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Marinaki, AM, Champion, M, Kurian, MA, Simmonds, HA, Marie, S, Vincent, MF, van den Berghe, G, Duley, JA and Fairbanks, LD (2004) Adenylosuccinate lyase deficiency - First British case. Nucleosides Nucleotides & Nucleic Acids, 23 8-9: 1231-1233. doi:10.1081/NCN-200027494 103   10 Cited 12 times in Scopus12 0
Marinaki, AM, Ansari, A, Duley, JA, Arenas, M, Sumi, S, Lewis, CM, Shobowale-Bakre, EM, Escuredo, E, Fairbanks, LD and Sanderson, JD (2004) Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase). Pharmacogenetics, 14 3: 181-187. doi:10.1097/01.fpc0000114709.42625.5d 273   179 Cited 196 times in Scopus196 0
Marinaki, AM, Sumi, S, Arenas, M, Fairbanks, L, Harihara, S, Shimizu, K, Ueta, A and Duley, JA (2004) Allele frequency of inosine triphosphate pyrophosphatase gene polymorphisms in a Japanese population. Nucleosides Nucleotides & Nucleic Acids, 23 8-9: 1399-1401. doi:10.1081/NCN-200027641 76   18 Cited 17 times in Scopus17 3
Carrey, EA, Smolenski, RT, Edbury, SM, Laurence, A, Marinaki, AM, Duley, JA, Zhu, LM, Goldsmith, DJA and Simmonds, HA (2004) An unusual pyridine nucleotide accumulating in erythrocytes: Its identity and positive correlation with degree of renal failure. Nucleosides Nucleotides & Nucleic Acids, 23 8-9: 1135-1139. doi:10.1081/NCN-200027391 37   7 Cited 7 times in Scopus7 0
Fairbanks, LD, Marinaki, AM, Carrey, EA, Hammans, SR and Duley, JA (2002) Deoxyuridine accumulation in urine in thymidine phosphorylase deficiency (MNGIE). Journal of Inherited Metabolic Disease, 25 7: 603-604. doi:10.1023/A:1022007827133 65   10 Cited 12 times in Scopus12 0
Duley, JA, Marinaki, AM, Arenas, M and Florin, THJ (2006) Do ITPA and TPMT genotypes predict the development of side effects to AZA?. Gut, 55 7: 1048-1048. 37   4 Cited 6 times in Scopus6
Sumi, S, Marinaki, AM, Arenas, M, Fairbanks, L, Shobowale-Bakre, M, Rees, DC, Thein, SL, Ansari, A, Sanderson, J, De Abreu, RA, Simmonds, HA and Duley, JA (2002) Genetic basis of inosine triphosphate pyrophosphohydrolase deficiency. Human Genetics, 111 4-5: 360-367. doi:10.1007/s00439-002-0798-z 166   129 Cited 139 times in Scopus139 3
Arenas, M, Duley, JA, Ansari, A, Shobowale-Bakre, EA, Fairbanks, L, Soon, SY, Sanderson, J and Marinaki, AM (2004) Genetic determinants of the pre- and post-azathioprine therapy thiopurine methyltransferase activity phenotype. Nucleosides Nucleotides & Nucleic Acids, 23 8-9: 1403-1405. doi:10.1081/NCN-200027643 47   14 Cited 17 times in Scopus17 0
Marinaki, AM, Arenas, M, Khan, ZH, Lewis, CM, Shobowale-Bakre, EM, Escuredo, E, Fairbanks, LD, Mayberry, JF, Wicks, AC, Ansari, A, Sanderson, J and Duley, JA (2003) Genetic determinants of the thiopurine methyltransferase intermediate activity phenotype in British Asians and Caucasians. Pharmacogenetics, 13 2: 97-105. doi:10.1097/00008571-200302000-00006 70   37 Cited 40 times in Scopus40 0
Arenas, M, Simpson, G, Lewis, CM, Shobowale-Bakre, EM, Escuredo, E, Fairbanks, LD, Duley, JA, Ansari, A, Sanderson, JD and Marinaki, AM (2005) Genetic variation in the MTHFR gene influences thiopurine methyltransferase activity. Clinical Chemistry, 51 12: 2371-2374. doi:10.1373/clinchem.2005.053157 54   29 Cited 29 times in Scopus29 0
Marinaki, AM, Duley, JA, Arenas, M, Ansari, A, Sumi, S, Lewis, CM, Shobowale-Bakre, M, Fairbanks, LD and Sanderson, J (2004) Mutation in the ITPA gene predicts intolerance to azathioprine. Nucleosides Nucleotides & Nucleic Acids, 23 8-9: 1393-1397. doi:10.1081/NCN-200027639 65   30 Cited 37 times in Scopus37 3
Carrey, EA, Smolenski, RT, Edbury, SM, Laurence, A, Marinaki, AM, Duley, JA, Zhu, LM, Goldsmith, DJA and Simmonds, HA (2003) Origin and characteristics of an unusual pyridine nucleotide accumulating in erythrocytes: positive correlation with degree of renal failure. Clinica Chimica Acta, 335 1-2: 117-129. doi:10.1016/S0009-8981(03)00294-8 43   19 Cited 18 times in Scopus18 0
Khan, ZH, Marinaki, AM, Bakre, MS, Duley, JA, Mayberry, JF and Wicks, AC (2000). Thiopurine methyltransferase activity and genetic polymorphism among British Asian patients with inflammatory bowel disease.. In: Gastroenterology. , , (A333-A333). .     0