Xiaoxi Sun

Effects on fertility of immunizing mice with anti-idiotypic antibodies to porcine zona pellucida antigen.

[Effect of cyclosporin A on the growth of human first trimester cytotrophoblasts in vitro].

[C3d molecular adjuvant increases the immunity of human chorionic gonadotropin beta DNA contraceptive vaccination and changes its immune response from Th1 to Th2].

Transformation of epithelial ovarian cancer stemlike cells into mesenchymal lineage via EMT results in cellular heterogeneity and supports tumor engraftment.

[Efficiency of multi-round fluorescence in situ hybridization and its influencing factors in preimplantation genetic diagnosis].

Non-invasive metabolomic profiling of day 3 embryo culture media using near-infrared spectroscopy to assess the development potential of embryos.

Polymorphisms of pentanucleotide repeats (tttta)n in the promoter of CYP11A1 and their relationships to polycystic ovary syndrome (PCOS) risk: a meta-analysis.

A retrospective analysis of the effect of salpingectomy on serum antiMüllerian hormone level and ovarian reserve.

Quadrivalent asymmetry in reciprocal translocation carriers predicts meiotic segregation patterns in cleavage stage embryos.

The Ser680Asn polymorphism in the follicle-stimulating hormone receptor gene is associated with the ovarian response in controlled ovarian hyperstimulation.

Smad7 maintains epithelial phenotype of ovarian cancer stem-like cells and supports tumor colonization by mesenchymal-epithelial transition.

MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro.

Association of skewed X chromosome inactivation and idiopathic recurrent spontaneous abortion: a systematic review and meta-analysis.

The association of serum estradiol level with outcomes of clomiphene citrate/human menopausal gonadotropin ovarian stimulation for in vitro fertilization and embryo transfer.

Non-invasive metabolomic profiling of embryo culture media and morphology grading to predict implantation outcome in frozen-thawed embryo transfer cycles.

Mutations in TUBB8 and Human Oocyte Meiotic Arrest.

Lectin binding of human sperm associates with DEFB126 mutation and serves as a potential biomarker for subfertility.

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

Genetic variations in the 3'-untranslated region of SLC18A2 are associated with serum FSH concentration in polycystic ovary syndrome patients and regulate gene expression in vitro.

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

Integrins β1 and β3 are biomarkers of uterine condition for embryo transfer.

Improved cryotolerance and developmental competence of human oocytes matured in vitro by transient hydrostatic pressure treatment prior to vitrification.

Anordrin Eliminates Tamoxifen Side Effects without Changing Its Antitumor Activity.

A Retrospective Study of Cytogenetic Results From Amniotic Fluid in 5328 Fetuses With Abnormal Obstetric Sonographic Findings.

High oestradiol concentration after ovarian stimulation is associated with lower maternal serum beta-HCG concentration and neonatal birth weight.

Maternal and neonatal morbidity: repeat Cesarean versus a trial of labour after previous Cesarean delivery.

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

The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers.

Transfer of Fresh versus Frozen Embryos in Ovulatory Women.

In Vitro Modeling of Human Germ Cell Development Using Pluripotent Stem Cells.

Analysis of segregation patterns of quadrivalent structures and the effect on genome stability during meiosis in reciprocal translocation carriers.

Expression of ENPP3 in human cyclic endometrium: a novel molecule involved in embryo implantation.

Screening of miRNAs in human follicular fluid reveals an inverse relationship between microRNA-663b expression and blastocyst formation.

Comparative analysis of human sperm glycocalyx from different freezability ejaculates by lectin microarray and identification of ABA as sperm freezability biomarker.

Comparison of the effect of immediate versus delayed transfer following a stimulated IVF cycle on the ongoing pregnancy rate of frozen-thawed embryo transfer cycles: a study protocol for a randomised controlled trial.

The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility.

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

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

Mutations in and cause female infertility characterised by early embryonic arrest.

BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers.

A pannexin 1 channelopathy causes human oocyte death.

Chronic exposure to environmental concentrations of phenanthrene impairs zebrafish reproduction.

Long-read sequencing and haplotype linkage analysis enabled preimplantation genetic testing for patients carrying pathogenic inversions.

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

MicroRNA-451 is downregulated in the follicular fluid of women with endometriosis and influences mouse and human embryonic potential.

Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations.

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

MicroRNA expression profile analysis in sperm reveals hsa-mir-191 as an auspicious omen of in vitro fertilization.

Ovarian endometrioma infiltrating neutrophils orchestrate immunosuppressive microenvironment.

Resolvin E1 in Follicular Fluid Acts as a Potential Biomarker and Improves Oocyte Developmental Competence by Optimizing Cumulus Cells.

Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest.

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

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

Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology.

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

17β-estradiol promotes bone marrow mesenchymal stem cell migration mediated by chemokine upregulation.

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

Effects of euploid blastocyst morphological development on reproductive outcomes.

Disruption in causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest.

Comparison of PGS2.0 versus conventional embryo morphology evaluation for patients with recurrent pregnancy loss: a study protocol for a multicentre randomised trial.

Oocyte Vitrification Temporarily Turns on Oxidation-Reduction Process Genes in Mouse Preimplantation Embryos.

Conventional ICSI improves the euploid embryo rate in male reciprocal translocation carriers.

Monozygotic dichorionic-diamniotic pregnancies following single frozen-thawed blastocyst transfer: a retrospective case series.

Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses.

Transcriptomic analysis of endometrial receptivity for a genomic diagnostics model of Chinese women.

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

Meiotic Heterogeneity of Trivalent Structure and Interchromosomal Effect in Blastocysts With Robertsonian Translocations.

Progesterone activates the cyclic AMP-protein kinase A signalling pathway by upregulating in fertile men.

Next-Generation Sequencing Is More Efficient at Detecting Mosaic Embryos and Improving Pregnancy Outcomes than Single-Nucleotide Polymorphism Array Analysis.

Immediate versus delayed frozen embryo transfer in patients following a stimulated IVF cycle: a randomised controlled trial.

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

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

Authors' response to Scriven's Letter to the Editor (Journal of Assisted Reproduction and Genetics; https://doi.org/10.1007/s10815-021-02139).

Modified strict sperm morphology threshold aids in the clinical selection of conventional fertilization (IVF) or intracytoplasmic sperm injection (ICSI).

A comprehensive and universal approach for embryo testing in patients with different genetic disorders.

PPOS Protocol Effectively Improves the IVF Outcome Without Increasing the Recurrence Rate in Early Endometrioid Endometrial Cancer and Atypical Endometrial Hyperplasia Patients After Fertility Preserving Treatment.

Live Birth with or without Preimplantation Genetic Testing for Aneuploidy.

Gankyrin has a potential role in embryo implantation via activation of STAT3.

Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis.

Complete androgen insensitivity syndrome caused by a novel mutation in the androgen receptor gene and its mechanism.

Sperm-specific protein ACTL7A as a biomarker for fertilization outcomes of assisted reproductive technology.

The clinical efficiency of transcriptome-based endometrial receptivity assessment (Tb-ERA) in Chinese patients with recurrent implantation failure (RIF): A study protocol for a prospective randomized controlled trial.

Re-denudation of residual cumulus cells on day 3 increases the accuracy of cell-free DNA detection in spent embryo culture medium.

Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping.

Analysis of the risk of complications during pregnancy in pregnant women with assisted reproductive technology: a retrospective study using registry linkage from 2013 to 2018 in Shanghai, China.

Combined Preimplantation Genetic Testing for Genetic Kidney Disease: Genetic Risk Identification, Assisted Reproductive Cycle, and Pregnancy Outcome Analysis.

Preimplantation genetic testing for aneuploidy in severe male factor infertility: protocol for a multicenter randomised controlled trial.

Can the combination of time-lapse parameters and clinical features predict embryonic ploidy status or implantation?

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

The use of frozen embryos and frozen sperm have complementary IVF outcomes: a retrospective analysis in couples experiencing IVF/Donor and IVF/Husband.

Long-term maintenance of human endometrial epithelial stem cells and their therapeutic effects on intrauterine adhesion.

Investigation of the role of X chromosome inactivation and androgen receptor CAG repeat polymorphisms in patients with recurrent pregnancy loss: a prospective case-control study.

The mechanism of acentrosomal spindle assembly in human oocytes.

A novel frameshift variant of LMX1A that leads to autosomal dominant non-syndromic sensorineural hearing loss: functional characterization of the C-terminal domain in LMX1A.

Elevated histone demethylase KDM5C increases recurrent miscarriage risk by preventing trophoblast proliferation and invasion.

A novel noninvasive prenatal testing method for chromosomal rearrangements using maternal circulating cell-free foetal DNA.

Karyopherin α deficiency contributes to human preimplantation embryo arrest.

A Novel System for the Detection of Spontaneous Abortion-Causing Aneuploidy and Its Erroneous Chromosome Origins through the Combination of Low-Pass Copy Number Variation Sequencing and NGS-Based STR Tests.

ADGB variants cause asthenozoospermia and male infertility.

Impacts of vitrification on the transcriptome of human ovarian tissue in patients with gynecological cancer.

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

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

Bi-allelic variants in ASTL cause abnormal fertilization or oocyte maturation defects.

Loss of ACTL7A causes small head sperm by defective acrosome-acroplaxome-manchette complex.

Growth hormone supplementation during ovarian stimulation in women with advanced maternal age undergoing preimplantation genetic testing for Aneuploidy.

A prospective study to evaluate whether serum kisspeptin is a marker predictive of the first-trimester miscarriage of women who conceive in IVF.

Clinical outcomes of fetal selective reduction in dichorionic triplet pregnancies.

The morphokinetic signature of human blastocysts with mosaicism and the clinical outcomes following transfer of embryos with low-level mosaicism.

Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertility.

Endometrial transcriptome profiling of patients with recurrent implantation failure during hormone replacement therapy cycles.

Comparing blastocyst euploid rates between the progestin-primed and gonadotrophin-releasing hormone antagonist protocols in aneuploidy genetic testing: a randomised trial protocol.

Immediate versus delayed single blastocyst transfer following the first stimulated IVF cycle in the freeze-all strategy: a study protocol for a randomised controlled trial.

Comprehensive preimplantation genetic testing for balanced insertional translocation carriers.