-
1
-
-
33746588738
-
The epidemiology of multiple sclerosis in Europe
-
Pugliatti, M. et al. The epidemiology of multiple sclerosis in Europe. Eur. J. Neurol. 13, 700-722 (2006).
-
(2006)
Eur. J. Neurol.
, vol.13
, pp. 700-722
-
-
Pugliatti, M.1
-
2
-
-
33749059726
-
The neurobiology of multiple sclerosis: Genes, inflammation, and neurodegeneration
-
Hauser, S. L. & Oksenberg, J. R. The neurobiology of multiple sclerosis: genes, inflammation, and neurodegeneration. Neuron 52, 61-76 (2006).
-
(2006)
Neuron
, vol.52
, pp. 61-76
-
-
Hauser, S.L.1
Oksenberg, J.R.2
-
4
-
-
73549089256
-
Multiple sclerosis: Distribution of inflammatory cells in newly forming lesions
-
Henderson, A. P., Barnett, M. H., Parratt, J. D. & Prineas, J. W. Multiple sclerosis: distribution of inflammatory cells in newly forming lesions. Ann. Neurol. 66, 739-753 (2009).
-
(2009)
Ann. Neurol.
, vol.66
, pp. 739-753
-
-
Henderson, A.P.1
Barnett, M.H.2
Parratt, J.D.3
Prineas, J.W.4
-
5
-
-
39549105607
-
Pathological heterogeneity of idiopathic central nervous system inflammatory demyelinating disorders
-
Lucchinetti, C. Pathological heterogeneity of idiopathic central nervous system inflammatory demyelinating disorders. Curr. Top. Microbiol. Immunol. 318, 19-43 (2008).
-
(2008)
Curr. Top. Microbiol. Immunol.
, vol.318
, pp. 19-43
-
-
Lucchinetti, C.1
-
6
-
-
39049163500
-
Homogeneity of active demyelinating lesions in established multiple sclerosis
-
Breij, E. C. et al. Homogeneity of active demyelinating lesions in established multiple sclerosis. Ann. Neurol. 63, 16-25 (2008).
-
(2008)
Ann. Neurol.
, vol.63
, pp. 16-25
-
-
Breij, E.C.1
-
7
-
-
0013950284
-
Risk of multiple sclerosis related to age at migration to israel
-
Alter, M., Leibowitz, U. & Speer, J. Risk of multiple sclerosis related to age at migration to israel. Arch. Neurol. 15, 234-237 (1996).
-
(1996)
Arch. Neurol.
, vol.15
, pp. 234-237
-
-
Alter, M.1
Leibowitz, U.2
Speer, J.3
-
8
-
-
0015240061
-
On the risk of multiple sclerosis according to age at migration to South Africa
-
Dean, G. & Kurtzke, J. F. On the risk of multiple sclerosis according to age at migration to South Africa. Br. Med. J. 3, 725-729 (1971).
-
(1971)
Br. Med. J.
, vol.3
, pp. 725-729
-
-
Dean, G.1
Kurtzke, J.F.2
-
9
-
-
28544450418
-
Role of return migration in the emergence of multiple sclerosis in the French west indies
-
Cabre, P. et al. Role of return migration in the emergence of multiple sclerosis in the French west indies. Brain 128, 2899-2910 (2005).
-
(2005)
Brain
, vol.128
, pp. 2899-2910
-
-
Cabre, P.1
-
10
-
-
33745728408
-
Differential twin concordance for multiple sclerosis by latitude of birthplace
-
Islam, T. et al. Differential twin concordance for multiple sclerosis by latitude of birthplace. Ann. Neurol. 60, 56-64 (2006).
-
(2006)
Ann. Neurol.
, vol.60
, pp. 56-64
-
-
Islam, T.1
-
11
-
-
34547616817
-
Childhood sun exposure influences risk of multiple sclerosis in monozygotic twins
-
Islam, T., Gauderman, W. J., Cozen, W. & Mack, T. M. Childhood sun exposure influences risk of multiple sclerosis in monozygotic twins. Neurology 69, 381-388 (2007).
-
(2007)
Neurology
, vol.69
, pp. 381-388
-
-
Islam, T.1
Gauderman, W.J.2
Cozen, W.3
MacK, T.M.4
-
12
-
-
69549122678
-
Explaining multiple sclerosis prevalence by ultraviolet exposure: A geospatial analysis
-
Beretich, B. D. & Beretich, T. M. Explaining multiple sclerosis prevalence by ultraviolet exposure: a geospatial analysis. Mult. Scler. 15, 891-898 (2009).
-
(2009)
Mult. Scler.
, vol.15
, pp. 891-898
-
-
Beretich, B.D.1
Beretich, T.M.2
-
13
-
-
12344314461
-
Timing of birth and risk of multiple sclerosis: Population based study
-
Willer, C. J. et al. Timing of birth and risk of multiple sclerosis: population based study. BMJ 330, 120 (2005).
-
(2005)
BMJ
, vol.330
, pp. 120
-
-
Willer, C.J.1
-
14
-
-
31544468078
-
Seasonal fluctuation of multiple sclerosis births in Sardinia
-
Sotgiu, S. et al. Seasonal fluctuation of multiple sclerosis births in Sardinia. J. Neurol. 253, 38-44 (2006).
-
(2006)
J. Neurol.
, vol.253
, pp. 38-44
-
-
Sotgiu, S.1
-
15
-
-
73349138876
-
HLA-DRB1 and month of birth in multiple sclerosis
-
Ramagopalan, S. V. et al. HLA-DRB1 and month of birth in multiple sclerosis. Neurology 73, 2107-2111 (2009).
-
(2009)
Neurology
, vol.73
, pp. 2107-2111
-
-
Ramagopalan, S.V.1
-
16
-
-
33749681309
-
Sex ratio of multiple sclerosis in Canada: A longitudinal study
-
Orton, S. M. et al. Sex ratio of multiple sclerosis in Canada: a longitudinal study. Lancet Neurol. 5, 932-936 (2006).
-
(2006)
Lancet Neurol.
, vol.5
, pp. 932-936
-
-
Orton, S.M.1
-
17
-
-
0034044360
-
Multiple sclerosis in time and space\geographic clues to cause
-
Kurtzke, J. F. Multiple sclerosis in time and space\geographic clues to cause. J. Neurovirol. 6 (Suppl. 2), S134-S140 (2000).
-
(2000)
J. Neurovirol.
, vol.6
, Issue.SUPPL. 2
-
-
Kurtzke, J.F.1
-
18
-
-
33748088131
-
Evidence of early childhood as the susceptibility period in multiple sclerosis: Space-time cluster analysis in a Sardinian population
-
Pugliatti, M. et al. Evidence of early childhood as the susceptibility period in multiple sclerosis: space-time cluster analysis in a Sardinian population. Am. J. Epidemiol. 164, 326-333 (2006).
-
(2006)
Am. J. Epidemiol.
, vol.164
, pp. 326-333
-
-
Pugliatti, M.1
-
19
-
-
45549092100
-
The genetics of multiple sclerosis: SNPs to pathways to pathogenesis
-
Oksenberg, J. R., Baranzini, S. E., Sawcer, S. & Hauser, S. L. The genetics of multiple sclerosis: SNPs to pathways to pathogenesis. Nat. Rev. Genet. 9, 516-526 (2008).
-
(2008)
Nat. Rev. Genet.
, vol.9
, pp. 516-526
-
-
Oksenberg, J.R.1
Baranzini, S.E.2
Sawcer, S.3
Hauser, S.L.4
-
20
-
-
76549242470
-
Familial occurrence of multiple sclerosis and its implications
-
Mackay, R. P. Familial occurrence of multiple sclerosis and its implications. Arch. Neurol. Psychiatry 64, 155-157 (1950).
-
(1950)
Arch. Neurol. Psychiatry
, vol.64
, pp. 155-157
-
-
MacKay, R.1
-
21
-
-
0001694546
-
Familial and conjugal multiple sclerosis
-
Schapira, K., Poskanzer, D. C. & Miller, H. Familial and conjugal multiple sclerosis. Brain 86, 315-332 (1963).
-
(1963)
Brain
, vol.86
, pp. 315-332
-
-
Schapira, K.1
Poskanzer, D.C.2
Miller, H.3
-
22
-
-
0025089312
-
Multiple sclerosis sibling pairs: Clustered onset and familial predisposition
-
Doolittle, T. H. et al. Multiple sclerosis sibling pairs: clustered onset and familial predisposition. Neurology 40, 1546-1552 (1990).
-
(1990)
Neurology
, vol.40
, pp. 1546-1552
-
-
Doolittle, T.H.1
-
23
-
-
0029874022
-
Age-adjusted recurrence risks for relatives of patients with multiple sclerosis
-
Robertson, N. P. et al. Age-adjusted recurrence risks for relatives of patients with multiple sclerosis. Brain 119, 449-455 (1996).
-
(1996)
Brain
, vol.119
, pp. 449-455
-
-
Robertson, N.P.1
-
24
-
-
0025019555
-
Linkage strategies for genetically complex traits. I. Multilocus models
-
Risch, N. Linkage strategies for genetically complex traits. I. Multilocus models. Am. J. Hum. Genet. 46, 222-228 (1990).
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
25
-
-
0027164123
-
Familial recurrence risks and inheritance of multiple sclerosis
-
Sadovnick, A. D. Familial recurrence risks and inheritance of multiple sclerosis. Curr. Opin. Neurol. Neurosurg. 6, 189-194 (1993).
-
(1993)
Curr. Opin. Neurol. Neurosurg.
, vol.6
, pp. 189-194
-
-
Sadovnick, A.D.1
-
26
-
-
0032231780
-
Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting
-
Guo, S. W. inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting. Am. J. Hum. Genet. 63, 252-258 (1998).
-
(1998)
Am. J. Hum. Genet.
, vol.63
, pp. 252-258
-
-
Guo, S.W.1
-
27
-
-
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
-
28
-
-
77649289047
-
What role for genetics in the prediction of multiple sclerosis?
-
Sawcer, S., Ban, M., wason, J. & Dudbridge, F. what role for genetics in the prediction of multiple sclerosis? Ann. Neurol. 67, 3-10 (2010).
-
(2010)
Ann. Neurol.
, vol.67
, pp. 3-10
-
-
Sawcer, S.1
Ban, M.2
Wason, J.3
Dudbridge, F.4
-
29
-
-
0030903014
-
Risks of multiple sclerosis in relatives of patients in Flanders, Belgium
-
Carton, H. et al. Risks of multiple sclerosis in relatives of patients in Flanders, Belgium. J. Neurol. Neurosurg. Psychiatry 62, 329-333 (1997).
-
(1997)
J. Neurol. Neurosurg. Psychiatry
, vol.62
, pp. 329-333
-
-
Carton, H.1
-
30
-
-
0029121088
-
A genetic basis for familial aggregation in multiple sclerosis
-
Ebers, G. C., Sadovnick, A. D. & Risch, N. J. A genetic basis for familial aggregation in multiple sclerosis. Nature 377, 150-151 (1995).
-
(1995)
Nature
, vol.377
, pp. 150-151
-
-
Ebers, G.C.1
Sadovnick, A.D.2
Risch, N.J.3
-
31
-
-
0030007661
-
Evidence for genetic basis of multiple sclerosis
-
The Canadian Collaborative Study Group
-
Sadovnick, A. D., Ebers, G. C., Dyment, D. A. & Risch, N. J. Evidence for genetic basis of multiple sclerosis. The Canadian Collaborative Study Group. Lancet 347, 1728-1730 (1996).
-
(1996)
Lancet
, vol.347
, pp. 1728-1730
-
-
Sadovnick, A.D.1
Ebers, G.C.2
Dyment, D.A.3
Risch, N.J.4
-
32
-
-
0033674248
-
Conjugal multiple sclerosis: Population-based prevalence and recurrence risks in offspring
-
Ebers, G. C., Yee, I. M., Sadovnick, A. D. & Duquette, P. Conjugal multiple sclerosis: population-based prevalence and recurrence risks in offspring. Ann. Neurol. 48, 927-931 (2000).
-
(2000)
Ann. Neurol.
, vol.48
, pp. 927-931
-
-
Ebers, G.C.1
Yee, I.M.2
Sadovnick, A.D.3
Duquette, P.4
-
33
-
-
0033549026
-
Familial factors influence disability in MS multiplex families
-
Brassat, D. et al. Familial factors influence disability in MS multiplex families. Neurology 52, 1632-1636 (1999).
-
(1999)
Neurology
, vol.52
, pp. 1632-1636
-
-
Brassat, D.1
-
34
-
-
0036151386
-
Genetic basis for clinical expression in multiple sclerosis
-
Barcellos, L. F. et al. Genetic basis for clinical expression in multiple sclerosis. Brain 125, 150-158 (2002).
-
(2002)
Brain
, vol.125
, pp. 150-158
-
-
Barcellos, L.F.1
-
35
-
-
33846566857
-
Familial effects on the clinical course of multiple sclerosis
-
Hensiek, A. E. et al. Familial effects on the clinical course of multiple sclerosis. Neurology 68, 376-383 (2007).
-
(2007)
Neurology
, vol.68
, pp. 376-383
-
-
Hensiek, A.E.1
-
36
-
-
38049170558
-
An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus
-
DeLuca, G. C. et al. An extremes of outcome strategy provides evidence that multiple sclerosis severity is determined by alleles at the HLA-DRB1 locus. Proc. Natl Acad. Sci. USA 104, 20896-20901 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 20896-20901
-
-
Deluca, G.C.1
-
37
-
-
0242268416
-
Twin concordance and sibling recurrence rates in multiple sclerosis
-
Willer, C. J., Dyment, D. A., Risch, N. J., Sadovnick, A. D. & Ebers, G. C. Twin concordance and sibling recurrence rates in multiple sclerosis. Proc. Natl Acad. Sci. USA 100, 12877-12882 (2003).
-
(2003)
Proc. Natl Acad. Sci. USA
, vol.100
, pp. 12877-12882
-
-
Willer, C.J.1
Dyment, D.A.2
Risch, N.J.3
Sadovnick, A.D.4
Ebers, G.C.5
-
38
-
-
25844442849
-
Concordance for multiple sclerosis in Danish twins: An update of a nationwide study
-
Hansen, T. et al. Concordance for multiple sclerosis in Danish twins: an update of a nationwide study. Mult. Scler. 11, 504-510 (2005).
-
(2005)
Mult. Scler.
, vol.11
, pp. 504-510
-
-
Hansen, T.1
-
39
-
-
66149186884
-
Twin studies and the heritability of MS: A conclusion
-
Hawkes, C. H. & Macgregor, A. J. Twin studies and the heritability of MS: a conclusion. Mult. Scler. 15, 661-667 (2009).
-
(2009)
Mult. Scler.
, vol.15
, pp. 661-667
-
-
Hawkes, C.H.1
MacGregor, A.J.2
-
41
-
-
26044433609
-
Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis
-
Booth, D. R. et al. Gene expression and genotyping studies implicate the interleukin 7 receptor in the pathogenesis of primary progressive multiple sclerosis. J. Mol. Med. 83, 822-830 (2005).
-
(2005)
J. Mol. Med.
, vol.83
, pp. 822-830
-
-
Booth, D.R.1
-
42
-
-
34548368541
-
Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis
-
Lundmark, F. et al. variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis. Nat. Genet. 39, 1108-1113 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1108-1113
-
-
Lundmark, F.1
-
43
-
-
34548351247
-
Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis
-
Gregory, S. G. et al. interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis. Nat. Genet. 39, 1083-1091 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1083-1091
-
-
Gregory, S.G.1
-
44
-
-
23944499790
-
A high-density screen for linkage in multiple sclerosis
-
Sawcer, S. et al. A high-density screen for linkage in multiple sclerosis. Am. J. Hum. Genet. 77, 454-467 (2005).
-
(2005)
Am. J. Hum. Genet.
, vol.77
, pp. 454-467
-
-
Sawcer, S.1
-
45
-
-
35748981184
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
Burton, P. R. et al. Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat. Genet. 39, 1329-1337 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 1329-1337
-
-
Burton, P.R.1
-
46
-
-
34548299105
-
Risk alleles for multiple sclerosis identified by a genome-wide study
-
International Multiple Sclerosis Genetics Consortium
-
International Multiple Sclerosis Genetics Consortium. Risk alleles for multiple sclerosis identified by a genome-wide study. N. Engl. J. Med. 357, 851-862 (2007).
-
(2007)
N. Engl. J. Med.
, vol.357
, pp. 851-862
-
-
-
47
-
-
55849139823
-
Identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms
-
Comabella, M. et al. identification of a novel risk locus for multiple sclerosis at 13q31.3 by a pooled genome-wide scan of 500,000 single nucleotide polymorphisms. PLoS ONE 3, e3490 (2008).
-
(2008)
PLoS ONE
, vol.3
-
-
Comabella, M.1
-
48
-
-
58949099391
-
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
-
Baranzini, S. E. et al. Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Hum. Mol. Genet. 18, 767-778 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 767-778
-
-
Baranzini, S.E.1
-
49
-
-
67649881102
-
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
-
Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)
-
Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene). Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nat. Genet. 41, 824-828 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 824-828
-
-
-
50
-
-
76049083598
-
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
-
Jakkula, E. et al. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Am. J. Hum. Genet. 86, 285-291 (2010).
-
(2010)
Am. J. Hum. Genet.
, vol.86
, pp. 285-291
-
-
Jakkula, E.1
-
51
-
-
77952884985
-
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
-
Sanna, S. et al. variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. Nat. Genet. 42, 495-497 (2010).
-
(2010)
Nat. Genet.
, vol.42
, pp. 495-497
-
-
Sanna, S.1
-
52
-
-
49849091315
-
Refining genetic associations in multiple sclerosis
-
International Multiple Sclerosis Genetics Consortium (iMSGC)
-
International Multiple Sclerosis Genetics Consortium (iMSGC). Refining genetic associations in multiple sclerosis. Lancet Neurol. 7, 567-569 (2008).
-
(2008)
Lancet Neurol.
, vol.7
, pp. 567-569
-
-
-
53
-
-
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
-
54
-
-
66249086434
-
Risk alleles for multiple sclerosis in multiplex families
-
D'Netto, M. J. et al. Risk alleles for multiple sclerosis in multiplex families. Neurology 72, 1984-1988 (2009).
-
(2009)
Neurology
, vol.72
, pp. 1984-1988
-
-
D'Netto, M.J.1
-
55
-
-
74049085453
-
Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis
-
Hoppenbrouwers, I. A. et al. Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis. J. Hum. Genet. 54, 676-680 (2009).
-
(2009)
J. Hum. Genet.
, vol.54
, pp. 676-680
-
-
Hoppenbrouwers, I.A.1
-
56
-
-
59149093148
-
The expanding genetic overlap between multiple sclerosis and type i diabetes
-
International Multiple Sclerosis Genetics Consortium (iMSGC)
-
International Multiple Sclerosis Genetics Consortium (iMSGC). The expanding genetic overlap between multiple sclerosis and type i diabetes. Genes Immun. 10, 11-14 (2009).
-
(2009)
Genes Immun.
, vol.10
, pp. 11-14
-
-
-
57
-
-
77950544633
-
Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci
-
International Multiple Sclerosis Genetics Consortium (iMSGC)
-
International Multiple Sclerosis Genetics Consortium (iMSGC). Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. Hum. Mol. Genet. 19, 953-962 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.19
, pp. 953-962
-
-
-
58
-
-
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
-
59
-
-
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
-
60
-
-
63149109244
-
Soluble iL?2RA levels in multiple sclerosis subjects and the effect of soluble iL?2RA on immune responses
-
Maier, L. M. et al. Soluble iL?2RA levels in multiple sclerosis subjects and the effect of soluble iL?2RA on immune responses. J. Immunol. 182, 1541-1547 (2009).
-
(2009)
J. Immunol.
, vol.182
, pp. 1541-1547
-
-
Maier, L.M.1
-
61
-
-
65549084289
-
Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
-
Baranzini, S. E. et al. Pathway and network-based analysis of genome-wide association studies in multiple sclerosis. Hum. Mol. Genet. 18, 2078-2090 (2009).
-
(2009)
Hum. Mol. Genet.
, vol.18
, pp. 2078-2090
-
-
Baranzini, S.E.1
-
62
-
-
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
-
63
-
-
59149098926
-
CD226 Gly307Ser association with multiple autoimmune diseases
-
Hafler, J. P. et al. CD226 Gly307Ser association with multiple autoimmune diseases. Genes Immun. 10, 5-10 (2009).
-
(2009)
Genes Immun.
, vol.10
, pp. 5-10
-
-
Hafler, J.P.1
-
64
-
-
74249098458
-
Autoimmune disease classification by inverse association with SNP alleles
-
Sirota, M., Schaub, M. A., Batzoglou, S., Robinson, W. H. & Butte, A. J. Autoimmune disease classification by inverse association with SNP alleles. PLoS Genet. 5, e1000792 (2009).
-
(2009)
PLoS Genet.
, vol.5
-
-
Sirota, M.1
Schaub, M.A.2
Batzoglou, S.3
Robinson, W.H.4
Butte, A.J.5
-
65
-
-
38649133304
-
The developing mosaic of autoimmune disease risk
-
Maier, L. M. & Hafler, D. A. The developing mosaic of autoimmune disease risk. Nat. Genet. 40, 131-132 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 131-132
-
-
Maier, L.M.1
Hafler, D.A.2
-
66
-
-
69349102624
-
Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
-
Dendrou, C. A. et al. Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource. Nat. Genet. 41, 1011-1015 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 1011-1015
-
-
Dendrou, C.A.1
-
67
-
-
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
-
68
-
-
34547140875
-
The human disease network
-
Goh, K. I. et al. The human disease network. Proc. Natl Acad. Sci. USA 104, 8685-8690 (2007).
-
(2007)
Proc. Natl Acad. Sci. USA
, vol.104
, pp. 8685-8690
-
-
Goh, K.I.1
-
69
-
-
33845545435
-
The modular nature of genetic diseases
-
Oti, M. & Brunner, H. G. The modular nature of genetic diseases. Clin. Genet. 71, 1-11 (2007).
-
(2007)
Clin. Genet.
, vol.71
, pp. 1-11
-
-
Oti, M.1
Brunner, H.G.2
-
70
-
-
71149114052
-
The biological coherence of human phenome databases
-
Oti, M., Huynen, M. A. & Brunner, H. G. The biological coherence of human phenome databases. Am. J. Hum. Genet. 85, 801-808 (2009).
-
(2009)
Am. J. Hum. Genet.
, vol.85
, pp. 801-808
-
-
Oti, M.1
Huynen, M.A.2
Brunner, H.G.3
-
71
-
-
34447521460
-
Human disease classification in the postgenomic era: A complex systems approach to human pathobiology
-
Loscalzo, J., Kohane, I. & Barabasi, A. L. Human disease classification in the postgenomic era: a complex systems approach to human pathobiology. Mol. Syst. Biol. 3, 124 (2007).
-
(2007)
Mol. Syst. Biol.
, vol.3
, pp. 124
-
-
Loscalzo, J.1
Kohane, I.2
Barabasi, A.L.3
-
72
-
-
40749089626
-
Structural variation of chromosomes in autism spectrum disorder
-
Marshall, C. R. et al. Structural variation of chromosomes in autism spectrum disorder. Am. J. Hum. Genet. 82, 477-488 (2008).
-
(2008)
Am. J. Hum. Genet.
, vol.82
, pp. 477-488
-
-
Marshall, C.R.1
-
73
-
-
67650735159
-
Genomic copy number variation, human health, and disease
-
Wain, L. V., Armour, J. A. & Tobin, M. D. Genomic copy number variation, human health, and disease. Lancet 374, 340-350 (2009).
-
(2009)
Lancet
, vol.374
, pp. 340-350
-
-
Wain, L.V.1
Armour, J.A.2
Tobin, M.D.3
-
74
-
-
70350221909
-
Copy number variation in human health, disease, and evolution
-
Zhang, F., Gu, W., Hurles, M. E. & Lupski, J. R. Copy number variation in human health, disease, and evolution. Annu. Rev. Genomics Hum. Genet. 10, 451-481 (2009).
-
(2009)
Annu. Rev. Genomics Hum. Genet.
, vol.10
, pp. 451-481
-
-
Zhang, F.1
Gu, W.2
Hurles, M.E.3
Lupski, J.R.4
-
75
-
-
61849115785
-
Copy number variation in the human genome and its implication in autoimmunity
-
Schaschl, H., Aitman, T. J. & vyse, T. J. Copy number variation in the human genome and its implication in autoimmunity. Clin. Exp. Immunol. 156, 12-16 (2009).
-
(2009)
Clin. Exp. Immunol.
, vol.156
, pp. 12-16
-
-
Schaschl, H.1
Aitman, T.J.2
Vyse, T.J.3
-
76
-
-
77950329947
-
Evidence for polygenic susceptibility to multiple sclerosis. the shape of things to come
-
International Multiple Sclerosis Genetics Consortium (iMSGC)
-
International Multiple Sclerosis Genetics Consortium (iMSGC). 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
-
-
-
77
-
-
55449120805
-
Genetic mapping in human disease
-
Altshuler, D., Daly, M. J. & Lander, E. S. Genetic mapping in human disease. Science 322, 881-888 (2008).
-
(2008)
Science
, vol.322
, pp. 881-888
-
-
Altshuler, D.1
Daly, M.J.2
Lander, E.S.3
-
78
-
-
16844366786
-
Genome wide strategies for detecting multiple loci that influence complex diseases
-
Marchini, J., Donnelly, P. & Cardon, L. R. Genome wide strategies for detecting multiple loci that influence complex diseases. Nat. Genet. 37, 413-417 (2005).
-
(2005)
Nat. Genet.
, vol.37
, pp. 413-417
-
-
Marchini, J.1
Donnelly, P.2
Cardon, L.R.3
-
79
-
-
34347338776
-
A genomic pathway approach to a complex disease: Axon guidance and Parkinson disease
-
Lesnick, T. G. et al. A genomic pathway approach to a complex disease: axon guidance and Parkinson disease. PLoS Genet. 3, e98 (2007).
-
(2007)
PLoS Genet.
, vol.3
-
-
Lesnick, T.G.1
-
80
-
-
53649098737
-
Pathway analysis of seven common diseases assessed by genome-wide association
-
Torkamani, A., Topol, E. J. & Schork, N. J. Pathway analysis of seven common diseases assessed by genome-wide association. Genomics 92, 265-272 (2008).
-
(2008)
Genomics
, vol.92
, pp. 265-272
-
-
Torkamani, A.1
Topol, E.J.2
Schork, N.J.3
-
81
-
-
65949107547
-
Common genetic variation and human traits
-
Goldstein, D. B. Common genetic variation and human traits. N. Engl. J. Med. 360, 1696-1698 (2009).
-
(2009)
N. Engl. J. Med.
, vol.360
, pp. 1696-1698
-
-
Goldstein, D.B.1
-
82
-
-
50149102578
-
Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event
-
Corvol, J. C. et al. Abrogation of T cell quiescence characterizes patients at high risk for multiple sclerosis after the initial neurological event. Proc. Natl Acad. Sci. USA 105, 11839-11844 (2008).
-
(2008)
Proc. Natl Acad. Sci. USA
, vol.105
, pp. 11839-11844
-
-
Corvol, J.C.1
-
83
-
-
71849098862
-
Integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: A weighted genetic risk score
-
De Jager, P. L. et al. integration of genetic risk factors into a clinical algorithm for multiple sclerosis susceptibility: a weighted genetic risk score. Lancet Neurol. 8, 1111-1119 (2009).
-
(2009)
Lancet Neurol.
, vol.8
, pp. 1111-1119
-
-
De Jager, P.L.1
-
84
-
-
65249131713
-
Rare variants of IFIH1, a gene Implicated in antiviral responses, protect against type 1 diabetes
-
Nejentsev, S., walker, N., Riches, D., Egholm, M. & Todd, J. A. Rare variants of IFIH1, a gene Implicated in antiviral responses, protect against type 1 diabetes. Science 324, 387-389 (2009).
-
(2009)
Science
, vol.324
, pp. 387-389
-
-
Nejentsev, S.1
Walker, N.2
Riches, D.3
Egholm, M.4
Todd, J.A.5
-
85
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson, S. P., wang, K., Krantz, I., Hakonarson, H. & Goldstein, D. B. Rare variants create synthetic genome-wide associations. PLoS Biol. 8, e1000294 (2010).
-
(2010)
PLoS Biol.
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
86
-
-
77951836633
-
Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis
-
Baranzini, S. E. et al. Genome, epigenome and RNA sequences of monozygotic twins discordant for multiple sclerosis. Nature 464, 1351-1356 (2010).
-
(2010)
Nature
, vol.464
, pp. 1351-1356
-
-
Baranzini, S.E.1
-
87
-
-
77950475726
-
Whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy
-
Lupski, J. R. et al. whole-genome sequencing in a patient with Charcot-Marie-Tooth neuropathy. N. Engl. J. Med. 362, 1181-1191 (2010).
-
(2010)
N. Engl. J. Med.
, vol.362
, pp. 1181-1191
-
-
Lupski, J.R.1
-
88
-
-
77951799158
-
Analysis of genetic inheritance in a family quartet by whole-genome sequencing
-
Roach, J. C. et al. Analysis of genetic inheritance in a family quartet by whole-genome sequencing. Science 328, 636-639 (2010).
-
(2010)
Science
, vol.328
, pp. 636-639
-
-
Roach, J.C.1
-
89
-
-
67349179231
-
From genes to function: The next challenge to understanding multiple sclerosis
-
Fugger, L., Friese, M. A. & Bell, J. I. From genes to function: the next challenge to understanding multiple sclerosis. Nat. Rev. Immunol. 9, 408-417 (2009).
-
(2009)
Nat. Rev. Immunol.
, vol.9
, pp. 408-417
-
-
Fugger, L.1
Friese, M.A.2
Bell, J.I.3
-
90
-
-
34447508481
-
Environmental risk factors for multiple sclerosis. Part ii: Noninfectious factors
-
Ascherio, A. & Munger, K. L. Environmental risk factors for multiple sclerosis. Part ii: noninfectious factors. Ann. Neurol. 61, 504-513 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 504-513
-
-
Ascherio, A.1
Munger, K.L.2
-
91
-
-
77949873898
-
Vitamin D controls T cell antigen receptor signaling and activation of human T cells
-
Von Essen, M. R. et al. vitamin D controls T cell antigen receptor signaling and activation of human T cells. Nat. Immunol. 11, 344-349 (2010).
-
(2010)
Nat. Immunol.
, vol.11
, pp. 344-349
-
-
Von Essen, M.R.1
-
92
-
-
66549129834
-
Immunomodulatory effects of vitamin D in multiple sclerosis
-
Correale, J., Ysrraelit, M. C. & Gaitan, M. I. immunomodulatory effects of vitamin D in multiple sclerosis. Brain 132, 1146-1160 (2009).
-
(2009)
Brain
, vol.132
, pp. 1146-1160
-
-
Correale, J.1
Ysrraelit, M.C.2
Gaitan, M.I.3
-
93
-
-
68949140898
-
Vitamin D status is positively correlated with regulatory T cell function in patients with multiple sclerosis
-
Smolders, J. et al. vitamin D status is positively correlated with regulatory T cell function in patients with multiple sclerosis. PLoS ONE 4, e6635 (2009).
-
(2009)
PLoS ONE
, vol.4
-
-
Smolders, J.1
-
94
-
-
61449102631
-
Expression of the multiple sclerosis-associated MHC class ii allele HLA-DRB1*1501 is regulated by vitamin D
-
Ramagopalan, S. V. et al. Expression of the multiple sclerosis-associated MHC class ii allele HLA-DRB1*1501 is regulated by vitamin D. PLoS Genet. 5, e1000369 (2009).
-
(2009)
PLoS Genet.
, vol.5
-
-
Ramagopalan, S.V.1
-
95
-
-
77950910418
-
Uv radiation suppresses experimental autoimmune encephalomyelitis independent of vitamin D production
-
Becklund, B. R., Severson, K. S., vang, S. V. & DeLuca, H. F. Uv radiation suppresses experimental autoimmune encephalomyelitis independent of vitamin D production. Proc. Natl Acad. Sci. USA 107, 6418-6423 (2010).
-
(2010)
Proc. Natl Acad. Sci. USA
, vol.107
, pp. 6418-6423
-
-
Becklund, B.R.1
Severson, K.S.2
Vang, S.V.3
Deluca, H.F.4
-
96
-
-
34247590137
-
Environmental risk factors for multiple sclerosis. Part i: The role of infection
-
Ascherio, A. & Munger, K. L. Environmental risk factors for multiple sclerosis. Part i: the role of infection. Ann. Neurol. 61, 288-299 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 288-299
-
-
Ascherio, A.1
Munger, K.L.2
-
97
-
-
34447504060
-
A specific viral cause of multiple sclerosis: One virus, one disease
-
Lipton, H. L., Liang, Z., Hertzler, S. & Son, K. N. A specific viral cause of multiple sclerosis: one virus, one disease. Ann. Neurol. 61, 514-523 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 514-523
-
-
Lipton, H.L.1
Liang, Z.2
Hertzler, S.3
Son, K.N.4
-
98
-
-
0035956494
-
Epstein-Barr virus antibodies and risk of multiple sclerosis: A prospective study
-
Ascherio, A. et al. Epstein-Barr virus antibodies and risk of multiple sclerosis: a prospective study. JAMA 286, 3083-3088 (2001).
-
(2001)
JAMA
, vol.286
, pp. 3083-3088
-
-
Ascherio, A.1
-
99
-
-
18244378502
-
Identification of Epstein-Barr virus proteins as putative targets of the immune response in multiple sclerosis
-
Cepok, S. et al. identification of Epstein-Barr virus proteins as putative targets of the immune response in multiple sclerosis. J. Clin. Invest. 115, 1352-1360 (2005).
-
(2005)
J. Clin. Invest.
, vol.115
, pp. 1352-1360
-
-
Cepok, S.1
-
100
-
-
36549034729
-
Dysregulated Epstein-Barr virus infection in the multiple sclerosis brain
-
Serafini, B. et al. Dysregulated Epstein-Barr virus infection in the multiple sclerosis brain. J. Exp. Med. 204, 2899-2912 (2007).
-
(2007)
J. Exp. Med.
, vol.204
, pp. 2899-2912
-
-
Serafini, B.1
-
101
-
-
67049158616
-
Epstein-Barr virus and multiple sclerosis
-
Salvetti, M., Giovannoni, G. & Aloisi, F. Epstein-Barr virus and multiple sclerosis. Curr. Opin. Neurol. 22, 201-206 (2009).
-
(2009)
Curr. Opin. Neurol.
, vol.22
, pp. 201-206
-
-
Salvetti, M.1
Giovannoni, G.2
Aloisi, F.3
-
102
-
-
0345327729
-
Smoking is a risk factor for multiple sclerosis
-
Riise, T., Nortvedt, M. W. & Ascherio, A. Smoking is a risk factor for multiple sclerosis. Neurology 61, 1122-1124 (2003).
-
(2003)
Neurology
, vol.61
, pp. 1122-1124
-
-
Riise, T.1
Nortvedt, M.W.2
Ascherio, A.3
-
103
-
-
70349305736
-
Tobacco smoking, but not Swedish snuff use, increases the risk of multiple sclerosis
-
Hedstrom, A. K., Baarnhielm, M., Olsson, T. & Alfredsson, L. Tobacco smoking, but not Swedish snuff use, increases the risk of multiple sclerosis. Neurology 73, 696-701 (2009).
-
(2009)
Neurology
, vol.73
, pp. 696-701
-
-
Hedstrom, A.K.1
Baarnhielm, M.2
Olsson, T.3
Alfredsson, L.4
-
104
-
-
9144269888
-
Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans
-
Oksenberg, J. R. et al. Mapping multiple sclerosis susceptibility to the HLA-DR locus in African Americans. Am. J. Hum. Genet. 74, 160-167 (2004).
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 160-167
-
-
Oksenberg, J.R.1
-
105
-
-
0037371325
-
HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course
-
Barcellos, L. F. et al. HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence. On disease course. Am. J. Hum. Genet. 72, 710-716 (2003).
-
(2003)
Am. J. Hum. Genet.
, vol.72
, pp. 710-716
-
-
Barcellos, L.F.1
-
106
-
-
26444469579
-
Complex interactions among MHC haplotypes in multiple sclerosis: Susceptibility and resistance
-
Dyment, D. A. et al. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. Hum. Mol. Genet. 14, 2019-2026 (2005).
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2019-2026
-
-
Dyment, D.A.1
-
107
-
-
33749515298
-
Functional epistasis on a common MHC haplotype associated with multiple sclerosis
-
Gregersen, J. W. et al. Functional epistasis on a common MHC haplotype associated with multiple sclerosis. Nature 443, 574-577 (2006).
-
(2006)
Nature
, vol.443
, pp. 574-577
-
-
Gregersen, J.W.1
-
108
-
-
54049103212
-
Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis
-
Caillier, S. J. et al. Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis. J. Immunol. 181, 5473-5480 (2008).
-
(2008)
J. Immunol.
, vol.181
, pp. 5473-5480
-
-
Caillier, S.J.1
-
109
-
-
38549083107
-
HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis
-
Brynedal, B. et al. HLA-A confers an HLA-DRB1 independent influence on the risk of multiple sclerosis. PLoS ONE 2, e664 (2007).
-
(2007)
PLoS ONE
, vol.2
-
-
Brynedal, B.1
-
110
-
-
34147167634
-
A second major histocompatibility complex susceptibility locus for multiple sclerosis
-
Yeo, T. W. et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Ann. Neurol. 61, 228-236 (2007).
-
(2007)
Ann. Neurol.
, vol.61
, pp. 228-236
-
-
Yeo, T.W.1
-
111
-
-
55549104692
-
+ T cells in multiple sclerosis
-
+ T cells in multiple sclerosis. Nat. Med. 14, 1227-1235 (2008).
-
(2008)
Nat. Med.
, vol.14
, pp. 1227-1235
-
-
Friese, M.A.1
-
112
-
-
67650052034
-
Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis
-
Lorentzen, A. R. et al. Killer immunoglobulin-like receptor ligand HLA-Bw4 protects against multiple sclerosis. Ann. Neurol. 65, 658-666 (2009).
-
(2009)
Ann. Neurol.
, vol.65
, pp. 658-666
-
-
Lorentzen, A.R.1
-
113
-
-
73249122274
-
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases
-
Rioux, J. D. et al. Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases. Proc. Natl Acad. Sci. USA 106, 18680-18685 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 18680-18685
-
-
Rioux, J.D.1
-
114
-
-
67249117049
-
Potential etiologic and functional implications of genome-wide association loci for human diseases and traits
-
Hindorff, L. A. et al. Potential etiologic and functional implications of genome-wide association loci for human diseases and traits. Proc. Natl Acad. Sci. USA 106, 9362-9367 (2009).
-
(2009)
Proc. Natl Acad. Sci. USA
, vol.106
, pp. 9362-9367
-
-
Hindorff, L.A.1
-
116
-
-
65249164859
-
Validating, augmenting and refining genome? wide association signals
-
Ioannidis, J. P., Thomas, G. & Daly, M. J. validating, augmenting and refining genome? wide association signals. Nat. Rev. Genet. 10, 318-329 (2009).
-
(2009)
Nat. Rev. Genet.
, vol.10
, pp. 318-329
-
-
Ioannidis, J.P.1
Thomas, G.2
Daly, M.J.3
-
117
-
-
70349956433
-
Finding the missing heritability of complex diseases
-
Manolio, T. A. et al. Finding the missing heritability of complex diseases. Nature 461, 747-753 (2009).
-
(2009)
Nature
, vol.461
, pp. 747-753
-
-
Manolio, T.A.1
-
119
-
-
67749091014
-
Age of onset in concordant twins and other relative pairs with multiple sclerosis
-
Sadovnick, A. D. et al. Age of onset in concordant twins and other relative pairs with multiple sclerosis. Am. J. Epidemiol. 170, 289-296 (2009).
-
(2009)
Am. J. Epidemiol.
, vol.170
, pp. 289-296
-
-
Sadovnick, A.D.1
-
120
-
-
40849094272
-
Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis
-
Byun, E. et al. Genome-wide pharmacogenomic analysis of the response to interferon beta therapy in multiple sclerosis. Arch. Neurol. 65, 337-344 (2008).
-
(2008)
Arch. Neurol.
, vol.65
, pp. 337-344
-
-
Byun, E.1
-
121
-
-
68549085471
-
Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis
-
Comabella, M. et al. Genome-wide scan of 500,000 single-nucleotide polymorphisms among responders and nonresponders to interferon beta therapy in multiple sclerosis. Arch. Neurol. 66, 972-978 (2009).
-
(2009)
Arch. Neurol.
, vol.66
, pp. 972-978
-
-
Comabella, M.1
-
122
-
-
58849146101
-
1HMR spectroscopy and MRi measures
-
1HMR spectroscopy and MRi measures. Brain 132, 250-259 (2009).
-
(2009)
Brain
, vol.132
, pp. 250-259
-
-
Okuda, D.T.1
-
123
-
-
74249092274
-
Multiple sclerosis pharmacogenomics: Maximizing efficacy of therapy
-
Pappas, D. J. & Oksenberg, J. R. Multiple sclerosis pharmacogenomics: maximizing efficacy of therapy. Neurology 74 (Suppl. 1), S62-S69 (2010).
-
(2010)
Neurology
, vol.74
, Issue.SUPPL. 1
-
-
Pappas, D.J.1
Oksenberg, J.R.2
-
124
-
-
77249176523
-
HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in western Australia
-
Wu, J. S. et al. HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in western Australia. J. Neuroimmunol. 219, 109-113 (2010).
-
(2010)
J. Neuroimmunol.
, vol.219
, pp. 109-113
-
-
Wu, J.S.1
|