-
1
-
-
84862747867
-
The genetics of multiple sclerosis: An up-To-date review
-
Gourraud, P.A., Harbo, H.F., Hauser, S.L. & Baranzini, S.E. The genetics of multiple sclerosis: An up-To-date review. Immunol. Rev. 248, 87-103 (2012
-
(2012)
Immunol. Rev
, vol.248
, pp. 87-103
-
-
Gourraud, P.A.1
Harbo, H.F.2
Hauser, S.L.3
Baranzini, S.E.4
-
4
-
-
32344446192
-
Multiple sclerosis in stepsiblings: Recurrence risk and ascertainment
-
Dyment, D.A., Yee, I.M., Ebers, G.C. & Sadovnick, A.D. Multiple sclerosis in stepsiblings: Recurrence risk and ascertainment. J. Neurol. Neurosurg. Psychiatry 77, 258-259 (2006
-
(2006)
J. Neurol. Neurosurg. Psychiatry
, vol.77
, pp. 258-259
-
-
Dyment, D.A.1
Yee, I.M.2
Ebers, G.C.3
Sadovnick, A.D.4
-
5
-
-
58649108766
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
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
-
44
-
-
84863845193
-
-
Howie, B., Marchini, J & Stephens, M. Genotype imputation with thousands of genomes. G3 1, 457-470 (2011
-
(2011)
Genotype Imputation With Thousands Of Genomes
, vol.G3
, Issue.1
, pp. 457-470
-
-
Howie, B.1
Marchini, J.2
Stephens, M.3
-
45
-
-
77953808087
-
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
-
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
-
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
|