| The human RNA-binding protein and E3 ligase MEX-3C binds the MEX-3–recognition element (MRE) motif with high affinity L Yang, C Wang, F Li, J Zhang, A Nayab, J Wu, Y Shi, Q Gong Journal of Biological Chemistry 292 (39), 16221-16234, 2017 | 26 | 2017 |
| Case report: biallelic variant in the tRNA methyltransferase domain of the AlkB homolog 8 causes syndromic intellectual disability A Waqas, A Nayab, S Shaheen, S Abbas, M Latif, MM Rafeeq, ... Frontiers in Genetics 13, 878274, 2022 | 16 | 2022 |
| Targeted exome sequencing identified a novel frameshift variant in the PGAM2 gene causing glycogen storage disease type X A Nayab, Q Alam, OR Alzahrani, R Khan, S Sarfaraz, AA Albaz, ... European Journal of Medical Genetics 64 (9), 104283, 2021 | 13 | 2021 |
| Clinical genetics of spondylocostal dysostosis: A mini review M Umair, M Younus, S Shafiq, A Nayab, M Alfadhel Frontiers in Genetics 13, 996364, 2022 | 8 | 2022 |
| Crystal Structure of Urate Oxidase from Bacillus Subtilis 168 A Nayab, SA Moududee, Y Shi, Y Jiang, Q Gong Crystallography Reports 64, 1126-1133, 2019 | 3 | 2019 |
| Expanding the Genetic and Mutation Spectrum of ASPM-associated Neurodevelopmental Disorders T Afsar, S Khan, A Nayab, A Waqas, A Mahmood, M Umair, S Razak Journal of Disability Research 2 (3), 24-31, 2023 | | 2023 |
| A Novel Variant in the PAX4 Gene Causes Maturity-Onset Diabetes of the Young (MODY), Type IX with Neurodevelopmental Disorder T Afsar, A Waqas, A Nayab, S Abbas, A Mahmood, M Umair, S Razak Journal of Disability Research 2 (2), 18-24, 2023 | | 2023 |
| Uncovering the genetic basis of hyperphosphatasia with impaired intellectual development syndrome type 2: identification of a novel biallelic nonsense mutation in PIGO gene A Nayab, S Andleeb, S Zeb, HY Manzoor, Z Zehri, A Mahmood, H Khan, ... Growth 3, 6, 2023 | | 2023 |
