Zhou Zhou

发表

Polymorphisms of the DNA Repair Genes XPD and XRCC1 and the Risk of Age-Related Cataract Development in Han Chinese

Binbin Wang, Xu Ma, Shanshan Hu, 2011, Current eye research.

Comparison of optical quality after implantable collamer lens implantation and wavefront-guided laser in situ keratomileusis.

Min Li, Zhou Zhou, Hongting Liu, 2018, International journal of ophthalmology.

Genetic factors as potential molecular markers of human oocyte and embryo quality

Qing Sang, Lei Wang, Zhou Zhou, 2021, Journal of Assisted Reproduction and Genetics.

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation

B. Li, Ling Wu, Y. Kuang, 2019, Human Genetics.

Identification of a missense mutation in MIP gene via mutation analysis of a Guangxi Zhuang ethnic pedigree with congenital nuclear cataracts.

Zhou Zhou, Li Li, Lu Lu, 2018, Experimental and therapeutic medicine.

A novel mutation in GJA8 causing congenital cataract–microcornea syndrome in a Chinese pedigree

Binbin Wang, Jing Wang, Xu Ma, 2010, Molecular vision.

Mutation analysis of congenital cataract in a Chinese family identified a novel missense mutation in the connexin 46 gene (GJA3)

Binbin Wang, Xu Ma, Shanshan Hu, 2010, Molecular vision.

A novel mutation in the connexin 46 (GJA3) gene associated with congenital cataract in a Chinese pedigree

Binbin Wang, Jing Wang, Xu Ma, 2011, Molecular vision.

A novel splicing variant in DNAH8 causes asthenozoospermia

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Journal of Assisted Reproduction and Genetics.

The physiological and pathological mechanisms of early embryonic development

Qing Sang, Zhou Zhou, Jian Mu, 2022, Fundamental Research.

Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility.

G. Lin, Xiangli Niu, Juan-zi Shi, 2020, American journal of human genetics.

The identification of novel mutations in PLCZ1 responsible for human fertilization failure and a therapeutic intervention by artificial oocyte activation.

Ling Wu, Y. Kuang, Zheng Yan, 2020, Molecular human reproduction.

Novel mutations in genes encoding subcortical maternal complex proteins may cause human embryonic developmental arrest.

Zhaogui Sun, Qiaoli Li, Suying Liu, 2018, Reproductive biomedicine online.

Comparison of Femtosecond Laser-Assisted Cataract Surgery and Conventional Phacoemulsification in Shallow Anterior Chambers and Glaucoma

Min Li, S. Zeng, Zhou Zhou, 2020, Journal of ophthalmology.

Genetic variations and polymorphisms in the ezrin gene are associated with age-related cataract

Shanshan Hu, Yanhua Qi, N. Zhang, 2013, Molecular vision.

Genetic variations in GJA3, GJA8, LIM2, and age-related cataract in the Chinese population: a mutation screening study

Chunmei Zhang, Binbin Wang, Xu Ma, 2011, Molecular vision.

Identification of Novel Mutations in CDC20: Expanding the Mutational Spectrum for Female Infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2021, Frontiers in Cell and Developmental Biology.

A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility

Congjian Xu, Qing Sang, Xiaoxi Sun, 2021, Journal of Assisted Reproduction and Genetics.

Homozygous variants in PANX1 cause human oocyte death and female infertility

Qiaoli Li, Qing Sang, Ronggui Qu, 2021, European Journal of Human Genetics.

Bi-allelic Missense Pathogenic Variants in TRIP13Cause Female Infertility Characterized by Oocyte Maturation Arrest.

Ling Wu, Y. Kuang, Zheng Yan, 2020, American journal of human genetics.

Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure

Ling Wu, Y. Kuang, Zheng Yan, 2019, Clinical genetics.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure.

Ling Wu, Qiaoli Li, Da Li, 2021, Human reproduction.

Homozygous mutations in REC114 cause female infertility characterised by multiple pronuclei formation and early embryonic arrest

Ling Wu, Qiaoli Li, Y. Kuang, 2019, Journal of Medical Genetics.

Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Journal of Assisted Reproduction and Genetics.

Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest.

Qiaoli Li, Y. Kuang, Zheng Yan, 2017, American journal of human genetics.

Improving genetic diagnosis of Mendelian disease with RNA sequencing: a narrative review

Qing Sang, Lei Wang, Zhou Zhou, 2021, Journal of Bio-X Research.

Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome

Ling Wu, Y. Kuang, Zheng Yan, 2020, Journal of Assisted Reproduction and Genetics.

Identification of a novel homozygous mutation in the MYO15A gene in a Kazakh family with non-syndromic hearing loss.

Biaobang Chen, Zhou Zhou, Jian Mu, 2019, International journal of pediatric otorhinolaryngology.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility

Ling Wu, Qiaoli Li, Da Li, 2018, European Journal of Human Genetics.

Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation

Ling Wu, Y. Kuang, Zheng Yan, 2019, Human Genetics.

Genetic analysis of the FOXL2 gene using quantitative real-time PCR in Chinese patients with blepharophimosis-ptosis-epicanthus inversus syndrome

Binbin Wang, Jing Wang, Xu Ma, 2011, Molecular vision.

A novel homozygous missense variant in BTG4 causes zygotic cleavage failure and female infertility

Qiaoli Li, Yifan Zhou, Qing Sang, 2021, Journal of Assisted Reproduction and Genetics.

Major intrinsic protein (MIP) polymorphism is associated with age-related cataract in Chinese

Binbin Wang, Xu Ma, Shanshan Hu, 2011, Molecular vision.

Karyopherin α deficiency contributes to human preimplantation embryo arrest

Ling Wu, Y. Miyamoto, Qiaoli Li, 2023, The Journal of clinical investigation.