Clustering of disease features within 512 multicase rheumatoid arthritis families.
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Replication of putative candidate-gene associations with rheumatoid arthritis in >4,000 samples from North America and Sweden: association of susceptibility with PTPN22, CTLA4, and PADI4Data for Genetic Analysis Workshop (GAW) 15 Problem 2, genetic causes of rheumatoid arthritis and associated traitsEvidence of linkage to chromosome 1 for early age of onset of rheumatoid arthritis and HLA marker DRB1 genotype in NARAC dataIdentifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association.A two-dimensional genome scan for rheumatoid arthritis susceptibility lociA large-scale rheumatoid arthritis genetic study identifies association at chromosome 9q33.2.A towards-multidimensional screening approach to predict candidate genes of rheumatoid arthritis based on SNP, structural and functional annotations.Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes.More powerful haplotype sharing by accounting for the mode of inheritance.PTPN22 genetic variation: evidence for multiple variants associated with rheumatoid arthritisChallenges comparing functional limitations in rheumatoid arthritis and ankylosing spondylitisEvidence for interaction between 5-hydroxytryptamine (serotonin) receptor 2A and MHC type II molecules in the development of rheumatoid arthritis.How do autoimmune diseases cluster in families? A systematic review and meta-analysis.Several regions in the major histocompatibility complex confer risk for anti-CCP-antibody positive rheumatoid arthritis, independent of the DRB1 locusGenetic vectors as a tool in association studies: definitions and application for study of rheumatoid arthritisCopy number variation in Y chromosome multicopy genes is linked to a paternal parent-of-origin effect on CNS autoimmune disease in female offspringGene-gene and gene-environment interactions involving HLA-DRB1, PTPN22, and smoking in two subsets of rheumatoid arthritisProtective effect of noninherited maternal HLA-DR antigens on rheumatoid arthritis development.One- and two-locus models for mapping rheumatoid arthritis-susceptibility genes on chromosome 6.The MHC2TA -168A/G polymorphism and risk for rheumatoid arthritis: a meta-analysis of 6861 patients and 9270 controls reveals no evidence for associationTwo independent alleles at 6q23 associated with risk of rheumatoid arthritisFamily history of rheumatoid arthritis: an old concept with new developments.Genome-wide association study identifies distinct genetic contributions to prognosis and susceptibility in Crohn's disease.Association of the 6q23 region with the rate of joint destruction in rheumatoid arthritis.High-density SNP analysis of 642 Caucasian families with rheumatoid arthritis identifies two new linkage regions on 11p12 and 2q33.Beyond disease susceptibility-Leveraging genome-wide association studies for new insights into complex disease biology.The kaleidoscope of autoimmunity: multiple autoimmune syndromes and familial autoimmunityAssociation analysis of TNFR2, VDR, A2M, GSTT1, GSTM1, and ACE genes with rheumatoid arthritis in South Asians and Caucasians of East Midlands in the United Kingdom
P2860
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P2860
Clustering of disease features within 512 multicase rheumatoid arthritis families.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Clustering of disease features within 512 multicase rheumatoid arthritis families.
@en
type
label
Clustering of disease features within 512 multicase rheumatoid arthritis families.
@en
prefLabel
Clustering of disease features within 512 multicase rheumatoid arthritis families.
@en
P2093
P356
P1476
Clustering of disease features within 512 multicase rheumatoid arthritis families.
@en
P2093
Damini Jawaheer
Lindsey A Criswell
Raymond F Lum
P304
P356
10.1002/ART.20066
P577
2004-03-01T00:00:00Z