Dr Rashid Hussain

Research Associate

School of Pharmacy and Biomedical Science

College of Health


Year Citation
2025 Ricos, M. G., Cole, B. A., Hussain, R., Rychkov, G. Y., Shaukat, Z., Pilati, N., . . . Lippiat, J. D. (2025). Identification of new KCNT1-epilepsy drugs by In silico, cell, and drosophila modeling. Annals Of Neurology, online(6), 1-14.
DOI
2024 Hussain, R., Lim, C. X., Shaukat, Z., Islam, A., Caseley, E. A., Lippiat, J. D., . . . Dibbens, L. M. (2024). Drosophila expressing mutant human KCNT1 transgenes make an effective tool for targeted drug screening in a whole animal model of KCNT1-epilepsy. Scientific Reports, 14(1, article no. 3357), 3357-1-3357-12.
DOI Scopus8 WoS8 Europe PMC8
2024 Islam, A., Shaukat, Z., Hussain, R., Ricos, M. G., Dibbens, L. M., & Gregory, S. L. (2024). Aneuploidy is linked to neurological phenotypes through oxidative stress. Journal of Molecular Neuroscience, 74(2, article no. 50), 1-11.
DOI Scopus1 WoS1
2024 Saidin, A., Cherepnalkovski, A. P., Shaukat, Z., Arsov, T., Hussain, R., Roberts, B. J., . . . Dibbens, L. M. (2024). A novel pathogenic TUBA1A variant in a Croatian infant is linked to a severe tubulinopathy with Walker-Warburg-like features. Genes, 15(8), 1-11.
DOI
2023 Islam, A., Shaukat, Z., Newman, D. L., Hussain, R., Ricos, M. G., Dibbens, L., & Gregory, S. L. (2023). Chromosomal instability causes sensitivity to polyamines and one-carbon metabolism. Metabolites, 13(5, article no. 642), 1-14.
DOI Scopus2 WoS3 Europe PMC6
2022 Islam, A., Shaukat, Z., Hussain, R., & Gregory, S. L. (2022). One-carbon and polyamine metabolism as cancer therapy targets. Biomolecules, 12(12, article no. 1902), 1-24.
DOI Scopus17 WoS16 Europe PMC14
2022 Shaukat, Z., Byard, R. W., Vink, R., Hussain, R., Ricos, M. G., & Dibbens, L. M. (2022). Investigating genetic variants in microRNA regulators of Neurokinin-1 receptor in sudden infant death syndrome. Acta Paediatrica, 112(2), 4 pages.
DOI Scopus1 Europe PMC1
2022 Rychkov, G. Y., Shaukat, Z., Lim, C. X., Hussain, R., Roberts, B. J., Bonardi, C. M., . . . Dibbens, L. M. (2022). Functional effects of Epilepsy associated KCNT1 mutations suggest pathogenesis via aberrant inhibitory neuronal activity. International Journal of Molecular Sciences, 23(23, article no. 15133), 1-14.
DOI Scopus10 WoS9 Europe PMC12
2016 Shaukat, Z., Liu, D., Hussain, R., Khan, M., & Gregory, S. (2016). The role of JNK signalling in responses to oxidative DNA damage. Current drug targets, 17(2), 154-163.
DOI Scopus26 WoS24 Europe PMC23
2015 Liu, D., Shaukat, Z., Hussain, R., Khan, M., & Gregory, S. (2015). Drosophila as a model for chromosomal instability. AIMS Genetics, 2(1), 1-12.
DOI WoS21
2014 Shaukat, Z., Liu, D., Choo, A., Hussain, R., O'Keefe, L., Richards, R., . . . Gregory, S. (2014). Chromosomal instability causes sensitivity to metabolic stress. Oncogene, 34(31), 4044-4055.
DOI Scopus37 WoS36 Europe PMC37
2009 Niazi, G., Shaukat, Z., Masood, K., & Hussain, R. (2009). Novel human pathological mutations. Gene symbol: F9. Disease: Haemophilia B.. Human Genetics, 126(2), 332.
Scopus1

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