Bin Li

发表

Pregnancy and neonatal outcomes of morphologically grade CC blastocysts: are they of clinical value?

Ling Wu, Zheng Yan, Q. Lyu, 2020, Archives of Gynecology and Obstetrics.

Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest.

Y. Kuang, Zheng Yan, Ruizhi Feng, 2016, American journal of human genetics.

Does the cell number of 0PN embryos on day 3 affect pregnancy and neonatal outcomes following single blastocyst transfer?

Ling Wu, Zheng Yan, Q. Lyu, 2022, BMC Pregnancy and Childbirth.

Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos

Zhaogui Sun, Y. Kuang, Zheng Yan, 2016, Journal of Medical Genetics.

A novel splicing variant in DNAH8 causes asthenozoospermia

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

Homozygous Mutations in WEE2 Cause Fertilization Failure and Female Infertility.

Ling Wu, Qiaoli Li, Y. Kuang, 2018, American journal of human genetics.

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

B. Li, E. Nogales, Mohan L Gupta, 2016, The New England journal of medicine.

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 PLCZ1 cause male infertility due to fertilization failure or poor fertilization.

Ling Wu, Y. Kuang, Zheng Yan, 2020, Human reproduction.

Mutations in NLRP2 and NLRP5 cause female infertility characterised by early embryonic arrest

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

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.

A pannexin 1 channelopathy causes human oocyte death

Ling Wu, Qiang Sun, Qiaoli Li, 2019, Science Translational Medicine.

Pregnancy and neonatal outcomes of artificial oocyte activation in patients undergoing frozen–thawed embryo transfer: a 6-year population-based retrospective study

Y. Kuang, Zheng Yan, Q. Lyu, 2019, Archives of Gynecology and Obstetrics.

Efficacy of artificial oocyte activation in patients with embryo developmental problems: a sibling oocyte control study

Ling Wu, Zheng Yan, Q. Lyu, 2021, Archives of Gynecology and Obstetrics.

Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development

Ling Wu, Qiaoli Li, Juan-zi Shi, 2020, Protein & Cell.

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 mutations and structural deletions in TUBB8: expanding mutational and phenotypic spectrum of patients with arrest in oocyte maturation, fertilization or early embryonic development

Qiaoli Li, Da Li, Y. Kuang, 2017, 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.

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility

Ling Wu, Da Li, Y. Kuang, 2019, Journal of Human 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.

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.

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.

Hepatic Gadd45β promotes hyperglycemia and glucose intolerance through DNA demethylation of PGC-1α

Xuejin Chen, Ling Wu, Yan Lu, 2021, The Journal of experimental medicine.

Metabolomics analysis of follicular fluid in ovarian endometriosis women receiving progestin-primed ovary stimulation protocol for in vitro fertilization

Ling Wu, Haiyan Guo, Q. Lyu, 2023, Scientific Reports.

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.

Novel mutations in ZP1: Expanding the mutational spectrum associated with empty follicle syndrome in infertile women

Ling Wu, Y. Kuang, Zheng Yan, 2020, Clinical genetics.

Karyopherin α deficiency contributes to human preimplantation embryo arrest

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

Novel mutations in PATL2: expanding the mutational spectrum and corresponding phenotypic variability associated with female infertility

Ling Wu, Da Li, Y. Kuang, 2019, Journal of Human Genetics.