Liying Yan

Poor intracytoplasmic sperm injection outcome in infertile males with azoospermia factor c microdeletions.

Association of TRB3 Q84R polymorphism with polycystic ovary syndrome in Chinese women.

In vitro maturation of cumulus-partially enclosed immature human oocytes by priming with gonadotropin.

Effects of combined epidermal growth factor, brain-derived neurotrophic factor and insulin-like growth factor-1 on human oocyte maturation and early fertilized and cloned embryo development.

Successful reprogramming of differentiated cells by somatic cell nuclear transfer, using in vitro-matured oocytes with a modified activation method.

Prenatal diagnosis and postnatal followup of partial trisomy 13q and partial monosomy 10p: a case report and review of the literature.

Excessive intrauterine fluid cause aberrant implantation and pregnancy outcome in mice.

Whole-genome analysis of 5-hydroxymethylcytosine and 5-methylcytosine at base resolution in the human brain.

Advances in preimplantation genetic diagnosis/screening.

The DNA methylation landscape of human early embryos.

Validation of multiple annealing and looping-based amplification cycle sequencing for 24-chromosome aneuploidy screening of cleavage-stage embryos.

Mesenchymal Stem Cells Enhance Angiogenesis and Follicle Survival in Human Cryopreserved Ovarian Cortex Transplantation.

Effect of vitrification at the germinal vesicle stage on the global methylation status in mouse oocytes subsequently matured in vitro.

Identification of a human subcortical maternal complex.

Mesenchymal Stem Cells Facilitate In Vitro Development of Human Preantral Follicle.

High-fat diets exaggerate endocrine and metabolic phenotypes in a rat model of DHEA-induced PCOS.

Human single follicle growth in vitro from cryopreserved ovarian tissue after slow freezing or vitrification.

Validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of blastocysts.

Fractalkine restores the decreased expression of StAR and progesterone in granulosa cells from patients with polycystic ovary syndrome.

Clinical applications of MARSALA for preimplantation genetic diagnosis of spinal muscular atrophy.

Re-analysis of aneuploidy blastocysts with an inner cell mass and different regional trophectoderm cells.

Testosterone Represses Estrogen Signaling by Upregulating miR-22: A Mechanism for Imbalanced Steroid Hormone Production in Preeclampsia.

Mesenchymal stem cell-derived angiogenin promotes primodial follicle survival and angiogenesis in transplanted human ovarian tissue.

[Advance in the methods of preimplantation genetic diagnosis for single gene diseases].

Single-cell DNA methylome sequencing of human preimplantation embryos.

Activation of hedgehog signaling and its association with cisplatin resistance in ovarian epithelial tumors.

Tracing the temporal-spatial transcriptome landscapes of the human fetal digestive tract using single-cell RNA-sequencing.

Transcriptome analysis of PCOS arrested 2-cell embryos.

Publisher Correction: Tracing the temporal-spatial transcriptome landscapes of the human fetal digestive tract using single-cell RNA-sequencing.

Endometrial miR-543 Is Downregulated During the Implantation Window in Women With Endometriosis-Related Infertility.

Identifying normal embryos from reciprocal translocation carriers by whole chromosome haplotyping.

The present and future of whole-exome sequencing in studying and treating human reproductive disorders.

Transcriptome Landscape of Human Folliculogenesis Reveals Oocyte and Granulosa Cell Interactions.

Single-cell multiomics sequencing and analyses of human colorectal cancer.

Risk of miscarriage in women with endometriosis undergoing IVF fresh cycles: a retrospective cohort study.

Epigenetic Regulation and Risk Factors During the Development of Human Gametes and Early Embryos.

Genetic testing and PGD for unexplained recurrent fetal malformations with MAGEL2 gene mutation.

Genetic analysis and preimplantation genetic diagnosis of Chinese Marfan syndrome patients.

Trio-whole-exome sequencing and preimplantation genetic diagnosis for unexplained recurrent fetal malformations.

scHaplotyper: haplotype construction and visualization for genetic diagnosis using single cell DNA sequencing data.

A novel homozygous mutation of phospholipase C zeta leading to defective human oocyte activation and fertilization failure.

Bioinspired l-Proline Oligomers for the Cryopreservation of Oocytes Controlling Ice Growth.

Novel PGD strategy based on single sperm linkage analysis for carriers of single gene pathogenic variant and chromosome reciprocal translocation.

Single-cell transcriptome analysis of the novel coronavirus (SARS-CoV-2) associated gene ACE2 expression in normal and non-obstructive azoospermia (NOA) human male testes.

A strategy using SNP linkage analysis for monogenic diseases PGD combined with HLA typing.

Effect of serum 25-hydroxyvitamin D levels on sperm quality and assisted reproductive technology outcomes for men of infertile Chinese couples.

Effects of oocyte vitrification on the behaviors and physiological indexes of aged first filial generation mice.

A novel pathogenic mutation in FBN2 associated with congenital contractural arachnodactyly for preimplantation genetic diagnosis.

SARS-CoV-2 Entry Factors: and Are Expressed in Peri-Implantation Embryos and the Maternal-Fetal Interface.

Effects of vitrification and cryostorage duration on single-cell RNA-Seq profiling of vitrified-thawed human metaphase II oocytes.

Dissecting the epigenomic dynamics of human fetal germ cell development at single-cell resolution.

Integrated multi-omics reveal epigenomic disturbance of assisted reproductive technologies in human offspring.

The methylome of a human polar body reflects that of its sibling oocyte and its aberrance may indicate poor embryo development.

Epigenetic consequences of hormonal interactions between opposite-sex twin fetuses.

Single-cell multiomics sequencing reveals the functional regulatory landscape of early embryos.

Clinical application of an NGS-based method in the preimplantation genetic testing for Duchenne muscular dystrophy.

Age-related changes in human conventional semen parameters and sperm chromatin structure assay-defined sperm DNA/chromatin integrity.

A comprehensive PGT-M strategy for ADPKD patients with de novo PKD1 mutations using affected embryo or gametes as proband.