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The Pharmacogenomics Journal|March 2, 2005
Functional analysis of genetic variants in the human concentrative nucleoside transporter 3 (CNT3; SLC28A3)I Badagnani, W Chan, R A Castro, et al.
The Pharmacogenomics Journal|July 19, 2006
Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversityS Fuselli, R H Gilman, S J Chanock, et al.
The Pharmacogenomics Journal|September 27, 2006
Clozapine-induced agranulocytosis in schizophrenic Caucasians: confirming clues for associations with human leukocyte class I and II antigensM Dettling, I Cascorbi, C Opgen-Rhein, et al.
The Pharmacogenomics Journal|June 9, 2005
Association of CYP2A6*1B genetic variant with the amount of smoking in French adults from the Stanislas cohortN Gambier, A-M Batt, B Marie, et al.
The Pharmacogenomics Journal|September 14, 2006
Genetic variation at the CYP2C locus and its association with torsemide biotransformationS V Vormfelde, M Schirmer, M R Toliat, et al.
The Pharmacogenomics Journal|September 14, 2006
ABCB1 genotype and PGP expression, function and therapeutic drug response: a critical review and recommendations for future researchG D Leschziner, T Andrew, M Pirmohamed, et al.
The Pharmacogenomics Journal|May 11, 2005
Common VKORC1 and GGCX polymorphisms associated with warfarin doseM Wadelius, L Y Chen, K Downes, et al.
The Pharmacogenomics Journal|June 25, 2022
A machine learning model using SNPs obtained from a genome-wide association study predicts the onset of vincristine-induced peripheral neuropathyHiroki Yamada, Rio Ohmori, Naoto Okada, et al.
The Pharmacogenomics Journal|June 18, 2021
The impact of pharmacogenetic testing in patients exposed to polypharmacy: a scoping reviewErika L Meaddough, Sara M Sarasua, Tracy K Fasolino, et al.
The Pharmacogenomics Journal|May 19, 2022
Exome sequencing allows detection of relevant pharmacogenetic variants in epileptic patientsSimon Verdez, Quentin Thomas, Philippine Garret, et al.
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