A homozygous FANCM frameshift pathogenic variant causes male infertility H Yin, H Ma, S Hussain, H Zhang, X Xie, L Jiang, X Jiang, F Iqbal, ... Genetics in Medicine 21 (1), 62-70, 2019 | 98 | 2019 |
Specific Deletion of Cdh2 in Sertoli Cells Leads to Altered Meiotic Progression and Subfertility of Mice X Jiang, T Ma, Y Zhang, H Zhang, S Yin, W Zheng, L Wang, Z Wang, ... Biology of reproduction 92 (3), 79, 1-12, 2015 | 64 | 2015 |
The evolutionarily conserved genes: Tex37, Ccdc73, Prss55 and Nxt2 are dispensable for fertility in mice M Khan, N Jabeen, T Khan, HMJ Hussain, A Ali, R Khan, L Jiang, T Li, ... Scientific Reports 8 (1), 4975, 2018 | 48 | 2018 |
Histone acetyltransferase KAT8 is essential for mouse oocyte development by regulating reactive oxygen species levels S Yin, X Jiang, H Jiang, Q Gao, F Wang, S Fan, T Khan, N Jabeen, ... Development 144 (12), 2165-2174, 2017 | 43 | 2017 |
A TOP6BL mutation abolishes meiotic DNA double-strand break formation and causes human infertility Y Jiao, S Fan, N Jabeen, H Zhang, R Khan, G Murtaza, H Jiang, A Ali, Y Li, ... Science Bulletin 65 (24), 2120-2129, 2020 | 22 | 2020 |
Novel Loss-of-Function Mutations in DNAH1 Displayed Different Phenotypic Spectrum in Humans and Mice R Khan, Q Zaman, J Chen, M Khan, A Ma, J Zhou, B Zhang, A Ali, ... Frontiers in Endocrinology 12, 765639, 2021 | 14 | 2021 |
The deubiquitinating gene Usp29 is dispensable for fertility in male mice Z Huang, M Khan, J Xu, T Khan, H Ma, R Khan, HMJ Hussain, X Jiang, ... Science China Life Sciences 62, 544-552, 2019 | 9 | 2019 |
Whole exome sequencing identifies a novel dominant missense mutation underlying leukonychia in a Pakistani family T Khan, M Khan, A Yousaf, S Khan, M Naeem, A Shah, G Murtaza, A Ali, ... Journal of Human Genetics 63 (10), 1071-1076, 2018 | 8 | 2018 |
Whole exome sequencing revealed a novel nonsense variant in the GNRHR gene causing normosmic hypogonadotropic hypogonadism in a Pakistani family HMJ Hussain, G Murtaza, X Jiang, R Khan, M Khan, MBS Kakakhel, ... Hormone Research in Paediatrics 91 (1), 9-16, 2019 | 7 | 2019 |
A novel NPHP4 homozygous missense variant identified in infertile brothers with multiple morphological abnormalities of the sperm flagella A Ali, A Unar, Z Muhammad, S Dil, B Zhang, H Sadaf, M Khan, M Ali, ... Journal of Assisted Reproduction and Genetics 41 (1), 109-120, 2024 | 5 | 2024 |
Inactivation of testis-specific gene C4orf46 is dispensable for spermatogenesis and fertility in mouse B Shah, R Khan, W Shah, A Aftab, M Khan, S Dil, Q Shi Mammalian Genome 32 (5), 364-370, 2021 | 5 | 2021 |
Deficiency in a special dynein DNAH12 causes male infertility by impairing DNAH1 and DNALI1 recruitment in humans and mice M Yang, HMJ Hussain, M Khan, Z Muhammad, J Zhou, A Ma, X Huang, ... bioRxiv, 2024.06. 20.599934, 2024 | 2 | 2024 |