Lin Zhao

发表

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.

Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest.

Ling Wu, Qiaoli Li, Y. Kuang, 2022, Genetics in medicine : official journal of the American College of Medical Genetics.

Integrated single-cell RNA-seq and DNA methylation reveal the effects of air pollution in patients with recurrent spontaneous abortion

Yan Gu, Fuxiang Chen, Fujia Chen, 2022, Clinical Epigenetics.

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.

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.

Homozygous variants in PANX1 cause human oocyte death and female infertility

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

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.

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.

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 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.

ADGB variants cause asthenozoospermia and male infertility

Ling Wu, Qiaoli Li, Y. Kuang, 2023, Human Genetics.

Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects

Ling Wu, Qiaoli Li, Juan-zi Shi, 2023, Genome Biology.

FBXO43 variants in patients with female infertility characterized by early embryonic arrest.

Qiaoli Li, Juan-zi Shi, Qing Sang, 2021, Human reproduction.

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.

Integrated single-cell RNA-seq and DNA methylation reveal the effects of air pollution in patients with recurrent spontaneous abortion

Yan Gu, Fuxiang Chen, Jing Du, 2022, Clinical Epigenetics.

Karyopherin α deficiency contributes to human preimplantation embryo arrest

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

Bi‐allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility

Qiaoli Li, Juan-zi Shi, Qing Sang, 2023, EMBO molecular medicine.