Ohnishi Yozo | Laboratory For Cardiovascular Disease Center For Genomic Medicine
スポンサーリンク
概要
関連著者
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OHNISHI Yozo
Laboratory for SNP Analysis, RIKEN Center for Genomic Medicine
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Ohnishi Yozo
Laboratory Of Molecular Medicine Human Genome Center Institute Of Medical Science The University Of
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Ohnishi Yozo
Inst. Of Physical And Chemical Res. (riken) Tokyo Jpn
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Ohnishi Yozo
Laboratory For Cardiovascular Diseases Snp Research Center The Institute Of Physical And Chemical Re
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Ohnishi Yozo
Laboratory For Snp Analysis Riken Center For Genomic Medicine
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Ohno Yoichi
Department Of Internal Medicine School Of Medicine Keio University
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Nagane Yutaka
Department Of Urology Sanai Hospital
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Tanaka Toshihiro
Laboratory for Cardiovascular Diseases, Center for Genomic Medicine, RIKEN
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Akiba Takashi
Department Of Medicine Kidney Center Tokyo Women's Medical University
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Takei Takashi
東京女子医科大学 腎臓病総合医療センター
著作論文
- New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
- Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
- Association of a single-nucleotide polymorphism in the immunoglobulin μ-binding protein 2 gene with immunoglobulin A nephropathy
- Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients
- Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy
- A high-throughput SNP typing system for genome-wide association studies
- Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21
- SNP projects in Japan
- High-density single-nucleotide polymorphism (SNP) map in the 96-kb region containing the entire human DiGeorge syndrome critical region 2 (DGCR2) gene at 22q11.2
- Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome