메뉴 건너뛰기




Volumn 45, Issue 11, 2013, Pages 1353-1362

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis

(193)  Beecham, Ashley H a   Patsopoulos, Nikolaos A b,c,d,e   Xifara, Dionysia K f   Davis, Mary F g   Kemppinen, Anu h   Cotsapas, Chris e,i   Shah, Tejas S j   Spencer, Chris f   Booth, David k   Goris, An l   Oturai, Annette m   Saarela, Janna n   Fontaine, Bertrand o   Hemmer, Bernhard p,q,r   Martin, Claes s   Zipp, Frauke t   D'Alfonso, Sandra u   Martinelli Boneschi, Filippo v   Taylor, Bruce w   Harbo, Hanne F x,y   more..


Author keywords

[No Author keywords available]

Indexed keywords

CD6 ANTIGEN; HERPESVIRUS ENTRY MEDIATOR LIGAND; LYMPHOCYTE FUNCTION ASSOCIATED ANTIGEN 3; STAT4 PROTEIN;

EID: 84887058596     PISSN: 10614036     EISSN: 15461718     Source Type: Journal    
DOI: 10.1038/ng.2770     Document Type: Article
Times cited : (1127)

References (47)
  • 5
    • 58649108766 scopus 로고    scopus 로고
    • Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions
    • Hemminki, K., Li, X., Sundquist, J., Hillert, J. & Sundquist, K. Risk for multiple sclerosis in relatives and spouses of patients diagnosed with autoimmune and related conditions. Neurogenetics 10, 5-11 (2009
    • (2009) Neurogenetics , vol.10 , pp. 5-11
    • Hemminki, K.1    Li, X.2    Sundquist, J.3    Hillert, J.4    Sundquist, K.5
  • 6
    • 0015492877 scopus 로고
    • HL-A antigens and multiple sclerosis
    • Jersild, C., Svejgaard, A. & Fog, T. HL-A antigens and multiple sclerosis. Lancet 1, 1240-1241 (1972
    • (1972) Lancet , vol.1 , pp. 1240-1241
    • Jersild, C.1    Svejgaard, A.2    Fog, T.3
  • 7
    • 34548299105 scopus 로고    scopus 로고
    • Risk alleles for multiple sclerosis identified by a genomewide study
    • International Multiple Sclerosis Genetics Consortium
    • International Multiple Sclerosis Genetics Consortium. Risk alleles for multiple sclerosis identified by a genomewide study. N. Engl. J. Med. 357, 851-862 (2007
    • (2007) N. Engl. J. Med , vol.357 , pp. 851-862
  • 8
    • 67649876123 scopus 로고    scopus 로고
    • Meta-Analysis of genome scans and replication identify CD6 IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
    • De Jager, P.L. et al. Meta-Analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Nat. Genet. 41, 776-782 (2009
    • (2009) Nat. Genet , vol.41 , pp. 776-782
    • De Jager, P.L.1
  • 9
    • 80051684615 scopus 로고    scopus 로고
    • Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
    • International Multiple Sclerosis Genetics Consortium & Wellcome Trust Case Control Consortium 2
    • International Multiple Sclerosis Genetics Consortium & Wellcome Trust Case Control Consortium 2. Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 476, 214-219 (2011
    • (2011) Nature , vol.476 , pp. 214-219
  • 10
    • 84255194782 scopus 로고    scopus 로고
    • Genome-wide meta-Analysis identifies novel multiple sclerosis susceptibility loci
    • Patsopoulos, N.A. et al. Genome-wide meta-Analysis identifies novel multiple sclerosis susceptibility loci. Ann. Neurol. 70, 897-912 (2011
    • (2011) Ann. Neurol , vol.70 , pp. 897-912
    • Patsopoulos, N.A.1
  • 11
    • 77950329947 scopus 로고    scopus 로고
    • Evidence for polygenic susceptibility to multiple sclerosis-The shape of things to come
    • International Multiple Sclerosis Genetics Consortium
    • International Multiple Sclerosis Genetics Consortium. Evidence for polygenic susceptibility to multiple sclerosis-The shape of things to come. Am. J. Hum. Genet. 86, 621-625 (2010
    • (2010) Am. J. Hum. Genet , vol.86 , pp. 621-625
  • 12
    • 70449470314 scopus 로고    scopus 로고
    • The genetics of autoimmune diseases: A networked perspective
    • Baranzini, S.E. The genetics of autoimmune diseases: A networked perspective. Curr. Opin. Immunol. 21, 596-605 (2009
    • (2009) Curr. Opin. Immunol , vol.21 , pp. 596-605
    • Baranzini, S.E.1
  • 13
    • 80052325959 scopus 로고    scopus 로고
    • Pervasive sharing of genetic effects in autoimmune disease
    • Cotsapas, C. et al. Pervasive sharing of genetic effects in autoimmune disease. PLoS Genet. 7, e1002254 (2011
    • (2011) PLoS Genet , vol.7
    • Cotsapas, C.1
  • 14
    • 79960279940 scopus 로고    scopus 로고
    • Promise and pitfalls of the Immunochip
    • Cortes, A. & Brown, M.A. Promise and pitfalls of the Immunochip. Arthritis Res. Ther. 13, 101 (2011
    • (2011) Arthritis Res. Ther , vol.13 , pp. 101
    • Cortes, A.1    Brown, M.A.2
  • 15
    • 84868336049 scopus 로고    scopus 로고
    • Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease
    • Jostins, L. et al. Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease. Nature 491, 119-124 (2012
    • (2012) Nature , vol.491 , pp. 119-124
    • Jostins, L.1
  • 16
    • 69649109364 scopus 로고    scopus 로고
    • Circos: An information aesthetic for comparative genomics
    • Krzywinski, M. et al. Circos: An information aesthetic for comparative genomics. Genome Res. 19, 1639-1645 (2009
    • (2009) Genome Res , vol.19 , pp. 1639-1645
    • Krzywinski, M.1
  • 17
    • 0033534627 scopus 로고    scopus 로고
    • Bcl10 is involved in t(1;14)(p22;q32) of MALT B cell lymphoma and mutated in multiple tumor types
    • Willis, T.G. et al. Bcl10 is involved in t(1;14)(p22;q32) of MALT B cell lymphoma and mutated in multiple tumor types. Cell 96, 35-45 (1999
    • (1999) Cell , vol.96 , pp. 35-45
    • Willis, T.G.1
  • 18
    • 70350011787 scopus 로고    scopus 로고
    • NF-κB a potential therapeutic target for the treatment of multiple sclerosis
    • Yan, J. & Greer, J.M. NF-κB, a potential therapeutic target for the treatment of multiple sclerosis. CNS Neurol. Disord. Drug Targets 7, 536-557 (2008
    • (2008) CNS Neurol. Disord. Drug Targets , vol.7 , pp. 536-557
    • Yan, J.1    Greer, J.M.2
  • 19
    • 34250681374 scopus 로고    scopus 로고
    • CARD-Bcl10-Malt1 signalosomes: Missing link to NF-κB
    • Wegener, E. & Krappmann, D. CARD-Bcl10-Malt1 signalosomes: Missing link to NF-κB. Sci. STKE 2007, pe21 (2007
    • (2007) Sci. STKE , vol.2007
    • Wegener, E.1    Krappmann, D.2
  • 20
    • 84860317030 scopus 로고    scopus 로고
    • Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles
    • Fairfax, B.P. et al. Genetics of gene expression in primary immune cells identifies cell type-specific master regulators and roles of HLA alleles. Nat. Genet. 44, 502-510 (2012
    • (2012) Nat. Genet , vol.44 , pp. 502-510
    • Fairfax, B.P.1
  • 21
    • 84874779411 scopus 로고    scopus 로고
    • Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
    • Lill, C.M. et al. Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. J. Med. Genet. 50, 140-143 (2013
    • (2013) J. Med. Genet , vol.50 , pp. 140-143
    • Lill, C.M.1
  • 22
    • 58949100205 scopus 로고    scopus 로고
    • IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production
    • Maier, L.M. et al. IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production. PLoS Genet. 5, e1000322 (2009
    • (2009) PLoS Genet , vol.5
    • Maier, L.M.1
  • 23
    • 84870502629 scopus 로고    scopus 로고
    • Bayesian refinement of association signals for 14 loci in 3 common diseases
    • Maller, J.B. et al. Bayesian refinement of association signals for 14 loci in 3 common diseases. Nat. Genet. 44, 1294-1301 (2012
    • (2012) Nat. Genet , vol.44 , pp. 1294-1301
    • Maller, J.B.1
  • 24
    • 77955405475 scopus 로고    scopus 로고
    • Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
    • McLaren, W. et al. Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 26, 2069-2070 (2010
    • (2010) Bioinformatics , vol.26 , pp. 2069-2070
    • McLaren, W.1
  • 25
    • 84865261493 scopus 로고    scopus 로고
    • TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis
    • Gregory, A.P. et al. TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis. Nature 488, 508-511 (2012
    • (2012) Nature , vol.488 , pp. 508-511
    • Gregory, A.P.1
  • 26
    • 65249155425 scopus 로고    scopus 로고
    • The role of the CD58 locus in multiple sclerosis
    • De Jager, P.L. et al. The role of the CD58 locus in multiple sclerosis. Proc. Natl. Acad. Sci. USA 106, 5264-5269 (2009
    • (2009) Proc. Natl. Acad. Sci. USA , vol.106 , pp. 5264-5269
    • De Jager, P.L.1
  • 27
    • 84878375851 scopus 로고    scopus 로고
    • Serum levels of LIGHT in MS
    • Malmeström, C. et al. Serum levels of LIGHT in MS. Mult. Scler. 19, 871-876 (2013
    • (2013) Mult. Scler , vol.19 , pp. 871-876
    • Malmeström, C.1
  • 28
    • 84865790047 scopus 로고    scopus 로고
    • An integrated encyclopedia of DNA elements in the human genome
    • ENCODE Project Consortium
    • ENCODE Project Consortium. An integrated encyclopedia of DNA elements in the human genome. Nature 489, 57-74 (2012
    • (2012) Nature , vol.489 , pp. 57-74
  • 29
    • 84865777825 scopus 로고    scopus 로고
    • Linking disease associations with regulatory information in the human genome
    • Schaub, M.A., Boyle, A.P., Kundaje, A., Batzoglou, S. & Snyder, M. Linking disease associations with regulatory information in the human genome. Genome Res. 22, 1748-1759 (2012
    • (2012) Genome Res , vol.22 , pp. 1748-1759
    • Schaub, M.A.1    Boyle, A.P.2    Kundaje, A.3    Batzoglou, S.4    Snyder, M.5
  • 30
    • 78651237647 scopus 로고    scopus 로고
    • Identifying a high fraction of the human genome to be under selective constraint using GERP++
    • Davydov, E.V. et al. Identifying a high fraction of the human genome to be under selective constraint using GERP++. PLoS Comput. Biol. 6, e1001025 (2010
    • (2010) PLoS Comput. Biol , vol.6
    • Davydov, E.V.1
  • 31
    • 57249114505 scopus 로고    scopus 로고
    • SNAP: A web-based tool for identification and annotation of proxy SNPs using HapMap
    • Johnson, A.D. et al. SNAP: A web-based tool for identification and annotation of proxy SNPs using HapMap. Bioinformatics 24, 2938-2939 (2008
    • (2008) Bioinformatics , vol.24 , pp. 2938-2939
    • Johnson, A.D.1
  • 32
    • 84869060864 scopus 로고    scopus 로고
    • Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants
    • Juran, B.D. et al. Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants. Hum. Mol. Genet. 21, 5209-5221 (2012
    • (2012) Hum. Mol. Genet , vol.21 , pp. 5209-5221
    • Juran, B.D.1
  • 33
    • 84866924593 scopus 로고    scopus 로고
    • Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis
    • Liu, J.Z. et al. Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis. Nat. Genet. 44, 1137-1141 (2012
    • (2012) Nat. Genet , vol.44 , pp. 1137-1141
    • Liu, J.Z.1
  • 34
    • 82255192188 scopus 로고    scopus 로고
    • Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
    • Trynka, G. et al. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat. Genet. 43, 1193-1201 (2011
    • (2011) Nat. Genet , vol.43 , pp. 1193-1201
    • Trynka, G.1
  • 35
    • 84870531924 scopus 로고    scopus 로고
    • High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis
    • Eyre, S. et al. High-density genetic mapping identifies new susceptibility loci for rheumatoid arthritis. Nat. Genet. 44, 1336-1340 (2012
    • (2012) Nat. Genet , vol.44 , pp. 1336-1340
    • Eyre, S.1
  • 36
    • 84870512735 scopus 로고    scopus 로고
    • Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity
    • Tsoi, L.C. et al. Identification of 15 new psoriasis susceptibility loci highlights the role of innate immunity. Nat. Genet. 44, 1341-1348 (2012
    • (2012) Nat. Genet , vol.44 , pp. 1341-1348
    • Tsoi, L.C.1
  • 37
    • 84869021173 scopus 로고    scopus 로고
    • Seven newly identified loci for autoimmune thyroid disease
    • Cooper, J.D. et al. Seven newly identified loci for autoimmune thyroid disease. Hum. Mol. Genet. 21, 5202-5208 (2012
    • (2012) Hum. Mol. Genet , vol.21 , pp. 5202-5208
    • Cooper, J.D.1
  • 38
    • 70349629969 scopus 로고    scopus 로고
    • Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
    • Ban, M. et al. Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. Eur. J. Hum. Genet. 17, 1309-1313 (2009
    • (2009) Eur. J. Hum. Genet , vol.17 , pp. 1309-1313
    • Ban, M.1
  • 39
    • 78649699944 scopus 로고    scopus 로고
    • A non-synonymous SNP within membrane metalloendopeptidase-like 1 (MMEL1) is associated with multiple sclerosis
    • Ban, M. et al. A non-synonymous SNP within membrane metalloendopeptidase- like 1 (MMEL1) is associated with multiple sclerosis. Genes Immun. 11, 660-664 (2010
    • (2010) Genes Immun , vol.11 , pp. 660-664
    • Ban, M.1
  • 40
    • 84863505871 scopus 로고    scopus 로고
    • Opticall: A robust genotype-calling algorithm for rare, low-frequency andcommon variants
    • Shah, T.S. et al. optiCall: A robust genotype-calling algorithm for rare, low-frequency andcommon variants. Bioinformatics 28, 1598-1603 (2012
    • (2012) Bioinformatics , vol.28 , pp. 1598-1603
    • Shah, T.S.1
  • 41
    • 34548292504 scopus 로고    scopus 로고
    • PLINK: A tool set for whole-genome association and population-based linkage analyses
    • Purcell, S. et al. PLINK: A tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559-575 (2007
    • (2007) Am. J. Hum. Genet , vol.81 , pp. 559-575
    • Purcell, S.1
  • 42
    • 71149112981 scopus 로고    scopus 로고
    • Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies
    • Browning, B.L. & Yu, Z. Simultaneous genotype calling and haplotype phasing improves genotype accuracy and reduces false-positive associations for genome-wide association studies. Am. J. Hum. Genet. 85, 847-861 (2009
    • (2009) Am. J. Hum. Genet , vol.85 , pp. 847-861
    • Browning, B.L.1    Yu, Z.2
  • 43
    • 34347344976 scopus 로고    scopus 로고
    • A new multipoint method for genome-wide association studies by imputation of genotypes
    • Marchini, J., Howie, B., Myers, S., McVean, G. & Donnelly, P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet. 39, 906-913 (2007
    • (2007) Nat. Genet , vol.39 , pp. 906-913
    • Marchini, J.1    Howie, B.2    Myers, S.3    McVean, G.4    Donnelly, P.5
  • 45
    • 77953808087 scopus 로고    scopus 로고
    • Genotype imputation for genome-wide association studies
    • Marchini, J. & Howie, B. Genotype imputation for genome-wide association studies. Nat. Rev. Genet. 11, 499-511 (2010
    • (2010) Nat. Rev. Genet , vol.11 , pp. 499-511
    • Marchini, J.1    Howie, B.2
  • 46
    • 77951751034 scopus 로고    scopus 로고
    • Meta-Analysis and imputation refines the association of 15q25 with smoking quantity
    • Liu, J.Z. et al. Meta-Analysis and imputation refines the association of 15q25 with smoking quantity. Nat. Genet. 42, 436-440 (2010
    • (2010) Nat. Genet , vol.42 , pp. 436-440
    • Liu, J.Z.1
  • 47
    • 77956534324 scopus 로고    scopus 로고
    • ANNOVAR: Functional annotation of genetic variants from high-Throughput sequencing data
    • Wang, K., Li, M. & Hakonarson, H. ANNOVAR: Functional annotation of genetic variants from high-Throughput sequencing data. Nucleic Acids Res. 38, e164 (2010
    • (2010) Nucleic Acids Res , vol.38
    • Wang, K.1    Li, M.2    Hakonarson, H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.