Nakamura Yusuke | 東京大学医科学研究所ヒトゲノム解析センターゲノムシークエンス解析分野

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OE-294 A Functional Variation in a Gene Encoding One of Galectin-2 Binding Proteins Confers Risk of Myocardial Infarction in Asian Populations(OE50,Coronary Circulation/Chronic Coronary Disease (Basic/Clinical) (IHD),Oral Presentation (English),The 73rd A
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)
FRS-004 Large Scale SNPs Association Study to Identify Genes Confer Risk of Myocardial Infarction(FRS1,New Molecules for Cardiovascular Regulation (M),Featured Research Session (English),The 73rd Annual Scientific Meeting of The Japanese Circulation Socie
New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population
A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction
PJ-152 A functional SNP in the Proteasome Subunit Alpha Type 6 Gene confers Risk of Myocardial Infarction in Japanese Population(Acute myocardial infarction, basic-2, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
OJ-212 Identification of a Novel non-coding RNA, MIAT, that Confers Risk of Myocardial Infarction(Genetics/Genetically engineered models/Gene therapy-2(H/M), The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Critical roles of T-LAK cell-originated protein kinase in cytokinesis
Involvement of kinesin family member 2C/mitotic centromere-associated kinesin overexpression in mammary carcinogenesis
Impact of CYP2D6^*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapy
Automated SNPs typing system based on the Invader assay
Orphan receptor tyrosine kinase ROR2 as a potential therapeutic target for osteosarcoma
Activation of an estrogen/estrogen receptor signaling by BIG3 through its inhibitory effect on nuclear transport of PHB2/REA in breast cancer
Involvement of G-patch domain containing 2 overexpression in breast carcinogenesis
Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population
5αDH-DOC (5α-dihydro-deoxycorticosterone) activates androgen receptor in castration-resistant prostate cancer
Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
Association between type 2 diabetes genetic susceptibility loci and visceral and subcutaneous fat area as determined by computed tomography
A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis
SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population
Genetic variations in the CYP17A1 and NT5C2 genes are associated with a reduction in visceral and subcutaneous fat areas in Japanese women
Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area
Association of variations in the FTO, SCG3 and MTMR9 genes with metabolic syndrome in a 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
Impact of LIMK1, MMP2 and TNF-α variations for intracranial aneurysm in Japanese population
A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population
Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis
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

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