Paul J Thornalley
Director and Chief Scientific Officer
Professor Paul J Thornalley received his BSc Chemistry from the University of Manchester, Manchester, UK, in 1979 and D Phil Biochemistry in 1982 from University of Oxford, Oxford, UK. He was Scientific Director, Diabetes Research Center, Qatar Biomedical Research Institute, Hamad Bin Khalifa University (HBKU), Doha, Qatar. Qatar, from 2018 – 2023 and Adjunct Professor, College of Health & Life Sciences, HBKU, Doha, Qatar, from 2023 – 2025.
He is a leading researcher and advocate in studies of the pathogenesis associated with hyperglycemia and also the reactive glucose-derived metabolite, methylglyoxal, and its metabolism by glyoxalase 1 (Glo1) of the glyoxalase system – in which he is considered founding investigator. He recently developed the “Hexokinase-linked glycolytic overload and unscheduled glycolysis” hypothesis of hyperglycemia-induced impaired incretin effect and pathogenesis in hepatic and peripheral insulin resistance, beta-cell glucotoxicity, type 2 diabetes and diabetic vascular complications. He also identified increased methylglyoxal as a major physiological activator of the unfolded protein response. He originated the strategy for development of small molecule inducers of Glo1 expression or “Glo1 inducer” therapeutics for treatment of insulin resistance and microvascular complications of diabetes. This was proven effective in correcting insulin resistance in subjects living with overweight and obesity in clinical trial. He is founder and Chair of the Reactive Metabolites in Diabetes Study Group, 2014 – date. He has 586 research publications with over 46,000 citations; h-index 112 (Google Scholar) and in the top 1% of scientists globally by citation number (AD Scientific index).
Some recent papers
- Naila Rabbani and Paul J Thornalley (2021) Protein glycation – emerging evidence as biomarkers of metabolic dysfunction and early-stage decline in health in the era of precision medicine. Redox Biology 42, 101920.
- Murphy, M.P., Bayir, H., Belousov, V., Chang, C.J., Davies, K.J.A., Davies, M.J., Dick, T.P., Finkel, T., Forman, H.J., Janssen-Heininger, Y., Gems, D., Kagan, V.E., Kalyanaraman, B., Larsson, N.-G., Milne, G.L., Nyström, T., Poulsen, H.E., Radi, R., Van Remmen, H., Schumacker, P.T., Thornalley, P.J., Toyokuni, S., Winterbourn, C.C., Yin, H. and Halliwell, B. (2022) CONSENSUS STATEMENT Guidelines for measuring reactive oxygen species and oxidative damage in cells and in vivo. Nature Metabolism 4, 651 – 662
- Xue, M., Rabbani, N. and Thornalley, P.J. (2024) Increased cellular protein modification by methylglyoxal activates three sensors of the unfolded protein response. Redox Biol. 65, 103025.
- Al-Saei, A.N.J.M., Eldine, W.N., Rajpoot, K., Arshad, N., Al-Shammari, A.R., Kamal, M., Al-Shabeeb Akil, A., Fakhro, K.A., Thornalley, P.J. and Rabbani, N. (2023) Validation of plasma protein glycation and oxidation biomarkers for the diagnosis of autism. Molecular Psychiatry 29, 653 – 659.
- Rabbani, N. and Thornalley, P.J. (2024) Hexokinase-linked glycolytic overload and unscheduled glycolysis in hyperglycemia-induced pathogenesis in insulin resistance, beta-cell glucotoxicity and diabetic vascular complications. Frontiers in Endocrinology 14, 268308.
- Rabbani, N. and Thornalley, P.J. (2024) Unravelling the impaired incretin effect in obesity and type 2 diabetes: key role of hyperglycemia-induced unscheduled glycolysis and glycolytic overload. Diabetes Res. Clin. Pract., 217, 111905
- Solaiman, B., Ghaly, M., Househ, M., Ismail, S., Mifsud, B., Thornalley, P. J. and Dieng, F. (2025) Research Guidelines for Healthcare AI Development. Available at http://dx.doi.org/10.2139/ssrn.5216892