Associated Papers
Intronic hexanucleotide repeat expansion in TYMS in monozygotic twins with congenital progressive universal melanosis.
Kanchanasutthiyakorn S et al.
Biomedical Reports, 2025
StarPhase: Comprehensive Phase-Aware Pharmacogenomic Diplotyper for Long-Read Sequencing Data.
Holt JM et al.
Biorxiv : the Preprint Server for Biology, 2024
39713404 (PubMed )
Supplement: media-1.pdf
UGT1A1 Genetic Variations and a Haplotype Associated with Neonatal Hyperbilirubinemia in Indonesian Population.
Wisnumurti DA et al.
Biomed Research International, 2018
Analysis of uridine diphosphate glucuronosyl transferase 1A1 gene mutations in neonates with unconjugated hyperbilirubinemia.
Guo XH et al.
Genetics and Molecular Research : Gmr, 2016
Pharmacogenetics of CYP2B6, CYP2A6 and UGT2B7 in HIV treatment in African populations: focus on efavirenz and nevirapine.
Čolić A et al.
Drug Metabolism Reviews, 2015
Do single nucleotide polymorphisms in xenobiotic metabolizing genes determine breast cancer susceptibility and treatment outcomes?
Singh V et al.
Cancer Investigation, 2008
Predicting drug response and toxicity based on gene polymorphisms.
Robert J et al.
Critical Reviews in Oncology/hematology, 2005
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