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Biomarkers in Medicine|January 22, 2015
Getting the best out of thiopurine therapy: thiopurine S-methyltransferase and beyondSteven Chung Ming Fong, Paul Andrew Blaker, Monica Arenas-Hernandez, et al.
The Journal of Investigative Dermatology|April 6, 2007
Polymorphisms in folate, pyrimidine, and purine metabolism are associated with efficacy and toxicity of methotrexate in psoriasisEmanuela Campalani, Monica Arenas, Anthony M Marinaki, et al.
Clinical Kidney Journal|December 21, 2016
Adenine phosphoribosyltransferase deficiency in the United Kingdom: two novel mutations and a cross-sectional surveyGowrie S Balasubramaniam, Monica Arenas-Hernandez, Emilia Escuredo, et al.
Inflammatory Bowel Diseases|June 4, 2008
Further experience with the use of 6-thioguanine in patients with Crohn's diseaseAzhar Ansari, Tim Elliott, Farina Fong, et al.
Diagnostic Microbiology and Infectious Disease|February 11, 2021
Understanding false positives and the detection of SARS-CoV-2 using the Cepheid Xpert Xpress SARS-CoV-2 and BD MAX SARS-CoV-2 assaysDhammika H Navarathna, Shawn Sharp, Janell Lukey, et al.
Orphanet Journal of Rare Diseases|December 3, 2010
The diagnosis of inherited metabolic diseases by microarray gene expression profilingMonica Arenas Hernandez, Reiner Schulz, Tracy Chaplin, et al.
Pharmacogenetics|May 29, 2004
Adverse drug reactions to azathioprine therapy are associated with polymorphism in the gene encoding inosine triphosphate pyrophosphatase (ITPase)Anthony M Marinaki, Azhar Ansari, John A Duley, et al.
Pharmacogenetics and Genomics|April 15, 2008
Trinucleotide repeat variants in the promoter of the thiopurine S-methyltransferase gene of patients exhibiting ultra-high enzyme activityRebecca L Roberts, Richard B Gearry, Michael V Bland, et al.
Molecular Genetics and Metabolism|November 2, 2024
cPMP rescue of a neonate with severe molybdenum cofactor deficiency after serendipitous early diagnosis, and characterisation of a novel MOCS1 variantBernd C Schwahn, Claire Hart, Louisa Ann Smith, et al.
Human Genetics|October 18, 2002
Genetic basis of inosine triphosphate pyrophosphohydrolase deficiencySatoshi Sumi, Anthony M Marinaki, Monica Arenas, et al.
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