Kamatani Naoyuki | 理化学研究所ゲノム医科学研究センター循環器疾患研究チーム

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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
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
PJ-756 Aliskiren Reduces Leukocyte Recruitment in Acute Vascular Inflammation via Oxidative Stress-dependent, but Blood Pressure Independent Mechanisms(PJ127,Intravascular Imagings 2 (I),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The
Arterial Stiffness in Patients with Non-Diabetic Chronic Kidney Disease (CKD)
Aortic Arch Calcification and Arterial Stiffness are Independent Factors for Diastolic Left Ventricular Dysfunction in Chronic Hemodialysis Patients
Low-Dose Losartan Therapy Reduces Proteinuria in Normotensive Patients with Immunoglobulin A Nephropathy
PJ-224 Primal role of intracellular zinc in PKC-dependent monocyte signalling and adhesive interaction(Atherosclerosis, basic(06)(IHD),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese
Variations in the FTO gene are associated with severe obesity in the Japanese
Similarity of the allele frequency and linkage disequilibrium pattern of single nucleotide polymorphisms in drug-related gene loci between Thai and northern East Asian populations : implications for tagging SNP selection in Thais
Clinical assessment of atherosclerotic parameters and cardiac function in chronic hemodialysis patients
Successful steroid treatment of a patient with autosomal dominant polycystic kidney disease complicated by sarcoidosis
Clinical effects of calcium channel blockers and renin-angiotensin-aldosterone system inhibitors on changes in the estimated glomerular filtration rate in patients with polycystic kidney disease
Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility
Effect of the antiplatelet agent cilostazol on endovascular inflammatory biochemical parameters and the clinical symptoms of peripheral artery disease and restless legs syndrome in hemodialysis patients
Dexamethasone increases the phosphorylation of nephrin in cultured podocytes
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
Induction of remission following a single dose of rituximab alone in a patient with minimal change nephrotic syndrome
Identification of independent risk loci for Graves' disease within the MHC in the Japanese population
Long-term beneficial effects of angiotensin-converting enzyme inhibitor and angiotensin receptor blocker therapy for patients with advanced immunoglobulin A nephropathy and impaired renal function
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
Clinical outcomes in patients with chronic kidney disease : a 5-year retrospective cohort study at a University Hospital in Japan
Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population
Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a 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
Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the association
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
A case of acute renal failure after exercise with renal hypouricemia demonstrated compound heterozygous mutations of uric acid transporter 1
Comparison of inhibitors of renin-angiotensin-aldosterone system (RAS) and combination therapy of steroids plus RAS inhibitors for patients with advanced immunoglobulin A nephropathy and impaired renal function
Circulating levels of soluble α-Klotho in patients with chronic kidney disease
pHCR : a Parallel Haplotype Configuration Reduction algorithm for haplotype interaction analysis

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