Xiaoxi Sun

Shanghai JiAi Genetics & IVF Institute, Fudan University

Research Area

Biography

Xiaoxi Sun has not added Biography.
If you are Xiaoxi Sun and would like to personalize this page please email our Author Liaison for assistance.

JoVE Journal Publications

ArticleTotal : 1	Year
Publication title	2024

Other Publications

Article	Year
Effects on fertility of immunizing mice with anti-idiotypic antibodies to porcine zona pellucida antigen. Journal of reproductive immunology\| PubMed ID: 11839397	2002
[Effect of cyclosporin A on the growth of human first trimester cytotrophoblasts in vitro]. Zhonghua fu chan ke za zhi\| PubMed ID: 11953067	2002
[C3d molecular adjuvant increases the immunity of human chorionic gonadotropin beta DNA contraceptive vaccination and changes its immune response from Th1 to Th2]. Zhonghua yi xue za zhi\| PubMed ID: 14642077	2003
Transformation of epithelial ovarian cancer stemlike cells into mesenchymal lineage via EMT results in cellular heterogeneity and supports tumor engraftment. Molecular medicine (Cambridge, Mass.)\| PubMed ID: 22801793	2012
[Efficiency of multi-round fluorescence in situ hybridization and its influencing factors in preimplantation genetic diagnosis]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics\| PubMed ID: 24078563	2013
Non-invasive metabolomic profiling of day 3 embryo culture media using near-infrared spectroscopy to assess the development potential of embryos. Acta biochimica et biophysica Sinica\| PubMed ID: 24140649	2013
Polymorphisms of pentanucleotide repeats (tttta)n in the promoter of CYP11A1 and their relationships to polycystic ovary syndrome (PCOS) risk: a meta-analysis. Molecular biology reports\| PubMed ID: 24610422	2014
A retrospective analysis of the effect of salpingectomy on serum antiMüllerian hormone level and ovarian reserve. American journal of obstetrics and gynecology\| PubMed ID: 25046807	2015
Quadrivalent asymmetry in reciprocal translocation carriers predicts meiotic segregation patterns in cleavage stage embryos. Reproductive biomedicine online\| PubMed ID: 25131559	2014
The Ser680Asn polymorphism in the follicle-stimulating hormone receptor gene is associated with the ovarian response in controlled ovarian hyperstimulation. Clinical endocrinology\| PubMed ID: 25132286	2015
Smad7 maintains epithelial phenotype of ovarian cancer stem-like cells and supports tumor colonization by mesenchymal-epithelial transition. Molecular medicine reports\| PubMed ID: 25333457	2015
MiRNA-320 in the human follicular fluid is associated with embryo quality in vivo and affects mouse embryonic development in vitro. Scientific reports\| PubMed ID: 25732513	2015
Association of skewed X chromosome inactivation and idiopathic recurrent spontaneous abortion: a systematic review and meta-analysis. Reproductive biomedicine online\| PubMed ID: 26096034	2015
The association of serum estradiol level with outcomes of clomiphene citrate/human menopausal gonadotropin ovarian stimulation for in vitro fertilization and embryo transfer. Reproductive biology and endocrinology : RB&E\| PubMed ID: 26444856	2015
Non-invasive metabolomic profiling of embryo culture media and morphology grading to predict implantation outcome in frozen-thawed embryo transfer cycles. Journal of assisted reproduction and genetics\| PubMed ID: 26463877	2015
Mutations in TUBB8 and Human Oocyte Meiotic Arrest. The New England journal of medicine\| PubMed ID: 26789871	2016
Lectin binding of human sperm associates with DEFB126 mutation and serves as a potential biomarker for subfertility. Scientific reports\| PubMed ID: 26832966	2016
Mutations in TUBB8 cause a multiplicity of phenotypes in human oocytes and early embryos. Journal of medical genetics\| PubMed ID: 27273344	2016
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. Human reproduction (Oxford, England)\| PubMed ID: 27354380	2016
Mutations in PADI6 Cause Female Infertility Characterized by Early Embryonic Arrest. American journal of human genetics\| PubMed ID: 27545678	2016
Integrins β1 and β3 are biomarkers of uterine condition for embryo transfer. Journal of translational medicine\| PubMed ID: 27782833	2016
Improved cryotolerance and developmental competence of human oocytes matured in vitro by transient hydrostatic pressure treatment prior to vitrification. Cryobiology\| PubMed ID: 28057448	2017
Anordrin Eliminates Tamoxifen Side Effects without Changing Its Antitumor Activity. Scientific reports\| PubMed ID: 28266626	2017
A Retrospective Study of Cytogenetic Results From Amniotic Fluid in 5328 Fetuses With Abnormal Obstetric Sonographic Findings. Journal of ultrasound in medicine : official journal of the American Institute of Ultrasound in Medicine\| PubMed ID: 28523762	2017
High oestradiol concentration after ovarian stimulation is associated with lower maternal serum beta-HCG concentration and neonatal birth weight. Reproductive biomedicine online\| PubMed ID: 28606454	2017
Maternal and neonatal morbidity: repeat Cesarean versus a trial of labour after previous Cesarean delivery. Clinical and investigative medicine. Medecine clinique et experimentale\| PubMed ID: 28653615	2017
Biallelic Mutations in PATL2 Cause Female Infertility Characterized by Oocyte Maturation Arrest. American journal of human genetics\| PubMed ID: 28965849	2017
The establishment and application of preimplantation genetic haplotyping in embryo diagnosis for reciprocal and Robertsonian translocation carriers. BMC medical genomics\| PubMed ID: 29041973	2017
Transfer of Fresh versus Frozen Embryos in Ovulatory Women. The New England journal of medicine\| PubMed ID: 29320646	2018
In Vitro Modeling of Human Germ Cell Development Using Pluripotent Stem Cells. Stem cell reports\| PubMed ID: 29398481	2018
Analysis of segregation patterns of quadrivalent structures and the effect on genome stability during meiosis in reciprocal translocation carriers. Human reproduction (Oxford, England)\| PubMed ID: 29579270	2018
Expression of ENPP3 in human cyclic endometrium: a novel molecule involved in embryo implantation. Reproduction, fertility, and development\| PubMed ID: 29614240	2018
Screening of miRNAs in human follicular fluid reveals an inverse relationship between microRNA-663b expression and blastocyst formation. Reproductive biomedicine online\| PubMed ID: 29703434	2018
Comparative analysis of human sperm glycocalyx from different freezability ejaculates by lectin microarray and identification of ABA as sperm freezability biomarker. Clinical proteomics\| PubMed ID: 29719495	2018
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 r... BMJ open\| PubMed ID: 29773699	2018
The comprehensive mutational and phenotypic spectrum of TUBB8 in female infertility. European journal of human genetics : EJHG\| PubMed ID: 30297906	2019
Novel mutations in WEE2: Expanding the spectrum of mutations responsible for human fertilization failure. Clinical genetics\| PubMed ID: 30628060	2019
Novel mutations in ZP1, ZP2, and ZP3 cause female infertility due to abnormal zona pellucida formation. Human genetics\| PubMed ID: 30810869	2019
Mutations in and cause female infertility characterised by early embryonic arrest. Journal of medical genetics\| PubMed ID: 30877238	2019
BasePhasing: a highly efficient approach for preimplantation genetic haplotyping in clinical application of balanced translocation carriers. BMC medical genomics\| PubMed ID: 30885195	2019
A pannexin 1 channelopathy causes human oocyte death. Science translational medicine\| PubMed ID: 30918116	2019
Chronic exposure to environmental concentrations of phenanthrene impairs zebrafish reproduction. Ecotoxicology and environmental safety\| PubMed ID: 31254851	2019
Long-read sequencing and haplotype linkage analysis enabled preimplantation genetic testing for patients carrying pathogenic inversions. Journal of medical genetics\| PubMed ID: 31439719	2019
Homozygous mutations in cause female infertility characterised by multiple pronuclei formation and early embryonic arrest. Journal of medical genetics\| PubMed ID: 31704776	2020
MicroRNA-451 is downregulated in the follicular fluid of women with endometriosis and influences mouse and human embryonic potential. Reproductive biology and endocrinology : RB&E\| PubMed ID: 31744497	2019
Expanding the genetic and phenotypic spectrum of female infertility caused by TLE6 mutations. Journal of assisted reproduction and genetics\| PubMed ID: 31897846	2020
The identification of novel mutations in PLCZ1 responsible for human fertilization failure and a therapeutic intervention by artificial oocyte activation. Molecular human reproduction\| PubMed ID: 31953539	2020
MicroRNA expression profile analysis in sperm reveals hsa-mir-191 as an auspicious omen of in vitro fertilization. BMC genomics\| PubMed ID: 32066367	2020
Ovarian endometrioma infiltrating neutrophils orchestrate immunosuppressive microenvironment. Journal of ovarian research\| PubMed ID: 32334621	2020
Resolvin E1 in Follicular Fluid Acts as a Potential Biomarker and Improves Oocyte Developmental Competence by Optimizing Cumulus Cells. Frontiers in endocrinology\| PubMed ID: 32373069	2020
Bi-allelic Missense Pathogenic Variants in TRIP13 Cause Female Infertility Characterized by Oocyte Maturation Arrest. American journal of human genetics\| PubMed ID: 32473092	2020
Homozygous Mutations in BTG4 Cause Zygotic Cleavage Failure and Female Infertility. American journal of human genetics\| PubMed ID: 32502391	2020
Identification novel mutations in TUBB8 in female infertility and a novel phenotype of large polar body in oocytes with TUBB8 mutations. Journal of assisted reproduction and genetics\| PubMed ID: 32524331	2020
Expanded carrier screening in Chinese patients seeking the help of assisted reproductive technology. Molecular genetics & genomic medicine\| PubMed ID: 32573981	2020
Biallelic mutations in CDC20 cause female infertility characterized by abnormalities in oocyte maturation and early embryonic development. Protein & cell\| PubMed ID: 32666501	2020
17β-estradiol promotes bone marrow mesenchymal stem cell migration mediated by chemokine upregulation. Biochemical and biophysical research communications\| PubMed ID: 32800343	2020
Novel mutations in LHCGR (luteinizing hormone/choriogonadotropin receptor): expanding the spectrum of mutations responsible for human empty follicle syndrome. Journal of assisted reproduction and genetics\| PubMed ID: 32860205	2020
Effects of euploid blastocyst morphological development on reproductive outcomes. Reproductive biology\| PubMed ID: 32861682	2020
Disruption in causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest. Science advances\| PubMed ID: 32923619	2020
Comparison of PGS2.0 versus conventional embryo morphology evaluation for patients with recurrent pregnancy loss: a study protocol for a multicentre randomised trial. BMJ open\| PubMed ID: 33033011	2020
Oocyte Vitrification Temporarily Turns on Oxidation-Reduction Process Genes in Mouse Preimplantation Embryos. Reproductive sciences (Thousand Oaks, Calif.)\| PubMed ID: 33067752	2021
Conventional ICSI improves the euploid embryo rate in male reciprocal translocation carriers. Journal of assisted reproduction and genetics\| PubMed ID: 33230615	2021
Monozygotic dichorionic-diamniotic pregnancies following single frozen-thawed blastocyst transfer: a retrospective case series. BMC pregnancy and childbirth\| PubMed ID: 33302917	2020
Characterization of Copy-Number Variations and Possible Candidate Genes in Recurrent Pregnancy Losses. Genes\| PubMed ID: 33499090	2021
Transcriptomic analysis of endometrial receptivity for a genomic diagnostics model of Chinese women. Fertility and sterility\| PubMed ID: 33589135	2021
A novel homozygous variant in ZP2 causes abnormal zona pellucida formation and female infertility. Journal of assisted reproduction and genetics\| PubMed ID: 33604805	2021
Meiotic Heterogeneity of Trivalent Structure and Interchromosomal Effect in Blastocysts With Robertsonian Translocations. Frontiers in genetics\| PubMed ID: 33679881	2021
Progesterone activates the cyclic AMP-protein kinase A signalling pathway by upregulating in fertile men. The Journal of international medical research\| PubMed ID: 33752482	2021
Next-Generation Sequencing Is More Efficient at Detecting Mosaic Embryos and Improving Pregnancy Outcomes than Single-Nucleotide Polymorphism Array Analysis. The Journal of molecular diagnostics : JMD\| PubMed ID: 33781963	2021
Immediate versus delayed frozen embryo transfer in patients following a stimulated IVF cycle: a randomised controlled trial. Human reproduction (Oxford, England)\| PubMed ID: 33885131	2021
Novel biallelic mutations in MEI1: expanding the phenotypic spectrum to human embryonic arrest and recurrent implantation failure. Human reproduction (Oxford, England)\| PubMed ID: 34037756	2021
FBXO43 variants in patients with female infertility characterized by early embryonic arrest. Human reproduction (Oxford, England)\| PubMed ID: 34052850	2021
Authors' response to Scriven's Letter to the Editor (Journal of Assisted Reproduction and Genetics; https://doi.org/10.1007/s10815-021-02139). Journal of assisted reproduction and genetics\| PubMed ID: 34086148	2021
Modified strict sperm morphology threshold aids in the clinical selection of conventional fertilization (IVF) or intracytoplasmic sperm injection (ICSI). Asian journal of andrology\| PubMed ID: 34135171	2022
A comprehensive and universal approach for embryo testing in patients with different genetic disorders. Clinical and translational medicine\| PubMed ID: 34323405	2021
PPOS Protocol Effectively Improves the IVF Outcome Without Increasing the Recurrence Rate in Early Endometrioid Endometrial Cancer and Atypical Endometrial Hyperplasia Patients After Fertili... Frontiers in medicine\| PubMed ID: 34386503	2021
Live Birth with or without Preimplantation Genetic Testing for Aneuploidy. The New England journal of medicine\| PubMed ID: 34818479	2021
Gankyrin has a potential role in embryo implantation via activation of STAT3. Reproduction (Cambridge, England)\| PubMed ID: 35038312	2022
Identifying Balanced Chromosomal Translocations in Human Embryos by Oxford Nanopore Sequencing and Breakpoints Region Analysis. Frontiers in genetics\| PubMed ID: 35116057	2021
Complete androgen insensitivity syndrome caused by a novel mutation in the androgen receptor gene and its mechanism. Clinica chimica acta; international journal of clinical chemistry\| PubMed ID: 35351434	2022
Sperm-specific protein ACTL7A as a biomarker for fertilization outcomes of assisted reproductive technology. Asian journal of andrology\| PubMed ID: 35532568	2022
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 r... Contemporary clinical trials communications\| PubMed ID: 35669489	2022
Re-denudation of residual cumulus cells on day 3 increases the accuracy of cell-free DNA detection in spent embryo culture medium. Journal of assisted reproduction and genetics\| PubMed ID: 35672538	2022
Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping. Journal of medical genetics\| PubMed ID: 35710108	2023
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, Ch... BMC pregnancy and childbirth\| PubMed ID: 35764962	2022
Combined Preimplantation Genetic Testing for Genetic Kidney Disease: Genetic Risk Identification, Assisted Reproductive Cycle, and Pregnancy Outcome Analysis. Frontiers in medicine\| PubMed ID: 35783601	2022
Preimplantation genetic testing for aneuploidy in severe male factor infertility: protocol for a multicenter randomised controlled trial. BMJ open\| PubMed ID: 35831058	2022
Can the combination of time-lapse parameters and clinical features predict embryonic ploidy status or implantation? Reproductive biomedicine online\| PubMed ID: 35918244	2022
Heterozygous loss-of-function variants in LHX8 cause female infertility characterized by oocyte maturation arrest. Genetics in medicine : official journal of the American College of Medical Genetics\| PubMed ID: 36029299	2022
The use of frozen embryos and frozen sperm have complementary IVF outcomes: a retrospective analysis in couples experiencing IVF/Donor and IVF/Husband. BMC pregnancy and childbirth\| PubMed ID: 36258180	2022
Long-term maintenance of human endometrial epithelial stem cells and their therapeutic effects on intrauterine adhesion. Cell & bioscience\| PubMed ID: 36258228	2022
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. BMC pregnancy and childbirth\| PubMed ID: 36324098	2022
The mechanism of acentrosomal spindle assembly in human oocytes. Science (New York, N.Y.)\| PubMed ID: 36395215	2022
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. Human molecular genetics\| PubMed ID: 36519758	2023
Elevated histone demethylase KDM5C increases recurrent miscarriage risk by preventing trophoblast proliferation and invasion. Cell death discovery\| PubMed ID: 36550096	2022
A novel noninvasive prenatal testing method for chromosomal rearrangements using maternal circulating cell-free foetal DNA. Clinical and translational medicine\| PubMed ID: 36610059	2023
Karyopherin α deficiency contributes to human preimplantation embryo arrest. The Journal of clinical investigation\| PubMed ID: 36647821	2023
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-... Journal of clinical medicine\| PubMed ID: 36902595	2023
ADGB variants cause asthenozoospermia and male infertility. Human genetics\| PubMed ID: 36995441	2023
Impacts of vitrification on the transcriptome of human ovarian tissue in patients with gynecological cancer. Frontiers in genetics\| PubMed ID: 37007967	2023
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects. Genome biology\| PubMed ID: 37024973	2023
Bi-allelic pathogenic variants in PABPC1L cause oocyte maturation arrest and female infertility. EMBO molecular medicine\| PubMed ID: 37052235	2023
Bi-allelic variants in ASTL cause abnormal fertilization or oocyte maturation defects. Human molecular genetics\| PubMed ID: 37133443	2023
Loss of ACTL7A causes small head sperm by defective acrosome-acroplaxome-manchette complex. Reproductive biology and endocrinology : RB&E\| PubMed ID: 37667331	2023
Growth hormone supplementation during ovarian stimulation in women with advanced maternal age undergoing preimplantation genetic testing for Aneuploidy. Journal of ovarian research\| PubMed ID: 37858247	2023
A prospective study to evaluate whether serum kisspeptin is a marker predictive of the first-trimester miscarriage of women who conceive in IVF. Journal of assisted reproduction and genetics\| PubMed ID: 37935913	2024
Clinical outcomes of fetal selective reduction in dichorionic triplet pregnancies. Journal of the Chinese Medical Association : JCMA\| PubMed ID: 37962135	2024
The morphokinetic signature of human blastocysts with mosaicism and the clinical outcomes following transfer of embryos with low-level mosaicism. Journal of ovarian research\| PubMed ID: 38195558	2024
Bi-allelic missense variants in MEI4 cause preimplantation embryonic arrest and female infertility. Human genetics\| PubMed ID: 38252283	2024
Endometrial transcriptome profiling of patients with recurrent implantation failure during hormone replacement therapy cycles. Frontiers in endocrinology\| PubMed ID: 38352249	2023
Comparing blastocyst euploid rates between the progestin-primed and gonadotrophin-releasing hormone antagonist protocols in aneuploidy genetic testing: a randomised trial protocol. BMJ open\| PubMed ID: 38521533	2024
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. BMJ open\| PubMed ID: 38719320	2024
Comprehensive preimplantation genetic testing for balanced insertional translocation carriers. Journal of medical genetics\| PubMed ID: 38802138	2024