Works by Cao, Yunxia


Results: 208
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    Preimplantation genetic testing for monogenic disorders (PGT-M) offers an alternative strategy to prevent children from being born with hereditary neurological diseases or metabolic diseases dominated by nervous system phenotypes: a retrospective study.

    Published in:
    Journal of Assisted Reproduction & Genetics, 2024, v. 41, n. 5, p. 1245, doi. 10.1007/s10815-024-03057-1
    By:
    • Zou, Weiwei;
    • Li, Min;
    • Wang, Xiaolei;
    • Lu, Hedong;
    • Hao, Yan;
    • Chen, Dawei;
    • Zhu, Shasha;
    • Ji, Dongmei;
    • Zhang, Zhiguo;
    • Zhou, Ping;
    • Cao, Yunxia
    Publication type:
    Article
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    Polymorphisms of mtDNA in the D-loop region moderate the associations of BMI with HOMA-IR and HOMA-β among women with polycystic ovary syndrome: a cross-sectional study.

    Published in:
    Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 8, p. 1983, doi. 10.1007/s10815-023-02843-7
    By:
    • He, Shitao;
    • Ji, Dongmei;
    • Liu, Yajing;
    • Deng, Xiaohong;
    • Zou, Weiwei;
    • Liang, Dan;
    • Du, Yinan;
    • Zong, Kai;
    • Jiang, Tingting;
    • Li, Mengzhu;
    • Zhang, Dongyang;
    • Yue, Xinyu;
    • Tao, Fangbiao;
    • Cao, Yunxia;
    • Liang, Chunmei
    Publication type:
    Article
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    Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos.

    Published in:
    Journal of Assisted Reproduction & Genetics, 2023, v. 40, n. 7, p. 1689, doi. 10.1007/s10815-023-02761-8
    By:
    • Tang, Fei;
    • Gao, Yang;
    • Li, KuoKuo;
    • Tang, DongDong;
    • Hao, Yan;
    • Lv, Mingrong;
    • Wu, Huan;
    • Cheng, Huiru;
    • Fei, Jia;
    • Jin, Zhiping;
    • Wang, Chao;
    • Xu, Yuping;
    • Wei, Zhaolian;
    • Zhou, Ping;
    • Zhang, Zhiguo;
    • He, Xiaojin;
    • Cao, Yunxia
    Publication type:
    Article
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    A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens.

    Published in:
    Journal of Assisted Reproduction & Genetics, 2020, v. 37, n. 6, p. 1421, doi. 10.1007/s10815-020-01779-6
    By:
    • 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
    Publication type:
    Article
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    Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans.

    Published in:
    Human Mutation, 2022, v. 43, n. 12, p. 2079, doi. 10.1002/humu.24475
    By:
    • Wang, Guanxiong;
    • Zhu, Xiaoyu;
    • Gao, Yang;
    • Lv, Mingrong;
    • Li, Kuokuo;
    • Tang, Dongdong;
    • Wu, Huan;
    • Xu, Chuan;
    • Geng, Hao;
    • Shen, Qunshan;
    • Zha, Xiaomin;
    • Duan, Zongliu;
    • Zhang, Jingjing;
    • Hua, Rong;
    • Tao, Fangbiao;
    • Zhou, Ping;
    • Wei, Zhaolian;
    • Cao, Yunxia;
    • Guo, Rui;
    • He, Xiaojin
    Publication type:
    Article
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    Cover, Volume 43, Issue 3.

    Published in:
    Human Mutation, 2022, v. 43, n. 3, p. i, doi. 10.1002/humu.24361
    By:
    • Gao, Yang;
    • Wu, Huan;
    • Xu, Yuping;
    • Shen, Qunshan;
    • Xu, Chuan;
    • Geng, Hao;
    • Lv, Mingrong;
    • Tan, Qing;
    • Li, Kuokuo;
    • Tang, Dongdong;
    • Song, Bing;
    • Zhou, Ping;
    • Wei, Zhaolian;
    • He, Xiaojin;
    • Cao, Yunxia
    Publication type:
    Article
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