Associated Papers
A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population.
Poon KS et al.
Bmc Research Notes, 2022
Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance.
Cagiada M et al.
Molecular Biology and Evolution, 2021
33779753 (PubMed )
Supplement: msab095_supplementary_data.zip › __MAVE-metaanalysis__SI__44__lindorff__2020__.pdf
Massively parallel variant characterization identifies NUDT15 alleles associated with thiopurine toxicity.
Suiter CC et al.
Proceedings of the National Academy of Sciences of the United States of America, 2020
Association of Genetic Variants in NUDT15 With Thiopurine-Induced Myelosuppression in Patients With Inflammatory Bowel Disease.
Walker GJ et al.
Jama, 2019
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