-
1
-
-
2042437650
-
Initial sequencing and analysis of the human genome
-
International Human Genome Sequencing Consortium. Initial sequencing and analysis of the human genome. Nature 2001;409: 860-921.
-
(2001)
Nature
, vol.409
, pp. 860-921
-
-
-
2
-
-
0035895505
-
The sequence of the human genome
-
Venter JC, Adams MD, Myers EW, Li PW, Mural RJ, Sutton GG, et al. The sequence of the human genome. Science 2001; 291:1304-51.
-
(2001)
Science
, vol.291
, pp. 1304-1351
-
-
Venter, J.C.1
Adams, M.D.2
Myers, E.W.3
Li, P.W.4
Mural, R.J.5
Sutton, G.G.6
-
3
-
-
0034727107
-
A SNP map of the human genome generated by reduced representation shotgun sequencing
-
Altschuler D, Pollara VJ, Cowles CR, Van Etten WJ, Baldwin J, Linton L, et al. A SNP map of the human genome generated by reduced representation shotgun sequencing. Nature 2000;407: 513-6.
-
(2000)
Nature
, vol.407
, pp. 513-516
-
-
Altschuler, D.1
Pollara, V.J.2
Cowles, C.R.3
Van Etten, W.J.4
Baldwin, J.5
Linton, L.6
-
4
-
-
0035865322
-
A map of human sequence variation containing 1.42 million single nucleotide polymorphisms
-
International SNP Map Working Group. A map of human sequence variation containing 1.42 million single nucleotide polymorphisms. Nature 2001;409:928-33.
-
(2001)
Nature
, vol.409
, pp. 928-933
-
-
-
5
-
-
0033936872
-
Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays
-
Fan J-B, Chen X, Halushka MK, Berno A, Huang X, Ryder T, et al. Parallel genotyping of human SNPs using generic high-density oligonucleotide tag arrays. Genome Res 2000;10:853-60.
-
(2000)
Genome Res
, vol.10
, pp. 853-860
-
-
Fan, J.-B.1
Chen, X.2
Halushka, M.K.3
Berno, A.4
Huang, X.5
Ryder, T.6
-
6
-
-
0036594904
-
A strategy for the rapid discovery of disease markers using the MassArray system
-
Rodi CP, Darnhofer-Patel B, Stanssen P, Zabeau M, Van den Boom D. A strategy for the rapid discovery of disease markers using the MassArray system. Biotechniques 2002;32:S62-9.
-
(2002)
Biotechniques
, vol.32
-
-
Rodi, C.P.1
Darnhofer-Patel, B.2
Stanssen, P.3
Zabeau, M.4
Van Den Boom, D.5
-
7
-
-
0036275126
-
BeadArray technology: Enabling an accurate cost-effective approach to high-throughput genotyping
-
Oliphant A, Barker DL, Stuelpnagel JR, Chee MS. BeadArray technology: enabling an accurate cost-effective approach to high-throughput genotyping. Biotechniques 2002;32:S56-61.
-
(2002)
Biotechniques
, vol.32
-
-
Oliphant, A.1
Barker, D.L.2
Stuelpnagel, J.R.3
Chee, M.S.4
-
8
-
-
0037421590
-
Pharmacogenomics: Drug disposition, drug targets, and side effects
-
Evans WE, McLeod HL. Pharmacogenomics: drug disposition, drug targets, and side effects. N Engl J Med 2003;348:538-49.
-
(2003)
N Engl J Med
, vol.348
, pp. 538-549
-
-
Evans, W.E.1
McLeod, H.L.2
-
9
-
-
0032524383
-
Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome
-
Wang DG, Fan J-B, Siao CJ, Berno A, Young P, Sapolsky R, et al. Large-scale identification, mapping, and genotyping of single-nucleotide polymorphisms in the human genome. Science 1998; 280:1077-82.
-
(1998)
Science
, vol.280
, pp. 1077-1082
-
-
Wang, D.G.1
Fan, J.-B.2
Siao, C.J.3
Berno, A.4
Young, P.5
Sapolsky, R.6
-
10
-
-
0026780282
-
Microsatellites for linkage analysis of complex traits
-
Hearne CM, Ghosh S, Todd JA. Microsatellites for linkage analysis of complex traits. Trends Genet 1992;8:288-94.
-
(1992)
Trends Genet
, vol.8
, pp. 288-294
-
-
Hearne, C.M.1
Ghosh, S.2
Todd, J.A.3
-
11
-
-
0028333697
-
Linkage disequilibrium in growing and stable populations
-
Slatkin M. Linkage disequilibrium in growing and stable populations. Genetics 1994;137:331-6.
-
(1994)
Genetics
, vol.137
, pp. 331-336
-
-
Slatkin, M.1
-
12
-
-
0033780104
-
How many diseases does it take to map a gene with SNPs?
-
Weiss KM, Terwilliger JD. How many diseases does it take to map a gene with SNPs? Nature Genet 2000;26:151-7.
-
(2000)
Nature Genet
, vol.26
, pp. 151-157
-
-
Weiss, K.M.1
Terwilliger, J.D.2
-
13
-
-
0034758045
-
Genomewide scans of complex human diseases: True linkage is hard to find
-
Altmüller J, Palmer LJ, Fischer G, Scherb H, Wjst M. Genomewide scans of complex human diseases: true linkage is hard to find. Am J Hum Genet 2001;69:936-50.
-
(2001)
Am J Hum Genet
, vol.69
, pp. 936-950
-
-
Altmüller, J.1
Palmer, L.J.2
Fischer, G.3
Scherb, H.4
Wjst, M.5
-
14
-
-
0035257236
-
Association study designs for complex diseases
-
Cardon LR, Bell JI. Association study designs for complex diseases. Nature Rev Genet 2001;2:91-9.
-
(2001)
Nature Rev Genet
, vol.2
, pp. 91-99
-
-
Cardon, L.R.1
Bell, J.I.2
-
15
-
-
0035654137
-
Assessing genetic variation: Genotyping single nucleotide polymorphisms
-
Syvänen A-C. Assessing genetic variation: genotyping single nucleotide polymorphisms. Nature Rev Genet 2001;2:930-42.
-
(2001)
Nature Rev Genet
, vol.2
, pp. 930-942
-
-
Syvänen, A.-C.1
-
16
-
-
0035776497
-
Methods for genotyping single nucleotide polymorphisms
-
Kwok P-Y. Methods for genotyping single nucleotide polymorphisms. Annu Rev Genomics Hum Genet 2001;2:235-58.
-
(2001)
Annu Rev Genomics Hum Genet
, vol.2
, pp. 235-258
-
-
Kwok, P.-Y.1
-
17
-
-
0036590151
-
Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools
-
Norton N, Williams NM, Williams HJ, Spurlock G, Kirov G, Morris DW, et al. Universal, robust, highly quantitative SNP allele frequency measurement in DNA pools. Hum Genet 2002; 110:471-8.
-
(2002)
Hum Genet
, vol.110
, pp. 471-478
-
-
Norton, N.1
Williams, N.M.2
Williams, H.J.3
Spurlock, G.4
Kirov, G.5
Morris, D.W.6
-
18
-
-
0033006003
-
Allelic discrimination using fluorogenic probes and the 5′ nuclease assay
-
Livak KJ. Allelic discrimination using fluorogenic probes and the 5′ nuclease assay. Genet Anal 1999;14:143-9.
-
(1999)
Genet Anal
, vol.14
, pp. 143-149
-
-
Livak, K.J.1
-
19
-
-
0031983834
-
Multicolor molecular beacons for allele discrimination
-
Tyagi S, Bratu DP, Kramer FR. Multicolor molecular beacons for allele discrimination. Nature Biotechnol 1998;16:49-53.
-
(1998)
Nature Biotechnol
, vol.16
, pp. 49-53
-
-
Tyagi, S.1
Bratu, D.P.2
Kramer, F.R.3
-
20
-
-
0036598550
-
SNPstream UHT: Ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery
-
Bell PA, Chaturvedi S, Gelfand CA, Huang CY, Kochersperger M, Kopla R, et al. SNPstream UHT: Ultra-high throughput SNP genotyping for pharmacogenomics and drug discovery. Biotechniques 2002;32:S70-7.
-
(2002)
Biotechniques
, vol.32
-
-
Bell, P.A.1
Chaturvedi, S.2
Gelfand, C.A.3
Huang, C.Y.4
Kochersperger, M.5
Kopla, R.6
-
21
-
-
0037099042
-
Multiplex SNP genotyping in pooled DNA samples by a four-colour microarray system
-
Lindroos K, Sigurdsson S, Johansson K, Rönnblom L, Syvänen A-C. Multiplex SNP genotyping in pooled DNA samples by a four-colour microarray system. Nucleic Acids Res 2002;30:e70.
-
(2002)
Nucleic Acids Res
, vol.30
-
-
Lindroos, K.1
Sigurdsson, S.2
Johansson, K.3
Rönnblom, L.4
Syvänen, A.-C.5
-
23
-
-
0037308263
-
The genetics of inflammatory bowel disease
-
Bonen DK, Cho JH. The genetics of inflammatory bowel disease. Gastroenterology 2003;124:521-36.
-
(2003)
Gastroenterology
, vol.124
, pp. 521-536
-
-
Bonen, D.K.1
Cho, J.H.2
-
24
-
-
10144222650
-
Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitis
-
Ohmen JD, Yang HY, Yamamoto KK, Zhao HY, Ma Y, Bentley LG, et al. Susceptibility locus for inflammatory bowel disease on chromosome 16 has a role in Crohn's disease, but not in ulcerative colitis. Hum Mol Genet 1996;5:1679-83.
-
(1996)
Hum Mol Genet
, vol.5
, pp. 1679-1683
-
-
Ohmen, J.D.1
Yang, H.Y.2
Yamamoto, K.K.3
Zhao, H.Y.4
Ma, Y.5
Bentley, L.G.6
-
25
-
-
17144472209
-
American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12
-
Brant SR, Fu Y, Fields CT, Baltazar R, Ravenhill G, Pickles MR, et al. American families with Crohn's disease have strong evidence for linkage to chromosome 16 but not chromosome 12. Gastroenterology 1998;115:1056-61.
-
(1998)
Gastroenterology
, vol.115
, pp. 1056-1061
-
-
Brant, S.R.1
Fu, Y.2
Fields, C.T.3
Baltazar, R.4
Ravenhill, G.5
Pickles, M.R.6
-
26
-
-
0032424067
-
Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16
-
Cavanaugh JA, Callen DF, Wilson SR, Stanford PM, Sraml ME, Gorska M, et al. Analysis of Australian Crohn's disease pedigrees refines the localization for susceptibility to inflammatory bowel disease on chromosome 16. Ann Hum Genet 1998;62: 291-8.
-
(1998)
Ann Hum Genet
, vol.62
, pp. 291-298
-
-
Cavanaugh, J.A.1
Callen, D.F.2
Wilson, S.R.3
Stanford, P.M.4
Sraml, M.E.5
Gorska, M.6
-
27
-
-
13144261748
-
Identification of novel susceptibility loci for inflammatory bowel disease on chromosome 1p, 3q, and 4q: Evidence for epistasis between Ip and IBD1
-
Cho JH, Nicolae DL, Gold LH, Fields CT, LaBuda MC, Rohal PM, et al. Identification of novel susceptibility loci for inflammatory bowel disease on chromosome 1p, 3q, and 4q: evidence for epistasis between Ip and IBD1. Proc Natl Acad Sci USA 1998;95:7502-7.
-
(1998)
Proc Natl Acad Sci USA
, vol.95
, pp. 7502-7507
-
-
Cho, J.H.1
Nicolae, D.L.2
Gold, L.H.3
Fields, C.T.4
LaBuda, M.C.5
Rohal, P.M.6
-
28
-
-
17144456849
-
Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16
-
Curran ME, Lau KF, Hampe J, Schreiber S, Bridger S, Macpherson AJS, et al. Genetic analysis of inflammatory bowel disease in a large European cohort supports linkage to chromosomes 12 and 16. Gastroenterology 1998;115:1066-71.
-
(1998)
Gastroenterology
, vol.115
, pp. 1066-1071
-
-
Curran, M.E.1
Lau, K.F.2
Hampe, J.3
Schreiber, S.4
Bridger, S.5
Macpherson, A.J.S.6
-
29
-
-
0032784580
-
Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus: A GISC study
-
Annese V, Latiano A, Bovio P, Forabosco P, Piepoli A, Lombardi G, et al. Genetic analysis in Italian families with inflammatory bowel disease supports linkage to the IBD1 locus: a GISC study. Eur J Hum Genet 1999;7:567-73.
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 567-573
-
-
Annese, V.1
Latiano, A.2
Bovio, P.3
Forabosco, P.4
Piepoli, A.5
Lombardi, G.6
-
30
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
IBD International Genetics Consortium. International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am J Hum Genet 2001;68:1165-71.
-
(2001)
Am J Hum Genet
, vol.68
, pp. 1165-1171
-
-
-
31
-
-
0032231756
-
Linkage and association between inflammatory bowel disease and a locus on chromosome 12
-
Duerr RH, Barmada MM, Zhang L, Davis S, Preston RA, Chensny LJ, et al. Linkage and association between inflammatory bowel disease and a locus on chromosome 12. Am J Hum Genet 1998;63:95-100.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 95-100
-
-
Duerr, R.H.1
Barmada, M.M.2
Zhang, L.3
Davis, S.4
Preston, R.A.5
Chensny, L.J.6
-
32
-
-
0033358425
-
A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort
-
Hampe J, Schreiber S, Shaw SH, Lau KF, Bridger S, Macpherson AJS, et al. A genomewide analysis provides evidence for novel linkages in inflammatory bowel disease in a large European cohort. Am J Hum Genet 1999;64:808-16.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 808-816
-
-
Hampe, J.1
Schreiber, S.2
Shaw, S.H.3
Lau, K.F.4
Bridger, S.5
Macpherson, A.J.S.6
-
33
-
-
0032926240
-
Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple nonparametric analyses
-
Yang H, Plevy SE, Taylor K, Tyan D, Fischel-Ghodsian N, McElree C, et al. Linkage of Crohn's disease to the major histocompatibility complex region is detected by multiple nonparametric analyses. Gut 1999;44:519-26.
-
(1999)
Gut
, vol.44
, pp. 519-526
-
-
Yang, H.1
Plevy, S.E.2
Taylor, K.3
Tyan, D.4
Fischel-Ghodsian, N.5
McElree, C.6
-
34
-
-
0035895992
-
Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-κB
-
Ogura Y, Inohara N, Benito A, Chen FF, Yamaoka S, Nunez G. Nod2, a Nod1/Apaf-1 family member that is restricted to monocytes and activates NF-κB. J Biol Chem 2001;276:4812-8.
-
(2001)
J Biol Chem
, vol.276
, pp. 4812-4818
-
-
Ogura, Y.1
Inohara, N.2
Benito, A.3
Chen, F.F.4
Yamaoka, S.5
Nunez, G.6
-
35
-
-
0035951792
-
Human Nodi confers responsiveness to bacterial lipopolysaccharides
-
Inohara N, Ogura Y, Chen FF, Muto A, Nunez G. Human Nodi confers responsiveness to bacterial lipopolysaccharides. J Biol Chem 2001;276:2551-4.
-
(2001)
J Biol Chem
, vol.276
, pp. 2551-2554
-
-
Inohara, N.1
Ogura, Y.2
Chen, F.F.3
Muto, A.4
Nunez, G.5
-
36
-
-
0031925362
-
Activation of nuclear factor kappa B in inflammatory bowel disease
-
Schreiber S, Nikolaus S, Hampe J. Activation of nuclear factor kappa B in inflammatory bowel disease. Gut 1998;42:477-84.
-
(1998)
Gut
, vol.42
, pp. 477-484
-
-
Schreiber, S.1
Nikolaus, S.2
Hampe, J.3
-
37
-
-
0035897904
-
Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations
-
Hampe J, Cuthbert A, Croucher PJ, Mirza MM, Mascheretti S, Fisher S, et al. Association between insertion mutation in NOD2 gene and Crohn's disease in German and British populations. Lancet 2001;357:1925-8.
-
(2001)
Lancet
, vol.357
, pp. 1925-1928
-
-
Hampe, J.1
Cuthbert, A.2
Croucher, P.J.3
Mirza, M.M.4
Mascheretti, S.5
Fisher, S.6
-
38
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot JP, Chamaillard M, Zouali H, Lesage S, Cezard JP, Belaiche J, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature 2001; 411:599-603.
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
-
39
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura Y, Bonen DK, Inohara N, Nicolae DL, Chen FF, Ramos R, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature 2001;411:603-6.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
-
40
-
-
0036202885
-
The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease
-
Cuthbert AP, Fisher SA, Mirza MM, King K, Hampe J, Croucher PJ, et al. The contribution of NOD2 gene mutations to the risk and site of disease in inflammatory bowel disease. Gastroenterology 2002;122:867-74.
-
(2002)
Gastroenterology
, vol.122
, pp. 867-874
-
-
Cuthbert, A.P.1
Fisher, S.A.2
Mirza, M.M.3
King, K.4
Hampe, J.5
Croucher, P.J.6
-
41
-
-
0036202336
-
The molecular classification of the clinical manifestations of Crohn's disease
-
Ahmad T, Armuzzi A, Bunce M, Mulcahy-Hawes K, Marshall SE, Orchard TR, et al. The molecular classification of the clinical manifestations of Crohn's disease. Gastroenterology 2002;122: 854-66.
-
(2002)
Gastroenterology
, vol.122
, pp. 854-866
-
-
Ahmad, T.1
Armuzzi, A.2
Bunce, M.3
Mulcahy-Hawes, K.4
Marshall, S.E.5
Orchard, T.R.6
-
42
-
-
0037221395
-
Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan
-
Bonen DK, Ogura Y, Nicolae DL, Inohara N, Saab L, Tsuyoshi T, et al. Crohn's disease-associated NOD2 variants share a signaling defect in response to lipopolysaccharide and peptidoglycan. Gastroenterology 2003;124:140-7.
-
(2003)
Gastroenterology
, vol.124
, pp. 140-147
-
-
Bonen, D.K.1
Ogura, Y.2
Nicolae, D.L.3
Inohara, N.4
Saab, L.5
Tsuyoshi, T.6
-
43
-
-
0027366623
-
Oxidative metabolism of omeprazole in human liver microsomes: Cosegregation with S-mephenytoin 4′-hydroxylation
-
Chiba K, Kobayashi K, Manabe K, Tani M, Kamataki T, Ishizaki T. Oxidative metabolism of omeprazole in human liver microsomes: cosegregation with S-mephenytoin 4′-hydroxylation. J Pharmacol Exp Ther 1993;266:52-9.
-
(1993)
J Pharmacol Exp Ther
, vol.266
, pp. 52-59
-
-
Chiba, K.1
Kobayashi, K.2
Manabe, K.3
Tani, M.4
Kamataki, T.5
Ishizaki, T.6
-
44
-
-
0028923801
-
Oxidative metabolism of lansoprazole by human liver cytochromes P450
-
Pichard L, Curi-Pedrosa R, Bonfils C, Jacqz-Aigrain Domergue J, Joyeux H. Oxidative metabolism of lansoprazole by human liver cytochromes P450. Mol Pharmacol 1995;47:410-8.
-
(1995)
Mol Pharmacol
, vol.47
, pp. 410-418
-
-
Pichard, L.1
Curi-Pedrosa, R.2
Bonfils, C.3
Jacqz-Aigrain Domergue, J.4
Joyeux, H.5
-
45
-
-
12644315063
-
Pharmacokinetics of omeprazole (a substrate of CYP2C19) and comparison with two mutant alleles, C gamma P2C19m1 in exon 5 and C gamma P2C19m2 in exon 4, in Japanese subjects
-
Ieiri I, Kubota T, Urae A, Kimura M, Wada Y, Mamiya K, et al. Pharmacokinetics of omeprazole (a substrate of CYP2C19) and comparison with two mutant alleles, C gamma P2C19m1 in exon 5 and C gamma P2C19m2 in exon 4, in Japanese subjects. Clin Pharmacol Ther 1996;59:647-53.
-
(1996)
Clin Pharmacol Ther
, vol.59
, pp. 647-653
-
-
Ieiri, I.1
Kubota, T.2
Urae, A.3
Kimura, M.4
Wada, Y.5
Mamiya, K.6
-
46
-
-
0034864471
-
CYP2C19 genotype and pharmacokinetics of three proton-pump inhibitors in healthy subjects
-
Sakai T, Aoyama N, Kita T, Sakaeda T, Nishiguchi K, Nishitora Y, et al. CYP2C19 genotype and pharmacokinetics of three proton-pump inhibitors in healthy subjects. Pharm Res 2001;18: 721-7.
-
(2001)
Pharm Res
, vol.18
, pp. 721-727
-
-
Sakai, T.1
Aoyama, N.2
Kita, T.3
Sakaeda, T.4
Nishiguchi, K.5
Nishitora, Y.6
-
47
-
-
0028260641
-
The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans
-
De Morais SMF, Wilkinson GR, Blaisdell J, Nakamura K, Goldstein JA. The major genetic defect responsible for the polymorphism of S-mephenytoin metabolism in humans. J Biol Chem 1994;269:15419-22.
-
(1994)
J Biol Chem
, vol.269
, pp. 15419-15422
-
-
De Morais, S.M.F.1
Wilkinson, G.R.2
Blaisdell, J.3
Nakamura, K.4
Goldstein, J.A.5
-
48
-
-
0028044085
-
Identification of a new genetic defect responsible for the polymorphism of S-mephenytoin metabolism in Japanese
-
De Morais SMF, Wilkinson GR, Blaisdell J, Meyer UA, Nakamura K, Goldstein JA. Identification of a new genetic defect responsible for the polymorphism of S-mephenytoin metabolism in Japanese. Mol Pharmacol 1994;46:594-8.
-
(1994)
Mol Pharmacol
, vol.46
, pp. 594-598
-
-
De Morais, S.M.F.1
Wilkinson, G.R.2
Blaisdell, J.3
Meyer, U.A.4
Nakamura, K.5
Goldstein, J.A.6
-
49
-
-
0022178173
-
Interethnic differences in genetic polymorphism of debrisoquin and mephenytoin hydroxylation between Japanese and Caucasian population
-
Nakamura K, Goto F, Ray WA, McAllister CB, Jacqz E, Wilkinson GR, et al. Interethnic differences in genetic polymorphism of debrisoquin and mephenytoin hydroxylation between Japanese and Caucasian population. Clin Pharmacol Ther 1985;38:402-8.
-
(1985)
Clin Pharmacol Ther
, vol.38
, pp. 402-408
-
-
Nakamura, K.1
Goto, F.2
Ray, W.A.3
McAllister, C.B.4
Jacqz, E.5
Wilkinson, G.R.6
-
50
-
-
0026506140
-
Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and S-mephenytoin
-
Bertilsson L, Lou Y-Q, Du YL, Liu Y, Kuang TY, Liao XM, et al. Pronounced differences between native Chinese and Swedish populations in the polymorphic hydroxylations of debrisoquin and S-mephenytoin. Clin Pharmacol Ther 1992;51:388-97.
-
(1992)
Clin Pharmacol Ther
, vol.51
, pp. 388-397
-
-
Bertilsson, L.1
Lou, Y.-Q.2
Du, Y.L.3
Liu, Y.4
Kuang, T.Y.5
Liao, X.M.6
-
51
-
-
0027208084
-
Why are diazepam metabolism and polymorphic S-mephenytoin hydroxylation associated with each other in white and Korean populations but not in Chinese population
-
Bertilsson L, Kalow W. Why are diazepam metabolism and polymorphic S-mephenytoin hydroxylation associated with each other in white and Korean populations but not in Chinese population. Clin Pharmacol Ther 1993;53:608-10.
-
(1993)
Clin Pharmacol Ther
, vol.53
, pp. 608-610
-
-
Bertilsson, L.1
Kalow, W.2
-
52
-
-
0033851533
-
Effects of omeprazole on intragastric pH and plasma gastrin levels are dependent on the CYP2C19 polymorphism
-
Sagar M, Tybring G, Dahl M-L, Bertilsson L, Seensalu R. Effects of omeprazole on intragastric pH and plasma gastrin levels are dependent on the CYP2C19 polymorphism. Gastroenterology 2000;119:670-6.
-
(2000)
Gastroenterology
, vol.119
, pp. 670-676
-
-
Sagar, M.1
Tybring, G.2
Dahl, M.-L.3
Bertilsson, L.4
Seensalu, R.5
-
53
-
-
0035208525
-
Effect of high-dose lansoprazole on intragastric pH in subjects who are homozygous extensive metabolizers of cytochrome P4502C19
-
Furuta T, Shirai N, Xiao F, Ohashi K, Ishizaki T. Effect of high-dose lansoprazole on intragastric pH in subjects who are homozygous extensive metabolizers of cytochrome P4502C19. Clin Pharmacol Ther 2001;70:484-92.
-
(2001)
Clin Pharmacol Ther
, vol.70
, pp. 484-492
-
-
Furuta, T.1
Shirai, N.2
Xiao, F.3
Ohashi, K.4
Ishizaki, T.5
-
54
-
-
0036795262
-
Effect of cytochrome P4502C19 genotypic differences on cure rates for gastroesophageal reflux disease by lansoprazole
-
Furuta T, Shirai N, Watanabe F, Honda S, Takeuchi K, Iida T, et al. Effect of cytochrome P4502C19 genotypic differences on cure rates for gastroesophageal reflux disease by lansoprazole. Clin Pharmacol Ther 2002;72:453-60.
-
(2002)
Clin Pharmacol Ther
, vol.72
, pp. 453-460
-
-
Furuta, T.1
Shirai, N.2
Watanabe, F.3
Honda, S.4
Takeuchi, K.5
Iida, T.6
-
55
-
-
0029895783
-
Allelic variation of human serotonin transporter gene expression
-
Heils A, Teufel A, Petri S, Stober G, Riederer P, Bengel D, et al. Allelic variation of human serotonin transporter gene expression. J Neurochem 1996;66:2621-4.
-
(1996)
J Neurochem
, vol.66
, pp. 2621-2624
-
-
Heils, A.1
Teufel, A.2
Petri, S.3
Stober, G.4
Riederer, P.5
Bengel, D.6
-
56
-
-
0033532309
-
Functional analysis of a novel human serotonin transporter gene promoter in immortalized raphe cells
-
Mortensen OV, Thomassen M, Larsen MB, Whittemore SR, Wiborg O. Functional analysis of a novel human serotonin transporter gene promoter in immortalized raphe cells. Mol Brain Res 1999;68:141-8.
-
(1999)
Mol Brain Res
, vol.68
, pp. 141-148
-
-
Mortensen, O.V.1
Thomassen, M.2
Larsen, M.B.3
Whittemore, S.R.4
Wiborg, O.5
-
57
-
-
0036325415
-
Serotonin-transporter polymorphism pharmacogenetics in diarrhea-predominant irritable bowel syndrome
-
Camilleri M, Atanasova E, Carlson PJ, Ahmad U, Kim HJ, Viramontes BE, et al. Serotonin-transporter polymorphism pharmacogenetics in diarrhea-predominant irritable bowel syndrome. Gastroenterology 2002;123:425-32.
-
(2002)
Gastroenterology
, vol.123
, pp. 425-432
-
-
Camilleri, M.1
Atanasova, E.2
Carlson, P.J.3
Ahmad, U.4
Kim, H.J.5
Viramontes, B.E.6
-
58
-
-
0037012338
-
Osteopontin identified as lead marker of colon cancer progression, using pooled sample expression profiling
-
Agrawal D, Chen T, Irby R, Quackenbush J, Chambers AF, Szabo M, et al. Osteopontin identified as lead marker of colon cancer progression, using pooled sample expression profiling. J Natl Cancer Inst 2002;94:513-21.
-
(2002)
J Natl Cancer Inst
, vol.94
, pp. 513-521
-
-
Agrawal, D.1
Chen, T.2
Irby, R.3
Quackenbush, J.4
Chambers, A.F.5
Szabo, M.6
-
59
-
-
13344259990
-
Mapping of a susceptibility locus for Crohn's disease on chromosome 16
-
Hugot JP, Laurent-Puig P, Gower-Rousseau C, Olson JM, Lee JC, Beaugerie L, et al. Mapping of a susceptibility locus for Crohn's disease on chromosome 16. Nature 1996;379:821-3.
-
(1996)
Nature
, vol.379
, pp. 821-823
-
-
Hugot, J.P.1
Laurent-Puig, P.2
Gower-Rousseau, C.3
Olson, J.M.4
Lee, J.C.5
Beaugerie, L.6
-
60
-
-
16044373177
-
Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
-
Satsangi J, Parkes M, Louis E, Hashimoto L, Kato N, Welsh K, et al. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nat Genet 1996;14:199-202.
-
(1996)
Nat Genet
, vol.14
, pp. 199-202
-
-
Satsangi, J.1
Parkes, M.2
Louis, E.3
Hashimoto, L.4
Kato, N.5
Welsh, K.6
-
61
-
-
0033358520
-
Linkage of inflammatory bowel disease to human chromosome 6p
-
Hampe J, Shaw SH, Saiz R, Leysens N, Lantermann A, Mascheretti S, et al. Linkage of inflammatory bowel disease to human chromosome 6p. Am J Hum Genet 1999;65:1647-55.
-
(1999)
Am J Hum Genet
, vol.65
, pp. 1647-1655
-
-
Hampe, J.1
Shaw, S.H.2
Saiz, R.3
Leysens, N.4
Lantermann, A.5
Mascheretti, S.6
-
62
-
-
0033228538
-
A genome-wide search identifies potential new susceptibility loci for Crohn's disease
-
Ma Y, Ohmen JD, Li Z, Bentley LG, McElree C, Pressman S, et al. A genome-wide search identifies potential new susceptibility loci for Crohn's disease. Inflamm Bowel Dis 1999;5:271-8.
-
(1999)
Inflamm Bowel Dis
, vol.5
, pp. 271-278
-
-
Ma, Y.1
Ohmen, J.D.2
Li, Z.3
Bentley, L.G.4
McElree, C.5
Pressman, S.6
-
63
-
-
0033927387
-
High-density genome scan in Crohn's disease shows confirmed linkage to chromosome 14q11-12
-
Duerr RH, Barmada M, Zhang L, Pfutzer R, Weeks DE. High-density genome scan in Crohn's disease shows confirmed linkage to chromosome 14q11-12. Am J Hum Genet 2000;66:1857-62.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1857-1862
-
-
Duerr, R.H.1
Barmada, M.2
Zhang, L.3
Pfutzer, R.4
Weeks, D.E.5
-
64
-
-
0033910870
-
Genome-wide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci
-
Rioux JD, Silverberg MS, Daly MJ, Steinhart AH, McLeod RS, Griffiths AM, et al. Genome-wide search in Canadian families with inflammatory bowel disease reveals two novel susceptibility loci. Am J Hum Genet 2000;66:1863-70.
-
(2000)
Am J Hum Genet
, vol.66
, pp. 1863-1870
-
-
Rioux, J.D.1
Silverberg, M.S.2
Daly, M.J.3
Steinhart, A.H.4
McLeod, R.S.5
Griffiths, A.M.6
-
65
-
-
0029587180
-
Use of omeprazole as probe drug for CYP2C19 phenotype in Swedish Caucasians: Comparison with S-mephenytoin hydroxylation phenotype and CYP2C19 genotype
-
Chang M, Dahl ML, Tybring G, Götharsson E, Bertilsson L. Use of omeprazole as probe drug for CYP2C19 phenotype in Swedish Caucasians: comparison with S-mephenytoin hydroxylation phenotype and CYP2C19 genotype. Pharmacogenetics 1995;5: 358-63.
-
(1995)
Pharmacogenetics
, vol.5
, pp. 358-363
-
-
Chang, M.1
Dahl, M.L.2
Tybring, G.3
Götharsson, E.4
Bertilsson, L.5
|