Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs.
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Yusuke Nakamura | Naoyuki Kamatani | Manabu Kawamoto | Masayoshi Harigai | Yusuke Nakamura | T. Kitamoto | A. Sekine | E. Inoue | N. Kamatani | S. Saito | M. Harigai | A. Iida | Susumu Saito | Akihiro Sekine | Takuya Kitamoto | Aritoshi Iida | Akifumi Kogame | Eisuke Inoue | M. Kawamoto | Akifumi Kogame
[1] Hadar I. Avi-Itzhak,et al. Selection of Minimum Subsets of Single Nucleotide Polymorphisms to Capture Haplotype Block Diversity , 2003, Pacific Symposium on Biocomputing.
[2] Judy H. Cho,et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease , 2001, Nature.
[3] R Judson,et al. Notes from the SNP vs. haplotype front. , 2001, Pharmacogenomics.
[4] A. Taniguchi,et al. Polymorphisms in the methylenetetrahydrofolate reductase gene were associated with both the efficacy and the toxicity of methotrexate used for the treatment of rheumatoid arthritis, as evidenced by single locus and haplotype analyses. , 2002, Pharmacogenetics.
[5] T. Kitamoto,et al. Catalog of 320 single nucleotide polymorphisms (SNPs) in 20 quinone oxidoreductase and sulfotransferase genes , 2001, Journal of Human Genetics.
[6] Charles R Cantor,et al. The use of MassARRAY technology for high throughput genotyping. , 2002, Advances in biochemical engineering/biotechnology.
[7] S. P. Fodor,et al. Blocks of Limited Haplotype Diversity Revealed by High-Resolution Scanning of Human Chromosome 21 , 2001, Science.
[8] Elizabeth M. Smigielski,et al. dbSNP: a database of single nucleotide polymorphisms , 2000, Nucleic Acids Res..
[9] K. Kondo,et al. Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8 , 2002, Journal of Human Genetics.
[10] Yusuke Nakamura,et al. JSNP: a database of common gene variations in the Japanese population , 2002, Nucleic Acids Res..
[11] Tom H. Lindner,et al. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus , 2000, Nature Genetics.
[12] R S Judson,et al. Complex promoter and coding region beta 2-adrenergic receptor haplotypes alter receptor expression and predict in vivo responsiveness. , 2000, Proceedings of the National Academy of Sciences of the United States of America.
[13] P. Donnelly,et al. A new statistical method for haplotype reconstruction from population data. , 2001, American journal of human genetics.
[14] L. Excoffier,et al. Maximum-likelihood estimation of molecular haplotype frequencies in a diploid population. , 1995, Molecular biology and evolution.
[15] P. Corey,et al. Incidence of Adverse Drug Reactions in Hospitalized Patients , 2012 .
[16] Jennifer Couzin,et al. HapMap Launched With Pledges of $100 Million , 2002, Science.
[17] S. Gabriel,et al. The Structure of Haplotype Blocks in the Human Genome , 2002, Science.
[18] P. Deloukas,et al. The impact of SNP density on fine-scale patterns of linkage disequilibrium. , 2004, Human molecular genetics.
[19] Zhaohui S. Qin,et al. Partition-ligation-expectation-maximization algorithm for haplotype inference with single-nucleotide polymorphisms. , 2002, American journal of human genetics.
[20] Yusuke Nakamura,et al. Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface , 2003, Journal of Human Genetics.
[21] B. Neri,et al. Clinical, genetic, and pharmacogenetic applications of the Invader assay. , 1999, Molecular diagnosis : a journal devoted to the understanding of human disease through the clinical application of molecular biology.
[22] Howard L McLeod,et al. Pharmacogenomics--drug disposition, drug targets, and side effects. , 2003, The New England journal of medicine.
[23] A. Sekine,et al. Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8 , 2002, Journal of Human Genetics.
[24] U. Meyer. Pharmacogenetics and adverse drug reactions , 2000, The Lancet.
[25] Mourad Sahbatou,et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease , 2001, Nature.
[26] 浦野 和子. Polymorphisms in the methylenetetrahydrofolate reductase gene were associated with both the efficacy and the toxicity of methotrexate used for the treatment of rheumatoid arthritis, as evidenced by single locus and haplotype analyses , 2003 .
[27] T. Morisaki,et al. Determination of probability distribution of diplotype configuration (diplotype distribution) for each subject from genotypic data using the EM algorithm. , 2002, Annals of human genetics.
[28] N E Morton,et al. Genetic epidemiology of single-nucleotide polymorphisms. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[29] Jennifer Couzin,et al. Human genome. HapMap launched with pledges of $100 million. , 2002, Science.
[30] M. Daly,et al. High-resolution haplotype structure in the human genome , 2001, Nature Genetics.
[31] Frank Dudbridge,et al. Haplotype tagging for the identification of common disease genes , 2001, Nature Genetics.
[32] E. Boerwinkle,et al. Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase. , 1998, American journal of human genetics.
[33] Yusuke Nakamura,et al. A high-throughput SNP typing system for genome-wide association studies , 2001, Journal of Human Genetics.
[34] L. Kruglyak. Prospects for whole-genome linkage disequilibrium mapping of common disease genes , 1999, Nature Genetics.
[35] J. Long,et al. An E-M algorithm and testing strategy for multiple-locus haplotypes. , 1995, American journal of human genetics.
[36] A. Sekine,et al. Catalog of 238 variations among six human genes encoding solute carriers (hSLCs) in the Japanese population , 2002, Journal of Human Genetics.
[37] M. Relling,et al. Pharmacogenomics: translating functional genomics into rational therapeutics. , 1999, Science.
[38] A. Chakravarti,et al. Linkage disequilibrium and haplotype diversity in the genes of the renin-angiotensin system: findings from the family blood pressure program. , 2003, Genome research.
[39] D. Nickerson,et al. Variation is the spice of life , 2001, Nature Genetics.
[40] T. Morisaki,et al. Determination of probability distribution of diplotype configuration (diplotype distribution) for each subject from genotypic data using the EM algorithm , 2002 .
[41] Sinead B. O'Leary,et al. Genetic variation in the 5q31 cytokine gene cluster confers susceptibility to Crohn disease , 2001, Nature Genetics.
[42] A. Taniguchi,et al. Adverse effects of sulfasalazine in patients with rheumatoid arthritis are associated with diplotype configuration at the N-acetyltransferase 2 gene. , 2002, The Journal of rheumatology.
[43] A. Sekine,et al. Catalog of 258 single-nucleotide polymorphisms (SNPs) in genes encoding three organic anion transporters, three organic anion-transporting polypeptides, and three NADH:ubiquinone oxidoreductase flavoproteins , 2001, Journal of Human Genetics.