| A DNAH17 missense variant causes flagella destabilization and asthenozoospermia B Zhang, H Ma, T Khan, A Ma, T Li, H Zhang, J Gao, J Zhou, Y Li, C Yu, ... Journal of Experimental Medicine 217 (2), 2020 | 112 | 2020 |
| 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 | 95 | 2019 |
| RPL10L is required for male meiotic division by compensating for RPL10 during meiotic sex chromosome inactivation in mice L Jiang, T Li, X Zhang, B Zhang, C Yu, Y Li, S Fan, X Jiang, T Khan, ... Current Biology 27 (10), 1498-1505. e6, 2017 | 91 | 2017 |
| Syncytins expressed in human placental trophoblast RM Roberts, T Ezashi, LC Schulz, J Sugimoto, DJ Schust, T Khan, J Zhou Placenta, 2021 | 60 | 2021 |
| 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 |
| MOF influences meiotic expansion of H2AX phosphorylation and spermatogenesis in mice H Jiang, Q Gao, W Zheng, S Yin, L Wang, L Zhong, A Ali, T Khan, Q Hao, ... PLoS genetics 14 (5), e1007300, 2018 | 37 | 2018 |
| The product of BMP-directed differentiation protocols for human primed pluripotent stem cells is placental trophoblast and not amnion AS Seetharam, HTH Vu, S Choi, T Khan, MA Sheridan, T Ezashi, ... Stem Cell Reports 17 (6), 1289-1302, 2022 | 21 | 2022 |
| Single Nucleus RNA Sequence (snRNAseq) Analysis of the Spectrum of Trophoblast Lineages Generated From Human Pluripotent Stem Cells in vitro T Khan, AS Seetharam, J Zhou, NJ Bivens, DJ Schust, T Ezashi, G Tuteja, ... Frontiers in Cell and Developmental Biology 9, 695248, 2021 | 17 | 2021 |
| A novel stop-gain mutation in ARMC2 is associated with multiple morphological abnormalities of the sperm flagella I Khan, S Dil, H Zhang, B Zhang, T Khan, A Zeb, J Zhou, S Nawaz, ... Reproductive BioMedicine Online 43 (5), 913-919, 2021 | 11 | 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 |
| Leveraging Optimized Transcriptomic and Personalized Stem Cell Technologies to Better Understand Syncytialization Defects in Preeclampsia S Choi, T Khan, RM Roberts, DJ Schust Frontiers in Genetics 13, 872818, 2022 | 2 | 2022 |
| Fluorescence-activated nuclear sorting (FANS) of nuclei from in vitro-generated syncytiotrophoblast T Khan, JJ Whyte, LC Schulz, RM Roberts Placenta, 2024 | | 2024 |
