Yang Zeng

发表

Identification of two novel pathogenic variants of the NR1H4 gene in intrahepatic cholestasis of pregnancy patients

Huai Liu, Yang Zou, H. Lai, 2022, BMC medical genomics.

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.

Whole-exome sequencing expands the roles of novel mutations of organic anion transporting polypeptide, ATP-binding cassette transporter, and receptor genes in intrahepatic cholestasis of pregnancy

Xiaoying Wu, Xianxian Liu, Yang Zou, 2022, Frontiers in Genetics.

Novel biallelic mutations in PADI6 in patients with early embryonic arrest

Zheng Yan, Qing Sang, Lei Wang, 2022, Journal of Human Genetics.

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.

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.

Developing and characterising Ricinus communis SSR markers by data mining of whole-genome sequences

Xingchu Yan, Xuekun Zhang, J. Xu, 2014, Molecular Breeding.

Genetic screening in patients with ovarian dysfunction

K. Choy, Ling Wu, Qingyuan Li, 2022, Clinical 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.

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.

ADGB variants cause asthenozoospermia and male infertility

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

CCDC28A deficiency causes sperm head defects, reduced sperm motility and male infertility in mice

Qing Sang, Ronggui Qu, Biaobang Chen, 2024, Cellular and molecular life sciences : CMLS.