| Item Type | Name |
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Concept
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Genetic Variation
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Academic Article
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Genetic variations in the gene encoding ELMO1 are associated with susceptibility to diabetic nephropathy.
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Academic Article
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Multiplex PCR-based real-time invader assay (mPCR-RETINA): a novel SNP-based method for detecting allelic asymmetries within copy number variation regions.
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Academic Article
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Association analysis of genetic variants in IL23R, ATG16L1 and 5p13.1 loci with Crohn's disease in Japanese patients.
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Academic Article
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Japanese population structure, based on SNP genotypes from 7003 individuals compared to other ethnic groups: effects on population-based association studies.
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Academic Article
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A model of prediction system for adverse cardiovascular reactions by calcineurin inhibitors among patients with renal transplants using gene-based single-nucleotide polymorphisms.
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Academic Article
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Independent and population-specific association of risk variants at the IRGM locus with Crohn's disease.
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Academic Article
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Expression of novel molecules, MICAL2-PV (MICAL2 prostate cancer variants), increases with high Gleason score and prostate cancer progression.
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Academic Article
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Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease.
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Academic Article
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Common variants on 14q32 and 13q12 are associated with DLBCL susceptibility.
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Academic Article
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Common variants at 11q12, 10q26 and 3p11.2 are associated with prostate cancer susceptibility in Japanese.
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Academic Article
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A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.
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Academic Article
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Whole-genome sequencing and comprehensive variant analysis of a Japanese individual using massively parallel sequencing.
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Academic Article
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Optineurin mutations in Japanese amyotrophic lateral sclerosis.
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Academic Article
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Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations.
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Academic Article
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Genetic differences in the two main groups of the Japanese population based on autosomal SNPs and haplotypes.
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Academic Article
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Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
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Academic Article
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Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.
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Academic Article
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Pharmacogenomics and patient care: one size does not fit all.
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Academic Article
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CYP2D6 genotyping for functional-gene dosage analysis by allele copy number detection.
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Academic Article
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A genome-wide association study identifies two susceptibility loci for duodenal ulcer in the Japanese population.
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Academic Article
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Haplotypes with copy number and single nucleotide polymorphisms in CYP2A6 locus are associated with smoking quantity in a Japanese population.
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Academic Article
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Identification of a novel non-coding RNA, MIAT, that confers risk of myocardial infarction.
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Academic Article
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Association between genetic variation in the gene for death-associated protein-3 (DAP3) and adult asthma.
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Academic Article
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Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patients.
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Academic Article
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Genetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitus.
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Academic Article
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Variations in the FTO gene are associated with severe obesity in the Japanese.
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Academic Article
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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
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Academic Article
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MOCSphaser: a haplotype inference tool from a mixture of copy number variation and single nucleotide polymorphism data.
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Academic Article
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Genetic variation in PSCA is associated with susceptibility to diffuse-type gastric cancer.
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Academic Article
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Absence of mutation in the NOD2/CARD15 gene among 483 Japanese patients with Crohn's disease.
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Academic Article
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Genome-wide association study of chemotherapeutic agent-induced severe neutropenia/leucopenia for patients in Biobank Japan.
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Academic Article
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Catalog of 238 variations among six human genes encoding solute carriers ( hSLCs) in the Japanese population.
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Academic Article
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Variation in the gene encoding Krüppel-like factor 7 influences body fat: studies of 14 818 Danes.
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Academic Article
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DNA variations in human and medical genetics: 25 years of my experience.
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Academic Article
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Catalog of 605 single-nucleotide polymorphisms (SNPs) among 13 genes encoding human ATP-binding cassette transporters: ABCA4, ABCA7, ABCA8, ABCD1, ABCD3, ABCD4, ABCE1, ABCF1, ABCG1, ABCG2, ABCG4, ABCG5, and ABCG8.
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Academic Article
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906 variations among 27 genes encoding cytochrome P450 (CYP) enzymes and aldehyde dehydrogenases (ALDHs) in the Japanese population.
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Academic Article
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Identification of 779 genetic variations in eight genes encoding members of the ATP-binding cassette, subfamily C (ABCC/MRP/CFTR.
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Academic Article
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Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.
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Academic Article
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Impact of allele copy number of polymorphisms in FCGR3A and FCGR3B genes on susceptibility to ulcerative colitis.
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Academic Article
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Catalog of 178 variations in the Japanese population among eight human genes encoding G protein-coupled receptors (GPCRs).
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Academic Article
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Catalog of 680 variations among eight cytochrome p450 ( CYP) genes, nine esterase genes, and two other genes in the Japanese population.
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Academic Article
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Amino acid substitution in HCV core region and genetic variation near the IL28B gene affect viral dynamics during telaprevir, peginterferon and ribavirin treatment.
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Academic Article
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VAV3 mediates resistance to breast cancer endocrine therapy.
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Academic Article
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An algorithm for inferring complex haplotypes in a region of copy-number variation.
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Academic Article
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Three hundred twenty-six genetic variations in genes encoding nine members of ATP-binding cassette, subfamily B (ABCB/MDR/TAP), in the Japanese population.
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Academic Article
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Establishment of CYP2D6 reference samples by multiple validated genotyping platforms.
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Academic Article
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An association study of asthma and related phenotypes with polymorphisms in negative regulator molecules of the TLR signaling pathway.
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Academic Article
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Catalog of 77 single-nucleotide polymorphisms (SNPs) in the carbohydrate sulfotransferase 1 (CHST1) and carbohydrate sulfotransferase 3 (CHST3) genes.
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Academic Article
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Amino acid substitution in HCV core/NS5A region and genetic variation near IL28B gene affect treatment efficacy to interferon plus ribavirin combination therapy.
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Academic Article
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Elevated expression of protein regulator of cytokinesis 1, involved in the growth of breast cancer cells.
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Academic Article
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Amino acid substitution in hepatitis C virus core region and genetic variation near the interleukin 28B gene predict viral response to telaprevir with peginterferon and ribavirin.
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Academic Article
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Importance of gastric cancer for the diagnosis and surveillance of Japanese Lynch syndrome patients.
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Academic Article
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Large-scale genome-wide association study in a Japanese population identifies novel susceptibility loci across different diseases.
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