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Volumn 40, Issue 4, 2003, Pages 321-328

Genetic Variation and Hematology: Single-Nucleotide Polymorphisms, Haplotypes, and Complex Disease

Author keywords

[No Author keywords available]

Indexed keywords

6 MERCAPTOPURINE DERIVATIVE; AZATHIOPRINE; MERCAPTOPURINE; TIOGUANINE;

EID: 0142094492     PISSN: 00371963     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0037-1963(03)00198-7     Document Type: Article
Times cited : (13)

References (77)
  • 1
    • 0032495656 scopus 로고    scopus 로고
    • Granulocytosis causing sickle-cell crisis
    • Abboud M, Laver J, Blau CA: Granulocytosis causing sickle-cell crisis. Lancet 351:959, 1998
    • (1998) Lancet , vol.351 , pp. 959
    • Abboud, M.1    Laver, J.2    Blau, C.A.3
  • 2
    • 0032898380 scopus 로고    scopus 로고
    • Thiopurine methyltransferase alleles in British and Ghanaian populations
    • Ameyaw MM, Collie-Duguid ES, Powrie RH, et al: Thiopurine methyltransferase alleles in British and Ghanaian populations. Hum Mol Genet 8:367-370, 1999
    • (1999) Hum Mol Genet , vol.8 , pp. 367-370
    • Ameyaw, M.M.1    Collie-Duguid, E.S.2    Powrie, R.H.3
  • 3
    • 0032212759 scopus 로고    scopus 로고
    • Thiopurine methyltransferase genotype predicts therapy-limiting severe toxicity from azathioprine
    • Black AJ, McLeod HL, Capell HA, et al: Thiopurine methyltransferase genotype predicts therapy-limiting severe toxicity from azathioprine. Ann Intern Med 129:716-718, 1998
    • (1998) Ann Intern Med , vol.129 , pp. 716-718
    • Black, A.J.1    McLeod, H.L.2    Capell, H.A.3
  • 4
    • 0037373275 scopus 로고    scopus 로고
    • Discovering genotypes underlying human phenotypes: Past successes for mendelian disease, future approaches for complex disease
    • Botstein D, Risch N: Discovering genotypes underlying human phenotypes: past successes for mendelian disease, future approaches for complex disease. Nat Genet 33:228-237, 2003 (suppl)
    • (2003) Nat Genet , vol.33 , Issue.SUPPL. , pp. 228-237
    • Botstein, D.1    Risch, N.2
  • 5
    • 0034753547 scopus 로고    scopus 로고
    • Rethinking genetic strategies to study complex diseases
    • Brookes AJ: Rethinking genetic strategies to study complex diseases. Trends Mol Med 7:512-516, 2001
    • (2001) Trends Mol Med , vol.7 , pp. 512-516
    • Brookes, A.J.1
  • 6
    • 0032991552 scopus 로고    scopus 로고
    • Characterization of single-nucleotide polymorphisms in coding regions of human genes
    • Cargill M, Altshuler D, Ireland J, et al: Characterization of single-nucleotide polymorphisms in coding regions of human genes. Nat Genet 22:231-238, 1999
    • (1999) Nat Genet , vol.22 , pp. 231-238
    • Cargill, M.1    Altshuler, D.2    Ireland, J.3
  • 7
    • 0031867595 scopus 로고    scopus 로고
    • Are sickle cell disease patients with stroke genetically predisposed to the event by inheriting a tendency to high tumor necrosis factor levels?
    • Carroll JE, McKie V, Kutlar A: Are sickle cell disease patients with stroke genetically predisposed to the event by inheriting a tendency to high tumor necrosis factor levels? Am J Hematol 58:250, 1998
    • (1998) Am J Hematol , vol.58 , pp. 250
    • Carroll, J.E.1    McKie, V.2    Kutlar, A.3
  • 8
    • 0036667399 scopus 로고    scopus 로고
    • Using genetic variation to study immunomodulation
    • Chanock S, Taylor JG: Using genetic variation to study immunomodulation. Curr Opin Pharmacol 2:463-469, 2002
    • (2002) Curr Opin Pharmacol , vol.2 , pp. 463-469
    • Chanock, S.1    Taylor, J.G.2
  • 9
    • 0032719023 scopus 로고    scopus 로고
    • SNPing away at innate immunity
    • Chanock SJ, Foster CB: SNPing away at innate immunity. J Clin Invest 104:369-370, 1999
    • (1999) J Clin Invest , vol.104 , pp. 369-370
    • Chanock, S.J.1    Foster, C.B.2
  • 10
    • 0035988621 scopus 로고    scopus 로고
    • One gene and one outcome? No way
    • Chanock S, Wacholder S: One gene and one outcome? No way. Trends Mol Med 8:266-269, 2002
    • (2002) Trends Mol Med , vol.8 , pp. 266-269
    • Chanock, S.1    Wacholder, S.2
  • 11
    • 0034799051 scopus 로고    scopus 로고
    • Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease
    • Chanock S: Candidate genes and single nucleotide polymorphisms (SNPs) in the study of human disease. Dis Markers 17:89-98, 2001
    • (2001) Dis Markers , vol.17 , pp. 89-98
    • Chanock, S.1
  • 12
    • 0037383961 scopus 로고    scopus 로고
    • Association between chronic disseminated candidiasis in adult acute leukemia and common IL 4 promoter haplotypes
    • Choi EH, Foster CB, Taylor JG, et al: Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes. J Infect Dis 187:1153-1156, 2003
    • (2003) J Infect Dis , vol.187 , pp. 1153-1156
    • Choi, E.H.1    Foster, C.B.2    Taylor, J.G.3
  • 13
    • 0036838809 scopus 로고    scopus 로고
    • A common haplotype of interleukin-4 gene IL4 is associated with severe respiratory syncytial virus disease in Korean children
    • Choi EH, Lee HJ, Yoo T, et al: A common haplotype of interleukin-4 gene IL4 is associated with severe respiratory syncytial virus disease in Korean children. J Infect Dis 186:1207-1211, 2002
    • (2002) J Infect Dis , vol.186 , pp. 1207-1211
    • Choi, E.H.1    Lee, H.J.2    Yoo, T.3
  • 14
    • 0035922669 scopus 로고    scopus 로고
    • Epidemiological methods for studying gene and environmental factors in complex diseases
    • a. Clayton D, McKeigue PM: Epidemiological methods for studying gene and environmental factors in complex diseases. Lancet 358:1356-1360, 2001
    • (2001) Lancet , vol.358 , pp. 1356-1360
    • Clayton, D.1    McKeigue, P.M.2
  • 15
    • 0032917646 scopus 로고    scopus 로고
    • The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations
    • Collie-Duguid ES, Pritchard SC, Powrie RH, et al: The frequency and distribution of thiopurine methyltransferase alleles in Caucasian and Asian populations. Pharmacogenetics 9:37-42, 1999
    • (1999) Pharmacogenetics , vol.9 , pp. 37-42
    • Collie-Duguid, E.S.1    Pritchard, S.C.2    Powrie, R.H.3
  • 16
    • 0030688004 scopus 로고    scopus 로고
    • Variations on a theme: Cataloging human DNA sequence variation
    • Collins FS, Guyer MS, Charkravarti A: Variations on a theme: Cataloging human DNA sequence variation. Science 278:1580-1581, 1997
    • (1997) Science , vol.278 , pp. 1580-1581
    • Collins, F.S.1    Guyer, M.S.2    Charkravarti, A.3
  • 17
    • 0033592988 scopus 로고    scopus 로고
    • Genetic epidemiology of single-nucleotide polymorphisms
    • Collins A, Lonjou C, Morton NE: Genetic epidemiology of single-nucleotide polymorphisms. Proc Natl Acad Sci USA 96:15173-15177, 1999
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 15173-15177
    • Collins, A.1    Lonjou, C.2    Morton, N.E.3
  • 18
    • 0037464588 scopus 로고    scopus 로고
    • A vision for the future of genomics research
    • Collins FS, Green ED, Guttmacher AE, et al: A vision for the future of genomics research. Nature 422:835-847, 2003
    • (2003) Nature , vol.422 , pp. 835-847
    • Collins, F.S.1    Green, E.D.2    Guttmacher, A.E.3
  • 19
    • 0033168459 scopus 로고    scopus 로고
    • Shattuck lecture - Medical and societal consequences of the Human Genome Project
    • Collins FS: Shattuck lecture - Medical and societal consequences of the Human Genome Project. N Engl J Med 341:28-37, 1999
    • (1999) N Engl J Med , vol.341 , pp. 28-37
    • Collins, F.S.1
  • 20
    • 0034791035 scopus 로고    scopus 로고
    • High-resolution haplotype structure in the human genome
    • Daly MJ, Rioux JD, Schaffner SF, et al: High-resolution haplotype structure in the human genome. Nat Genet 29:229-232, 2001
    • (2001) Nat Genet , vol.29 , pp. 229-232
    • Daly, M.J.1    Rioux, J.D.2    Schaffner, S.F.3
  • 21
    • 0036660410 scopus 로고    scopus 로고
    • Glutathione S-transferase genotypes genetic susceptibility, and outcome of therapy in childhood acute lymphoblastic leukemia
    • Davies SM, Bhatia S, Ross JA, et al: Glutathione S-transferase genotypes, genetic susceptibility, and outcome of therapy in childhood acute lymphoblastic leukemia. Blood 100:67-71, 2002
    • (2002) Blood , vol.100 , pp. 67-71
    • Davies, S.M.1    Bhatia, S.2    Ross, J.A.3
  • 22
    • 0035423158 scopus 로고    scopus 로고
    • Differing contribution of thiopurine methyltransferase to mercaptopurine versus thioguanine effects in human leukemic cells
    • Dervieux T, Blanco JG, Krynetski EY, et al: Differing contribution of thiopurine methyltransferase to mercaptopurine versus thioguanine effects in human leukemic cells. Cancer Res 61:5810-5816, 2001
    • (2001) Cancer Res , vol.61 , pp. 5810-5816
    • Dervieux, T.1    Blanco, J.G.2    Krynetski, E.Y.3
  • 23
    • 0037320652 scopus 로고    scopus 로고
    • Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor
    • Duan J, Wainwright MS, Comeron JM, et al: Synonymous mutations in the human dopamine receptor D2 (DRD2) affect mRNA stability and synthesis of the receptor. Hum Mol Genet 12:205-216, 2003
    • (2003) Hum Mol Genet , vol.12 , pp. 205-216
    • Duan, J.1    Wainwright, M.S.2    Comeron, J.M.3
  • 24
    • 0037345361 scopus 로고    scopus 로고
    • Genome-wide detection of LOH in prostate cancer using human SNP microarray technology
    • Dumur CI, Dechsukhum C, Ware JL, et al: Genome-wide detection of LOH in prostate cancer using human SNP microarray technology. Genomics 81:260-269, 2003
    • (2003) Genomics , vol.81 , pp. 260-269
    • Dumur, C.I.1    Dechsukhum, C.2    Ware, J.L.3
  • 25
    • 0029130796 scopus 로고
    • Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population
    • Excoffier L, Slatkin M: Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. Mol Biol Evol 12:921-927, 1995
    • (1995) Mol Biol Evol , vol.12 , pp. 921-927
    • Excoffier, L.1    Slatkin, M.2
  • 26
    • 0035154452 scopus 로고    scopus 로고
    • Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease
    • Fallin D, Cohen A, Essioux L, et al: Genetic analysis of case/control data using estimated haplotype frequencies: Application to APOE locus variation and Alzheimer's disease. Genome Res 11:143-151, 2001
    • (2001) Genome Res , vol.11 , pp. 143-151
    • Fallin, D.1    Cohen, A.2    Essioux, L.3
  • 27
    • 0032535301 scopus 로고    scopus 로고
    • Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease
    • Foster CB, Lehrnbecher T, Mol F, et al: Host defense molecule polymorphisms influence the risk for immune-mediated complications in chronic granulomatous disease. J Clin Invest 102:2146-2155, 1998
    • (1998) J Clin Invest , vol.102 , pp. 2146-2155
    • Foster, C.B.1    Lehrnbecher, T.2    Mol, F.3
  • 28
    • 0033619497 scopus 로고    scopus 로고
    • Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: Cohort study
    • Gabolde M, Guilloud-Bataille M, Feingold J, et al: Association of variant alleles of mannose binding lectin with severity of pulmonary disease in cystic fibrosis: Cohort study. BMJ 319:1166-1167, 1999
    • (1999) BMJ , vol.319 , pp. 1166-1167
    • Gabolde, M.1    Guilloud-Bataille, M.2    Feingold, J.3
  • 29
    • 18444369013 scopus 로고    scopus 로고
    • The structure of haplotype blocks in the human genome
    • Gabriel SB, Schaffner SF, Nguyen H, et al: The structure of haplotype blocks in the human genome. Science 296:2225-2229, 2002
    • (2002) Science , vol.296 , pp. 2225-2229
    • Gabriel, S.B.1    Schaffner, S.F.2    Nguyen, H.3
  • 30
    • 0036178075 scopus 로고    scopus 로고
    • Mannose-binding lectin (MBL) therapy in an MBL-deficient patient with severe cystic fibrosis lung disease
    • Garred P, Pressler T, Lanng S, et al: Mannose-binding lectin (MBL) therapy in an MBL-deficient patient with severe cystic fibrosis lung disease. Pediatr Pulmonol 33:201-207, 2002
    • (2002) Pediatr Pulmonol , vol.33 , pp. 201-207
    • Garred, P.1    Pressler, T.2    Lanng, S.3
  • 31
    • 0032695668 scopus 로고    scopus 로고
    • Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis
    • Garred P, Pressler T, Madsen HO, et al: Association of mannose-binding lectin gene heterogeneity with severity of lung disease and survival in cystic fibrosis. J Clin Invest 104:431-437, 1999
    • (1999) J Clin Invest , vol.104 , pp. 431-437
    • Garred, P.1    Pressler, T.2    Madsen, H.O.3
  • 32
    • 0035748530 scopus 로고    scopus 로고
    • Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients
    • Garred P, Voss A, Madsen HO, et al: Association of mannose-binding lectin gene variation with disease severity and infections in a population-based cohort of systemic lupus erythematosus patients. Genes Immun 2:442-450, 2001
    • (2001) Genes Immun , vol.2 , pp. 442-450
    • Garred, P.1    Voss, A.2    Madsen, H.O.3
  • 33
    • 0035071541 scopus 로고    scopus 로고
    • Screening a large reference sample to identify very low frequency sequence variants: Comparisons between two genes
    • Glatt CE, DeYoung JA, Delgado S, et al: Screening a large reference sample to identify very low frequency sequence variants: Comparisons between two genes. Nat Genet 27:435-438, 2001
    • (2001) Nat Genet , vol.27 , pp. 435-438
    • Glatt, C.E.1    DeYoung, J.A.2    Delgado, S.3
  • 34
    • 0032990407 scopus 로고    scopus 로고
    • Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis
    • Halushka MK, Fan JB, Bentley K, et al: Patterns of single-nucleotide polymorphisms in candidate genes for blood-pressure homeostasis. Nat Genet 22:239-247, 1999
    • (1999) Nat Genet , vol.22 , pp. 239-247
    • Halushka, M.K.1    Fan, J.B.2    Bentley, K.3
  • 35
    • 0036517472 scopus 로고    scopus 로고
    • A comprehensive review of genetic association studies
    • Hirschhorn JN, Lohmueller K, Byrne E, et al: A comprehensive review of genetic association studies. Genet Med 4:45-61, 2002
    • (2002) Genet Med , vol.4 , pp. 45-61
    • Hirschhorn, J.N.1    Lohmueller, K.2    Byrne, E.3
  • 36
    • 0042100284 scopus 로고    scopus 로고
    • Mannose-binding protein B allele confers protection against tuberculous meningitis
    • Hoal-Van Helden EG, Epstein J, Victor TC, et al: Mannose-binding protein B allele confers protection against tuberculous meningitis. Pediatr Res 45:459-464, 1999
    • (1999) Pediatr Res , vol.45 , pp. 459-464
    • Hoal-Van Helden, E.G.1    Epstein, J.2    Victor, T.C.3
  • 37
    • 0038107362 scopus 로고    scopus 로고
    • Distinct HLA associations by stroke subtype in children with sickle cell anemia
    • Hoppe C, Klitz W, Noble J, et al: Distinct HLA associations by stroke subtype in children with sickle cell anemia. Blood 101:2865-2869, 2003
    • (2003) Blood , vol.101 , pp. 2865-2869
    • Hoppe, C.1    Klitz, W.2    Noble, J.3
  • 38
    • 0034790092 scopus 로고    scopus 로고
    • A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anaemia
    • Hoppe C, Cheng S, Grow M, et al: A novel multilocus genotyping assay to identify genetic predictors of stroke in sickle cell anaemia. Br J Haematol 114:718-720, 2001
    • (2001) Br J Haematol , vol.114 , pp. 718-720
    • Hoppe, C.1    Cheng, S.2    Grow, M.3
  • 39
    • 0037699066 scopus 로고    scopus 로고
    • Genome-wide genetic characterization of bladder cancer: A comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis
    • Hoque MO, Lee CC, Cairns P, et al: Genome-wide genetic characterization of bladder cancer: A comparison of high-density single-nucleotide polymorphism arrays and PCR-based microsatellite analysis. Cancer Res 63:2216-2222, 2003
    • (2003) Cancer Res , vol.63 , pp. 2216-2222
    • Hoque, M.O.1    Lee, C.C.2    Cairns, P.3
  • 40
    • 0036075780 scopus 로고    scopus 로고
    • GSTT1 and CYP2E1 polymorphisms and trihalomethanes in drinking water: Effect on childhood leukemia
    • Infante-Rivard C, Amre D, Sinnett D: GSTT1 and CYP2E1 polymorphisms and trihalomethanes in drinking water: Effect on childhood leukemia. Environ Health Perspect 110: 591-593, 2002
    • (2002) Environ Health Perspect , vol.110 , pp. 591-593
    • Infante-Rivard, C.1    Amre, D.2    Sinnett, D.3
  • 41
    • 0033626025 scopus 로고    scopus 로고
    • Pharmacogenetics: A tool for individualizing antineoplastic therapy
    • Innocenti F, Iyer L, Ratain MJ: Pharmacogenetics: A tool for individualizing antineoplastic therapy. Clin Pharmacokinet 39:315-325, 2000
    • (2000) Clin Pharmacokinet , vol.39 , pp. 315-325
    • Innocenti, F.1    Iyer, L.2    Ratain, M.J.3
  • 42
    • 0034789532 scopus 로고    scopus 로고
    • Haplotype tagging for the identification of common disease genes
    • Johnson GC, Esposito L, Barratt BJ, et al: Haplotype tagging for the identification of common disease genes. Nat Genet 29:233-237, 2001
    • (2001) Nat Genet , vol.29 , pp. 233-237
    • Johnson, G.C.1    Esposito, L.2    Barratt, B.J.3
  • 43
    • 0036866625 scopus 로고    scopus 로고
    • Glutathione S-transferase P 1 genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukaemia
    • Krajinovic M, Labuda D, Sinnett D: Glutathione S-transferase P1 genetic polymorphisms and susceptibility to childhood acute lymphoblastic leukaemia. Pharmacogenetics 12:655-658, 2002
    • (2002) Pharmacogenetics , vol.12 , pp. 655-658
    • Krajinovic, M.1    Labuda, D.2    Sinnett, D.3
  • 44
    • 0037049795 scopus 로고    scopus 로고
    • Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia
    • Krajinovic M, Sinnett H, Richer C, et al: Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia, Int J Cancer 97:230-236, 2002
    • (2002) Int J Cancer , vol.97 , pp. 230-236
    • Krajinovic, M.1    Sinnett, H.2    Richer, C.3
  • 45
    • 0035094764 scopus 로고    scopus 로고
    • Variation is the spice of life
    • Kruglyak L, Nickerson DA: Variation is the spice of life. Nat Genet 27:234-236, 2001
    • (2001) Nat Genet , vol.27 , pp. 234-236
    • Kruglyak, L.1    Nickerson, D.A.2
  • 46
    • 0033039497 scopus 로고    scopus 로고
    • Prospects for whole-genome linkage disequilibrium mapping of common disease genes
    • Kruglyak L: Prospects for whole-genome linkage disequilibrium mapping of common disease genes, Nat Genet 22:139-144, 1999
    • (1999) Nat Genet , vol.22 , pp. 139-144
    • Kruglyak, L.1
  • 47
    • 2042437650 scopus 로고    scopus 로고
    • Initial sequencing and analysis of the human genome
    • Lander ES, Linton LM, Birren B, et al: Initial sequencing and analysis of the human genome. Nature 409:860-921, 2001
    • (2001) Nature , vol.409 , pp. 860-921
    • Lander, E.S.1    Linton, L.M.2    Birren, B.3
  • 48
    • 0034161456 scopus 로고    scopus 로고
    • Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease
    • Lane DA, Grant PJ: Role of hemostatic gene polymorphisms in venous and arterial thrombotic disease. Blood 95:1517-1532, 2000
    • (2000) Blood , vol.95 , pp. 1517-1532
    • Lane, D.A.1    Grant, P.J.2
  • 49
    • 0034425049 scopus 로고    scopus 로고
    • Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays
    • Lindblad-Toh K, Tanenbaum DM, Daly MJ, et al: Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays. Nat Biotechnol 18:1001-1005, 2000
    • (2000) Nat Biotechnol , vol.18 , pp. 1001-1005
    • Lindblad-Toh, K.1    Tanenbaum, D.M.2    Daly, M.J.3
  • 50
    • 0037312921 scopus 로고    scopus 로고
    • Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease
    • Lohmueller KE, Pearce CL, Pike M, et al: Meta-analysis of genetic association studies supports a contribution of common variants to susceptibility to common disease. Nat Genet 33:177-182, 2003
    • (2003) Nat Genet , vol.33 , pp. 177-182
    • Lohmueller, K.E.1    Pearce, C.L.2    Pike, M.3
  • 51
    • 0028044714 scopus 로고
    • Thiopurine methyltransferase activity in American white subjects and black subjects
    • McLeod HL, Lin JS, Scott EP, et al: Thiopurine methyltransferase activity in American white subjects and black subjects. Clin Pharmacol Ther 55:15-20, 1994
    • (1994) Clin Pharmacol Ther , vol.55 , pp. 15-20
    • McLeod, H.L.1    Lin, J.S.2    Scott, E.P.3
  • 52
    • 0035033019 scopus 로고    scopus 로고
    • Pharmacogenomics: Unlocking the human genome for better drug therapy
    • McLeod HL, Evans WE: Pharmacogenomics: Unlocking the human genome for better drug therapy. Annu Rev Pharmacol Toxicol 41:101-121, 2001
    • (2001) Annu Rev Pharmacol Toxicol , vol.41 , pp. 101-121
    • McLeod, H.L.1    Evans, W.E.2
  • 53
    • 0033434009 scopus 로고    scopus 로고
    • Ethnic differences in thiopurine methyltransferase pharmacogenetics: Evidence for allele specificity in Caucasian and Kenyan individuals
    • McLeod HL, Pritchard SC, Githang'a J, et al: Ethnic differences in thiopurine methyltransferase pharmacogenetics: Evidence for allele specificity in Caucasian and Kenyan individuals. Pharmacogenetics 9:773-776, 1999
    • (1999) Pharmacogenetics , vol.9 , pp. 773-776
    • McLeod, H.L.1    Pritchard, S.C.2    Githang'a, J.3
  • 54
    • 0037093083 scopus 로고    scopus 로고
    • Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation
    • Mullighan CG, Heatley S, Doherty K, et al: Mannose-binding lectin gene polymorphisms are associated with major infection following allogeneic hemopoietic stem cell transplantation. Blood 99:3524-3529, 2002
    • (2002) Blood , vol.99 , pp. 3524-3529
    • Mullighan, C.G.1    Heatley, S.2    Doherty, K.3
  • 55
    • 0035949107 scopus 로고    scopus 로고
    • Deficiency of mannose-binding lectin and burden of infection in children with malignancy: A prospective study
    • Neth O, Hann I, Turner MW, et al: Deficiency of mannose-binding lectin and burden of infection in children with malignancy: A prospective study. Lancet 358:614-618, 2001
    • (2001) Lancet , vol.358 , pp. 614-618
    • Neth, O.1    Hann, I.2    Turner, M.W.3
  • 56
    • 0031965089 scopus 로고    scopus 로고
    • Cerebrovascular accidents in sickle cell disease: Rates and risk factors
    • Ohene-Frempong K, Weiner SJ, Sleeper LA, et al: Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood 91:288-294, 1998
    • (1998) Blood , vol.91 , pp. 288-294
    • Ohene-Frempong, K.1    Weiner, S.J.2    Sleeper, L.A.3
  • 57
    • 0019949838 scopus 로고
    • Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster
    • Orkin SH, Kazazian HH Jr, Antonarakis SE, et al: Linkage of beta-thalassaemia mutations and beta-globin gene polymorphisms with DNA polymorphisms in human beta-globin gene cluster. Nature 296:627-631, 1982
    • (1982) Nature , vol.296 , pp. 627-631
    • Orkin, S.H.1    Kazazian H.H., Jr.2    Antonarakis, S.E.3
  • 58
    • 0035949119 scopus 로고    scopus 로고
    • Association between deficiency of mannose-binding lectin and severe infections after chemotherapy
    • Peterslund NA, Koch C, Jensenius JC, et al: Association between deficiency of mannose-binding lectin and severe infections after chemotherapy. Lancet 358:637-638, 2001
    • (2001) Lancet , vol.358 , pp. 637-638
    • Peterslund, N.A.1    Koch, C.2    Jensenius, J.C.3
  • 59
    • 0034969437 scopus 로고    scopus 로고
    • Are rare variants responsible for susceptibility to complex diseases?
    • Pritchard JK: Are rare variants responsible for susceptibility to complex diseases? Am J Hum Genet 69:124-137, 2001
    • (2001) Am J Hum Genet , vol.69 , pp. 124-137
    • Pritchard, J.K.1
  • 60
    • 0032906340 scopus 로고    scopus 로고
    • Sequence variation in the human angiotensin converting enzyme
    • Rieder MJ, Taylor SL, Clark AG, et al: Sequence variation in the human angiotensin converting enzyme. Nat Genet 22:59-62, 1999
    • (1999) Nat Genet , vol.22 , pp. 59-62
    • Rieder, M.J.1    Taylor, S.L.2    Clark, A.G.3
  • 61
    • 0029741063 scopus 로고    scopus 로고
    • The future of genetic studies of complex human diseases
    • Risch N, Merikangas K: The future of genetic studies of complex human diseases. Science 273:1516-1517, 1996
    • (1996) Science , vol.273 , pp. 1516-1517
    • Risch, N.1    Merikangas, K.2
  • 62
    • 0034927358 scopus 로고    scopus 로고
    • The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches
    • Risch N: The genetic epidemiology of cancer: Interpreting family and twin studies and their implications for molecular genetic approaches. Cancer Epidemiol Biomarkers Prev 10:733-741, 2001
    • (2001) Cancer Epidemiol Biomarkers Prev , vol.10 , pp. 733-741
    • Risch, N.1
  • 63
    • 0034660559 scopus 로고    scopus 로고
    • Searching for genetic determinants in the new millennium
    • Risch NJ: Searching for genetic determinants in the new millennium. Nature 405:847-856, 2000
    • (2000) Nature , vol.405 , pp. 847-856
    • Risch, N.J.1
  • 64
    • 0036633359 scopus 로고    scopus 로고
    • Genome-based pharmacogenetics and the pharmaceutical industry
    • RosesAD: Genome-based pharmacogenetics and the pharmaceutical industry. Nat Rev Drug Discov 1:541-549, 2002
    • (2002) Nat Rev Drug Discov , vol.1 , pp. 541-549
    • Roses, A.D.1
  • 65
    • 0035951501 scopus 로고    scopus 로고
    • The use of common genetic polymorphisms to enhance the epidemiologic study of environmental carcinogens
    • Rothman N, Wacholder S, Caporaso NE: The use of common genetic polymorphisms to enhance the epidemiologic study of environmental carcinogens. Biochim Biophys Acta 1471: C1-10, 2001
    • (2001) Biochim Biophys Acta , vol.1471
    • Rothman, N.1    Wacholder, S.2    Caporaso, N.E.3
  • 66
    • 0036155283 scopus 로고    scopus 로고
    • Score tests for association between traits and haplotypes when linkage phase is ambiguous
    • Schaid DJ, Rowland CM, Tines DE, et al: Score tests for association between traits and haplotypes when linkage phase is ambiguous. Am J Hum Genet 70:425-434, 2002
    • (2002) Am J Hum Genet , vol.70 , pp. 425-434
    • Schaid, D.J.1    Rowland, C.M.2    Tines, D.E.3
  • 67
    • 0035912152 scopus 로고    scopus 로고
    • Genetic susceptibility to venous thrombosis
    • Seligsohn U, Lubetsky A: Genetic susceptibility to venous thrombosis. N Engl J Med 344:1222-1231, 2001
    • (2001) N Engl J Med , vol.344 , pp. 1222-1231
    • Seligsohn, U.1    Lubetsky, A.2
  • 68
    • 0043175289 scopus 로고    scopus 로고
    • Chosing haplotype-tagging SNP based on unphased genotype data using a preliminary sample of the unrelated subjects with an example from the multiethnic cohort study
    • Stram D, Haiman C, Hirschhorn J, et al: Chosing haplotype-tagging SNP based on unphased genotype data using a preliminary sample of the unrelated subjects with an example from the multiethnic cohort study. Human Hered 55:27-36, 2003
    • (2003) Human Hered , vol.55 , pp. 27-36
    • Stram, D.1    Haiman, C.2    Hirschhorn, J.3
  • 69
    • 0037269170 scopus 로고    scopus 로고
    • Long-term study of the clinical significance of loss of heterozygosity in childhood acute lymphoblastic leukemia
    • Takeuchi S, Tsukasaki K, Bartram CR, et al: Long-term study of the clinical significance of loss of heterozygosity in childhood acute lymphoblastic leukemia. Leukemia 7:149-154, 2003
    • (2003) Leukemia , vol.7 , pp. 149-154
    • Takeuchi, S.1    Tsukasaki, K.2    Bartram, C.R.3
  • 70
    • 0034762644 scopus 로고    scopus 로고
    • Using genetic variation to study human disease
    • Taylor JG, Choi EH, Foster CB, et al: Using genetic variation to study human disease. Trends Mol Med 7:507-512, 2001
    • (2001) Trends Mol Med , vol.7 , pp. 507-512
    • Taylor, J.G.1    Choi, E.H.2    Foster, C.B.3
  • 71
    • 0037114628 scopus 로고    scopus 로고
    • Variants in the VCAM 1 gene and risk for symptomatic stroke in sickle cell disease
    • Taylor JG, Tang DC, Savage SA, et al: Variants in the VCAM1 gene and risk for symptomatic stroke in sickle cell disease. Blood 100:4303-4309, 2002
    • (2002) Blood , vol.100 , pp. 4303-4309
    • Taylor, J.G.1    Tang, D.C.2    Savage, S.A.3
  • 72
    • 0036154197 scopus 로고    scopus 로고
    • Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease
    • Taylor JG, Tang D, Foster CB, et al: Patterns of low-affinity immunoglobulin receptor polymorphisms in stroke and homozygous sickle cell disease. Am J Hematol 69:109-114, 2002
    • (2002) Am J Hematol , vol.69 , pp. 109-114
    • Taylor, J.G.1    Tang, D.2    Foster, C.B.3
  • 73
    • 0035895505 scopus 로고    scopus 로고
    • The sequence of the human genome
    • Venter JC, Adams MD, Myers EW, et al: The sequence of the human genome. Science 16:1304-1351, 2001
    • (2001) Science , vol.16 , pp. 1304-1351
    • Venter, J.C.1    Adams, M.D.2    Myers, E.W.3
  • 74
    • 0037196954 scopus 로고    scopus 로고
    • Study of genes and environmental factors in complex diseases
    • Wacholder S, Garcia-Closas M, Rothman N: Study of genes and environmental factors in complex diseases. Lancet 359:1155, 2002
    • (2002) Lancet , vol.359 , pp. 1155
    • Wacholder, S.1    Garcia-Closas, M.2    Rothman, N.3
  • 75
    • 0018822866 scopus 로고
    • Mercaptopurine pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity
    • Weinshilboum RM, Sladek SL: Mercaptopurine pharmacogenetics: Monogenic inheritance of erythrocyte thiopurine methyltransferase activity. Am J Hum Genet 32:651-662, 1980
    • (1980) Am J Hum Genet , vol.32 , pp. 651-662
    • Weinshilboum, R.M.1    Sladek, S.L.2
  • 76
    • 0034040532 scopus 로고    scopus 로고
    • Chronic granulomatous disease: Report on a national registry of 368 patients
    • Winkelstein JA, Marino MC, Johnston RB Jr, et al: Chronic granulomatous disease: Report on a national registry of 368 patients. Medicine (Baltimore) 79:155-169, 2000
    • (2000) Medicine (Baltimore) , vol.79 , pp. 155-169
    • Winkelstein, J.A.1    Marino, M.C.2    Johnston R.B., Jr.3
  • 77
    • 0033815541 scopus 로고    scopus 로고
    • Linkage disequilibrium mapping in populations of variable size using the decay of haplotype sharing and a stepwise-mutation model
    • Zhang S, Zhao H: Linkage disequilibrium mapping in populations of variable size using the decay of haplotype sharing and a stepwise-mutation model. Genet Epidemiol 19:S99-105, 2000 (suppl 1)
    • (2000) Genet Epidemiol , vol.19 , Issue.SUPPL. 1
    • Zhang, S.1    Zhao, H.2


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