about
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities.An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritisSLC22A4 and RUNX1: identification of RA susceptible genesAssociation of a single-nucleotide polymorphism in the immunoglobulin mu-binding protein 2 gene with immunoglobulin A nephropathyKnee Pain and Low Back Pain Additively Disturb Sleep in the General Population: A Cross-Sectional Analysis of the Nagahama StudyGastroesophageal reflux disease symptoms and dietary behaviors are significant correlates of short sleep duration in the general population: the Nagahama StudyMeta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese populationAn integrative study of the genetic, social and environmental determinants of chronic kidney disease characterized by tubulointerstitial damages in the North Central Region of Sri LankaGenetic polymorphisms of the human PNPLA3 gene are strongly associated with severity of non-alcoholic fatty liver disease in Japanese.LAMPLINK: detection of statistically significant SNP combinations from GWAS data.Myelin basic protein as a novel genetic risk factor in rheumatoid arthritis--a genome-wide study combined with immunological analysesAssociation of genetic polymorphisms with interferon-induced haematologic adverse effects in chronic hepatitis C patients.Large-scale East-Asian eQTL mapping reveals novel candidate genes for LD mapping and the genomic landscape of transcriptional effects of sequence variantsAssociation between the SERPING1 gene and age-related macular degeneration and polypoidal choroidal vasculopathy in JapaneseAnti-citrullinated peptide antibody-negative RA is a genetically distinct subset: a definitive study using only bone-erosive ACPA-negative rheumatoid arthritisRecent findings on genes associated with inflammatory disease.A multimedia intervention on cardiopulmonary resuscitation and advance directives.Application of permanents of square matrices for DNA identification in multiple-fatality casesAnti-citrullinated peptide/protein antibody (ACPA)-negative RA shares a large proportion of susceptibility loci with ACPA-positive RA: a meta-analysis of genome-wide association study in a Japanese population.Three missense variants of metabolic syndrome-related genes are associated with alpha-1 antitrypsin levelsCitrullinated proteins in rheumatoid arthritis.Peptidylarginine deiminase type 4, anticitrullinated peptide antibodies, and rheumatoid arthritis.Combined association of clinical and lifestyle factors with non-restorative sleep: The Nagahama Study.Genome-wide single nucleotide polymorphism analyses of rheumatoid arthritis.A burden of rare variants in BMPR2 and KCNK3 contributes to a risk of familial pulmonary arterial hypertension.Isotonic Regression Based-Method in Quantitative High-Throughput Screenings for Genotoxicity.Relationship Among Chlamydia and Mycoplasma Pneumoniae Seropositivity, IKZF1 Genotype and Chronic Obstructive Pulmonary Disease in A General Japanese Population: The Nagahama Study.Citrullination by peptidylarginine deiminase in rheumatoid arthritis.Human genetic variation database, a reference database of genetic variations in the Japanese population.Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis.Association between single-nucleotide polymorphisms in selectin genes and immunoglobulin A nephropathy.Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis.The Contribution of Genetic Architecture to the 10-Year Incidence of Age-Related Macular Degeneration in the Fellow Eye.The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population.FCRL3, an autoimmune susceptibility gene, has inhibitory potential on B-cell receptor-mediated signaling.A twin study of rheumatoid arthritis in the Japanese population.A prospective multicenter study on genome wide associations to ranibizumab treatment outcome for age-related macular degeneration.Comprehensive assessment of the expression of the SWI/SNF complex defines two distinct prognostic subtypes of ovarian clear cell carcinoma.Effects of smoking and shared epitope on the production of anti-citrullinated peptide antibody in a Japanese adult population.Ethnic differences in allele frequency of autoimmune-disease-associated SNPs.
P50
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P50
description
onderzoeker
@nl
researcher ORCID ID = 0000-0002-1587-630X
@en
name
Ryo Yamada
@ast
Ryo Yamada
@en
Ryo Yamada
@es
Ryo Yamada
@nl
type
label
Ryo Yamada
@ast
Ryo Yamada
@en
Ryo Yamada
@es
Ryo Yamada
@nl
prefLabel
Ryo Yamada
@ast
Ryo Yamada
@en
Ryo Yamada
@es
Ryo Yamada
@nl
P106
P108
P1153
7202185709
P31
P496
0000-0002-1587-630X