Literature DB >> 11752280

JSNP: a database of common gene variations in the Japanese population.

Mika Hirakawa1, Toshihiro Tanaka, Yoichi Hashimoto, Masako Kuroda, Toshihisa Takagi, Yusuke Nakamura.   

Abstract

JSNP is a repository of Japanese Single Nucleotide Polymorphism (SNP) data, begun in 2000 and developed through the Prime Minister's Millennium Project. The aim of this undertaking is to identify and collate up to 150 000 SNPs from the Japanese population, located in genes or in adjacent regions that might influence the coding sequence of the genes. The project has been carried out by a collaboration between the Human Genome Center (HGC) in the Institute of Medical Science (IMS) at the University of Tokyo and the Japan Science and Technology Corporation (JST). JSNP serves as both a storage site for the Japanese SNPs obtained from the ongoing project and as a facility for public dissemination to allow researchers access to high quality SNP data. A primary motivation of the project is the construction of a basic data set to identify relationships between polymorphisms and common diseases or the reaction to drugs. As such, emphasis has been placed on the identification of SNPs that lie in candidate regions which may affect phenotype but which would not necessarily directly cause disease. Unrestricted access to JSNP and any associated files is available at http://snp.ims.u-tokyo.ac.jp/.

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Year:  2002        PMID: 11752280      PMCID: PMC99126          DOI: 10.1093/nar/30.1.158

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN: 0305-1048            Impact factor:   16.971


  17 in total

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4.  dbSNP: the NCBI database of genetic variation.

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Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

5.  RefSeq and LocusLink: NCBI gene-centered resources.

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Journal:  Nucleic Acids Res       Date:  2001-01-01       Impact factor: 16.971

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Journal:  Science       Date:  2001-02-16       Impact factor: 47.728

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  71 in total

1.  HOWDY: an integrated database system for human genome research.

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3.  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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4.  Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations.

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6.  Designing a multistage, SNP-based, genome screen for common diseases.

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7.  Evaluation of microsatellite markers in association studies: a search for an immune-related susceptibility gene in sarcoidosis.

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Journal:  Immunogenetics       Date:  2005-01-27       Impact factor: 2.846

8.  PharmGKB: an integrated resource of pharmacogenomic data and knowledge.

Authors:  Li Gong; Ryan P Owen; Winston Gor; Russ B Altman; Teri E Klein
Journal:  Curr Protoc Bioinformatics       Date:  2008-09

9.  Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes.

Authors:  Akio Kanazawa; Syuuichi Tsukada; Akihiro Sekine; Tatsuhiko Tsunoda; Atsushi Takahashi; Atsunori Kashiwagi; Yasushi Tanaka; Tetsuya Babazono; Masafumi Matsuda; Kohei Kaku; Yasuhiko Iwamoto; Ryuzo Kawamori; Ryuichi Kikkawa; Yusuke Nakamura; Shiro Maeda
Journal:  Am J Hum Genet       Date:  2004-09-21       Impact factor: 11.025

10.  An association analysis between ApoA1 polymorphisms and the high-density lipoprotein (HDL) cholesterol level and myocardial infarction (MI) in Japanese.

Authors:  Keisuke Shioji; Toshifumi Mannami; Yoshihiro Kokubo; Yoichi Goto; Hiroshi Nonogi; Naoharu Iwai
Journal:  J Hum Genet       Date:  2004-07-17       Impact factor: 3.172

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