Xiaojin He

发表

Bi-allelic variants in human TCTE1/DRC5 cause asthenospermia and male infertility

P. Zhou, Yunxia Cao, Siyu Liu, 2022, European Journal of Human Genetics.

Loss of DRC1 function leads to multiple morphological abnormalities of the sperm flagella and male infertility in human and mouse

Yunxia Cao, Siyu Liu, Jintao Zhang, 2021, Human molecular genetics.

Star-shaped polymers for DNA sequencing by capillary electrophoresis.

Xiaojin He, Yuguo Ma, Cai Tie, 2011, Journal of chromatography. A.

Genetic study of Hormad1 and Hormad2 with non-obstructive azoospermia patients in the male Chinese population

X. Zuo, F. Zhou, P. Zhou, 2014, Journal of Assisted Reproduction and Genetics.

Application of atosiban in frozen-thawed cycle patients with different times of embryo transfers

P. Zhou, Yunxia Cao, Huan Wu, 2016, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

Diet, microbe, and autism: Cause or consequence?

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Cell Host & Microbe.

Association Study Between Polymorphisms of PRMT6, PEX10, SOX5, and Nonobstructive Azoospermia in the Han Chinese Population1

M. Wang, Yongyong Shi, Zhiqiang Li, 2014, Biology of reproduction.

No significant long-term complications from inadvertent exposure to gonadotropin-releasing hormone agonist during early pregnancy in mothers and offspring: a retrospective analysis

P. Zhou, Yunxia Cao, Huan Wu, 2020, Reproductive Biology and Endocrinology.

Performance evaluation of differential splicing analysis methods and splicing analytics platform construction

K. Xia, Kuokuo Li, Guihu Zhao, 2022, Nucleic acids research.

Efficacy of tripterygium glycosides (TG) in rheumatoid arthritis as a disease-modifying anti-rheumatic drug (DMARD) in combination with conventional DMARDs: A systematic review and meta-analysis of randomized controlled trials.

Xueping Zhou, Xiaojin He, Zheng Feng, 2022, Pharmacological research.

Prognosis of Congenital Anomalies in Conceptions Following In Vitro Fertilization: A Multicenter Retrospective Cohort Study in China

J. Qiao, Chuncheng Lu, Xiaojin He, 2022, Frontiers in Endocrinology.

Activation of MT1/MT2 to Protect Testes and Leydig Cells against Cisplatin-Induced Oxidative Stress through the SIRT1/Nrf2 Signaling Pathway

F. Tao, Xiaoyu Chen, Yunxia Cao, 2022, Cells.

Identification of deleterious variants in patients with male infertility due to idiopathic non-obstructive azoospermia

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Reproductive Biology and Endocrinology.

Non-invasive molecular biomarkers for predicting outcomes of micro-TESE in patients with idiopathic non-obstructive azoospermia

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Expert Reviews in Molecular Medicine.

Genetic association between PAX2 and mullerian duct anomalies in Han Chinese females

Binbin Wang, Jing Wang, Xiaojin He, 2016, Journal of Assisted Reproduction and Genetics.

Bi‐allelic mutations in MCIDAS and CCNO cause human infertility associated with abnormal gamete transport

F. Tao, Yiyuan Liu, Yunxia Cao, 2021, Clinical genetics.

Homozygous mutations in DZIP1 can induce asthenoteratospermia with severe MMAF

Chuanmao Zhang, L. Jin, H. Saiyin, 2020, Journal of Medical Genetics.

Novel bi-allelic variants in DNAH2 cause severe asthenoteratozoospermia with multiple morphological abnormalities of the flagella.

P. Zhou, Yunxia Cao, Huan Wu, 2021, Reproductive biomedicine online.

Bi-allelic Mutations in TTC21A Induce Asthenoteratospermia in Humans and Mice.

Shimin Zhao, P. Ray, L. Jin, 2019, American journal of human genetics.

Biallelic mutations in CFAP65 cause male infertility with multiple morphological abnormalities of the sperm flagella in humans and mice

P. Ray, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

Poor semen parameters are associated with abnormal methylation of imprinted genes in sperm DNA

Yunxia Cao, Xiaojin He, Zhaolian Wei, 2022, Reproductive Biology and Endocrinology.

Case Report: Novel Biallelic Mutations in ARMC4 Cause Primary Ciliary Dyskinesia and Male Infertility in a Chinese Family

Kuokuo Li, F. Tao, P. Zhou, 2021, Frontiers in Genetics.

Loss of function mutation in DNAH7 induces male infertility associated with abnormalities of the sperm flagella and mitochondria in human

Kuokuo Li, F. Tao, P. Zhou, 2022, Clinical genetics.

lethal, autosomal recessive neurodegenerative disease and leads to progressive impairment of movement and cognition. A couple with a proband child with calcium-independent group VI phospholipase A2 (PLA2G6)-associated INAD and a previous affected pregnancy sought pre-implantation genetic diagnosis

P. Zhou, Yunxia Cao, Huan Wu, 2019 .

Administration of atosiban in patients with endometriosis undergoing frozen-thawed embryo transfer: a prospective, randomized study.

P. Zhou, Yunxia Cao, Huan Wu, 2016, Fertility and sterility.

[Sperm chromatin integrity test for predicting the outcomes of IVF and ICSI].

Xiaojin He, Yun-xia Cao, Bing Song, 2011, Zhonghua nan ke xue = National journal of andrology.

Identification of Novel Biallelic TLE6 Variants in Female Infertility With Preimplantation Embryonic Lethality

P. Zhou, Yunxia Cao, Huan Wu, 2021, Frontiers in Genetics.

Altered mRNAs Profiles in the Testis of Patients With “Secondary Idiopathic Non-Obstructive Azoospermia”

Kuokuo Li, Yunxia Cao, Xiaojin He, 2022, Frontiers in Cell and Developmental Biology.

Novel variants in helicase for meiosis 1 lead to male infertility due to non-obstructive azoospermia

Kuokuo Li, Yunxia Cao, Xiaojin He, 2021, Reproductive Biology and Endocrinology.

Novel Variants in HFM1 Lead to Male Infertility Due to Non-obstructive Azoospermia

Kuokuo Li, Yunxia Cao, Xiaojin He, 2021 .

Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome.

J. Gécz, P. Zhou, Yunxia Cao, 2016, American journal of human genetics.

Bi-allelic Mutations in ARMC2 Lead to Severe Astheno-Teratozoospermia Due to Sperm Flagellum Malformations in Humans and Mice.

N. Thierry-Mieg, B. Conne, P. Ray, 2019, American journal of human genetics.

A homozygous nonsense mutation of PLCZ1 cause male infertility with oocyte activation deficiency

Yunxia Cao, Huan Wu, Xiaojin He, 2020, Journal of Assisted Reproduction and Genetics.

Novel variants in DNAH9 lead to nonsyndromic severe asthenozoospermia

Yunxia Cao, Xiaojin He, Junqiang Zhang, 2021, Reproductive Biology and Endocrinology.

A novel homozygous mutation in WDR19 induces disorganization of microtubules in sperm flagella and nonsyndromic asthenoteratospermia

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

A novel homozygous mutation in the meiotic gene MSH4 leading to male infertility due to non-obstructive azoospermia.

Yunxia Cao, Xiaojin He, Huiru Cheng, 2020, American journal of translational research.

Spermatogenesis Affects the Outcome of ICSI for Azoospermic Patients Rather Than Sperm Retrieval Method

P. Zhou, Xiaojin He, Zhiguo Zhang, 2010, Systems biology in reproductive medicine.

A novel hemizygous loss-of-function mutation in ADGRG2 causes male infertility with congenital bilateral absence of the vas deferens

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

Association of single nucleotide polymorphisms in the USF1, GTF2A1L and OR2W3 genes with non-obstructive azoospermia in the Chinese population

X. Zuo, F. Zhou, Xiaojin He, 2014, Journal of Assisted Reproduction and Genetics.

Altered miRNA profile in testis of post-cryptorchidopexy patients with non-obstructive azoospermia

Huan Wu, Xiaojin He, Xiansheng Zhang, 2018, Reproductive Biology and Endocrinology.

Novel Biallelic TLE6 Variants Induce Preimplantation Embryonic Lethality That Cannot be Rescued by IVF or ICSI

P. Zhou, Yunxia Cao, Huan Wu, 2021 .

Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.

J. Veltman, M. O’Bryan, P. Ray, 2021, American journal of human genetics.

Dehydroepiandrosterone plus climen supplementation shows better effects than dehydroepiandrosterone alone on infertility patients with diminished ovarian reserve of low-FSH level undergoing in-vitro fertilization cycles: a randomized controlled trial

P. Zhou, Yunxia Cao, Xiaojin He, 2016, Reproductive Biology and Endocrinology.

Deficiency of primate-specific SSX1 induced asthenoteratozoospermia in infertile men and cynomolgus monkey and tree shrew models.

Y. Li, Yong-Gang Yao, Zhixi Su, 2023, American journal of human genetics.

Patients with severe asthenoteratospermia carrying SPAG6 or RSPH3 mutations have a positive pregnancy outcome following intracytoplasmic sperm injection

P. Zhou, Yunxia Cao, Huan Wu, 2020, Journal of Assisted Reproduction and Genetics.

miR-323-3p regulates the steroidogenesis and cell apoptosis in polycystic ovary syndrome (PCOS) by targeting IGF-1.

Yunxia Cao, Xiaojin He, Zhiguo Zhang, 2019, Gene.

Exploration of molecular features of PCOS with different androgen levels and immune-related prognostic biomarkers associated with implantation failure

Yunxia Cao, Xiaojin He, Shuyu Meng, 2022, Frontiers in Endocrinology.

Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Kuokuo Li, Yunxia Cao, Huan Wu, 2021, Reproductive Biology and Endocrinology.

Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

Jingze Tan, Hongyan Wang, L. Jin, 2018, Journal of Human Genetics.

Homozygous variants in AKAP3 induce asthenoteratozoospermia and male infertility

L. Jin, Yunxia Cao, Huan Wu, 2022, Journal of Medical Genetics.

Biallelic mutations in CFAP54 cause male infertility with severe MMAF and NOA

L. Jin, Yunxia Cao, Huan Wu, 2023, Journal of Medical Genetics.

Novel FSIP2 Variants Induce Super-Length Mitochondrial Sheath and Asthenoteratozoospermia in Humans

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, International journal of biological sciences.

Correction to: Homozygous SPAG6 variants can induce nonsyndromic asthenoteratozoospermia with severe MMAF

Kuokuo Li, Yunxia Cao, Huan Wu, 2022, Reproductive Biology and Endocrinology.

Bi-allelic DNAH8 Variants Lead to Multiple Morphological Abnormalities of the Sperm Flagella and Primary Male Infertility.

M. Ikawa, P. Ray, L. Jin, 2020, American journal of human genetics.

Bi-allelic Mutations in TTC29 Cause Male Subfertility with Asthenoteratospermia in Humans and Mice.

L. Jin, Yunxia Cao, Huan Wu, 2019, American journal of human genetics.

Homozygous mutations in SPEF2 induce multiple morphological abnormalities of the sperm flagella and male infertility

Yong Zhu, L. Jin, Yunxia Cao, 2019, Journal of Medical Genetics.

Novel homozygous CFAP69 mutations in humans and mice cause severe asthenoteratospermia with multiple morphological abnormalities of the sperm flagella

Jian Wang, Jingze Tan, Hongyan Wang, 2018, Journal of Medical Genetics.

Mutations in PMFBP1 Cause Acephalic Spermatozoa Syndrome.

Qing-Yuan Sun, P. Zhou, Yunxia Cao, 2018, American journal of human genetics.

Artificial oocyte activation to improve reproductive outcomes in couples with various causes of infertility: a retrospective cohort study.

P. Zhou, Yunxia Cao, Xiaojin He, 2020, Reproductive biomedicine online.

Successful preimplantation genetic diagnosis by targeted next-generation sequencing on an ion torrent personal genome machine platform

P. Zhou, Yunxia Cao, Xiaojin He, 2018, Oncology letters.

SARS-CoV-2 and the reproductive system: assessment of risk and recommendations for infection control in reproductive departments

Yunxia Cao, Huan Wu, Xiaojin He, 2020, Systems biology in reproductive medicine.

Impact of the COVID-19 Pandemic on Partner Relationships and Sexual and Reproductive Health: Cross-Sectional, Online Survey Study

Yunxia Cao, Huan Wu, Xiaojin He, 2020, Journal of medical Internet research.

Novel DPY19L2 variants in globozoospermic patients and the overcoming this male infertility

Jie Yan, J. Qiao, Xiaojin He, 2018, Asian journal of andrology.

Genetic association study of RNF8 and BRDT variants with non-obstructive azoospermia in the Chinese Han population

X. Zuo, F. Zhou, Xiaojin He, 2015, Systems biology in reproductive medicine.

Genetic Variants in TEX15 Gene Conferred Susceptibility to Spermatogenic Failure in the Chinese Han Population

X. Zuo, Xuejun Zhang, Xiaojin He, 2012, Reproductive Sciences.

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

Yunxia Cao, Xiaojin He, G. Lin, 2021, American journal of human genetics.

Bi-allelic Loss-of-function Variants in CFAP58 Cause Flagellar Axoneme and Mitochondrial Sheath Defects and Asthenoteratozoospermia in Humans and Mice.

L. Jin, H. Saiyin, P. Zhou, 2020, American journal of human genetics.

DNALI1 deficiency causes male infertility with severe asthenozoospermia in humans and mice by disrupting the assembly of the flagellar inner dynein arms and fibrous sheath

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Cell Death & Disease.

Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.

Yunxia Cao, Huan Wu, Xiaojin He, 2021, American journal of human genetics.

A Novel Missense Variant of TP63 Heterozygously Present in Split-Hand/Foot Malformation

Xiaojin He, Zhiguo Zhang, D. Tang, 2020, BioMed research international.

Asymptomatic and Presymptomatic Infectors: Hidden Sources of COVID-19 Disease

Yunxia Cao, Xiaojin He, Xiaojin He, 2020, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Impact of the COVID-19 Pandemic on Partner Relationships and Sexual and Reproductive Health: Cross-Sectional, Online Survey Study (Preprint)

Yunxia Cao, Huan Wu, Xiaojin He, 2020 .

Association of genetic variants in SOHLH1 and SOHLH2 with non-obstructive azoospermia risk in the Chinese population.

F. Zhou, P. Zhou, Yunxia Cao, 2015, European journal of obstetrics, gynecology, and reproductive biology.

CREM Variants rs4934540 and rs2295415 Conferred Susceptibility to Nonobstructive Azoospermia Risk in the Chinese Population1

X. Zuo, F. Zhou, P. Zhou, 2014, Biology of reproduction.

Running title: CREM variants conferred susceptibility to NOA

X. Zuo, F. Zhou, P. Zhou, 2014 .

Biallelic loss‐of‐function mutations in SEPTIN4 (C17ORF47), encoding a conserved annulus protein, cause thin midpiece spermatozoa and male infertility in humans

Kuokuo Li, F. Tao, P. Zhou, 2022, Human mutation.

Novel biallelic mutations in SLC26A8 cause severe asthenozoospermia in humans owing to midpiece defects: Insights into a putative dominant genetic disease

Kuokuo Li, P. Zhou, Yunxia Cao, 2021, Human mutation.

Novel Mutations in X-Linked, USP26-Induced Asthenoteratozoospermia and Male Infertility

L. Jin, Yunxia Cao, Huan Wu, 2021, Cells.

NovelCFAP43 andCFAP44 mutations cause male infertility with multiple morphological abnormalities of the sperm flagella (MMAF).

P. Zhou, Yunxia Cao, Huan Wu, 2019, Reproductive biomedicine online.

A homozygous loss‐of‐function mutation in FBXO43 causes human non‐obstructive azoospermia

F. Tao, P. Zhou, Yiyuan Liu, 2021, Clinical genetics.

Novel HYDIN variants associated with male infertility in two Chinese families

Kuokuo Li, Yu-xia Cao, P. Zhou, 2023, Frontiers in Endocrinology.

Knowledge, Attitudes, and Practice Patterns Relating to Female Sexual Health Among Obstetricians and Gynecologists in China

Dan Zhang, Yunxia Cao, Xiaojin He, 2021, JAMA Network Open.

Genetic analysis of DACT1 in 100 Chinese Han women with Müllerian duct anomalies.

Binbin Wang, Jing Wang, Yunxia Cao, 2016, Reproductive biomedicine online.

Low sexual desire and hypoactive sexual desire disorder in Chinese women

Yunxia Cao, Xiaojin He, D. Tang, 2022, International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics.

Circular RNAs: Novel potential regulators in embryogenesis, female infertility, and pregnancy‐related diseases

C. Qian, Yunxia Cao, Xiaojin He, 2021, Journal of cellular physiology.

Biallelic mutations of CFAP251 cause sperm flagellar defects and human male infertility

Jingze Tan, Hongyan Wang, L. Jin, 2018, Journal of Human Genetics.

Polymorphisms of F2, PROC, PROZ, and F13A1 Genes are Associated With Recurrent Spontaneous Abortion in Chinese Han Women

Yunxia Cao, Xiaojin He, Wei Liu, 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.

Prevalence and risk factors of monochorionic diamniotic twinning after assisted reproduction: A six-year experience base on a large cohort of pregnancies

P. Zhou, Huan Wu, Xiaojin He, 2017, PloS one.

Influencing factors and predictive model of live birth involving low-grade blastocyst frozen–thawed transfer: a retrospective study

P. Zhou, Yunxia Cao, Xiaojin He, 2023, European Journal of Medical Research.

Novel deleterious splicing variant in HFM1 causes gametogenesis defect and recurrent implantation failure: concerning the risk of chromosomal abnormalities in embryos

Kuokuo Li, P. Zhou, Yunxia Cao, 2023, Journal of Assisted Reproduction and Genetics.

Sperm DNA integrity status is associated with DNA methylation signatures of imprinted genes and non-imprinted genes

P. Zhou, Yunxia Cao, Huan Wu, 2021, Journal of Assisted Reproduction and Genetics.

Homozygous mutation in SLO3 leads to severe asthenoteratozoospermia due to acrosome hypoplasia and mitochondrial sheath malformations

Kuokuo Li, F. Tao, P. Zhou, 2022, Reproductive Biology and Endocrinology.

Systematic Evaluation of Genetic Variants for Polycystic Ovary Syndrome in a Chinese Population

Yongyong Shi, Zhiqiang Li, P. Zhou, 2015, PloS one.

Sperm cryopreservation in the human sperm bank: 11-year results of the Chinese mainland sperm banking network

Xiaojin He, S. Dai, Zhiqiang Wang, 2022, Chinese Medical Journal.

Biallelic SUN5 Mutations Cause Autosomal-Recessive Acephalic Spermatozoa Syndrome.

J. Gécz, P. Zhou, Yunxia Cao, 2016, American journal of human genetics.

Homozygous missense mutation in CCDC155 disrupts the transmembrane distribution of CCDC155 and SUN1, resulting in non-obstructive azoospermia and premature ovarian insufficiency in humans

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2022, Human Genetics.

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study

P. Zhou, Yunxia Cao, Huan Wu, 2021, Journal of medical Internet research.

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study (Preprint)

P. Zhou, Yunxia Cao, Huan Wu, 2020 .

Sulfur dioxide may predominate in the adverse effects of ambient air pollutants on semen quality among the general population in Hefei, China.

Xiaojin He, Tailang Yin, P. Jia, 2023, Science of the Total Environment.

Bi-allelic variants in DNAH10 cause asthenoteratozoospermia and male infertility

Kuokuo Li, F. Tao, P. Zhou, 2021, Journal of Assisted Reproduction and Genetics.

A homozygous frameshift mutation in ADAD2 cause male infertility with spermatogenic impairments.

F. Tao, Yue Lv, L. Jin, 2023, Journal of genetics and genomics = Yi chuan xue bao.

Bi-allelic truncating variants in CFAP206 cause male infertility in human and mouse

N. Thierry-Mieg, Kuokuo Li, F. Tao, 2021, Human Genetics.

Homozygous loss-of-function mutations in FSIP2 cause male infertility with asthenoteratospermia.

Hongyan Wang, L. Jin, Yang Gao, 2019, Journal of genetics and genomics = Yi chuan xue bao.

PRDM9 gene polymorphism may not be associated with defective spermatogenesis in the Chinese Han population

X. Zuo, Xuejun Zhang, Huan Wu, 2013, Systems biology in reproductive medicine.

Retrospective Study to Compare Frozen-Thawed Embryo Transfer with Fresh Embryo Transfer on Pregnancy Outcome Following Intracytoplasmic Sperm Injection for Male Infertility

P. Zhou, Yunxia Cao, Huan Wu, 2018, Medical science monitor : international medical journal of experimental and clinical research.

Bi-allelic human TEKT3 mutations cause male infertility with oligoasthenoteratozoospermia due to acrosomal hypoplasia and reduced progressive motility.

Kuokuo Li, P. Zhou, Yiyuan Liu, 2023, Human molecular genetics.

Deficiency of X-linked TENT5D causes male infertility by disrupting the mRNA stability during spermatogenesis

Mohan Liu, Xiaojin He, Chunyu Liu, 2022, Cell Discovery.

Novel compound heterozygous variants in dynein axonemal heavy chain 17 cause asthenoteratospermia with sperm flagellar defects.

P. Zhou, Yunxia Cao, Xiaojin He, 2020, Journal of genetics and genomics = Yi chuan xue bao.

Ferroptosis in female reproductive diseases: from potential pathogenesis to therapy

Xiaojin He, Q. Xing, Yuping Xu, 2023 .

Differences in the Gut Microbiome of Women With and Without Hypoactive Sexual Desire Disorder: Case Control Study (Preprint)

P. Zhou, Yunxia Cao, Huan Wu, 2020 .

ACROSIN deficiency causes total fertilization failure in humans by preventing the sperm from penetrating the zona pellucida.

Kuokuo Li, Yiyuan Liu, Yunxia Cao, 2023, Human reproduction.

Prioritizing de novo potential non-canonical splicing variants in neurodevelopmental disorders

Kuokuo Li, Xiaomeng Wang, Guihu Zhao, 2023, EBioMedicine.

Homozygous deleterious variants in the C-terminal of TDRD5 impair spermiogenesis, causing severe oligoasthenoteratozoospermia in humans.

Mingxi Liu, Xiaojin He, Huiru Cheng, 2024, Andrology.

LRRC23 deficiency causes male infertility with idiopathic asthenozoospermia by disrupting the assembly of radial spokes

Yu-xia Cao, P. Zhou, Huan Wu, 2023, Clinical genetics.

Bi-allelic variants in chromatoid body protein TDRD6 cause spermiogenesis defects and severe oligoasthenoteratozoospermia in humans

Huan Wu, Xiaojin He, Yang Gao, 2024, Journal of Medical Genetics.