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Genetic susceptibility to adverse drug reactions
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scholarly article
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
review article
1 reference
stated in
Europe PubMed Central
title
Genetic susceptibility to adverse drug reactions
(English)
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
author name string
Pirmohamed M
series ordinal
1
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
Park BK
series ordinal
2
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
publication date
1 June 2001
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
published in
Trends in Pharmacological Sciences
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
volume
22
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
page(s)
298-305
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
issue
6
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
cites work
Incidence of adverse drug reactions in hospitalized patients: a meta-analysis of prospective studies
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Drug-related hospital admissions
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New active substances authorized in the United Kingdom between 1972 and 1994.
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Pharmacogenetics and pharmacogenomics: why is this relevant to the clinical geneticist?
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Getting the right drug into the right patient.
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Crossref
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7 January 2021
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Adverse drug reactions: definitions, diagnosis, and management
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Role of Drug Disposition in Drug Hypersensitivity: A Chemical, Molecular, and Clinical Perspective
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Adverse drug reactions
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Crossref
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Pharmacogenetics and adverse drug reactions
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A functional polymorphism of the cytochrome P450 1A2 (CYP1A2) gene: association with tardive dyskinesia in schizophrenia.
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Crossref
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Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications
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Crossref
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The genetic polymorphism of debrisoquine/sparteine metabolism--clinical aspects
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The role of cytochrome P450 enzymes in hepatic and extrahepatic human drug toxicity
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7 January 2021
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Association of CYP3A4 genotype with treatment-related leukemia
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Polymorphic human cytochrome P450 enzymes: an opportunity for individualized drug treatment
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Toxicogenetics in drug development
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Extension of a pilot study: impact from the cytochrome P450 2D6 polymorphism on outcome and costs associated with severe mental illness.
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Prevention of stroke in patients with nonvalvular atrial fibrillation
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Frequency of major complications of aspirin, warfarin, and intravenous heparin for secondary stroke prevention. A population-based study
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Hydroxylation of warfarin by human cDNA-expressed cytochrome P-450: a role for P-4502C9 in the etiology of (S)-warfarin-drug interactions
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Allelic variants of human cytochrome P450 2C9: baculovirus-mediated expression, purification, structural characterization, substrate stereoselectivity, and prochiral selectivity of the wild-type and I359L mutant forms.
1 reference
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Crossref
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7 January 2021
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Comparisons between in-vitro and in-vivo metabolism of (S)-warfarin: catalytic activities of cDNA-expressed CYP2C9, its Leu359 variant and their mixture versus unbound clearance in patients with the corresponding CYP2C9 genotypes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
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Cytochrome P450 polymorphisms are associated with reduced warfarin dose
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
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Human P450 metabolism of warfarin
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
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Warfarin usage: can safety be improved?
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Multicentre randomised study of computerised anticoagulant dosage. European Concerted Action on Anticoagulation.
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Oral anticoagulation self-management and management by a specialist anticoagulation clinic: a randomised cross-over comparison.
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Crossref
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Idiosyncratic drug reactions: a mechanistic evaluation of risk factors
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Crossref
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7 January 2021
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N-acetyltransferase
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Crossref
reference URL
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7 January 2021
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Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia
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Crossref
reference URL
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Pharmacogenetics: a tool for individualizing antineoplastic therapy
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Association analysis of drug metabolizing enzyme gene polymorphisms in HIV-positive patients with co-trimoxazole hypersensitivity
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Glutathione S-transferase mu genotype (GSTM1*0) in Alzheimer's patients with tacrine transaminitis
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The purine path to chemotherapy
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Molecular diagnosis of thiopurine S-methyltransferase deficiency: genetic basis for azathioprine and mercaptopurine intolerance
1 reference
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Crossref
reference URL
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7 January 2021
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Altered mercaptopurine metabolism, toxic effects, and dosage requirement in a thiopurine methyltransferase-deficient child with acute lymphocytic leukemia
1 reference
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Crossref
reference URL
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Azathioprine-induced myelosuppression in thiopurine methyltransferase deficient heart transplant recipient
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
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Genetic variation in response to 6-mercaptopurine for childhood acute lymphoblastic leukaemia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Mercaptopurine therapy intolerance and heterozygosity at the thiopurine S-methyltransferase gene locus
1 reference
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Crossref
reference URL
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High incidence of secondary brain tumours after radiotherapy and antimetabolites.
1 reference
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Crossref
reference URL
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Human erythrocyte thiopurine methyltransferase: radiochemical microassay and biochemical properties
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
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Polymorphisms in UDP glucuronosyltransferase genes: functional consequences and clinical relevance.
1 reference
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Crossref
reference URL
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based on heuristic
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Genetic predisposition to the metabolism of irinotecan (CPT-11). Role of uridine diphosphate glucuronosyltransferase isoform 1A1 in the glucuronidation of its active metabolite (SN-38) in human liver microsomes
1 reference
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7 January 2021
based on heuristic
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Phenotype-genotype correlation of in vitro SN-38 (active metabolite of irinotecan) and bilirubin glucuronidation in human liver tissue with UGT1A1 promoter polymorphism
1 reference
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Crossref
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7 January 2021
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P-glycoprotein in the blood-brain barrier of mice influences the brain penetration and pharmacological activity of many drugs
1 reference
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Crossref
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7 January 2021
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Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo
1 reference
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Crossref
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7 January 2021
based on heuristic
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Glucose-6-phosphate dehydrogenase deficiency
1 reference
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Crossref
reference URL
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A transcription-activating polymorphism in the ACHE promoter associated with acute sensitivity to anti-acetylcholinesterases.
1 reference
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Association between β2-adrenoceptor polymorphism and susceptibility to bronchodilator desensitisation in moderately severe stable asthmatics
1 reference
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Crossref
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7 January 2021
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Pharmacogenomics of psychiatric disorders
1 reference
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reference URL
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7 January 2021
based on heuristic
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Association of the MscI polymorphism of the dopamine D3 receptor gene with tardive dyskinesia in schizophrenia
1 reference
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Crossref
reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Ryanodine receptor mutations in malignant hyperthermia and central core disease
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
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Pharmacogenetics of cardiac K(+) channels
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
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MiRP1 forms IKr potassium channels with HERG and is associated with cardiac arrhythmia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
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A common polymorphism associated with antibiotic-induced cardiac arrhythmia
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Idiosyncratic drug reactions: the reactive metabolite syndromes
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Single nucleotide polymorphisms as tools in human genetics
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Complete sequence and gene map of a human major histocompatibility complex. The MHC sequencing consortium
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
An allelic polymorphism within the human tumor necrosis factor alpha promoter region is strongly associated with HLA A1, B8, and DR3 alleles
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Idiosyncratic drug reactions. Metabolic bioactivation as a pathogenic mechanism
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Investigation of mechanisms in toxic epidermal necrolysis induced by carbamazepine
1 reference
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https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic predisposition to phenytoin-induced birth defects
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
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Concordance of primary generalised epilepsy and carbamazepine hypersensitivity in monozygotic twins
1 reference
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7 January 2021
based on heuristic
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Anticonvulsant hypersensitivity syndrome. In vitro assessment of risk
1 reference
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Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Characterization of the microsomal epoxide hydrolase gene in patients with anticonvulsant adverse drug reactions
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Genetic analysis of microsomal epoxide hydrolase in patients with carbamazepine hypersensitivity
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
TNFalpha promoter region gene polymorphisms in carbamazepine-hypersensitive patients.
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
inferred from DOI database lookup
Interpretation of results from genetic studies of multifactorial diseases
1 reference
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reference URL
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7 January 2021
based on heuristic
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Pharmacogenetics and the practice of medicine
1 reference
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reference URL
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retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
1 reference
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reference URL
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7 January 2021
based on heuristic
inferred from DOI database lookup
Pharmacogenetics in the new patterns of healthcare delivery
1 reference
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reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
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7 January 2021
based on heuristic
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Testing drug response in the presence of genetic information: sampling issues for clinical trials
1 reference
stated in
Crossref
reference URL
https://api.crossref.org/works/10.1016%2FS0165-6147%2800%2901717-X
retrieved
7 January 2021
based on heuristic
inferred from DOI database lookup
Identifiers
DOI
10.1016/S0165-6147(00)01717-X
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
PubMed ID
11395158
1 reference
stated in
Europe PubMed Central
PubMed ID
11395158
retrieved
1 August 2017
ResearchGate publication ID
11944607
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