Item Type | Name |
Concept
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Polymorphism, Single Nucleotide
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Academic Article
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Association of solute carrier family 12 (sodium/chloride) member 3 with diabetic nephropathy, identified by genome-wide analyses of single nucleotide polymorphisms.
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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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Functional SNP in an Sp1-binding site of AGTRL1 gene is associated with susceptibility to brain infarction.
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Academic Article
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Association of VKORC1 and CYP2C9 polymorphisms with warfarin dose requirements in Japanese patients.
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Academic Article
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A SNP in the ABCC11 gene is the determinant of human earwax type.
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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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A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction.
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Academic Article
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Genome-wide detection and characterization of positive selection in human populations.
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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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Genome-wide association scan identifies a colorectal cancer susceptibility locus on 11q23 and replicates risk loci at 8q24 and 18q21.
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Academic Article
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Case-control association study of 65 candidate genes revealed a possible association of a SNP of HTR5A to be a factor susceptible to bipolar disease in Bulgarian population.
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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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A genome-wide association study identifies ITGA9 conferring risk of nasopharyngeal carcinoma.
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Academic Article
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Significant effect of polymorphisms in CYP2D6 and ABCC2 on clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients.
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Academic Article
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Criterion values for multiplex SNP genotyping by the invader assay.
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Academic Article
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Automated SNPs typing system based on the Invader assay.
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Academic Article
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Making a haplotype catalog with estimated frequencies based on SNP homozygotes.
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Academic Article
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Single nucleotide polymorphism in ABCG2 is associated with irinotecan-induced severe myelosuppression.
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Academic Article
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Functional variants in ADH1B and ALDH2 coupled with alcohol and smoking synergistically enhance esophageal cancer risk.
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Academic Article
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Association study of genetic polymorphism in ABCC4 with cyclophosphamide-induced adverse drug reactions in breast cancer patients.
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Academic Article
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The association of a nonsynonymous single-nucleotide polymorphism in TNFAIP3 with systemic lupus erythematosus and rheumatoid arthritis in the Japanese population.
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Academic Article
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Common variations in PSMD3-CSF3 and PLCB4 are associated with neutrophil count.
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Academic Article
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Genome-wide association study of intracranial aneurysm identifies three new risk loci.
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Academic Article
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Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand.
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Academic Article
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Functional SNP of ARHGEF10 confers risk of atherothrombotic stroke.
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Academic Article
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PADI4 polymorphism predisposes male smokers to rheumatoid arthritis.
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Academic Article
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Identification of evidence suggestive of an association with peripheral arterial disease at the OSBPL10 locus by genome-wide investigation in the Japanese population.
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Academic Article
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Common variation of IL28 affects gamma-GTP levels and inflammation of the liver in chronically infected hepatitis C virus patients.
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Academic Article
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A genome-wide association study identifies four susceptibility loci for keloid in the Japanese population.
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Academic Article
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Establishment of a standardized system to perform population structure analyses with limited sample size or with different sets of SNP genotypes.
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Academic Article
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Variation in TP63 is associated with lung adenocarcinoma susceptibility in Japanese and Korean populations.
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Academic Article
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Association of a novel long non-coding RNA in 8q24 with prostate cancer susceptibility.
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Academic Article
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A genome-wide association study reveals susceptibility variants for non-small cell lung cancer in the Korean population.
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Academic Article
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Impact of LIMK1, MMP2 and TNF-a variations for intracranial aneurysm in Japanese population.
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Academic Article
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Genome-wide associations and functional genomic studies of musculoskeletal adverse events in women receiving aromatase inhibitors.
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Academic Article
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Common variation in GPC5 is associated with acquired nephrotic syndrome.
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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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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.
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Academic Article
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A genome-wide association study identifies variants in the HLA-DP locus associated with chronic hepatitis B in Asians.
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Academic Article
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SNPs on chromosome 5p15.3 associated with myocardial infarction in Japanese population.
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Academic Article
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Genome-wide association study for C-reactive protein levels identified pleiotropic associations in the IL6 locus.
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Academic Article
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Genome-wide association study identifies a susceptibility locus for HCV-induced hepatocellular carcinoma.
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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 three loci associated with susceptibility to uterine fibroids.
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Academic Article
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Genome-wide association studies of tuberculosis in Asians identify distinct at-risk locus for young tuberculosis.
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Academic Article
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Genome-wide association study of epirubicin-induced leukopenia in Japanese patients.
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Academic Article
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Genome-wide association meta-analysis identifies new endometriosis risk loci.
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Academic Article
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Genome-wide association study identifies two susceptibility loci for exudative age-related macular degeneration in the Japanese population.
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Academic Article
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A genome-wide association study identifies novel loci for paclitaxel-induced sensory peripheral neuropathy in CALGB 40101.
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Academic Article
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Re: CYP2D6 genotype and tamoxifen response in postmenopausal women with endocrine-responsive breast cancer: the Breast International Group 1-98 trial.
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Academic Article
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Evaluating genetic risk for prostate cancer among Japanese and Latinos.
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Academic Article
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Variants of C-C motif chemokine 22 (CCL22) are associated with susceptibility to atopic dermatitis: case-control studies.
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Academic Article
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A genome-wide association study of nephrolithiasis in the Japanese population identifies novel susceptible Loci at 5q35.3, 7p14.3, and 13q14.1.
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Academic Article
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A genome-wide association study identifies three new risk loci for Kawasaki disease.
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Academic Article
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Genome-wide association study identifies eight new susceptibility loci for atopic dermatitis in the Japanese population.
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Academic Article
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SNPs in KCNQ1 are associated with susceptibility to type 2 diabetes in East Asian and European populations.
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Academic Article
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Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population.
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Academic Article
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Variation in the DEPDC5 locus is associated with progression to hepatocellular carcinoma in chronic hepatitis C virus carriers.
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Academic Article
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Multiple loci are associated with white blood cell phenotypes.
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Academic Article
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Inverse association of IL28B genotype and liver mRNA expression of genes promoting or suppressing antiviral state.
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Academic Article
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Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.
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Academic Article
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New sequence variants in HLA class II/III region associated with susceptibility to knee osteoarthritis identified by genome-wide association study.
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Academic Article
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A genome-wide association study in 19 633 Japanese subjects identified LHX3-QSOX2 and IGF1 as adult height loci.
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Academic Article
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A genome-wide association study identifies SNP in DCC is associated with gallbladder cancer in the Japanese population.
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Academic Article
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Meta-analysis identifies common variants associated with body mass index in east Asians.
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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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A genome-wide association study in the Japanese population identifies susceptibility loci for type 2 diabetes at UBE2E2 and C2CD4A-C2CD4B.
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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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A genome-wide association study identifies genetic variants in the CDKN2BAS locus associated with endometriosis in Japanese.
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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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Replication analysis of SNPs on 9p21.2 and 19p13.3 with amyotrophic lateral sclerosis in East Asians.
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Academic Article
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Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese.
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Academic Article
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Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk.
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Academic Article
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PlatinumCNV: a Bayesian Gaussian mixture model for genotyping copy number polymorphisms using SNP array signal intensity data.
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Academic Article
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A genome-wide association study of overall survival in pancreatic cancer patients treated with gemcitabine in CALGB 80303.
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Academic Article
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A genome-wide association study identifies locus at 10q22 associated with clinical outcomes of adjuvant tamoxifen therapy for breast cancer patients in Japanese.
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Academic Article
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Prostate cancer genomics, biology, and risk assessment through genome-wide association studies.
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Academic Article
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A genome-wide association study identified AFF1 as a susceptibility locus for systemic lupus eyrthematosus in Japanese.
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Academic Article
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A genome-wide association study identifies four genetic markers for hematological toxicities in cancer patients receiving gemcitabine therapy.
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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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Aromatase inhibitors, estrogens and musculoskeletal pain: estrogen-dependent T-cell leukemia 1A (TCL1A) gene-mediated regulation of cytokine expression.
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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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A genome-wide association study identifies two new susceptibility loci for lung adenocarcinoma in the Japanese population.
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Academic Article
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Meta-analysis identifies multiple loci associated with kidney function-related traits in east Asian populations.
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Academic Article
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Genome-wide association study identifies five new susceptibility loci for prostate cancer in the Japanese population.
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Academic Article
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Genome-wide association study identifies genetic determinants of warfarin responsiveness for Japanese.
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Academic Article
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Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.
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Academic Article
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Genome-wide association study identifies variations in 6p21.3 associated with nevirapine-induced rash.
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Academic Article
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CYP2B6 genotype is a strong predictor of systemic exposure to efavirenz in HIV-infected Zimbabweans.
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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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Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population.
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Academic Article
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A single-nucleotide polymorphism in ANK1 is associated with susceptibility to type 2 diabetes in Japanese populations.
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Academic Article
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Meta-analysis identifies six new susceptibility loci for atrial fibrillation.
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Academic Article
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Functional variants in NFKBIE and RTKN2 involved in activation of the NF-?B pathway are associated with rheumatoid arthritis in Japanese.
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Academic Article
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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.
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Academic Article
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A second generation human haplotype map of over 3.1 million SNPs.
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Academic Article
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SLC22A4 polymorphism and rheumatoid arthritis susceptibility: a replication study in a Japanese population and a metaanalysis.
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Academic Article
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Genome-wide association study of hematological and biochemical traits in a Japanese population.
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Academic Article
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A genome-wide association identified the common genetic variants influence disease severity in beta0-thalassemia/hemoglobin E.
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Academic Article
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Replication study for the association between four Loci identified by a genome-wide association study on European American subjects with type 1 diabetes and susceptibility to diabetic nephropathy in Japanese subjects with type 2 diabetes.
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Academic Article
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Genome-wide association study of pancreatic cancer in Japanese population.
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Academic Article
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IL28 variation affects expression of interferon stimulated genes and peg-interferon and ribavirin therapy.
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Academic Article
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Genome-wide association study of white blood cell count in 16,388 African Americans: the continental origins and genetic epidemiology network (COGENT).
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Academic Article
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Interstitial lung disease in gefitinib-treated Japanese patients with non-small-cell lung cancer: genome-wide analysis of genetic data.
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Academic Article
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Genome-wide association study identifies three new susceptibility loci for adult asthma in the Japanese population.
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Academic Article
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Genome-wide association study identifies HLA-DP as a susceptibility gene for pediatric asthma in Asian populations.
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Academic Article
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ORAI1 genetic polymorphisms associated with the susceptibility of atopic dermatitis in Japanese and Taiwanese populations.
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Academic Article
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Soluble MICA and a MICA variation as possible prognostic biomarkers for HBV-induced hepatocellular carcinoma.
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Academic Article
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Identification of a significant association of a single nucleotide polymorphism in TNXB with systemic lupus erythematosus in a Japanese population.
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Academic Article
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Lack of association between variations of PDE4D and ischemic stroke in the Japanese population.
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Academic Article
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A genome-wide association study identifies three new susceptibility loci for ulcerative colitis in the Japanese population.
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Academic Article
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Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1.
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Academic Article
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Association study of the polymorphisms on chromosome 12p13 with atherothrombotic stroke in the Japanese population.
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Academic Article
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Meta-analysis of published studies identified eight additional common susceptibility loci for Crohn's disease and ulcerative colitis.
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Academic Article
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A functional variant in ZNF512B is associated with susceptibility to amyotrophic lateral sclerosis in Japanese.
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Academic Article
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A genome-wide association study of chronic hepatitis B identified novel risk locus in a Japanese population.
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Academic Article
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Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma.
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Academic Article
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Merging pharmacometabolomics with pharmacogenomics using '1000 Genomes' single-nucleotide polymorphism imputation: selective serotonin reuptake inhibitor response pharmacogenomics.
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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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A genome-wide association study in the Japanese population confirms 9p21 and 14q23 as susceptibility loci for primary open angle glaucoma.
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Academic Article
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Association of common variants in TNFRSF13B, TNFSF13, and ANXA3 with serum levels of non-albumin protein and immunoglobulin isotypes in Japanese.
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Academic Article
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Genome-wide association analysis in asthma subjects identifies SPATS2L as a novel bronchodilator response gene.
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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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Nucleotide pyrophosphatase gene polymorphism associated with ossification of the posterior longitudinal ligament of the spine.
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Academic Article
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Single-nucleotide polymorphisms in the class II region of the major histocompatibility complex in Japanese patients with immunoglobulin A nephropathy.
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Academic Article
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Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21.
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Academic Article
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Catalog of 300 SNPs in 23 genes encoding G-protein coupled receptors.
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Academic Article
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Inference from the relationships between linkage disequilibrium and allele frequency distributions of 240 candidate SNPs in 109 drug-related genes in four Asian populations.
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Academic Article
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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.
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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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Functional SNPs in the lymphotoxin-alpha gene that are associated with susceptibility to myocardial infarction.
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Academic Article
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Fine-scale SNP map of an 11-kb genomic region at 22q13.1 containing the galectin-1 gene.
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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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Functional haplotypes of PADI4, encoding citrullinating enzyme peptidylarginine deiminase 4, are associated with rheumatoid arthritis.
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Academic Article
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Functional haplotypes of IL-12B are associated with childhood atopic asthma.
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Academic Article
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A functional single nucleotide polymorphism in mucin 1, at chromosome 1q22, determines susceptibility to diffuse-type gastric cancer.
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Academic Article
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Identification of 156 novel SNPs in 29 genes encoding G-protein coupled receptors.
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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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Functional single-nucleotide polymorphisms in the secretogranin III (SCG3) gene that form secretory granules with appetite-related neuropeptides are associated with obesity.
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Academic Article
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Association of single-nucleotide polymorphisms in MTMR9 gene with obesity.
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Academic Article
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Integration of cell line and clinical trial genome-wide analyses supports a polygenic architecture of Paclitaxel-induced sensory peripheral neuropathy.
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Academic Article
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A genome-wide association study identifies 2 susceptibility Loci for Crohn's disease in a Japanese population.
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Academic Article
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Association study of 71 European Crohn's disease susceptibility loci in a Japanese population.
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Academic Article
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Predictive value of the IL28B polymorphism on the effect of interferon therapy in chronic hepatitis C patients with genotypes 2a and 2b.
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Academic Article
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Influence of ITPA polymorphisms on decreases of hemoglobin during treatment with pegylated interferon, ribavirin, and telaprevir.
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Academic Article
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An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis.
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Academic Article
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Common variants in CASP3 confer susceptibility to Kawasaki disease.
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Academic Article
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The textile plot: a new linkage disequilibrium display of multiple-single nucleotide polymorphism genotype data.
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Academic Article
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Variants in KCNQ1 are associated with susceptibility to type 2 diabetes mellitus.
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Academic Article
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Identification of 45 novel SNPs in the 83-kb region containing peptidylarginine deiminase types 1 and 3 loci on chromosomal band 1p36.13.
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Academic Article
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Identification of 20 novel SNPs in the guanine nucleotide binding protein alpha 12 gene locus.
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Academic Article
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Association of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathy.
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Academic Article
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Impact of four loci on serum tamsulosin hydrochloride concentration.
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Academic Article
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High-density association study and nomination of susceptibility genes for hypertension in the Japanese National Project.
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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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Prediction of response to peginterferon-alfa-2b plus ribavirin therapy in Japanese patients infected with hepatitis C virus genotype 1b.
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Academic Article
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INSIG2 gene rs7566605 polymorphism is associated with severe obesity in Japanese.
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Academic Article
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Association of new loci identified in European genome-wide association studies with susceptibility to type 2 diabetes in the Japanese.
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Academic Article
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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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Academic Article
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Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.
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Academic Article
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Impact of PSCA variation on gastric ulcer susceptibility.
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Academic Article
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Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene.
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Academic Article
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A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.
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Academic Article
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Genome wide association study of age at menarche in the Japanese population.
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Academic Article
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Association of the RIP2 gene with childhood atopic asthma.
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Academic Article
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Functional polymorphism in the suppressor of cytokine signaling 1 gene associated with adult asthma.
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Academic Article
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ITPKC functional polymorphism associated with Kawasaki disease susceptibility and formation of coronary artery aneurysms.
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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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Screening of 336 single-nucleotide polymorphisms in 85 obesity-related genes revealed McKusick-Kaufman syndrome gene variants are associated with metabolic syndrome.
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Academic Article
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Association between obesity and polymorphisms in SEC16B, TMEM18, GNPDA2, BDNF, FAIM2 and MC4R in a Japanese population.
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Academic Article
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Regulatory polymorphisms in EGR2 are associated with susceptibility to systemic lupus erythematosus.
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Academic Article
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ITPA polymorphism affects ribavirin-induced anemia and outcomes of therapy--a genome-wide study of Japanese HCV virus patients.
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Academic Article
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HCV substitutions and IL28B polymorphisms on outcome of peg-interferon plus ribavirin combination therapy.
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Academic Article
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A genome-wide association study of HCV-induced liver cirrhosis in the Japanese population identifies novel susceptibility loci at the MHC region.
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Academic Article
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TSPYL5 SNPs: association with plasma estradiol concentrations and aromatase expression.
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Academic Article
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Genomewide association between GLCCI1 and response to glucocorticoid therapy in asthma.
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Academic Article
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Identification of a functional variant in SPLUNC1 associated with nasopharyngeal carcinoma susceptibility among Malaysian Chinese.
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Academic Article
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Identification of a functional variant in the MICA promoter which regulates MICA expression and increases HCV-related hepatocellular carcinoma risk.
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Academic Article
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High-density genotyping study identifies four new susceptibility loci for atopic dermatitis.
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Academic Article
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Analysis of single-nucleotide polymorphisms in Japanese rheumatoid arthritis patients shows additional susceptibility markers besides the classic shared epitope susceptibility sequences.
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Academic Article
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Association of the gene encoding wingless-type mammary tumor virus integration-site family member 5B (WNT5B) with type 2 diabetes.
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Academic Article
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A functional polymorphism in the 5' UTR of GDF5 is associated with susceptibility to osteoarthritis.
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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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Identification of sequence polymorphisms in CALM2 and analysis of association with hip osteoarthritis in a Japanese population.
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Academic Article
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Common genetic polymorphism of ITPA gene affects ribavirin-induced anemia and effect of peg-interferon plus ribavirin therapy.
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Academic Article
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The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.
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Academic Article
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Toward the establishment of a prediction system for the personalized treatment of chronic hepatitis C.
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Academic Article
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Whole-genome-wide association study in the Bulgarian population reveals HHAT as schizophrenia susceptibility gene.
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Academic Article
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Seven new loci associated with age-related macular degeneration.
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Academic Article
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Pathway analysis of genome-wide data improves warfarin dose prediction.
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Academic Article
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Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer.
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Academic Article
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Trans-ethnic meta-analysis of white blood cell phenotypes.
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Academic Article
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Functional promoter polymorphism in the TBX21 gene associated with aspirin-induced asthma.
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Academic Article
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A replication study for three nephrolithiasis loci at 5q35.3, 7p14.3 and 13q14.1 in the Japanese population.
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Academic Article
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High-resolution SNP map in the 55-kb region containing the selectin gene family on chromosome 1q24-q25.
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Academic Article
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Aromatase inhibitor-associated bone fractures: a case-cohort GWAS and functional genomics.
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Academic Article
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Polymorphisms in NRXN3, TFAP2B, MSRA, LYPLAL1, FTO and MC4R and their effect on visceral fat area in the Japanese population.
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Academic Article
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Catalog of 86 single-nucleotide polymorphisms (SNPs) in three uridine diphosphate glycosyltransferase genes: UGT2A1, UGT2B15, and UGT8.
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Academic Article
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CD40 ligand gene and Kawasaki disease.
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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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Association analysis of SLC22A4, SLC22A5 and DLG5 in Japanese patients with Crohn disease.
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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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Twenty single-nucleotide polymorphisms in four genes encoding cardiac ion channels.
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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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Thymic stromal lymphopoietin gene promoter polymorphisms are associated with susceptibility to bronchial asthma.
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Academic Article
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A functional SNP in ITIH3 is associated with susceptibility to myocardial infarction.
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Academic Article
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[SNP collection, pharmacogenomics, and the future of drug therapy].
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Academic Article
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Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy.
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Academic Article
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A functional single nucleotide polymorphism in the core promoter region of CALM1 is associated with hip osteoarthritis in Japanese.
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Academic Article
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Genome-wide association study identified SNP on 15q24 associated with bladder cancer risk in Japanese population.
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Academic Article
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High-density SNP map of human ITR, a gene associated with vascular remodeling.
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Academic Article
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Selective estrogen receptor modulators and pharmacogenomic variation in ZNF423 regulation of BRCA1 expression: individualized breast cancer prevention.
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Academic Article
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A polymorphism in MAPKAPK3 affects response to interferon therapy for chronic hepatitis C.
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Academic Article
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SNPs in BRAP associated with risk of myocardial infarction in Asian populations.
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Academic Article
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Genetic variants associated with angiotensin-converting enzyme inhibitor-associated angioedema.
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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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Genetic polymorphisms in the IL22 gene are associated with psoriasis vulgaris in a Japanese population.
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Academic Article
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Catalog of 668 SNPs detected among 31 genes encoding potential drug targets on the cell surface.
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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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Genetic variants associated with warfarin dose in African-American individuals: a genome-wide association study.
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Academic Article
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Association between single nucleotide polymorphisms within genes encoding sirtuin families and diabetic nephropathy in Japanese subjects with type 2 diabetes.
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Academic Article
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A polygenic risk score for breast cancer in women receiving tamoxifen or raloxifene on NSABP P-1 and P-2.
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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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Genome wide analysis of drug-induced torsades de pointes: lack of common variants with large effect sizes.
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Academic Article
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A single nucleotide polymorphism in activated Cdc42 associated tyrosine kinase 1 influences the interferon therapy in hepatitis C patients.
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Academic Article
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A functional SNP in CILP, encoding cartilage intermediate layer protein, is associated with susceptibility to lumbar disc disease.
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Academic Article
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A genome-wide association study of chemotherapy-induced alopecia in breast cancer patients.
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Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathy.
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Meta-analysis of genome-wide association studies identifies six new Loci for serum calcium concentrations.
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Inhaled corticosteroid treatment modulates ZNF432 gene variant's effect on bronchodilator response in asthmatics.
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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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Association of EMCN with susceptibility to rheumatoid arthritis in a Japanese population.
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Coding SNP in tenascin-C Fn-III-D domain associates with adult asthma.
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Germline variants and advanced colorectal adenomas: adenoma prevention with celecoxib trial genome-wide association study.
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Single nucleotide polymorphisms in TNFSF15 confer susceptibility to Crohn's disease.
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No association for Chinese HBV-related hepatocellular carcinoma susceptibility SNP in other East Asian populations.
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The BioBank Japan Project.
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High-resolution SNP map of ASPN, a susceptibility gene for osteoarthritis.
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Japanese single nucleotide polymorphism database for 267 possible drug-related genes.
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hzAnalyzer: detection, quantification, and visualization of contiguous homozygosity in high-density genotyping datasets.
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Associations of functional NLRP3 polymorphisms with susceptibility to food-induced anaphylaxis and aspirin-induced asthma.
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Association analysis of the NOD2 gene with susceptibility to graft-versus-host disease in a Japanese population.
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Genome-wide association study identifies a new SMAD7 risk variant associated with colorectal cancer risk in East Asians.
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HLA-DQB1*03 confers susceptibility to chronic hepatitis C in Japanese: a genome-wide association study.
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[BioBank Japan project].
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The construction of risk prediction models using GWAS data and its application to a type 2 diabetes prospective cohort.
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Impact of viral amino acid substitutions and host interleukin-28b polymorphism on replication and susceptibility to interferon of hepatitis C virus.
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A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population.
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Single-nucleotide polymorphisms in GALNT8 are associated with the response to interferon therapy for chronic hepatitis C.
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Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy.
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HLA-A SNPs and amino acid variants are associated with nasopharyngeal carcinoma in Malaysian Chinese.
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A functional SNP in EDG2 increases susceptibility to knee osteoarthritis in Japanese.
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A genome-wide association study identifies PLCL2 and AP3D1-DOT1L-SF3A2 as new susceptibility loci for myocardial infarction in Japanese.
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Population-genetic nature of copy number variations in the human genome.
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Functional variation in LGALS2 confers risk of myocardial infarction and regulates lymphotoxin-alpha secretion in vitro.
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A functional polymorphism in MMP-9 is associated with childhood atopic asthma.
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A single nucleotide polymorphism in KCNQ1 is associated with susceptibility to diabetic nephropathy in japanese subjects with type 2 diabetes.
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Association of STAT4 with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Japanese population.
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A single nucleotide polymorphism within the acetyl-coenzyme A carboxylase beta gene is associated with proteinuria in patients with type 2 diabetes.
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A functional SNP in PSMA6 confers risk of myocardial infarction in the Japanese population.
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Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome.
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Functional impact of IgA nephropathy-associated selectin gene haplotype on leukocyte-endothelial interaction.
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Associations of HLA-DP variants with hepatitis B virus infection in southern and northern Han Chinese populations: a multicenter case-control study.
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Thirteen single-nucleotide polymorphisms (SNPs) in the alcohol dehydrogenase 4 (ADH4) gene locus.
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Large-scale single-nucleotide polymorphism (SNP) and haplotype analyses, using dense SNP Maps, of 199 drug-related genes in 752 subjects: the analysis of the association between uncommon SNPs within haplotype blocks and the haplotypes constructed with haplotype-tagging SNPs.
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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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Citalopram and escitalopram plasma drug and metabolite concentrations: genome-wide associations.
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Pharmacoethnicity in Paclitaxel-Induced Sensory Peripheral Neuropathy.
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Genetic polymorphism regulating ORM1-like 3 (Saccharomyces cerevisiae) expression is associated with childhood atopic asthma in a Japanese population.
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Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms.
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Integrated pathway analysis of nasopharyngeal carcinoma implicates the axonemal dynein complex in the Malaysian cohort.
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Association of variations in HLA class II and other loci with susceptibility to EGFR-mutated lung adenocarcinoma.
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Pharmacogenomics and drug toxicity.
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Pharmacogenetic Discovery in CALGB (Alliance) 90401 and Mechanistic Validation of a VAC14 Polymorphism that Increases Risk of Docetaxel-Induced Neuropathy.
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Significant Effect of Polymorphisms in CYP2D6 on Response to Tamoxifen Therapy for Breast Cancer: A Prospective Multicenter Study.
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Accurate automated clustering of two-dimensional data for single-nucleotide polymorphism genotyping by a combination of clustering methods: evaluation by large-scale real data.
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Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study.
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SLCO1B1 polymorphisms and plasma estrone conjugates in postmenopausal women with ER+ breast cancer: genome-wide association studies of the estrone pathway.
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The vitamin D receptor gene as a determinant of survival in pancreatic cancer patients: Genomic analysis and experimental validation.
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GWAS identifies two novel colorectal cancer loci at 16q24.1 and 20q13.12.
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Beta-defensin 1, aryl hydrocarbon receptor and plasma kynurenine in major depressive disorder: metabolomics-informed genomics.
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Genome-wide association study identifies gastric cancer susceptibility loci at 12q24.11-12 and 20q11.21.
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Identification of two novel breast cancer loci through large-scale genome-wide association study in the Japanese population.
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Effect of CYP4F2, VKORC1, and CYP2C9 in Influencing Coumarin Dose: A Single-Patient Data Meta-Analysis in More Than 15,000 Individuals.
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Plasma or Serum: Which Is Preferable for Mutation Detection in Liquid Biopsy?
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Genome-wide association study of epilepsy in a Japanese population identified an associated region at chromosome 12q24.
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Application of targeted nanopore sequencing for the screening and determination of structural variants in patients with Lynch syndrome.
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