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2.Qin Y#, Zhang F, Chen ZJ*. BRCA2 in Ovarian Development and Function. N Engl J Med. 2019 Mar 14;380(11):1086.
3.Wang X, Zhang X, Dang Y, Li D, Lu G, Chan WY, Leung PCK, Zhao S,Qin Y*, Chen ZJ. Long noncoding RNA HCP5 participates in premature ovarian insufficiency by transcriptionally regulating MSH5 and DNA damage repair via YB1. Nucleic Acids Res. 2020 May 7;48(8):4480-4491.
4.Shao T#, Ke H#, Liu R, Xu L, Han S, Zhang X, Dang Y, Jiao X, Li W, Chen ZJ,Qin Y*, Zhao S*. Autophagy regulates differentiation of ovarian granulosa cells through degradation of WT1. Autophagy. 2022 Aug;18(8):1864-1878.
5.Yang Y#, Xu W#, Gao F#, Wen C, Zhao S, Yu Y, Jiao W, Mi X,Qin Y*, Chen ZJ*, Zhao S*. Transcription-replication conflicts in primordial germ cells necessitate the Fanconi anemia pathway to safeguard genome stability. Proc Natl Acad Sci U S A. 2022 Aug 23;119(34):e2203208119.
6.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 Jan 24;9(2):106.
7.Wang Y#, Guo T#, Ke H, Zhang Q, Li S, Luo W,Qin Y*. Pathogenic variants of meiotic double strand break (DSB) formation genes PRDM9 and ANKRD31 in premature ovarian insufficiency. Genet Med. 2021 Dec;23(12):2309-2315.
8.Jiao X, Ke H,Qin Y*, Chen ZJ*. Molecular Genetics of Premature Ovarian Insufficiency. Trends Endocrinol Metab. 2018 Nov;29(11):795-807.
9.Jiao X#, Zhang X#, Li N, Zhang D, Zhao S, Dang Y, Zanvit P, Jin W, Chen ZJ*, Chen W*,Qin Y*. Tregdeficiency-mediated TH1 response causes human premature ovarian insufficiency through apoptosis and steroidogenesis dysfunction of granulosa cells. Clin Transl Med. 2021 Jun;11(6):e448.
10.Zhang J, Yan L, Wang Y, Zhang S, Xu X, Dai Y, Zhao S, Li Z, Zhang Y, Xia G,Qin Y*, Zhang H*. In vivo and in vitro activation of dormant primordial follicles by EGF treatment in mouse and human. Clin Transl Med. 2020 Sep;10(5):e182.
11.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 Apr;113(4):845-852.
12.Li C#, Dang Y#, Li J, Li H, Zhu Y,Qin Y*. Preimplantation genetic testing is not a preferred recommendation for patients with X chromosome abnormalities. Hum Reprod. 2021 Aug 18;36(9):2612-2621.
13.Huang C, Guo T*,Qin Y*. Meiotic Recombination Defects and Premature Ovarian Insufficiency. Front Cell Dev Biol. 2021 Mar 8;9:652407.
14.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 Nov;235(11):8826-8838.
15.Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F*,Qin Y*, Chen X*. Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause. Hum Mol Genet. 2020 Sep 29;29(16):2698-2707.
16.Ke H, Hu J, Zhao L, Ding L, Jiao X*,Qin Y*. Impact of Thyroid Autoimmunity on Ovarian Reserve, Pregnancy Outcomes, and Offspring Health in Euthyroid Women Following In Vitro Fertilization/Intracytoplasmic Sperm Injection. Thyroid. 2020 Apr;30(4):588-597.
17.Luo W#, Guo T#, Li G, Liu R, Zhao S, Song M, Zhang L, Wang S, Chen ZJ,Qin Y*. Variants in Homologous Recombination Genes EXO1 and RAD51 Related with Premature Ovarian Insufficiency. J Clin Endocrinol Metab. 2020 Oct 1;105(10):dgaa505.
18.Zhang T#, Du X#, Zhao L#, He M, Lin L, Guo C, Zhang X, Han J, Yan H, Huang K, Sun G, Yan L, Zhou B, Xia G,Qin Y*, Wang C*. SIRT1 facilitates primordial follicle recruitment independent of deacetylase activity through directly modulating Akt1 and mTOR transcription. FASEB J. 2019 Dec;33(12):14703-14716.
19.Yang Y, Guo T, Liu R, Ke H, Xu W, Zhao S*,Qin Y*. FANCL gene mutations in premature ovarian insufficiency. Hum Mutat. 2020 May;41(5):1033-1041.