Hu TY - Search Results

1

Novel homozygous truncating variants in ZMYND15 causing severe oligozoospermia and their implications for male infertility.

Hu TY, Zhang H, Meng LL, Yuan SM, Tu CF, Du J, Lu GX, Lin G, Nie HC, Tan YQ. Hu TY, et al. Hum Mutat. 2021 Jan;42(1):31-36. doi: 10.1002/humu.24138. Epub 2020 Nov 15. Hum Mutat. 2021. PMID: 33169450

2

A novel homozygous frameshift mutation in MNS1 associated with severe oligoasthenoteratozoospermia in humans.

Li Y, Wang WL, Tu CF, Meng LL, Hu TY, Du J, Lin G, Nie HC, Tan YQ. Li Y, et al. Among authors: hu ty. Asian J Androl. 2021 Mar-Apr;23(2):197-204. doi: 10.4103/aja.aja_56_20. Asian J Androl. 2021. PMID: 33037173 Free PMC article.

3

Genetic underpinnings of asthenozoospermia.

Tu C, Wang W, Hu T, Lu G, Lin G, Tan YQ. Tu C, et al. Best Pract Res Clin Endocrinol Metab. 2020 Dec;34(6):101472. doi: 10.1016/j.beem.2020.101472. Epub 2020 Nov 6. Best Pract Res Clin Endocrinol Metab. 2020. PMID: 33191078 Review.

4

CFAP65 is required in the acrosome biogenesis and mitochondrial sheath assembly during spermiogenesis.

Wang W, Tian S, Nie H, Tu C, Liu C, Li Y, Li D, Yang X, Meng L, Hu T, Zhang Q, Du J, Fan L, Lu G, Lin G, Zhang F, Tan YQ. Wang W, et al. Hum Mol Genet. 2021 Nov 16;30(23):2240-2254. doi: 10.1093/hmg/ddab185. Hum Mol Genet. 2021. PMID: 34231842

5

Bi-allelic variants in DNHD1 cause flagellar axoneme defects and asthenoteratozoospermia in humans and mice.

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. Tan C, et al. Am J Hum Genet. 2022 Jan 6;109(1):157-171. doi: 10.1016/j.ajhg.2021.11.022. Epub 2021 Dec 20. Am J Hum Genet. 2022. PMID: 34932939 Free PMC article.

6

Biallelic CFAP61 variants cause male infertility in humans and mice with severe oligoasthenoteratozoospermia.

Hu T, Meng L, Tan C, Luo C, He WB, Tu C, Zhang H, Du J, Nie H, Lu GX, Lin G, Tan YQ. Hu T, et al. J Med Genet. 2023 Feb;60(2):144-153. doi: 10.1136/jmedgenet-2021-108249. Epub 2022 Apr 6. J Med Genet. 2023. PMID: 35387802

7

Novel homozygous variants in TTC12 cause male infertility with asthenoteratozoospermia owing to dynein arm complex and mitochondrial sheath defects in flagella.

Meng L, Liu Q, Tan C, Xu X, He W, Hu T, Tu C, Li Y, Du J, Zhang Q, Lu G, Fan LQ, Lin G, Nie H, Zhang H, Tan YQ. Meng L, et al. Front Cell Dev Biol. 2023 Jun 1;11:1184331. doi: 10.3389/fcell.2023.1184331. eCollection 2023. Front Cell Dev Biol. 2023. PMID: 37325566 Free PMC article.

8

A hemizygous loss-of-function variant in BCORL1 is associated with male infertility and oligoasthenoteratozoospermia.

Luo C, Chen Z, Meng L, Tan C, He W, Tu C, Du J, Lu GX, Lin G, Tan YQ, Hu TY. Luo C, et al. Among authors: hu ty. Clin Genet. 2024 Jul;106(1):27-36. doi: 10.1111/cge.14500. Epub 2024 Feb 11. Clin Genet. 2024. PMID: 38342987

9

The landscape of RNA binding proteins in mammalian spermatogenesis.

Li Y, Wang Y, Tan YQ, Yue Q, Guo Y, Yan R, Meng L, Zhai H, Tong L, Yuan Z, Li W, Wang C, Han S, Ren S, Yan Y, Wang W, Gao L, Tan C, Hu T, Zhang H, Liu L, Yang P, Jiang W, Ye Y, Tan H, Wang Y, Lu C, Li X, Xie J, Yuan G, Cui Y, Shen B, Wang C, Guan Y, Li W, Shi Q, Lin G, Ni T, Sun Z, Ye L, Vourekas A, Guo X, Lin M, Zheng K. Li Y, et al. Science. 2024 Oct 25;386(6720):eadj8172. doi: 10.1126/science.adj8172. Epub 2024 Oct 25. Science. 2024. PMID: 39208083

10

Blood-based diagnosis of pediatric tuberculosis: a prospective cohort study in South Africa and Dominican Republic.

Li L, Mao L, van der Zalm MM, Olivo J, Liu S, Vergara C, Palmer M, Shu Q, Demers AM, Lyon CJ, Goussard P, Schaaf HS, Hesseling AC, Nachman S, Pérez-Then E, Mitchell CD, Ghimenton E, Hu TY. Li L, et al. Among authors: hu ty. J Infect. 2025 Jan 2:106404. doi: 10.1016/j.jinf.2024.106404. Online ahead of print. J Infect. 2025. PMID: 39755278

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