スポンサーリンク
Laboratory for Medical Informatics, Center for Genomic Medicine, The Institute of Physical and Chemical Research (RIKEN) | 論文
- OE-009 Identification of a Locus on Chromosome 5p that Confers Risk of Coronary Artery Disease by Genome Wide Association Study(OE02,ACS/AMI (Basic) (IHD),Oral Presentation (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Society)
- Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy
- Genome-wide association study to identify genes related to myocardial infarction
- A high-throughput SNP typing system for genome-wide association studies in patients with myocardial infarction
- SNP projects in Japan
- Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus
- Lack of Association of LRP5 and LRP6 Polymorphisms with Type 2 Diabetes Mellitus in the Japanese Population
- Association Study of the Effect of WFS1 Polymorphisms on Risk of Type 2 Diabetes in Japanese Population
- Association of Serum MCP-1 Concentration and MCP-1 Polymorphism with Insulin Resistance in Japanese Individuals with Obese type 2 Diabetes
- A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
- Membrane Localization of Protein-Tyrosine Phosphatase 1B is Essential for its Activation of Sterol Regulatory Element-Binding Protein-1 Gene Expression and Consequent Hypertriglyceridaemia
- Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
- Gene-based SNP discovery as part of the Japanese Millennium Genome Project : identification of 190 562 genetic variations in the human genome
- Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
- Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
- SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
- Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
- Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility
- Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes
- Making a haplotype catalog with estimated frequencies based on SNP homozygotes