Yi, Luo, Keli, Yang, Xiaoyi, Lu, Guang-Xiu, Lin, Ge, Gong, Fei

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Novel loss‐of‐function mutation in MCM8 causes premature ovarian insufficiency von Zhang, Ya‐Xin, He, Wen‐Bin, Xiao, Wen‐Juan, Meng, Lan‐Lan, Tan, Chen, Du, Juan, Lu, Guang‐Xiu, Lin, Ge, Tan, Yue‐Qiu

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Next‐generation sequence‐based preimplantation genetic testing for monogenic disease resulting from maternal mosaicism von Hu, Xiao, He, Wen‐Bin, Zhang, Shuo‐Ping, Luo, Ke‐Li, Gong, Fei, Dai, Jing, Zhang, Yi, Wan, Zhen‐Xing, Li, Wen, Yuan, Shi‐Min, Tan, Yue‐Qiu, Lu, Guang‐Xiu, Lin, Ge, Du, Juan

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Novel mutations of PKD genes in Chinese patients suffering from autosomal dominant polycystic kidney disease and seeking assisted reproduction von He, Wen-Bin, Xiao, Wen-Juan, Tan, Yue-Qiu, Zhao, Xiao-Meng, Li, Wen, Zhang, Qian-Jun, Zhong, Chang-Gao, Li, Xiu-Rong, Hu, Liang, Lu, Guang-Xiu, Lin, Ge, Du, Juan

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Abnormalities in centrosome number in human embryos and embryonic stem cells von Gu, Yi-Fan, OuYang, Qi, Dai, Can, Lu, Chang-Fu, Lin, Ge, Gong, Fei, Lu, Guang-Xiu

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