A homozygous KASH5 frameshift mutation causes diminished ovarian reserve, recurrent miscarriage, and non-obstructive azoospermia in humans by Xiaoning Hou, Xiaoning Hou, Xiaoning Hou, Xiaoning Hou, Aurang Zeb, Aurang Zeb, Aurang Zeb, Aurang Zeb, Sobia Dil, Sobia Dil, Sobia Dil, Sobia Dil, Jianteng Zhou, Jianteng Zhou, Jianteng Zhou, Jianteng Zhou, Huan Zhang, Huan Zhang, Huan Zhang, Huan Zhang, Baolu Shi, Baolu Shi, Baolu Shi, Baolu Shi, Zubair Muhammad, Zubair Muhammad, Zubair Muhammad, Zubair Muhammad, Ihsan Khan, Ihsan Khan, Ihsan Khan, Ihsan Khan, Qamar Zaman, Qamar Zaman, Qamar Zaman, Qamar Zaman, Wasim Akbar Shah, Wasim Akbar Shah, Wasim Akbar Shah, Wasim Akbar Shah, Xiaohua Jiang, Xiaohua Jiang, Xiaohua Jiang, Xiaohua Jiang, Limin Wu, Limin Wu, Limin Wu, Limin Wu, Hui Ma, Hui Ma, Hui Ma, Hui Ma, Qinghua Shi, Qinghua Shi, Qinghua Shi, Qinghua Shi

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A homozygous missense variant in DND1 causes non-obstructive azoospermia in humans by Xuefeng Xie, Mazhar Khan, Muhammad Zubair, Abbas Khan, Ranjha Khan, Jianteng Zhou, Yuanwei Zhang, Muzafar Said, Sher Ali Khan, Qamar Zaman, Ghulam Murtaza, Muzamil Ahmad Khan, Wei Liu, Xiaoning Hou, Huan Zhang, Bo Xu, Xiaohua Jiang, Shun Bai, Qinghua Shi

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A novel recombination protein C12ORF40/REDIC1 is required for meiotic crossover formation by Suixing Fan, Yuewen Wang, Hanwei Jiang, Xiaohua Jiang, Jianteng Zhou, Yuying Jiao, Jingwei Ye, Zishuo Xu, Yue Wang, Xuefeng Xie, Huan Zhang, Yang Li, Wei Liu, Xiangjun Zhang, Hui Ma, Baolu Shi, Yuanwei Zhang, Muhammad Zubair, Wasim Shah, Zhipeng Xu, Bo Xu, Qinghua Shi

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Pathogenic relationship between phenotypes of ARPKD and novel compound heterozygous mutations of PKHD1 by Xinrong Zhang, Xinrong Zhang, Xinrong Zhang, Jiebin Wu, Jiebin Wu, Jianteng Zhou, Jie Liang, Jie Liang, Jie Liang, Yu Han, Yu Han, Yu Han, Yunmeng Qi, Yunmeng Qi, Yunmeng Qi, Tao Zhu, Dejian Yuan, Zuobin Zhu, Zuobin Zhu, Jingfang Zhai, Jingfang Zhai, Jingfang Zhai, Jingfang Zhai

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Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice by Ao Ma, Jianteng Zhou, Haider Ali, Tanveer Abbas, Imtiaz Ali, Zubair Muhammad, Sobia Dil, Jing Chen, Xiongheng Huang, Hui Ma, Daren Zhao, Beibei Zhang, Yuanwei Zhang, Wasim Shah, Basit Shah, Ghulam Murtaza, Furhan Iqbal, Muzammil Ahmad Khan, Asad Khan, Qing Li, Bo Xu, Limin Wu, Huan Zhang, Qinghua Shi

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Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans by Junyan Liu, Fazal Rahim, Jianteng Zhou, Suixing Fan, Hanwei Jiang, Changping Yu, Jing Chen, Jianze Xu, Gang Yang, Wasim Shah, Muhammad Zubair, Asad Khan, Yang Li, Basit Shah, Daren Zhao, Furhan Iqbal, Xiaohua Jiang, Tonghang Guo, Peng Xu, Bo Xu, Limin Wu, Hui Ma, Yuanwei Zhang, Huan Zhang, Qinghua Shi

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