Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms - Wikidata - awgldk - TriplyDB

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms

Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms

http://www.wikidata.org/entity/Q33378475

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Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS Revealing the genetic basis of multiple sclerosis: are we there yet?Genetic implication of a novel thiamine transporter in human hypertension.Association between Tumor Necrosis Factor- α-308 G/A Polymorphism and Multiple Sclerosis: A Systematic Review and Meta-Analysis Epistasis and immunity: the role of genetic interactions in autoimmune diseases A genome-wide association study in progressive multiple sclerosis SNP-based analysis of the HLA locus in Japanese multiple sclerosis patients.Network-based multiple sclerosis pathway analysis with GWAS data from 15,000 cases and 30,000 controls.Estimates of array and pool-construction variance for planning efficient DNA-pooling genome wide association studies Pooled genome-wide analysis to identify novel risk loci for pediatric allergic asthma Genetic burden in multiple sclerosis families Refining the association of MHC with multiple sclerosis in African Americans.IL7Rα contributes to experimental autoimmune encephalomyelitis through altered T cell responses and nonhematopoietic cell lineages Ultra high throughput sequencing excludes MDH1 as candidate gene for RP28-linked retinitis pigmentosa Advances and challenges in biomarker development for type 1 diabetes prediction and prevention using omic technologies Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome Cost-effective genome-wide estimation of allele frequencies from pooled DNA in Atlantic salmon (Salmo salar L.).A genome-wide integrative genomic study localizes genetic factors influencing antibodies against Epstein-Barr virus nuclear antigen 1 (EBNA-1).Genome-wide association studies in neurology.Association of SNPs of CD40 gene with multiple sclerosis in Russians.Contribution of genome-wide association studies to scientific research: a pragmatic approach to evaluate their impact.Genetic Variants Underlying Risk of Intracranial Aneurysms: Insights from a GWAS in Portugal.Genetic determinants of risk and progression in multiple sclerosis.GWAS signals across the HLA regions: revealing a clue for common etiology underlying infectious tumors and other immunity diseases Aggregation of multiple sclerosis genetic risk variants in multiple and single case families.Tumor necrosis factor polymorphisms associated with tumor necrosis factor production influence the risk of idiopathic intermediate uveitis.A PheWAS approach in studying HLA-DRB1*1501.IL12A, MPHOSPH9/CDK2AP1 and RGS1 are novel multiple sclerosis susceptibility loci.Genetic risk variants in African Americans with multiple sclerosis ZFAT gene variant association with multiple sclerosis in the Arabian Gulf population: A genetic basis for gender-associated susceptibility Association between type 1 diabetes and GWAS SNPs in the southeast US Caucasian population Genes associated with multiple sclerosis: 15 and counting.Potential impact of B cells on T cell function in multiple sclerosis The genetics of multiple sclerosis: an up-to-date review.From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A.Decoding multiple sclerosis: an update on genomics and future directions.A review of genome-wide association studies for multiple sclerosis: classical and hypothesis-driven approaches.Identifying patient subtypes in multiple sclerosis and tailoring immunotherapy: challenges for the future.Tolerance of activated pathogenic CD4+ T cells by transcriptional targeting of dendritic cells.

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Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms

http://www.wikidata.org/entity/Q33378475

description

2008 nî lūn-bûn

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2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

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2008 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Identification of a novel risk ...... ingle nucleotide polymorphisms

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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type

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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Identification of a novel risk ...... ingle nucleotide polymorphisms

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Arcadi Navarro

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BiomarkerMS Study Group

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Carlos Morcillo

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Cristina Lopez

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David W Craig

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Manuel Comabella

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Montse Camiña-Tato

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P2860

c-Myc-regulated microRNAs modulate E2F1 expression

Novel mutations in the PEX12 gene of patients with a peroxisome biogenesis disorder

Risk alleles for multiple sclerosis identified by a genomewide study

SNP analysis to results (SNPator): a web-based environment oriented to statistical genomics analyses upon SNP data.

The E2F1-3 transcription factors are essential for cellular proliferation.

New diagnostic criteria for multiple sclerosis: guidelines for research protocols.

Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients.

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.

Identification of the genetic basis for complex disorders by use of pooling-based genomewide single-nucleotide-polymorphism association studies

Peroxisome biogenesis disorders: the role of peroxisomes and metabolic dysfunction in developing brain.

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10

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Xavier Montalban

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multiple sclerosis

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