Associated Papers
The frequency of NUDT15 rs116855232 and its impact on mercaptopurine-induced toxicity in Syrian children with acute lymphoblastic leukemia.
Muhammad M et al.
Frontiers in Oncology, 2024
Nudix hydrolase 15 (NUDT15) loss-of-function variants in an Australian inflammatory bowel disease population.
Afrin S et al.
Internal Medicine Journal, 2022
Long-read HiFi sequencing of NUDT15: Phased full-gene haplotyping and pharmacogenomic allele discovery.
Scott ER et al.
Human Mutation, 2022
A direct sequencing assay for pharmacogenetic testing of thiopurine-intolerant NUDT15 alleles in an Asian population.
Poon KS et al.
Bmc Research Notes, 2022
Nudix Hydroxylase 15 Mutations Strongly Predict Thiopurine-Induced Leukopenia Across Different Asian Ethnicities: Implications for Screening in a Diverse Population.
Khoo XH et al.
Frontiers in Medicine, 2022
Impact of NUDT15 genetics on severe thiopurine-related hematotoxicity in patients with European ancestry.
Schaeffeler E et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics, 2019
30728528 (PubMed )
Supplement: 41436_2019_448_MOESM1_ESM.pdf
The Nudix Hydrolase 15 (NUDT15) Gene Variants among Jordanian Arab Population
Jarrar YB et al.
Asian Pacific Journal of Cancer Prevention : Apjcp, 2019
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