| 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 | 104 | 2020 |
| 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 | 34 | 2021 |
| 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 | 19 | 2020 |
| Novel frameshift mutation in STK33 is associated with asthenozoospermia and multiple morphological abnormalities of the flagella H Ma, B Zhang, A Khan, D Zhao, A Ma, J Zhou, I Khan, K Khan, H Zhang, ... Human Molecular Genetics 30 (21), 1977-1984, 2021 | 18 | 2021 |
| Biological and Phytochemicals Properties of Monotheca buxifolia: An Unexplored Medicinal Plant I Khan, JS Ali, I Ul-Haq, M Zia Pharmaceutical Chemistry Journal 54, 293-301, 2020 | 17 | 2020 |
| Biallelic Variants in CFAP61 Cause Multiple Morphological Abnormalities of the Flagella and Male Infertility A Ma, A Zeb, I Ali, D Zhao, A Khan, B Zhang, J Zhou, R Khan, H Zhang, ... Frontiers in Cell and Developmental Biology 9, 803818, 2022 | 15 | 2022 |
| 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 | 13 | 2021 |
| Antimicrobial, cytotoxic, phytochemical and biological properties of crude extract and solid phase fractions of Monotheca buxifolia JS Ali, I Khan, M Zia Advances in Traditional Medicine 20, 115-122, 2020 | 13 | 2020 |
| Biallelic HFM1 variants cause non-obstructive azoospermia with meiotic arrest in humans by impairing crossover formation to varying degrees X Xie, G Murtaza, Y Li, J Zhou, J Ye, R Khan, L Jiang, I Khan, M Zubair, ... Human Reproduction 37 (7), 1664-1677, 2022 | 12 | 2022 |
| A recurrent homozygous missense mutation in CCDC103 causes asthenoteratozoospermia due to disorganized dynein arms M Zubair, R Khan, A Ma, U Hameed, M Khan, T Abbas, R Ahmad, JT Zhou, ... Asian Journal of Andrology 24 (3), 255-259, 2022 | 11 | 2022 |
| Normal spermatogenesis and fertility in Ddi1 (DNA damage inducible 1) mutant mice A Yousaf, Y Wu, R Khan, W Shah, I Khan, Q Shi, X Jiang Reproductive Biology 20 (4), 520-524, 2020 | 10 | 2020 |
| 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 | 8 | 2021 |
| In silico analysis of a novel pathogenic variant c.7G > A in C14orf39 gene identified by WES in a Pakistani family with azoospermia H Ali, A Unar, M Zubair, S Dil, F Ullah, I Khan, A Hussain, Q Shi Molecular Genetics and Genomics 297 (3), 719-730, 2022 | 6 | 2022 |
| M1AP interacts with the mammalian ZZS complex and promotes male meiotic recombination Y Li, Y Wu, I Khan, J Zhou, Y Lu, J Ye, J Liu, X Xie, C Hu, H Jiang, S Fan, ... EMBO reports 24 (2), e55778, 2023 | 5 | 2023 |
| Antioxidant, cytotoxicity, protein kinase inhibition and antibacterial activities of Fragaria× ananassa leaves. I Khan, S Tabassum, M Ikram, M Zia Pakistan Journal of Pharmaceutical Sciences 31 (4), 2018 | 5 | 2018 |
| A novel homozygous variant in homologous recombination repair gene ZSWIM7 causes azoospermia in males and primary ovarian insufficiency in females S Hussain, S Nawaz, I Khan, N Khan, S Hussain, I Ullah, KA Fakhro, ... European Journal of Medical Genetics 65 (11), 104629, 2022 | 4 | 2022 |
| Testis-specific fascin component FSCN3 is dispensable for mouse spermatogenesis and fertility H Ali, A Unar, S Dil, I Ali, K Khan, I Khan, Q Shi Molecular Biology Reports 49 (7), 6261-6268, 2022 | 4 | 2022 |
| Identification and Functional Investigation of Novel Heterozygous HELQ Mutations in Patients with Sertoli Cell-only Syndrome G Murtaza, L Yang, I Khan, A Unar, M Khan, Z Huan, R Khan, Q Shi Genetic Testing and Molecular Biomarkers 25 (10), 654-659, 2021 | 4 | 2021 |
| A Comprehensive Review on Various Aspects of Genetic Disorders A Khan, I Khan, K Zahid, G Nabi Journal of Biology and Life Science 6 (2), 110-118, 2015 | 3 | 2015 |
| A novel homozygous TSGA10 missense variant causes acephalic spermatozoa syndrome in a Pakistani family K Khan, X Zhang, S Dil, I Khan, A Unar, J Ye, A Zeb, M Zubair, W Shah, ... Basic and Clinical Andrology 34 (1), 4, 2024 | | 2024 |
