Kubo Michiaki | Laboratory For Genotyping Development Center For Genomic Medicine

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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)
Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population
Impact of CYP2D6^*10 on recurrence-free survival in breast cancer patients receiving adjuvant tamoxifen therapy
Association of genetic polymorphisms in SLCO1B3 and ABCC2 with docetaxel-induced leukopenia
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
Profile of Participants and Genotype Distributions of 108 Polymorphisms in a Cross-Sectional Study of Associations of Genotypes With Lifestyle and Clinical Factors : A Project in the Japan Multi-Institutional Collaborative Cohort (J-MICC) Study
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
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
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
Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population
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
Effect of the PPARG2 Pro12Ala Polymorphism and Clinical Risk Factors for Diabetes Mellitus on HbA1c in the Japanese General Population
A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese
Associations Between hOGG1 Ser326Cys Polymorphism and Increased Body Mass Index and Fasting Glucose Level in the Japanese General Population

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