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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2008 1
2010 1
2011 1
2012 3
2013 5
2014 6
2015 8
2016 10
2017 18
2018 26
2019 39
2020 47
2021 18
2022 29
2023 15
2024 7

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211 results

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Page 1
The mechanism of acentrosomal spindle assembly in human oocytes.
Wu T, Dong J, Fu J, Kuang Y, Chen B, Gu H, Luo Y, Gu R, Zhang M, Li W, Dong X, Sun X, Sang Q, Wang L. Wu T, et al. Among authors: kuang y. Science. 2022 Nov 18;378(6621):eabq7361. doi: 10.1126/science.abq7361. Epub 2022 Nov 18. Science. 2022. PMID: 36395215
Karyopherin α deficiency contributes to human preimplantation embryo arrest.
Wang W, Miyamoto Y, Chen B, Shi J, Diao F, Zheng W, Li Q, Yu L, Li L, Xu Y, Wu L, Mao X, Fu J, Li B, Yan Z, Shi R, Xue X, Mu J, Zhang Z, Wu T, Zhao L, Wang W, Zhou Z, Dong J, Li Q, Jin L, He L, Sun X, Lin G, Kuang Y, Wang L, Sang Q. Wang W, et al. Among authors: kuang y. J Clin Invest. 2023 Jan 17;133(2):e159951. doi: 10.1172/JCI159951. J Clin Invest. 2023. PMID: 36647821 Free PMC article.
Mutations in TUBB8 and Human Oocyte Meiotic Arrest.
Feng R, Sang Q, Kuang Y, Sun X, Yan Z, Zhang S, Shi J, Tian G, Luchniak A, Fukuda Y, Li B, Yu M, Chen J, Xu Y, Guo L, Qu R, Wang X, Sun Z, Liu M, Shi H, Wang H, Feng Y, Shao R, Chai R, Li Q, Xing Q, Zhang R, Nogales E, Jin L, He L, Gupta ML Jr, Cowan NJ, Wang L. Feng R, et al. Among authors: kuang y. N Engl J Med. 2016 Jan 21;374(3):223-32. doi: 10.1056/NEJMoa1510791. N Engl J Med. 2016. PMID: 26789871 Free PMC article.
Large-scale analysis of de novo mutations identifies risk genes for female infertility characterized by oocyte and early embryo defects.
Li Q, Zhao L, Zeng Y, Kuang Y, Guan Y, Chen B, Xu S, Tang B, Wu L, Mao X, Sun X, Shi J, Xu P, Diao F, Xue S, Bao S, Meng Q, Yuan P, Wang W, Ma N, Song D, Xu B, Dong J, Mu J, Zhang Z, Fan H, Gu H, Li Q, He L, Jin L, Wang L, Sang Q. Li Q, et al. Among authors: kuang y. Genome Biol. 2023 Apr 6;24(1):68. doi: 10.1186/s13059-023-02894-0. Genome Biol. 2023. PMID: 37024973 Free PMC article.
ADGB variants cause asthenozoospermia and male infertility.
Qu R, Zhang Z, Wu L, Li Q, Mu J, Zhao L, Yan Z, Wang W, Zeng Y, Liu R, Dong J, Li Q, Sun X, Wang L, Sang Q, Chen B, Kuang Y. Qu R, et al. Among authors: kuang y. Hum Genet. 2023 Jun;142(6):735-748. doi: 10.1007/s00439-023-02546-0. Epub 2023 Mar 30. Hum Genet. 2023. PMID: 36995441
Mutations in CCIN cause teratozoospermia and male infertility.
Fan Y, Huang C, Chen J, Chen Y, Wang Y, Yan Z, Yu W, Wu H, Yang Y, Nie L, Huang S, Wang F, Wang H, Hua Y, Lyu Q, Kuang Y, Lei M. Fan Y, et al. Among authors: kuang y. Sci Bull (Beijing). 2022 Oct 31;67(20):2112-2123. doi: 10.1016/j.scib.2022.09.026. Epub 2022 Sep 26. Sci Bull (Beijing). 2022. PMID: 36546111 Free article.
211 results