骨・結合組織疾患
CATEGORY
2024.1.1
GWAS for systemic sclerosis identifies six novel susceptibility loci including one in the Fcγ receptor region
2023.1.30
Evidence of causality of low body mass index on risk of adolescent idiopathic scoliosis: a Mendelian randomization study
2023.1.23
Improved Genetic Prediction of the Risk of Knee Osteoarthritis using the Risk Factor-Based Polygenic Score
2023.1.5
Extracting immunological and clinical heterogeneity across autoimmune rheumatic diseases by cohort-wide immunophenotyping
2023.1.1
Genetic insights into ossification of the posterior longitudinal ligament of the spine
2022.1.31
Novel susceptibility loci for steroid-associated osteonecrosis of the femoral head in systemic lupus erythematosus
2022.1.28
Multi-ancestry genome-wide association analyses identify novel genetic mechanisms in rheumatoid arthritis
2022.1.19
Multi-trait and cross-population genome-wide association studies across autoimmune and allergic diseases identify shared and distinct genetic component
2022.1.13
Biological insights into systemic lupus erythematosus through an immune cell-specific transcriptome-wide association study
2021.1.8
Meta-analysis of 208370 East Asians identifies 113 susceptibility loci for systemic lupus erythematosus
2020.1.27
Association of the RPA3-UMAD1 locus with interstitial lung diseases complicated with rheumatoid arthritis in Japanese
2019.1.10
Identification of rare coding variants in TYK2 protective for rheumatoid arthritis in the Japanese population and their effects on cytokine signalling
2018.1.21
Genome-wide meta-analysis and replication studies in multiple ethnicities identify novel adolescent idiopathic scoliosis susceptibility loci
2018.1.19
Splicing variant of WDFY4 augments MDA5 signalling and the risk of clinically amyopathic dermatomyositis
2018.1.18
A multi-ethnic meta-analysis confirms the association of rs6570507 with adolescent idiopathic scoliosis
2018.1.4
Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density
2017.1.23
Genetic landscape of interactive effects of HLA-DRB1 alleles on susceptibility to ACPA(+) rheumatoid arthritis and ACPA levels in Japanese population
2017.1.18
Genome-wide Association Study of Idiopathic Osteonecrosis of the Femoral Head
2017.1.14
A functional variant in MIR4300HG, the host gene of microRNA MIR4300 is associated with progression of adolescent idiopathic scoliosis.
2017.1.9
Polygenic burdens on cell-specific pathways underlie the risk of rheumatoid arthritis
2016.1.12
Contribution of a Non-classical HLA Gene, HLA-DOA, to the Risk of Rheumatoid Arthritis
2016.1.6
High-density genotyping of immune-related loci identifies new SLE risk variants in individuals with Asian ancestry
2015.1.16
A Functional SNP in BNC2 Is Associated with Adolescent Idiopathic Scoliosis
2010.3.22
HLA-DRB1*0901 lowers anti-cyclic citrullinated peptide antibody levels in Japanese patients with rheumatoid arthritis
2015.1.7
Anti-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
2010.3.22
Association study of TRAF1-C5 polymorphisms with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in Japanese
2015.1.6
An association between amino acid position 74 of HLA-DRB1 and anti-citrullinated protein antibody levels in Japanese patients with anti-citrullinated protein antibody-positive rheumatoid arthritis
2009.3.22
A single nucleotide polymorphism in the IRF5 promoter region is associated with susceptibility to rheumatoid arthritis in the Japanese population
2014.1.1
Genetics of rheumatoid arthritis contributes to biology and drug discovery
2009.3.22
Contribution of a haplotype in the HLA region to anti-cyclic citrullinated peptide antibody positivity in rheumatoid arthritis, independently of HLA-DRB1
2014.1.9
A genome-wide association study identifies susceptibility loci for ossification of the posterior longitudinal ligament of the spine
2008.3.22
Functional SNPs in CD244 increase the risk of rheumatoid arthritis in a Japanese population
2013.1.27
PLD4 as a novel susceptibility gene for systemic sclerosis in a Japanese population
2008.3.22
SLC22A4 polymorphism and rheumatoid arthritis susceptibility: a replication study in a Japanese population and a metaanalysis
2013.1.24
Lumbar disc degeneration is linked to a carbohydrate sulfotransferase 3 variant
2008.3.22
A functional SNP in the NKX2.5-binding site of ITPR3 promoter is associated with susceptibility to systemic lupus erythematosus in Japanese population
2013.1.20
Identification of a susceptibility locus for severe adolescent idiopathic scoliosis on chromosome 17q24.3
2008.3.22
Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosis
2013.1.16
An association analysis of HLA-DRB1 with systemic lupus erythematosus and rheumatoid arthritis in a Japanese population: effects of *09:01 allele on disease phenotypes
2008.3.22
Association of STAT4 with susceptibility to rheumatoid arthritis and systemic lupus erythematosus in the Japanese population
2013.1.11
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosis
2007.1.1
A functional variant in FCRL3, encoding Fc receptor-like 3, is associated with rheumatoid arthritis and several autoimmunities
2012.1.24
Functional variants in NFKBIE and RTKN2 involved in activation of the NF-κB pathway are associated with rheumatoid arthritis in Japanese
2024.1.8
Genome-wide association studies for pelvic organ prolapse in the Japanese population
2012.1.11
Meta-analysis identifies nine new loci associated with rheumatoid arthritis in the Japanese population
2011.3.22
PADI4 polymorphism predisposes male smokers to rheumatoid arthritis
2011.3.22
The human AIRE gene at chromosome 21q22 is a genetic determinant for the predisposition to rheumatoid arthritis in Japanese population
2011.3.22
Common variants in a novel gene, FONG on chromosome 2q33.1 confer risk of osteoporosis in Japanese
2010.3.22
A regulatory variant in CCR6 is associated with rheumatoid arthritis susceptibility