| The molecular mechanism of sex hormones on Sertoli cell development and proliferation W Shah, R Khan, B Shah, A Khan, S Dil, W Liu, J Wen, X Jiang Frontiers in endocrinology 12, 648141, 2021 | 63 | 2021 |
| Novel loss‐of‐function variants in DNAH17 cause multiple morphological abnormalities of the sperm flagella in humans and mice B Zhang, I Khan, C Liu, A Ma, A Khan, Y Zhang, H Zhang, MBS Kakakhel, ... Clinical Genetics 99 (1), 176-186, 2021 | 43 | 2021 |
| Novel biallelic loss-of-function mutations in CFAP43 cause multiple morphological abnormalities of the sperm flagellum in Pakistani families I Khan, B Shah, S Dil, N Ullah, JT Zhou, DR Zhao, YW Zhang, XH Jiang, ... Asian Journal of Andrology 23 (6), 627-632, 2021 | 16 | 2021 |
| Loss-of-function mutations in CFAP57 cause multiple morphological abnormalities of the flagella in humans and mice A Ma, J Zhou, H Ali, T Abbas, I Ali, Z Muhammad, S Dil, J Chen, X Huang, ... JCI insight 8 (3), 2023 | 15 | 2023 |
| Evolutionarily conserved and testis-specific gene, 4930524B15Rik, is not essential for mouse spermatogenesis and fertility R Khan, J Ye, A Yousaf, W Shah, A Aftab, B Shah, Q Zaman, M Zubair, ... Molecular biology reports 47, 5207-5213, 2020 | 13 | 2020 |
| 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 |
| 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 |
| Loss-of-function variants in KCTD19 cause non-obstructive azoospermia in humans J Liu, F Rahim, J Zhou, S Fan, H Jiang, C Yu, J Chen, J Xu, G Yang, ... Iscience 26 (7), 2023 | 4 | 2023 |
| 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 | 3 | 2024 |
| A recessive ACTL7A founder variant leads to male infertility due to acrosome detachment in Pakistani Pashtuns J Zhou, B Zhang, A Zeb, A Ma, J Chen, D Zhao, F Rahim, R Khan, ... Clinical Genetics 104 (5), 564-570, 2023 | 2 | 2023 |
| Knockout of the family with sequence similarity 181, member A (Fam181a) gene does not impair spermatogenesis or male fertility in the mouse W Shah, R Khan, B Shah, S Dil, Q Shi Reproduction, Fertility and Development 33 (10), 674-681, 2021 | 2 | 2021 |
| Novel homozygous SPAG17 variants cause human male infertility through multiple morphological abnormalities of spermatozoal flagella related to axonemal microtubule doublets T Liu, F Rahim, ML Yang, M Uddin, JW Ye, I Ali, Y Raza, A Mansoor, ... Asian Journal of Andrology, 10.4103, 2024 | | 2024 |
| Cornichon protein CNIH4 is not essential for mice gametogenesis and fertility S Dil, J Ye, H Ma, A Unar, I Khan, A Ali, K Khan, Y Menglei, A Ma, B Shah, ... Developmental Biology 496, 15-23, 2023 | | 2023 |
