Takahashi Atsushi | Laboratory For Statistical Analysis Center For Genomic Medicine Riken

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著作論文

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)
Association of the MSX2 gene polymorphisms with ankylosing spondylitis in Japanese
New correction algorithms for multiple comparisons in case-control multilocus association studies based on haplotypes and diplotype configurations
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
Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction
Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients
Japanese single nucleotide polymorphism database for 267 possible drug-related genes
A genomewide linkage analysis of Kawasaki disease : evidence for linkage to chromosome 12
Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes
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
A founder mutation of CANT1 common in Korean and Japanese Desbuquois dysplasia
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
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
Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome
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
A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma
Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian population
pHCR : a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis
Role of Insulin Resistance in the Pathogenesis and Development of Type 2 Diabetes in WBN/Kob-Leprfa Rats
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese

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