中文

Journal Publications

[1]Wang X, Tan YQ*, Liu MF. Defective piRNA Processing and Azoospermia..N Engl J Med. 2022 Apr 28;386(17):1674-1675.
[2]Wang Y, Liu L, Tan C, Meng G, Meng L, Nie H, Du J, Lu GX, Lin G, He WB, Tan YQ*. Novel MEIOB variants cause primary ovarian insufficiency and non-obstructive azoospermia..Front Genet. 2022 Aug 5;13:936264., 2022
[3]Yuan S, Guo L, Cheng D, Li X, Hu H, Hu L, Lu G, Lin G, Gong F, Tan YQ*. The de novo aberration rate of prenatal karyotype was comparable between 1496 fetuses conceived via IVF/ICSI and 1396 fetuses from natural conception..J Assist Reprod Genet. 2022 Jul;39(7):1683-1689., 2022
[4]Wang W, Meng L, He J, Su L, Li Y, Tan C, Xu X, Nie H, Zhang H, Du J, Lu G, Luo M, Lin G, Tu C, Tan YQ*. Bi-allelic variants in SHOC1 cause non-obstructive azoospermia with meiosis arrest in humans and mice..Mol Hum Reprod. 2022 May 27;28(6):gaac015., 2022
[5]Xie C, Wang W, Tu C, Meng L, Lu G, Lin G, Lu LY, Tan YQ*. Meiotic recombination: insights into its mechanisms and its role in human reproduction with a special focus on non-obstructive azoospermia..Hum Reprod Update. 2022 May 25:dmac024., 2022
[6]Li L, Tan YQ*, Lu LY. Defective piRNA Processing and Azoospermia..N Engl J Med. 2022 Apr 28;386(17):1675-1676., 2022
[7]Hu T, Meng L, Tan C, Luo C, He WB, Tu C, Zhang H, Du J, Nie H, Lu GX, Lin G, Tan YQ*. Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia..J Med Genet. 2022 Apr 6:jmedgenet-2021-108249, 2022
[8]Tan C, Meng L, Lv M, He X, Sha Y, Tang D, Tan Y, Hu T, He W, Tu C, Nie H, Zhang H, Du J, Lu G, Fan LQ, Cao Y, Lin G, Tan YQ*. Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice..Am J Hum Genet, 2022, 109 (1) : 157-171.
[9]Tu C, Li H, Liu X, Wang Y, Li W, Meng L, Wang W, Li Y, Li D, Du J, Lu G, Lin G, Tan YQ*. TDRD7 participates in lens development and spermiogenesis by mediating autophagosome maturation.Autophagy, 2021, 17 (11) : 3848-3864.
[10]Tu C, Cong J, Zhang Q, He X, Zheng R, Yang X, Gao Y, Wu H, Lv M, Gu Y, Lu S, Liu C, Tian S, Meng L, Wang W, Tan C, Nie H, Li D, Zhang H, Gong F, Hu L, Lu G, Xu W, Lin G, Zhang F, Cao Y, Tan YQ*. Bi-allelic mutations of DNAH10 cause primary male infertility with asthenoteratozoospermia in humans and mice.Am J Hum Genet, 2021, 108 (8) : 1466.
[11]Liu C, Tu C, Wang L, Wu H, Houston BJ, Mastrorosa FK, Zhang W, Shen Y, Wang J, Tian S, Meng L, Cong J, Yang S, Jiang Y, Tang S, Zeng Y, Lv M, Lin G, Li J, Saiyin H, He X, Jin L, Touré A, Ray PF, Veltman JA, Shi Q, O'Bryan MK, Cao Y, Tan YQ*, Zhang F. Deleterious variants in X-linked CFAP47 induce asthenoteratozoospermia and primary male infertility.Am J Hum Genet, 2021, 108 (2) : 309-323.
[12]Lu S, Gu Y, Wu Y, Yang S, Li C, Meng L, Yuan W, Jiang T, Zhang X, Li Y, Wang C, Liu M, Ye L, Guo X, Shen H, Yang X, Tan Y*, Hu Z. Bi-allelic variants in human WDR63 cause male infertility via abnormal inner dynein arms assembly.Cell Discov, 2021, 7 (1) : 110.
[13]Hu TY, Zhang H, Meng LL, Yuan SM, Tu CF, Du J, Lu GX, Lin G, Nie HC, Tan YQ*. Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility[J].Hum Mutat., 2020: doi: 10.1002/humu.24138. Online ahead of print..
[14]Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ*. Genetic underpinnings of asthenozoospermia[J].Best Pract Res Clin Endocrinol Metab., 2020: 101472.
[15]Cheng D, Yuan S, Hu L, Yi D, Luo K, Gong F, Lu C, Lu G, Lin G, Tan YQ*. The genetic cause of intellectual deficiency and/or congenital malformations in two parental reciprocal translocation carriers and implications for assisted reproduction[J].J Assist Reprod Genet., 2020: doi: 10.1007/s10815-020-01986-1. Online ahead of print. PMID: 3309447..
[16]Li Y, Wang WL, Tu CF, Meng LL, Hu TY, Du J, Lin G, Nie HC, Tan YQ*. A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans[J].Asian J Androl., 2020: 19.doi: 10.4103/aja.aja_56_20.Online ahead of print. PMID: 33037173..
[17]Wang WL, Tu CF, Tan YQ*. Insight on multiple morphological abnormalities of sperm falgella in male infertility: what is new?.Asian J Androl, 2020, 22 (3) : 236-245.
[18]Tu C, Wang Y, Nie H, Meng L, Wang W, Li Y, Li D, Zhang H, Lu G, Lin G, Tan YQ*, Du J*. An M1AP homozygous splice-site mutation associated with severe oligozoospermia in a consanguineous family[J].Clin Genet, 2020, 97 (5) : 741-746.
[19]He WB, Tan C, Zhang YX, Meng LL, Gong F, Lu GX, Lin G, Du J, Tan YQ*. Homozygous variants in SYCP2L cause premature ovarian insufficiency.J Med Genet, 2020: doi: 10.1136/jmedgenet-2019-106789.
[20]Wang Y, Tu C, Nie H, Meng L, Li D, Wang W, Zhang H, Lu G, Lin G, Tan YQ*, Du J*. Novel DNAAF6 variants identified by whole-exome sequencing cause male infertility and primary ciliary dyskinesia[J].J Assist reprod Genet, 2020, 37 (4) : 811-820.

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