Associated Papers
Frequency of pharmacogenomic variation and medication exposures among All of Us Participants.
Haddad A et al.
Medrxiv : the Preprint Server for Health Sciences, 2024
Genetic profiling of NUDT15 in the Slovenian population.
Šmid A et al.
Pharmacogenomics, 2024
A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population.
Poon KS et al.
Bmc Research Notes, 2022
NUDT15 Genetic Variants in Chinese Han, Uighur, Kirghiz, and Dai Nationalities.
Zhang F et al.
Frontiers in Pediatrics, 2022
Pharmacogene Variation Consortium Gene Introduction: NUDT15.
Yang JJ et al.
Clinical Pharmacology and Therapeutics, 2019
30515762 (PubMed )
Supplement: CPT-105-1091-s001.xlsx › NUDT15_nomenclature_
Combination of common and novel rare NUDT15 variants improves predictive sensitivity of thiopurine-induced leukopenia in children with acute lymphoblastic leukemia.
Zhu Y et al.
Haematologica, 2018
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