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Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.
J Genet Genomics. 2024 Feb;51(2):252-255. doi: 10.1016/j.jgg.2023.03.013. Epub 2023 Apr 14.
J Genet Genomics. 2024.
PMID: 37062450
No abstract available.
Rare variants in GPR3 in POI patients: a case series with review of literature.
Ren S, Zhang F, Shang L, Yang X, Pan Y, Zhang X, Wu Y.
Ren S, et al. Among authors: pan y.
J Ovarian Res. 2023 Nov 3;16(1):210. doi: 10.1186/s13048-023-01282-3.
J Ovarian Res. 2023.
PMID: 37919810
Free PMC article.
Review.
Item in Clipboard
Rare variants in FANCA induce premature ovarian insufficiency.
Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, Li G, Shang L, Yang J, Jin L, Shi Q, Wu Y.
Yang X, et al. Among authors: pan y.
Hum Genet. 2019 Dec;138(11-12):1227-1236. doi: 10.1007/s00439-019-02059-9. Epub 2019 Sep 18.
Hum Genet. 2019.
PMID: 31535215
Free PMC article.
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Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.
Li G, Yang X, Wang L, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, Wu Y, Zhang X, Zhang F.
Li G, et al. Among authors: pan y.
J Med Genet. 2022 Jun;59(6):579-588. doi: 10.1136/jmedgenet-2020-107398. Epub 2021 Apr 22.
J Med Genet. 2022.
PMID: 33888552
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Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.
Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X.
Wang Y, et al. Among authors: pan y.
Mol Genet Genomic Med. 2022 Jan;10(1):e1820. doi: 10.1002/mgg3.1820. Epub 2021 Nov 29.
Mol Genet Genomic Med. 2022.
PMID: 34845858
Free PMC article.
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Temporal transcriptomic landscape of postnatal mouse ovaries reveals dynamic gene signatures associated with ovarian aging.
Zhou Z, Yang X, Pan Y, Shang L, Chen S, Yang J, Jin L, Zhang F, Wu Y.
Zhou Z, et al. Among authors: pan y.
Hum Mol Genet. 2021 Oct 13;30(21):1941-1954. doi: 10.1093/hmg/ddab163.
Hum Mol Genet. 2021.
PMID: 34137841
Free PMC article.
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A heterozygous hypomorphic mutation of Fanca causes impaired follicle development and subfertility in female mice.
Pan Y, Yang X, Zhang F, Chen S, Zhou Z, Yin H, Ma H, Shang L, Yang J, Li G, Wang Y, Jin L, Shi Q, Wu Y.
Pan Y, et al.
Mol Genet Genomics. 2021 Jan;296(1):103-112. doi: 10.1007/s00438-020-01730-5. Epub 2020 Oct 6.
Mol Genet Genomics. 2021.
PMID: 33025164
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