scholarly article | Q13442814 |
P356 | DOI | 10.1038/TPJ.2008.4 |
P2888 | exact match | https://scigraph.springernature.com/pub.10.1038/tpj.2008.4 |
P698 | PubMed publication ID | 18301416 |
P5875 | ResearchGate publication ID | 5551797 |
P2093 | author name string | L Li | |
A D Roses | |||
E H Lai | |||
M Mosteller | |||
M R Nelson | |||
S-A Bacanu | |||
C E Bowman | |||
M G Ehm | |||
P2860 | cites work | HLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinol | Q24555784 |
PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
Statistical significance for genomewide studies | Q24681264 | ||
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patients | Q28169189 | ||
Genetic variations in HLA-B region and hypersensitivity reactions to abacavir | Q28214097 | ||
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecan | Q28249001 | ||
Medical genetics: a marker for Stevens-Johnson syndrome | Q28254047 | ||
A new multipoint method for genome-wide association studies by imputation of genotypes | Q29547209 | ||
Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies | Q29616299 | ||
Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus | Q33882066 | ||
Risk of cardiovascular events associated with selective COX-2 inhibitors | Q34087109 | ||
Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavir | Q34117815 | ||
Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactions | Q34429480 | ||
Disease-specific target selection: a critical first step down the right road | Q36039820 | ||
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. | Q37161006 | ||
Adverse drug reactions: definitions, diagnosis, and management | Q40739350 | ||
Cytochrome P450 2E1 genotype and the susceptibility to antituberculosis drug-induced hepatitis | Q44385947 | ||
A Gilbert's syndrome UGT1A1 variant confers susceptibility to tranilast-induced hyperbilirubinemia. | Q44675167 | ||
Association of genetic variations in HLA-B region with hypersensitivity to abacavir in some, but not all, populations | Q44796890 | ||
Relevance of different UGT1A1 polymorphisms in irinotecan-induced toxicity: a molecular and clinical study of 75 patients | Q45009159 | ||
Case-only analysis of treatment-covariate interactions in clinical trials | Q46152923 | ||
Evaluating and improving power in whole-genome association studies using fixed marker sets. | Q53255191 | ||
A single-nucleotide polymorphism tagging set for human drug metabolism and transport | Q57309672 | ||
Design of Case-controls Studies with Unscreened Controls | Q58132458 | ||
P433 | issue | 1 | |
P304 | page(s) | 23-33 | |
P577 | publication date | 2008-02-26 | |
P1433 | published in | The Pharmacogenomics Journal | Q10534704 |
P1476 | title | Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions | |
P478 | volume | 9 |
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