Pharmacogenetic variants in the DPYD, TYMS, CDA and MTHFR genes are clinically significant predictors of fluoropyrimidine toxicity von Loganayagam, A, Arenas Hernandez, M, Corrigan, A, Fairbanks, L, Lewis, C M, Harper, P, Maisey, N, Ross, P, Sanderson, J D, Marinaki, A M

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Review article: malignancy on thiopurine treatment with special reference to inflammatory bowel disease von Smith, M. A., Irving, P. M., Marinaki, A. M., Sanderson, J. D.

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Novel pharmacogenetic markers for treatment outcome in azathioprine‐treated inflammatory bowel disease von SMITH, M. A., MARINAKI, A. M., ARENAS, M., SHOBOWALE‐BAKRE, M., LEWIS, C. M., ANSARI, A., DULEY, J., SANDERSON, J. D.

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Assessment of thiopurine methyltransferase enzyme activity is superior to genotype in predicting myelosuppression following azathioprine therapy in patients with inflammatory bowel... von WINTER, J. W., GAFFNEY, D., SHAPIRO, D, SPOONER, R. J., MARINAKI, A. M., SANDERSON, J. D., MILLS, P. R.

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Methotrexate polyglutamates as a marker of patient compliance and clinical response in psoriasis: a single-centre prospective study von Woolf, R.T., West, S.L., Arenas-Hernandez, M., Hare, N., Peters van Ton, A.M., Lewis, C.M., Marinaki, A.M., Barker, J.N.W.N, Smith, C.H.

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Mechanism of allopurinol induced TPMT inhibition von Blaker, P.A., Arenas-Hernandez, M., Smith, M.A., Shobowale-Bakre, E.A., Fairbanks, L., Irving, P.M., Sanderson, J.D., Marinaki, A.M.

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Genotyping before azathioprine administration in dermatology von Shipman, K. E., Shipman, A. R., Marinaki, A. M.

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unusual genetic variant in the MOCS1 gene leads to complete missplicing of an alternatively spliced exon in a patient with molybdenum cofactor deficiency von Arenas, M, Fairbanks, L. D, Vijayakumar, K, Carr, L, Escuredo, E, Marinaki, A. M

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The effect of pre‐operative anxiety on induction of anaesthesia with propofol von Morley, A. P., Papageorgiou, C. H., Marinaki, A. M., Cooper, D. J., Lewis, C. M.

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Pharmacogenetics of pemetrexed combination therapy in lung cancer: pathway analysis reveals novel toxicity associations von Corrigan, A, Walker, J L, Wickramasinghe, S, Hernandez, M A, Newhouse, S J, Folarin, A A, Lewis, C M, Sanderson, J D, Spicer, J, Marinaki, A M

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A practical guide to the use of thiopurines in oral medicine von Hullah, E. A., Blaker, P. A., Marinaki, A. M., Escudier, M. P., Sanderson, J. D.

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Do ITPA and TPMT genotypes predict the development of side effects to AZA? von Duley, J A, Marinaki, A M, Arenas, M, Florin, T H J

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Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency von SUMI, Satoshi, MARINAKI, Anthony M, SIMMONDS, H. Anne, DULEY, John A, ARENAS, Monica, FAIRBANKS, Lynette, SHOBOWALE-BAKRE, Monsor, REES, David C, SWEE LAY THEIN, ANSARI, Azhar, SANDERSON, Jeremy, DE ABREU, Ronney A

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Deoxyuridine accumulation in urine in thymidine phosphorylase deficiency (MNGIE) von Fairbanks, L. D., Marinaki, A. M., Carrey, E. A., Hammans, S. R., Duley, J. A.

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Does genetic variability in aldehyde oxidase and molybdenum cofactor sulfurase predict nonresponse to allopurinol? von Roberts, R. L., Zhang, M., Marinaki, A. M., Stamp, L. K.

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A biochemical mechanism for the role of allopurinol in TMPT inhibition von Blaker, P A, Arenas, M, Fairbanks, L, Irving, P, Marinaki, A M, Sanderson, J

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Pitfalls in the determination of mutant alleles of the thiopurine methyltransferase gene von Brouwer, C, Marinaki, A M, Lambooy, L H, Duley, J A, Shobowale-Bakre, M, De Abreu, R A

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Familial juvenile hyperuricaemic nephropathy von Fairbanks, L.D., Marinaki, A.M., Simmonds, H.A., Cameron, J.S.

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Recessive congenital methaemoglobinaemia type II, a new mutation which causes incorrect splicing in the NADH‐cytochrome b5 reductase gene von Owen, E. P., Berens, J., Marinaki, A. M., Ipp, H., Harley, E. H.

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Genetic basis of hemolytic anemia caused by pyrimidine 5′ nucleotidase deficiency von Marinaki, Anthony M., Escuredo, Emilia, Duley, John A., Simmonds, H. Anne, Amici, Adolfo, Naponelli, Valeria, Magni, Giulio, Seip, Martin, Ben-Bassat, Isaac, Harley, Eric H., Thein, Swee Lay, Rees, David C.

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