Yunxia Cao

发表

Genome-wide association study identifies eight new risk loci for polycystic ovary syndrome

Yuhua Shi, Han Zhao, Li You, 2012, Nature Genetics.

FABP4: a novel candidate gene for polycystic ovary syndrome

F. Zhang, Jingjing Liu, Binbin Wang, 2009, Endocrine.

Live birth after fresh embryo transfer vs elective embryo cryopreservation/frozen embryo transfer in women with polycystic ovary syndrome undergoing IVF (FreFro-PCOS): study protocol for a multicenter, prospective, randomized controlled clinical trial

B. Zhang, Zi-jiang Chen, X. Liang, 2014, Trials.

Lack of association between interleukin-1a gene (IL-1a) C (-889) T variant and polycystic ovary syndrome in chinese women

Jingjing Liu, Binbin Wang, Jing Wang, 2009, Endocrine.

Lack of an association between CYP1A1 gene Ile462Val polymorphism and polycystic ovary syndrome in Chinese

Jingjing Liu, Binbin Wang, Jing Wang, 2009, Endocrine.

Novel homozygous mutation in TUBB8 associated with oocyte maturation defect-2 in a consanguineous marriage family

Binbin Wang, Xu Ma, Yunxia Cao, 2020 .

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

B. Tang, Qing Liu, Wotu Tian, 2021, Movement disorders : official journal of the Movement Disorder Society.

Novel alanyl-tRNA synthetase 2 (AARS2) homozygous mutation in a consanguineous Chinese family with premature ovarian insufficiency.

Binbin Wang, Xu Ma, Yunxia Cao, 2019, Fertility and sterility.

A single nucleotide polymorphism in the MTOR gene is associated with recurrent spontaneous abortion in the Chinese female population

Xu Ma, Yunxia Cao, Chenzhi Zong, 2015, Systems biology in reproductive medicine.

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.

Binbin Wang, Jing Wang, Xu Ma, 2011, Human reproduction.

Mutational analysis of human bone morphogenetic protein 15 in Chinese women with polycystic ovary syndrome.

Jingjing Liu, Binbin Wang, Jing Wang, 2011, Metabolism: clinical and experimental.

Association of polymorphisms in the estrogen receptor β (ESR2) with unexplained recurrent spontaneous abortion (URSA) in Chinese population

Binbin Wang, Jing Wang, Xu Ma, 2012, Journal of Maternal-Fetal & Neonatal 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.

No association between polymorphisms in PTEN and primary ovarian insufficiency in a Han Chinese population

Binbin Wang, Jing Wang, Xu Ma, 2015, Reproductive Biology and Endocrinology.

Effect of melatonin on the clinical outcome of patients with repeated cycles after failed cycles of in vitro fertilization and intracytoplasmic sperm injection.

Kaijuan Wang, Zhiguo Zhang, Yunxia Cao, 2021, Zygote.

Upregulated HMGB1 levels in maternal–fetal interface of patients with unexplained recurrent spontaneous abortion from different sources

Yunxia Cao, Huijuan Zou, Cong Ma, 2021, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Interleukin 1 beta (IL-1β) promoter C [−511] T polymorphism but not C [+3953] T polymorphism is associated with polycystic ovary syndrome

Jingjing Liu, Binbin Wang, Jing Wang, 2010, Endocrine.

Identification of novel missense mutations of GDF9 in Chinese women with polycystic ovary syndrome.

Jingjing Liu, Binbin Wang, Jing Wang, 2010, Reproductive biomedicine online.

Frozen versus fresh single blastocyst transfer in ovulatory women: a multicentre, randomised controlled trial

Jia-yin Liu, Yimin Zhu, Zi-jiang Chen, 2019, The Lancet.

Polar Body Genome Transfer for Preventing the Transmission of Inherited Mitochondrial Diseases

Jianhong Zhu, Yunxia Cao, Dong-mei Ji, 2014, Cell.

Fresh versus Frozen Embryos for Infertility in the Polycystic Ovary Syndrome.

Zi-jiang Chen, Han Zhao, X. Liang, 2016, The New England journal of medicine.

Analysis of FOXO3 mutation in 114 Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

Micro-TESE surgery combined with ICSI regimen in the treatment of non-obstructive azoospermia patients and its effect analysis

Qiushuang Wang, Kaijuan Wang, Zhiguo Zhang, 2022, Zygote.

Consultation and treatment behaviour of infertile couples in China: a population-based study.

J. Qiao, Yimin Zhu, Rong Li, 2019, Reproductive biomedicine online.

Consanguineous familial study revealed biallelic FIGLA mutation associated with premature ovarian insufficiency

Binbin Wang, Jing Wang, Yunxia Cao, 2018, Journal of Ovarian Research.

A homozygous NOBOX truncating variant causes defective transcriptional activation and leads to primary ovarian insufficiency

Binbin Wang, Jing Wang, Kehkooi Kee, 2016, Human reproduction.

A dominant negative mutation at the ATP binding domain of AMHR2 is associated with a defective anti-Müllerian hormone signaling pathway.

Wei Zhang, Xueya Zhou, Binbin Wang, 2016, Molecular human reproduction.

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.

Sequence variants of KHDRBS1 as high penetrance susceptibility risks for primary ovarian insufficiency by mis-regulating mRNA alternative splicing

Binbin Wang, Jing Wang, Kehkooi Kee, 2017, Human reproduction.

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients.

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive Biomedicine Online.

Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).

Jianfeng Xu, Yongyong Shi, J. Qiao, 2012, Human molecular genetics.

Maternal heterozygous mutation in CHEK1 leads to mitotic arrest in human zygotes

Jie Na, Jia Ming, Haitao Li, 2021, Protein & cell.

Mutation analysis of the WNT4 gene in Han Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive biology and endocrinology : RB&E.

Mutation analysis of the WNT 4 gene in Han Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2011 .

Analysis of cyclin-dependent kinase inhibitor 1B mutation in Han Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

GPR3 may not be a potential candidate gene for premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2010, Reproductive biomedicine online.

Mutational analysis of SAL-Like 4 (SALL4) in Han Chinese women with premature ovarian failure.

Binbin Wang, Jing Wang, Xu Ma, 2009, Molecular human reproduction.

Vaginal progesterone gel is non-inferior to intramuscular progesterone in efficacy with acceptable tolerability for luteal phase support: A prospective, randomized, multicenter study in China.

J. Qiao, Yimin Zhu, Rong Li, 2019, European journal of obstetrics, gynecology, and reproductive biology.

A novel mutation of HOXA11 in a patient with septate uterus

Binbin Wang, Longfei Cheng, Jing Wang, 2017, Orphanet Journal of Rare Diseases.

A novel mutation of HOXA10 in a Chinese woman with a Mullerian duct anomaly.

Binbin Wang, Longfei Cheng, Jing Wang, 2011, Human reproduction.

Reproductive genetics A novel mutation of HOXA 10 in a Chinese woman with a Müllerian duct anomaly

Binbin Wang, Longfei Cheng, Jing Wang, 2011 .

Intracytoplasmic sperm injection (ICSI) versus conventional in vitro fertilisation (IVF) in couples with non-severe male infertility (NSMI-ICSI): protocol for a multicentre randomised controlled trial

B. Mol, Li Tang, Y. Lian, 2019, BMJ Open.

Human Papillomavirus Genome-Wide Identification of T-Cell Epitopes for Peptide Vaccine Development Against Cervical Cancer: An Integration of Computational Analysis and Experimental Assay

Bo Li, Yunxia Cao, Xianfang Zheng, 2015, J. Comput. Biol..

Current Studies of Mitochondrial Quality Control in the Preeclampsia

Yunxia Cao, Ruirui Hou, Yuanyuan Yang, 2022, Frontiers in Cardiovascular Medicine.

Association between exposure to airborne particulate matter less than 2.5 μm and human fecundity in China.

Ping Liu, J. Qiao, Yimin Zhu, 2020, Environment international.

Identification and functional analysis of a novel LHX1 mutation associated with congenital absence of the uterus and vagina

Xuegong Zhang, Xueya Zhou, Binbin Wang, 2017, Oncotarget.

Glutathione S-transferase A1 polymorphism and the risk of recurrent spontaneous abortion in Chinese Han population

Juan Liu, Binbin Wang, Jing Wang, 2014, Journal of Assisted Reproduction and Genetics.

Mutation analysis of FOXL2 gene in Chinese patients with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology.

A NANOS3 mutation linked to protein degradation causes premature ovarian insufficiency

G. Shi, Ying Xu, Yunxia Cao, 2013, Cell Death and Disease.

Epidemiology of infertility in China: a population‐based study

J. Qiao, Xiujuan Chen, Y. Zhu, 2018, BJOG : an international journal of obstetrics and gynaecology.

Downregulation of miR-320a/383-sponge-like long non-coding RNA NLC1-C (narcolepsy candidate-region 1 genes) is associated with male infertility and promotes testicular embryonal carcinoma cell proliferation

Xiaoyuan Song, H. Tian, Yunxia Cao, 2015, Cell Death and Disease.

A small increase in CHEK1 activity leads to the arrest of the first zygotic division in human

Jie Na, Jia Ming, Haitao Li, 2020, bioRxiv.

Association of 8q22.3 locus in Chinese Han with idiopathic premature ovarian failure (POF).

Jianfeng Xu, Yongyong Shi, J. Qiao, 2012, Human Molecular Genetics.

tRNA-derived fragment tRF-03357 promotes cell proliferation, migration and invasion in high-grade serous ovarian cancer

Yunxia Cao, Zhaolian Wei, Jing Wang, 2019 .

The miR-449b polymorphism, rs10061133 A>G, is associated with premature ovarian insufficiency

Binbin Wang, Jing Wang, Yunxia Cao, 2016, Menopause.

Haplotype analysis of chemokine CXCL12 polymorphisms and susceptibility to premature ovarian failure in Chinese women.

Binbin Wang, Jing Wang, Xu Ma, 2011, Human Reproduction.

New candidate gene POU5F1 associated with premature ovarian failure in Chinese patients.

Binbin Wang, Jing Wang, Xu Ma, 2011, Reproductive biomedicine online.

Effect of melatonin on the clinical outcome of patients with repeated cycles after failed cycles of in vitro fertilization and intracytoplasmic sperm injection.

Yu Cao, R. Huo, Kaijuan Wang, 2021, Zygote (Cambridge. Print).

Analyses of growth differentiation factor 9 (GDF9) and bone morphogenetic protein 15 (BMP15) mutation in Chinese women with premature ovarian failure

Binbin Wang, Jing Wang, Xu Ma, 2010, Clinical endocrinology.