Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions

scientific article published on 26 February 2008

Genome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1038/TPJ.2008.4
P2888exact matchhttps://scigraph.springernature.com/pub.10.1038/tpj.2008.4
P698PubMed publication ID18301416
P5875ResearchGate publication ID5551797

P2093author name stringL Li
A D Roses
E H Lai
M Mosteller
M R Nelson
S-A Bacanu
C E Bowman
M G Ehm
P2860cites workHLA-B*5801 allele as a genetic marker for severe cutaneous adverse reactions caused by allopurinolQ24555784
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Principal components analysis corrects for stratification in genome-wide association studiesQ27860975
Adverse drug reactions as cause of admission to hospital: prospective analysis of 18 820 patientsQ28169189
Genetic variations in HLA-B region and hypersensitivity reactions to abacavirQ28214097
Genetic variants in the UDP-glucuronosyltransferase 1A1 gene predict the risk of severe neutropenia of irinotecanQ28249001
Medical genetics: a marker for Stevens-Johnson syndromeQ28254047
A new multipoint method for genome-wide association studies by imputation of genotypesQ29547209
Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studiesQ29616299
Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locusQ33882066
Risk of cardiovascular events associated with selective COX-2 inhibitorsQ34087109
Association between presence of HLA-B*5701, HLA-DR7, and HLA-DQ3 and hypersensitivity to HIV-1 reverse-transcriptase inhibitor abacavirQ34117815
Adverse drug event surveillance and drug withdrawals in the United States, 1969-2002: the importance of reporting suspected reactionsQ34429480
Disease-specific target selection: a critical first step down the right roadQ36039820
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC.Q37161006
Adverse drug reactions: definitions, diagnosis, and managementQ40739350
Cytochrome P450 2E1 genotype and the susceptibility to antituberculosis drug-induced hepatitisQ44385947
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, populationsQ44796890
Relevance of different UGT1A1 polymorphisms in irinotecan-induced toxicity: a molecular and clinical study of 75 patientsQ45009159
Case-only analysis of treatment-covariate interactions in clinical trialsQ46152923
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 transportQ57309672
Design of Case-controls Studies with Unscreened ControlsQ58132458
P433issue1
P304page(s)23-33
P577publication date2008-02-26
P1433published inThe Pharmacogenomics JournalQ10534704
P1476titleGenome-wide approaches to identify pharmacogenetic contributions to adverse drug reactions
P478volume9

Reverse relations

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