Whole genome association study of rheumatoid arthritis using 27 039 microsatellites. - Test2 - elhamkhani - TriplyDB

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

http://www.wikidata.org/entity/Q34431672

about

Association study in the 5q31-32 linkage region for schizophrenia using pooled DNA genotyping Pooled DNA genotyping on Affymetrix SNP genotyping arrays Common variants in the COL4A4 gene confer susceptibility to lattice degeneration of the retina.Association analysis of the PIP4K2A gene on chromosome 10p12 and schizophrenia in the Irish study of high density schizophrenia families (ISHDSF) and the Irish case-control study of schizophrenia (ICCSS).Genome wide screen identifies microsatellite markers associated with acute adverse effects following radiotherapy in cancer patients Antiviral immune responses: triggers of or triggered by autoimmunity?Polymorphisms in genes controlling inflammation and tissue repair in rheumatoid arthritis: a case control study.A systems genetics approach provides a bridge from discovered genetic variants to biological pathways in rheumatoid arthritis.Interleukins and interleukin receptors in rheumatoid arthritis: Research, diagnostics and clinical implications.Potential of ayurgenomics approach in complex trait research: leads from a pilot study on rheumatoid arthritis The landscape of human STR variation.Epistatic interaction between FCRL3 and NFkappaB1 genes in Spanish patients with rheumatoid arthritis Fractioned DNA pooling: a new cost-effective strategy for fine mapping of quantitative trait loci.HLA Immune Function Genes in Autism.Translating genomic biomarkers into clinically useful diagnostics.Novel susceptibility genes in inflammatory bowel disease.Linkage analysis of anti-CCP levels as dichotomized and quantitative traits using GAW15 single-nucleotide polymorphism scan of NARAC families.Linkage disequilibrium between STRPs and SNPs across the human genome.Genome-wide association analysis with selective genotyping identifies candidate loci for adult height at 8q21.13 and 15q22.33-q23 in Mongolians A transmembrane polymorphism in FcgammaRIIb (FCGR2B) is associated with the production of anti-cyclic citrullinated peptide autoantibodies in Taiwanese RA.VarySysDB: a human genetic polymorphism database based on all H-InvDB transcripts Lack of association with high myopia and the MYP2 locus in the Japanese population by high resolution microsatellite analysis on chromosome 18.Hyperlink Management System and ID Converter System: enabling maintenance-free hyperlinks among major biological databases.Whole genome association study in a homogenous population in Shandong peninsula of China reveals JARID2 as a susceptibility gene for schizophrenia The discovery of human genetic variations and their use as disease markers: past, present and future.Immunogenetics of hematopoietic stem cell transplantation: the contribution of microsatellite polymorphism studies.Hunting for genes for hypertension: the Millennium Genome Project for Hypertension.Lessons from Genome-Wide Search for Disease-Related Genes with Special Reference to HLA-Disease Associations.Genome-wide screening for risk loci of idiopathic recurrent miscarriage in a Han Chinese population: a pilot study.Assessment of chromosome 19 for genetic association in severe chronic periodontitis.Kidney Diseases Enhance Expression of Tetraspanin-8: A Possible Protective Effect against Tubular Injury.Genomewide association analysis of human narcolepsy and a new resistance gene.Current concepts in the genetic diagnostics of rheumatoid arthritis.Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.Microsatellite scanning of the immunogenome associates MAPK14 and ELTD1 with graft-versus-host disease in hematopoietic stem cell transplantation.Estimating population haplotype frequencies from pooled DNA samples using PHASE algorithm.Selection pressure on human STR loci and its relevance in repeat expansion disease.Genomic DNA pooling for whole-genome association scans in complex disease: empirical demonstration of efficacy in rheumatoid arthritis.Haplotype-specific gene expression profiles in a telomeric major histocompatibility complex gene cluster and susceptibility to autoimmune diseases.Association 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

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

http://www.wikidata.org/entity/Q34431672

description

2005 nî lūn-bûn

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2005 թուականի Յուլիսին հրատարակուած գիտական յօդուած

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2005 թվականի հուլիսին հրատարակված գիտական հոդված

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2005年の論文

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年学术文章

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2005年學術文章

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name

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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type

label

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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prefLabel

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

@ast

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

@en

Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Human Molecular Genetics

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Whole genome association study of rheumatoid arthritis using 27 039 microsatellites.

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Akira Oka

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Atsuo Taniguchi

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Gen Tamiya

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Hideo Ishibashi

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Hidetoshi Inoko

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Hiroshi Hashimoto

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Hisashi Yamanaka

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Joji Mochida

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Kei Fujimoto

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Koh Furugaki

http://www.w3.org/2001/XMLSchema#string

P2860

Single nucleotide polymorphisms as tools in human genetics

Searching for genetic determinants in the new millennium

Identification of a novel gene and a common variant associated with uric acid nephrolithiasis in a Sardinian genetic isolate.

Identification of I kappa BL as the second major histocompatibility complex-linked susceptibility locus for rheumatoid arthritis

The structure of haplotype blocks in the human genome

The International HapMap Project

A comprehensive genetic map of the human genome based on 5,264 microsatellites

The WD repeat: a common architecture for diverse functions

Using haplotype blocks to map human complex trait loci

An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis

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2305-2321

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scholarly article

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10.1093/HMG/DDI234

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16

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14

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Tadashi Imanishi

Takashi Gojobori

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2005-07-06T00:00:00Z

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7744622

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