-
1
-
-
0025787909
-
Monitoring of adverse drug events in hospitals
-
Kennedy, D. L., Johnson, J. M. & Nightingale, S. L. Monitoring of adverse drug events in hospitals. J. Am. Med. Assoc. 266, 2878 (1991).
-
(1991)
J. Am. Med. Assoc.
, vol.266
, pp. 2878
-
-
Kennedy, D.L.1
Johnson, J.M.2
Nightingale, S.L.3
-
2
-
-
0031032055
-
Adverse drug events in hospitalized patients. Excess length of stay, extra costs, and attributable mortality
-
Classen, D. C., Pestotnik, S. L., Evans, R. S., Lloyd, J. F. & Burke, J. P. Adverse drug events in hospitalized patients. Excess length of stay, extra costs, and attributable mortality. J. Am. Med. Assoc. 277, 301-306 (1997).
-
(1997)
J. Am. Med. Assoc.
, vol.277
, pp. 301-306
-
-
Classen, D.C.1
Pestotnik, S.L.2
Evans, R.S.3
Lloyd, J.F.4
Burke, J.P.5
-
3
-
-
0033984792
-
Incidence and costs of adverse drug reactions during hospitalisation: Computerised monitoring versus stimulated spontaneous reporting
-
Dormann, H. et al. Incidence and costs of adverse drug reactions during hospitalisation: computerised monitoring versus stimulated spontaneous reporting. Drug Saf. 22, 161-168 (2000).
-
(2000)
Drug Saf.
, vol.22
, pp. 161-168
-
-
Dormann, H.1
-
4
-
-
0033518849
-
Postmarketing surveillance and adverse drug reactions: Current perspectives and future needs
-
Brewer, T. & Colditz, G. A. Postmarketing surveillance and adverse drug reactions: current perspectives and future needs. J. Am. Med. Assoc. 281, 824-829 (1999).
-
(1999)
J. Am. Med. Assoc.
, vol.281
, pp. 824-829
-
-
Brewer, T.1
Colditz, G.A.2
-
5
-
-
0035861049
-
Potential role of pharmacogenomics in reducing adverse drug reactions: A systematic review
-
Phillips, K. A., Veenstra, D. L., Oren, E., Lee, J. K. & Sadee, W. Potential role of pharmacogenomics in reducing adverse drug reactions: a systematic review. J. Am. Med. Assoc. 286, 2270-2279 (2001).
-
(2001)
J. Am. Med. Assoc.
, vol.286
, pp. 2270-2279
-
-
Phillips, K.A.1
Veenstra, D.L.2
Oren, E.3
Lee, J.K.4
Sadee, W.5
-
6
-
-
0242326280
-
-
1st edn (ed. Weber, W. W.) (Oxford Univ. Press, New York)
-
Motulsky, A. G., Harper, P. S., Bobrow, M. & Scriver, C. in Pharmacogenetics 1st edn (ed. Weber, W. W.) 1-20 (Oxford Univ. Press, New York, 1997).
-
(1997)
Pharmacogenetics
, pp. 1-20
-
-
Motulsky, A.G.1
Harper, P.S.2
Bobrow, M.3
Scriver, C.4
-
7
-
-
0013534209
-
The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine
-
Beutler, E., Dern, R. J. & Alving, A. S. The hemolytic effect of primaquine. VI. An in vitro test for sensitivity of erythrocytes to primaquine. J. Lab. Clin. Med. 45, 40-50 (1955).
-
(1955)
J. Lab. Clin. Med.
, vol.45
, pp. 40-50
-
-
Beutler, E.1
Dern, R.J.2
Alving, A.S.3
-
8
-
-
26444539817
-
Genetic control of isoniazid metabolism in man
-
Price-Evans, D. A., Manley, F. A. & McKusick, V. A. Genetic control of isoniazid metabolism in man. Br. Med. J. 2, 485-491 (1960).
-
(1960)
Br. Med. J.
, vol.2
, pp. 485-491
-
-
Price-Evans, D.A.1
Manley, F.A.2
McKusick, V.A.3
-
9
-
-
0001103663
-
Uber die Erbbedingtheit der intraindividuellen Konstantz der Isoniazidausscheidung beim Menshen (Untersuchen an eineiggen und zweieiggen Zwilligen)
-
Bönicke, R. & Lisboa, B. P. Uber die Erbbedingtheit der intraindividuellen Konstantz der Isoniazidausscheidung beim Menshen (Untersuchen an eineiggen und zweieiggen Zwilligen). Naturwissenschafften 44, 314 (1957).
-
(1957)
Naturwissenschafften
, vol.44
, pp. 314
-
-
Bönicke, R.1
Lisboa, B.P.2
-
10
-
-
0033569516
-
Pharmacogenomics: Translating functional genomics into rational therapeutics
-
Evans, W. E. & Relling, M. V. Pharmacogenomics: translating functional genomics into rational therapeutics. Science 286, 487-491 (1999).
-
(1999)
Science
, vol.286
, pp. 487-491
-
-
Evans, W.E.1
Relling, M.V.2
-
11
-
-
0034660560
-
Pharmacogenetics and the practice of medicine
-
Roses, A. D. Pharmacogenetics and the practice of medicine. Nature 405, 857-865 (2000).
-
(2000)
Nature
, vol.405
, pp. 857-865
-
-
Roses, A.D.1
-
12
-
-
0034638766
-
Pharmacogenetics and adverse drug reactions
-
Meyer, U. A. Pharmacogenetics and adverse drug reactions. Lancet 356, 1667-1671 (2000).
-
(2000)
Lancet
, vol.356
, pp. 1667-1671
-
-
Meyer, U.A.1
-
13
-
-
0018099670
-
Effect of acetylator phenotype on the rate at which procainamide induces antinuclear antibodies and the lupus syndrome
-
Woosley, R. L. et al. Effect of acetylator phenotype on the rate at which procainamide induces antinuclear antibodies and the lupus syndrome. N. Engl. J. Med. 298, 1157-1159 (1978).
-
(1978)
N. Engl. J. Med.
, vol.298
, pp. 1157-1159
-
-
Woosley, R.L.1
-
14
-
-
0026768271
-
Polymorphisms of N-acetyltransferase genes
-
Grant, D. M., Blum, M. & Meyer, U. A. Polymorphisms of N-acetyltransferase genes. Xenobiotica 22, 1073-1081 (1992).
-
(1992)
Xenobiotica
, vol.22
, pp. 1073-1081
-
-
Grant, D.M.1
Blum, M.2
Meyer, U.A.3
-
15
-
-
0017695082
-
Polymorphic hydroxylation of debrisoquine in man
-
Mahgoub, A., Idle, R. J., Dring, L. G., Lancaster, R. & Smith, R. L. Polymorphic hydroxylation of debrisoquine in man. Lancet 2, 584-586 (1977).
-
(1977)
Lancet
, vol.2
, pp. 584-586
-
-
Mahgoub, A.1
Idle, R.J.2
Dring, L.G.3
Lancaster, R.4
Smith, R.L.5
-
16
-
-
0018615011
-
Defective N-oxidation of sparteine in man: A new pharmacogenetic defect
-
Eichelbaum, M., Spannbrucker, N., Steincke, B. & Dengler, H. J. Defective N-oxidation of sparteine in man: a new pharmacogenetic defect. Eur. J. Clin. Pharmacol. 16, 183-187 (1979).
-
(1979)
Eur. J. Clin. Pharmacol.
, vol.16
, pp. 183-187
-
-
Eichelbaum, M.1
Spannbrucker, N.2
Steincke, B.3
Dengler, H.J.4
-
17
-
-
0033046088
-
Impact of ethnic origin and quinidine coadministration on codeine's disposition and pharmacodynamic effects
-
Caraco, Y., Sheller, J. & Wood, A. J. Impact of ethnic origin and quinidine coadministration on codeine's disposition and pharmacodynamic effects. J. Pharmacol. Exp. Ther. 290, 413-422 (1999).
-
(1999)
J. Pharmacol. Exp. Ther.
, vol.290
, pp. 413-422
-
-
Caraco, Y.1
Sheller, J.2
Wood, A.J.3
-
18
-
-
0025733250
-
Role of P450IID6, the target of the sparteine-debrisoquin oxidation polymorphism, in the metabolism of imipramine
-
Brosen, K., Zeugin, T. & Meyer, U. A. Role of P450IID6, the target of the sparteine-debrisoquin oxidation polymorphism, in the metabolism of imipramine. Clin. Pharmacol. Ther. 49, 609-617 (1991).
-
(1991)
Clin. Pharmacol. Ther.
, vol.49
, pp. 609-617
-
-
Brosen, K.1
Zeugin, T.2
Meyer, U.A.3
-
19
-
-
0025312448
-
The role of genetically determined polymorphic drug metabolism in the β-blockade produced by propafenone
-
Lee, J. T. et al. The role of genetically determined polymorphic drug metabolism in the β-blockade produced by propafenone. N. Engl. J. Med. 322, 1764-1768 (1990).
-
(1990)
N. Engl. J. Med.
, vol.322
, pp. 1764-1768
-
-
Lee, J.T.1
-
20
-
-
0020409410
-
Oxidation phenotype - A major determinant of metoprolol metabolism and response
-
Lennard, M. S. et al. Oxidation phenotype - a major determinant of metoprolol metabolism and response. N. Engl. J. Med. 307, 1558-1560 (1982).
-
(1982)
N. Engl. J. Med.
, vol.307
, pp. 1558-1560
-
-
Lennard, M.S.1
-
21
-
-
0030995879
-
Molecular mechanisms of genetic polymorphisms of drug metabolism
-
Meyer, U. A. & Zanger, U. M. Molecular mechanisms of genetic polymorphisms of drug metabolism. Annu. Rev. Pharmacol. Toxicol. 37, 269-296 (1997).
-
(1997)
Annu. Rev. Pharmacol. Toxicol.
, vol.37
, pp. 269-296
-
-
Meyer, U.A.1
Zanger, U.M.2
-
22
-
-
0033608466
-
Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications
-
Aithal, G. P., Day, C. P., Kesteven, P. J. & Daly, A. K. Association of polymorphisms in the cytochrome P450 CYP2C9 with warfarin dose requirement and risk of bleeding complications, Lancet 353, 717-719 (1999).
-
(1999)
Lancet
, vol.353
, pp. 717-719
-
-
Aithal, G.P.1
Day, C.P.2
Kesteven, P.J.3
Daly, A.K.4
-
23
-
-
0000140377
-
Effect of genetic differences in omeprazole metabolism on cure rates for Helicobacter pylori infection and peptic ulcer
-
Furuta, T. et al, Effect of genetic differences in omeprazole metabolism on cure rates for Helicobacter pylori infection and peptic ulcer. Ann. Intern. Med. 129, 1027-1030 (1998).
-
(1998)
Ann. Intern. Med.
, vol.129
, pp. 1027-1030
-
-
Furuta, T.1
-
24
-
-
0024308532
-
Methyltransferase pharmacogenetics
-
Weinshilboum, R. Methyltransferase pharmacogenetics. Pharmacol. Ther. 43, 77-90 (1989).
-
(1989)
Pharmacol. Ther.
, vol.43
, pp. 77-90
-
-
Weinshilboum, R.1
-
25
-
-
0034671387
-
Polymorphisms of UDP-glucuronosyltransferase gene and innotecan toxicity: A pharmacogenetic analysis
-
Ando, Y. et al. Polymorphisms of UDP-glucuronosyltransferase gene and innotecan toxicity: a pharmacogenetic analysis. Cancer Res. 60, 6921-6926 (2000).
-
(2000)
Cancer Res.
, vol.60
, pp. 6921-6926
-
-
Ando, Y.1
-
26
-
-
0035479494
-
Human cytosolic sulphotransferases: Genetics, characteristics, toxicological aspects
-
Glatt, H. et al. Human cytosolic sulphotransferases: genetics, characteristics, toxicological aspects. Mutat. Res. 482, 27-40 (2001).
-
(2001)
Mutat. Res.
, vol.482
, pp. 27-40
-
-
Glatt, H.1
-
27
-
-
50449146212
-
Prolonged apnea following injection of succinylcholine
-
Forbat, A., Lond, M. B., Lehmann, H. & Silk, E. Prolonged apnea following injection of succinylcholine. Lancet 2, 1067-1068 (1953).
-
(1953)
Lancet
, vol.2
, pp. 1067-1068
-
-
Forbat, A.1
Lond, M.B.2
Lehmann, H.3
Silk, E.4
-
28
-
-
0014739850
-
Genetic aspects of succinylcholine sensitivity
-
Whittaker, M. Genetic aspects of succinylcholine sensitivity. Anesthesiology 32, 143-150 (1970).
-
(1970)
Anesthesiology
, vol.32
, pp. 143-150
-
-
Whittaker, M.1
-
29
-
-
0026478902
-
Tricyclic antidepressant plasma levels after fluoxetine addition
-
Vandel, S. et al. Tricyclic antidepressant plasma levels after fluoxetine addition. Neuropsychobiology 25, 202-207 (1992).
-
(1992)
Neuropsychobiology
, vol.25
, pp. 202-207
-
-
Vandel, S.1
-
30
-
-
0027474601
-
Mechanism of the cardiotoxic actions of terfenadine
-
Woosley, R. L., Chen, Y., Freiman, J. P. & Gillis, R. A. Mechanism of the cardiotoxic actions of terfenadine. J. Am. Med. Assoc. 269, 1532-1536 (1993).
-
(1993)
J. Am. Med. Assoc.
, vol.269
, pp. 1532-1536
-
-
Woosley, R.L.1
Chen, Y.2
Freiman, J.P.3
Gillis, R.A.4
-
31
-
-
0033514320
-
Inhibition of P-glycoprotein-mediated drug transport: A unifying mechanism to explain the interaction between digoxin and quinidine
-
Fromm, M. F., Kim, R. B., Stein, C. M., Wilkinson, G. R. & Roden, D. M. Inhibition of P-glycoprotein-mediated drug transport: A unifying mechanism to explain the interaction between digoxin and quinidine. Circulation 99, 552-557 (1999).
-
(1999)
Circulation
, vol.99
, pp. 552-557
-
-
Fromm, M.F.1
Kim, R.B.2
Stein, C.M.3
Wilkinson, G.R.4
Roden, D.M.5
-
32
-
-
0032518290
-
P-glycoprotein transporter limits oral absorption and brain entry of HIV protease inhibitors
-
Kim, R. B. et al. P-glycoprotein transporter limits oral absorption and brain entry of HIV protease inhibitors. J. Clin. Invest. 101, 289-294 (1998).
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 289-294
-
-
Kim, R.B.1
-
33
-
-
0034724324
-
Functional polymorphisms of the human multidrug-resistance gene: Multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo
-
Hoffmeyer, S. et al. Functional polymorphisms of the human multidrug-resistance gene: multiple sequence variations and correlation of one allele with P-glycoprotein expression and activity in vivo. Proc. Natl Acad. Sci. USA 97, 3473-3478 (2000).
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 3473-3478
-
-
Hoffmeyer, S.1
-
34
-
-
3042772026
-
Identification of functionally variant MDR1 alleles among European Americans and African Americans
-
Kim, R. B. et al. Identification of functionally variant MDR1 alleles among European Americans and African Americans. Clin. Pharmacol. Ther. 70, 189-199 (2001).
-
(2001)
Clin. Pharmacol. Ther.
, vol.70
, pp. 189-199
-
-
Kim, R.B.1
-
35
-
-
0028229150
-
Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs
-
Schinkel, A. H. et al. Disruption of the mouse mdr1a P-glycoprotein gene leads to a deficiency in the blood-brain barrier and to increased sensitivity to drugs. Cell 77, 491-502 (1994).
-
(1994)
Cell
, vol.77
, pp. 491-502
-
-
Schinkel, A.H.1
-
36
-
-
0035071598
-
Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic, CYP3A5 expression
-
Kuehl, P. et al. Sequence diversity in CYP3A promoters and characterization of the genetic basis of polymorphic, CYP3A5 expression. Nature Genet. 27, 383-391 (2001).
-
(2001)
Nature Genet.
, vol.27
, pp. 383-391
-
-
Kuehl, P.1
-
37
-
-
0032169485
-
The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions
-
Lehmann, J. M. et al. The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions. J. Clin. Invest. 102, 1016-1023 (1998).
-
(1998)
J. Clin. Invest.
, vol.102
, pp. 1016-1023
-
-
Lehmann, J.M.1
-
38
-
-
0035918186
-
Orphan receptor promiscuity in the induction of cytochromes p450 by xenobiotics
-
Smirlis, D., Muangmoonchai, R., Edwards, M., Phillips, I. R. & Shephard, E. A. Orphan receptor promiscuity in the induction of cytochromes p450 by xenobiotics. J. Biol. Chem. 276, 12822-12826 (2001).
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 12822-12826
-
-
Smirlis, D.1
Muangmoonchai, R.2
Edwards, M.3
Phillips, I.R.4
Shephard, E.A.5
-
39
-
-
0035038919
-
The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux
-
Synold, T. W., Dussault, I. & Forman, B. M. The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux. Nature Med. 7, 584-590 (2001).
-
(2001)
Nature Med.
, vol.7
, pp. 584-590
-
-
Synold, T.W.1
Dussault, I.2
Forman, B.M.3
-
40
-
-
0033638960
-
Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR
-
Xie, W. et al. Reciprocal activation of xenobiotic response genes by nuclear receptors SXR/PXR and CAR. Genes Dev. 14, 3014-3023 (2000).
-
(2000)
Genes Dev.
, vol.14
, pp. 3014-3023
-
-
Xie, W.1
-
41
-
-
0034721159
-
Humanized xenobiotic response in mice expressing nuclear receptor SXR
-
Xie, W. et al. Humanized xenobiotic response in mice expressing nuclear receptor SXR. Nature 406, 435-439 (2000).
-
(2000)
Nature
, vol.406
, pp. 435-439
-
-
Xie, W.1
-
42
-
-
0007691164
-
Apolipoprotein E4 allele as a predictor of cholinergic deficits and treatment outcome in Alzheimer disease
-
Poirier, J. et al. Apolipoprotein E4 allele as a predictor of cholinergic deficits and treatment outcome in Alzheimer disease. Proc. Natl Acad. Sci. USA 92, 12260-12264 (1995).
-
(1995)
Proc. Natl. Acad. Sci. USA
, vol.92
, pp. 12260-12264
-
-
Poirier, J.1
-
43
-
-
0003425462
-
A common polymorphism associated with antibiotic-induced cardiac arrhythmia
-
Sesti, F. et al. A common polymorphism associated with antibiotic-induced cardiac arrhythmia. Proc. Natl Acad. Sci. USA 97, 10613-10618 (2000).
-
(2000)
Proc. Natl. Acad. Sci. USA
, vol.97
, pp. 10613-10618
-
-
Sesti, F.1
-
44
-
-
0033059209
-
Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment
-
Drazen. J. M. et al. Pharmacogenetic association between ALOX5 promoter genotype and the response to anti-asthma treatment. Nature Genet. 22, 168-170 (1999).
-
(1999)
Nature Genet.
, vol.22
, pp. 168-170
-
-
Drazen, J.M.1
-
45
-
-
19244371485
-
KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome
-
Donger, C. et al. KVLQT1 C-terminal missense mutation causes a forme fruste long-QT syndrome. Circulation 96, 2778-2781 (1997).
-
(1997)
Circulation
, vol.96
, pp. 2778-2781
-
-
Donger, C.1
-
46
-
-
0034083759
-
Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias
-
Napolitano, C. et al. Evidence for a cardiac ion channel mutation underlying drug-induced QT prolongation and life-threatening arrhythmias. J. Cardiovasc. Electrophysiol. 11, 691-696 (2000).
-
(2000)
J. Cardiovasc. Electrophysiol.
, vol.11
, pp. 691-696
-
-
Napolitano, C.1
-
47
-
-
0000800698
-
Frequency of ion channel mutations and polymorphisms in a large population of patients with drug-associated Long QT Syndrome
-
Yang, P. et al. Frequency of ion channel mutations and polymorphisms in a large population of patients with drug-associated Long QT Syndrome. Pacing Clin. Electrophys. 24, 579 (2001).
-
(2001)
Pacing Clin. Electrophys.
, vol.24
, pp. 579
-
-
Yang, P.1
-
48
-
-
0002587155
-
KS potassium channels
-
KS potassium channels. Circulation 100, 1-495 (1999).
-
(1999)
Circulation
, vol.100
, pp. 1-495
-
-
Wei, J.1
-
49
-
-
0025165779
-
An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels
-
Rigat, B. et al. An insertion/deletion polymorphism in the angiotensin I-converting enzyme gene accounting for half the variance of serum enzyme levels. J. Clin. Invest. 86, 1343-1346 (1990).
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 1343-1346
-
-
Rigat, B.1
-
50
-
-
0032542030
-
ACE(I/D) genotype as a predictor of the magnitude and duration of the response to an ACE inhibitor drug (enalaprilat) in humans
-
Ueda, S., Meredith, P. A., Morton, J. J., Connell, J. M. & Elliott, H. L. ACE(I/D) genotype as a predictor of the magnitude and duration of the response to an ACE inhibitor drug (enalaprilat) in humans. Circulation 98, 2148-2153 (1998).
-
(1998)
Circulation
, vol.98
, pp. 2148-2153
-
-
Ueda, S.1
Meredith, P.A.2
Morton, J.J.3
Connell, J.M.4
Elliott, H.L.5
-
51
-
-
0035957262
-
Pharmacogenetic interactions between β-blocker therapy and the angiotensin-converting enzyme deletion polymorphism in patients with congestive heart failure
-
McNamara, D. M. et al. Pharmacogenetic interactions between β-blocker therapy and the angiotensin-converting enzyme deletion polymorphism in patients with congestive heart failure. Circulation 106, 1644-1648 (2001).
-
(2001)
Circulation
, vol.106
, pp. 1644-1648
-
-
McNamara, D.M.1
-
52
-
-
0014403645
-
Genetic control of drug levels in man: Antipyrine
-
Vesell, E. S. & Page, J. G. Genetic control of drug levels in man: antipyrine. Science 161, 72-73 (1968).
-
(1968)
Science
, vol.161
, pp. 72-73
-
-
Vesell, E.S.1
Page, J.G.2
-
53
-
-
0034616930
-
Functional discovery via a compendium of expression profiles
-
Hughes, T. R. et al. Functional discovery via a compendium of expression profiles. Cell 102, 109-126 (2000).
-
(2000)
Cell
, vol.102
, pp. 109-126
-
-
Hughes, T.R.1
-
54
-
-
0035865322
-
A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms
-
Sachidanandam, R. et al. A map of human genome sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 409, 928-933 (2001).
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
Sachidanandam, R.1
-
55
-
-
0035919656
-
Haplotype variation and linkage disequilibrium in 313 human genes
-
Stephens, J. C. et al. Haplotype variation and linkage disequilibrium in 313 human genes. Science 293, 489-493 (2001).
-
(2001)
Science
, vol.293
, pp. 489-493
-
-
Stephens, J.C.1
-
56
-
-
0034929664
-
Notes from the SNP vs haplotype front
-
Judson, R. & Stephens, J. C. Notes from the SNP vs haplotype front. Pharmacogenomics 2, 7-10 (2001).
-
(2001)
Pharmacogenomics
, vol.2
, pp. 7-10
-
-
Judson, R.1
Stephens, J.C.2
-
57
-
-
0032030953
-
Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity
-
Otterness, D. M., Szumlanski, C. L., Wood, T. C. & Weinshilboum, R. M. Human thiopurine methyltransferase pharmacogenetics. Kindred with a terminal exon splice junction mutation that results in loss of activity. J. Clin. Invest. 101, 1036-1044 (1998).
-
(1998)
J. Clin. Invest.
, vol.101
, pp. 1036-1044
-
-
Otterness, D.M.1
Szumlanski, C.L.2
Wood, T.C.3
Weinshilboum, R.M.4
-
58
-
-
0034034158
-
Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia
-
McLeod, H. L., Krynetski, E. Y., Relling, M. V. & Evans, W. E. Genetic polymorphism of thiopurine methyltransferase and its clinical relevance for childhood acute lymphoblastic leukemia. Leukemia 14, 567-572 (2000).
-
(2000)
Leukemia
, vol.14
, pp. 567-572
-
-
McLeod, H.L.1
Krynetski, E.Y.2
Relling, M.V.3
Evans, W.E.4
-
59
-
-
0035286694
-
Ethical and legal implications of pharmacogenomics
-
Rothstein, M. A. & Epps, P. G. Ethical and legal implications of pharmacogenomics. Nature Rev. Genet. 2, 228-231 (2001).
-
(2001)
Nature Rev. Genet.
, vol.2
, pp. 228-231
-
-
Rothstein, M.A.1
Epps, P.G.2
-
60
-
-
0034940965
-
Consent and privacy in pharmacogenetic testing
-
Robertson, J. A. Consent and privacy in pharmacogenetic testing. Nature Genet. 28, 207-209 (2001).
-
(2001)
Nature Genet.
, vol.28
, pp. 207-209
-
-
Robertson, J.A.1
-
61
-
-
0025913812
-
Effect of enalapril on survival in patients with reduced left ventricular ejection fractions and congestive heart failure
-
The SOLVD Investigators
-
The SOLVD Investigators. Effect of enalapril on survival in patients with reduced left ventricular ejection fractions and congestive heart failure. N. Engl. J. Med. 325, 293-302 (1991).
-
(1991)
N. Engl. J. Med.
, vol.325
, pp. 293-302
-
-
-
62
-
-
0026786643
-
Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction. Results of the survival and ventricular enlargement trial
-
Pfeffer, M. A. et al. Effect of captopril on mortality and morbidity in patients with left ventricular dysfunction after myocardial infarction. Results of the survival and ventricular enlargement trial. N. Engl. J. Med. 327, 669-677 (1992).
-
(1992)
N. Engl. J. Med.
, vol.327
, pp. 669-677
-
-
Pfeffer, M.A.1
-
63
-
-
0029783337
-
Black Americans have an increased rate of angiotensin converting enzyme inhibitor-associated angioedema
-
Brown, N. J., Ray, W. A., Snowden, M. & Griffin, M. R. Black Americans have an increased rate of angiotensin converting enzyme inhibitor-associated angioedema. Clin. Pharmacol. Ther. 60, 8-13 (1996).
-
(1996)
Clin. Pharmacol. Ther.
, vol.60
, pp. 8-13
-
-
Brown, N.J.1
Ray, W.A.2
Snowden, M.3
Griffin, M.R.4
-
64
-
-
0030806877
-
Recurrent angiotensin-converting enzyme inhibitor-associated angioedema
-
Brown, N. J., Snowden, M. & Griffin, M. R. Recurrent angiotensin-converting enzyme inhibitor-associated angioedema. J. Am. Med. Assoc. 278, 232-233 (1997).
-
(1997)
J. Am. Med. Assoc.
, vol.278
, pp. 232-233
-
-
Brown, N.J.1
Snowden, M.2
Griffin, M.R.3
-
65
-
-
0027987849
-
Randomised trial of cholesterol lowering in 4,444 patients with coronary heart disease: The Scandinavian Simvastatin Survival Study (4S)
-
Scandinavian Simvastatin Survival Study Group
-
Scandinavian Simvastatin Survival Study Group. Randomised trial of cholesterol lowering in 4,444 patients with coronary heart disease: the Scandinavian Simvastatin Survival Study (4S). Lancet 344, 1383-1389 (1994).
-
(1994)
Lancet
, vol.344
, pp. 1383-1389
-
-
-
66
-
-
0028883828
-
Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia
-
West of Scotland Coronary Prevention Study Group
-
Shepherd, J. et al. Prevention of coronary heart disease with pravastatin in men with hypercholesterolemia. West of Scotland Coronary Prevention Study Group. N. Engl. J. Med. 333, 1301-1307 (1995).
-
(1995)
N. Engl. J. Med.
, vol.333
, pp. 1301-1307
-
-
Shepherd, J.1
-
67
-
-
0034046256
-
HMG-CoA reductase inhibitors and myotoxicity
-
Ucar, M., Mjorndal, T. & Dahlqvist, R. HMG-CoA reductase inhibitors and myotoxicity Drug Saf. 22, 441-457 (2000).
-
(2000)
Drug Saf.
, vol.22
, pp. 441-457
-
-
Ucar, M.1
Mjorndal, T.2
Dahlqvist, R.3
-
68
-
-
0032544336
-
Genetic variation as a guide to drug development
-
Kleyn, P. W. & Vesell, E. S. Genetic variation as a guide to drug development. Science 281, 1820-1821 (1998).
-
(1998)
Science
, vol.281
, pp. 1820-1821
-
-
Kleyn, P.W.1
Vesell, E.S.2
-
69
-
-
0032440352
-
The effects of genetic polymorphisms of CYP2C9 and CYP2C19 on phenytoin metabolism in Japanese adult patients with epilepsy: Studies in stereoselective hydroxylation and population pharmacokinetics
-
Mamiya, K. et al. The effects of genetic polymorphisms of CYP2C9 and CYP2C19 on phenytoin metabolism in Japanese adult patients with epilepsy: studies in stereoselective hydroxylation and population pharmacokinetics. Epilepsia 39, 1317-1323 (1998).
-
(1998)
Epilepsia
, vol.39
, pp. 1317-1323
-
-
Mamiya, K.1
-
70
-
-
0029658591
-
The role ofthe CYP2C9 Leu359 allelic variant in the tolbutamide polymorphism
-
Sullivan-Klose, T. H. et al. The role ofthe CYP2C9 Leu359 allelic variant in the tolbutamide polymorphism. Pharmacogenetics 6, 341-349 (1996).
-
(1996)
Pharmacogenetics
, vol.6
, pp. 341-349
-
-
Sullivan-Klose, T.H.1
-
71
-
-
0021684926
-
Mephenytoin hydroxylation deficiency in caucasians: Frequency of a new oxidative drug metabolism polymorphism
-
Wedlund, P. J., Aslanian, W. S., McAllister, C. B., Wilkinson, G. R. & Branch, R. A. Mephenytoin hydroxylation deficiency in caucasians: frequency of a new oxidative drug metabolism polymorphism. Clin. Pharmacol. Ther. 36, 773-780 (1984).
-
(1984)
Clin. Pharmacol. Ther.
, vol.36
, pp. 773-780
-
-
Wedlund, P.J.1
Aslanian, W.S.2
McAllister, C.B.3
Wilkinson, G.R.4
Branch, R.A.5
-
72
-
-
0029064096
-
Ultrarapid hydroxylation of debrisoquine in a Swedish population: Analysis of the molecular genetic basis
-
Dahl, M.-L., Johansson, I., Bertilsson, F., Ingelman-Sundberg, M. & Sjoeqvist, F. Ultrarapid hydroxylation of debrisoquine in a Swedish population: analysis of the molecular genetic basis. J. Pharmacol. Exp. Ther. 274, 516-520 (1995).
-
(1995)
J. Pharmacol. Exp. Ther.
, vol.274
, pp. 516-520
-
-
Dahl, M.-L.1
Johansson, I.2
Bertilsson, F.3
Ingelman-Sundberg, M.4
Sjoeqvist, F.5
-
73
-
-
0028809608
-
Pharmacogenetic, explanation for excessive β-blockade following timolol eye drops. Potential for oral-ophthalmic drug interaction
-
Edeki, T. I., He, H. & Wood, A. J. Pharmacogenetic, explanation for excessive β-blockade following timolol eye drops. Potential for oral-ophthalmic drug interaction. J. Am. Med. Assoc. 274, 1611-1613 (1995).
-
(1995)
J. Am. Med. Assoc.
, vol.274
, pp. 1611-1613
-
-
Edeki, T.I.1
He, H.2
Wood, A.J.3
-
74
-
-
0029035966
-
Stereoselective disposition of carvedilol is determined by CYP2D6
-
Zhou, H. H. & Wood, A. J. Stereoselective disposition of carvedilol is determined by CYP2D6. Clin. Pharmacol. Ther. 57, 518-524 (1995).
-
(1995)
Clin. Pharmacol. Ther.
, vol.57
, pp. 518-524
-
-
Zhou, H.H.1
Wood, A.J.2
-
75
-
-
0018086205
-
Hypotensive response to debrisoquine and hydroxylation phenotype
-
Idle, J. R., Maingoub, A., Lancaster, R. & Smith, R. L. Hypotensive response to debrisoquine and hydroxylation phenotype. Life Sci. 22, 979-984 (1978).
-
(1978)
Life Sci.
, vol.22
, pp. 979-984
-
-
Idle, J.R.1
Maingoub, A.2
Lancaster, R.3
Smith, R.L.4
-
76
-
-
0018013511
-
The hepatic toxicity of isoniazid among rapid and slow acetylators of the drug
-
Ellard, G. A., Mitchison, D. A., Girling, D. J., Nunn, A. J. & Fox, W. The hepatic toxicity of isoniazid among rapid and slow acetylators of the drug. Am. Rev. Respir. Dis. 118, 628-629 (1978).
-
(1978)
Am. Rev. Respir. Dis.
, vol.118
, pp. 628-629
-
-
Ellard, G.A.1
Mitchison, D.A.2
Girling, D.J.3
Nunn, A.J.4
Fox, W.5
-
77
-
-
0031715622
-
Reduced thiopurine methyltransferase activity and development of side effects of azathioprine treatment in patients with rheumatoid arthritis
-
Stolk, J. N. et al. Reduced thiopurine methyltransferase activity and development of side effects of azathioprine treatment in patients with rheumatoid arthritis. Arthritis Rheum. 41, 1858-1866 (1998).
-
(1998)
Arthritis Rheum.
, vol.41
, pp. 1858-1866
-
-
Stolk, J.N.1
-
78
-
-
0033915078
-
The effect of polymorphisms of the β(2)-adrenergic receptor on the response to regular use of albuterol in asthma
-
Israel, E. et al. The effect of polymorphisms of the β(2)-adrenergic receptor on the response to regular use of albuterol in asthma. Am. J. Respir. Crit. Care Med. 162, 75-80 (2000).
-
(2000)
Am. J. Respir. Crit. Care Med.
, vol.162
, pp. 75-80
-
-
Israel, E.1
-
79
-
-
0035843968
-
Novel polymorphisms in promoter region of ATP binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy
-
Lutucuta, S., Ballantyne, C. M., Elghannam, H., Gotto, A. M., Jr & Marian, A. J. Novel polymorphisms in promoter region of ATP binding cassette transporter gene and plasma lipids, severity, progression, and regression of coronary atherosclerosis and response to therapy. Circ. Res. 88, 969-973 (2001).
-
(2001)
Circ. Res.
, vol.88
, pp. 969-973
-
-
Lutucuta, S.1
Ballantyne, C.M.2
Elghannam, H.3
Gotto Jr., A.M.4
Marian, A.J.5
-
80
-
-
0032495541
-
The role of a common variant of the cholesteryl ester transfer protein gene in the progression of coronary atherosclerosis
-
The Regression Growth Evaluation Statin Study Group
-
Kuivenhoven, J. A. et al. The role of a common variant of the cholesteryl ester transfer protein gene in the progression of coronary atherosclerosis. The Regression Growth Evaluation Statin Study Group. N. Engl. J. Med. 338, 86-93 (1998).
-
(1998)
N. Engl. J. Med.
, vol.338
, pp. 86-93
-
-
Kuivenhoven, J.A.1
|