Sha Y - Search Results

1

CCDC9 is identified as a novel candidate gene of severe asthenozoospermia.

Sha Y, Xu Y, Wei X, Liu W, Mei L, Lin S, Ji Z, Wang X, Su Z, Qiu P, Chen J, Wang X. Sha Y, et al. Syst Biol Reprod Med. 2019 Dec;65(6):465-473. doi: 10.1080/19396368.2019.1655812. Epub 2019 Sep 10. Syst Biol Reprod Med. 2019. PMID: 31502483

2

A Case of Bilateral Testicular Tumors Subsequently Diagnosed as Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency.

Sha YK, Sha YW, Ding L, Liu WW, Song YQ, Lin J, He XM, Qiu PP, Zhang L, Li P. Sha YK, et al. Int J Fertil Steril. 2016 Jan-Mar;9(4):574-80. doi: 10.22074/ijfs.2015.4618. Epub 2015 Dec 23. Int J Fertil Steril. 2016. PMID: 26985347 Free PMC article.

3

Genetic factors contributing to human primary ciliary dyskinesia and male infertility.

Ji ZY, Sha YW, Ding L, Li P. Ji ZY, et al. Asian J Androl. 2017 Sep-Oct;19(5):515-520. doi: 10.4103/1008-682X.181227. Asian J Androl. 2017. PMID: 27270341 Free PMC article. Review.

4

A successful pregnancy by intracytoplasmic sperm injection using ejaculate sperm from an infertile man with 46, XX/46, XY true hermaphrodite.

Sha YW, Sha YK, Ding L, Lin SB, Ji ZY, Wang X, Song YQ, Li P. Sha YW, et al. Asian J Androl. 2017 Nov-Dec;19(6):721-722. doi: 10.4103/1008-682X.190329. Asian J Androl. 2017. PMID: 27905326 Free PMC article. No abstract available.

5

Diagnosis of a Chinese man with 45,X/46,X,i(Y)(q10)/47,X,i(Y) (q10) ×2 mosaic Turner syndrome.

Sha YW, Ding L, Ji ZY, Ge YS, Kong H, Zhang Q, Zhou YL, Li P. Sha YW, et al. Asian J Androl. 2018 Mar-Apr;20(2):205-207. doi: 10.4103/1008-682X.193162. Asian J Androl. 2018. PMID: 28091398 Free PMC article. No abstract available.

6

Comprehensive Genome Profiling of Single Sperm Cells by Multiple Annealing and Looping-Based Amplification Cycles and Next-Generation Sequencing from Carriers of Robertsonian Translocation.

Sha Y, Sha Y, Ji Z, Ding L, Zhang Q, Ouyang H, Lin S, Wang X, Shao L, Shi C, Li P, Song Y. Sha Y, et al. Ann Hum Genet. 2017 Mar;81(2):91-97. doi: 10.1111/ahg.12187. Ann Hum Genet. 2017. PMID: 28205220

7

Globozoospermic infertility associated with balanced DPY19L2 translocation/gene deletion at the chromosomal breakpoint.

Sha YW, Mei LB, Zheng LK, Tian RH, Ding L, Ji ZY, Zhang Q, Li P. Sha YW, et al. Asian J Androl. 2018 Mar-Apr;20(2):210-211. doi: 10.4103/1008-682X.196314. Asian J Androl. 2018. PMID: 28272055 Free PMC article. No abstract available.

8

Case study of a patient with cryptozoospermia associated with a recessive TEX15 nonsense mutation.

Wang X, Jin HR, Cui YQ, Chen J, Sha YW, Gao ZL. Wang X, et al. Asian J Androl. 2018 Jan-Feb;20(1):101-102. doi: 10.4103/1008-682X.194998. Asian J Androl. 2018. PMID: 28303806 Free PMC article. No abstract available.

9

DNAH1 gene mutations and their potential association with dysplasia of the sperm fibrous sheath and infertility in the Han Chinese population.

Sha Y, Yang X, Mei L, Ji Z, Wang X, Ding L, Li P, Yang S. Sha Y, et al. Fertil Steril. 2017 Jun;107(6):1312-1318.e2. doi: 10.1016/j.fertnstert.2017.04.007. Fertil Steril. 2017. PMID: 28577616 Free article.

10

A homozygous CEP135 mutation is associated with multiple morphological abnormalities of the sperm flagella (MMAF).

Sha YW, Xu X, Mei LB, Li P, Su ZY, He XQ, Li L. Sha YW, et al. Gene. 2017 Oct 30;633:48-53. doi: 10.1016/j.gene.2017.08.033. Epub 2017 Sep 1. Gene. 2017. PMID: 28866084

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