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For: Dou X, Guo T, Li G, Zhou L, Qin Y, Chen ZJ. Minichromosome maintenance complex component 8 mutations cause primary ovarian insufficiency. Fertil Steril 2016;106:1485-1489.e2. [PMID: 27573988 DOI: 10.1016/j.fertnstert.2016.08.018] [Cited by in Crossref: 23] [Cited by in F6Publishing: 20] [Article Influence: 3.8] [Reference Citation Analysis]
Number Citing Articles
1 Jiao X, Ke H, Qin Y, Chen Z. Molecular Genetics of Premature Ovarian Insufficiency. Trends in Endocrinology & Metabolism 2018;29:795-807. [DOI: 10.1016/j.tem.2018.07.002] [Cited by in Crossref: 70] [Cited by in F6Publishing: 62] [Article Influence: 17.5] [Reference Citation Analysis]
2 Wang F, Guo S, Li P. Two novel mutations in the MCM8 gene shared by two Chinese siblings with primary ovarian insufficiency and short stature. Mol Genet Genomic Med 2020;8:e1396. [PMID: 32652893 DOI: 10.1002/mgg3.1396] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
3 Huang C, Guo T, Qin Y. Meiotic Recombination Defects and Premature Ovarian Insufficiency. Front Cell Dev Biol 2021;9:652407. [PMID: 33763429 DOI: 10.3389/fcell.2021.652407] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
4 Liu R, Ke H, Shao T, Qin Y, Zhao S. TMEM150B is dispensable for oocyte maturation and female fertility in mouse. Sci Rep 2020;10:21381. [PMID: 33288838 DOI: 10.1038/s41598-020-78554-1] [Reference Citation Analysis]
5 Sun B, Yeh J. Onco-fertility and personalized testing for potential for loss of ovarian reserve in patients undergoing chemotherapy: proposed next steps for development of genetic testing to predict changes in ovarian reserve. Fertil Res Pract 2021;7:13. [PMID: 34193292 DOI: 10.1186/s40738-021-00105-7] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
6 Zhang X, Dang Y, Liu R, Zhao S, Ma J, Qin Y. MicroRNA-127-5p impairs function of granulosa cells via HMGB2 gene in premature ovarian insufficiency. J Cell Physiol 2020;235:8826-38. [PMID: 32391592 DOI: 10.1002/jcp.29725] [Cited by in Crossref: 5] [Cited by in F6Publishing: 6] [Article Influence: 2.5] [Reference Citation Analysis]
7 Li D, Xu W, Wang X, Dang Y, Xu L, Lu G, Chan WY, Leung PCK, Zhao S, Qin Y. lncRNA DDGC participates in premature ovarian insufficiency through regulating RAD51 and WT1. Mol Ther Nucleic Acids 2021;26:1092-106. [PMID: 34786213 DOI: 10.1016/j.omtn.2021.10.015] [Reference Citation Analysis]
8 Trofimova T, Lizneva D, Suturina L, Walker W, Chen Y, Azziz R, Layman LC. Genetic basis of eugonadal and hypogonadal female reproductive disorders. Best Practice & Research Clinical Obstetrics & Gynaecology 2017;44:3-14. [DOI: 10.1016/j.bpobgyn.2017.05.003] [Cited by in Crossref: 11] [Cited by in F6Publishing: 6] [Article Influence: 2.2] [Reference Citation Analysis]
9 Dondik Y, Lei Z, Gaskins J, Pagidas K. Minichromosome maintenance complex component 8 and 9 gene expression in the menstrual cycle and unexplained primary ovarian insufficiency. J Assist Reprod Genet 2019;36:57-64. [PMID: 30276597 DOI: 10.1007/s10815-018-1325-z] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 1.3] [Reference Citation Analysis]
10 Li J, Yu D, Liu L, Liang H, Ouyang Q, Liu Y. Structural study of the N-terminal domain of human MCM8/9 complex. Structure 2021:S0969-2126(21)00164-7. [PMID: 34043945 DOI: 10.1016/j.str.2021.05.006] [Reference Citation Analysis]
11 Veitia RA. Primary ovarian insufficiency, meiosis and DNA repair. Biomed J 2020;43:115-23. [PMID: 32381463 DOI: 10.1016/j.bj.2020.03.005] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
12 Zhang YX, He WB, Xiao WJ, Meng LL, Tan C, Du J, Lu GX, Lin G, Tan YQ. Novel loss-of-function mutation in MCM8 causes premature ovarian insufficiency. Mol Genet Genomic Med 2020;8:e1165. [PMID: 32048466 DOI: 10.1002/mgg3.1165] [Cited by in Crossref: 8] [Cited by in F6Publishing: 10] [Article Influence: 4.0] [Reference Citation Analysis]
13 Cioppi F, Rosta V, Krausz C. Genetics of Azoospermia. Int J Mol Sci 2021;22:3264. [PMID: 33806855 DOI: 10.3390/ijms22063264] [Cited by in Crossref: 4] [Cited by in F6Publishing: 5] [Article Influence: 4.0] [Reference Citation Analysis]
14 Xu X, Su S, Cao Y, Zhao S, Li W, Qin Y. Variation analysis of tousled like kinase 1 gene in patients with sporadic premature ovarian insufficiency. Gynecol Endocrinol 2020;36:33-5. [PMID: 31362519 DOI: 10.1080/09513590.2019.1630606] [Cited by in Crossref: 1] [Article Influence: 0.3] [Reference Citation Analysis]
15 Vo KCT, Kawamura K. Female Oncofertility: Current Understandings, Therapeutic Approaches, Controversies, and Future Perspectives. J Clin Med 2021;10:5690. [PMID: 34884393 DOI: 10.3390/jcm10235690] [Reference Citation Analysis]
16 Xu X, Zhang Y, Zhao S, Bian Y, Ning Y, Qin Y. Mutational analysis of theFAM175A gene in patients with premature ovarian insufficiency. Reprod Biomed Online 2019;38:943-50. [PMID: 31000350 DOI: 10.1016/j.rbmo.2019.02.006] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.3] [Reference Citation Analysis]
17 Ratnakumar A, Zimmerman SE, Jordan BA, Mar JC. Estrogen activates Alzheimer's disease genes. Alzheimers Dement (N Y) 2019;5:906-17. [PMID: 31890855 DOI: 10.1016/j.trci.2019.09.004] [Cited by in Crossref: 11] [Cited by in F6Publishing: 10] [Article Influence: 3.7] [Reference Citation Analysis]
18 Guo T, Zheng Y, Li G, Zhao S, Ma J, Qin Y. Novel pathogenic mutations in minichromosome maintenance complex component 9 (MCM9) responsible for premature ovarian insufficiency. Fertil Steril 2020;113:845-52. [PMID: 32145932 DOI: 10.1016/j.fertnstert.2019.11.015] [Cited by in Crossref: 10] [Cited by in F6Publishing: 7] [Article Influence: 5.0] [Reference Citation Analysis]
19 Kim S, Lee S, Park HT, Song JY, Kim T. Genomic Consideration in Chemotherapy-Induced Ovarian Damage and Fertility Preservation. Genes (Basel) 2021;12:1525. [PMID: 34680919 DOI: 10.3390/genes12101525] [Reference Citation Analysis]
20 Tang R, Yu Q. Novel variants in women with premature ovarian function decline identified via whole-exome sequencing. J Assist Reprod Genet 2020;37:2487-502. [PMID: 32789750 DOI: 10.1007/s10815-020-01919-y] [Cited by in Crossref: 5] [Cited by in F6Publishing: 5] [Article Influence: 2.5] [Reference Citation Analysis]
21 Dang Y, Wang X, Hao Y, Zhang X, Zhao S, Ma J, Qin Y, Chen ZJ. MicroRNA-379-5p is associate with biochemical premature ovarian insufficiency through PARP1 and XRCC6. Cell Death Dis 2018;9:106. [PMID: 29367615 DOI: 10.1038/s41419-017-0163-8] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 4.0] [Reference Citation Analysis]
22 Schmitz D, Ek WE, Berggren E, Höglund J, Karlsson T, Johansson Å. Genome-Wide Association Study of Estradiol Levels, and the Causal Effect of Estradiol on Bone Mineral Density. J Clin Endocrinol Metab 2021:dgab507. [PMID: 34255042 DOI: 10.1210/clinem/dgab507] [Cited by in F6Publishing: 2] [Reference Citation Analysis]
23 Yang Y, Zhao S, Qin Y. Response to “Should FANCL heterozygous pathogenic variants be considered as potentially causative of primary ovarian insufficiency?”. Human Mutation 2020;41:1700-1. [DOI: 10.1002/humu.24073] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]