-
2
-
-
54149084585
-
Multiple sclerosis
-
Compston A, Coles A Multiple sclerosis. Lancet 2008, 372:1502-1517.
-
(2008)
Lancet
, vol.372
, pp. 1502-1517
-
-
Compston, A.1
Coles, A.2
-
3
-
-
33749681309
-
Sex ratio of multiple sclerosis in Canada: a longitudinal study
-
the Canadian Collaborative Study
-
Orton SM, Herrera BM, Yee IM, et al. Sex ratio of multiple sclerosis in Canada: a longitudinal study. Lancet Neurol 2006, 5:932-936. the Canadian Collaborative Study.
-
(2006)
Lancet Neurol
, vol.5
, pp. 932-936
-
-
Orton, S.M.1
Herrera, B.M.2
Yee, I.M.3
-
4
-
-
0029874022
-
Age-adjusted recurrence risks for relatives of patients with multiple sclerosis
-
Robertson NP, Fraser M, Deans J, Clayton D, Walker N, Compston DA Age-adjusted recurrence risks for relatives of patients with multiple sclerosis. Brain 1996, 119:449-455.
-
(1996)
Brain
, vol.119
, pp. 449-455
-
-
Robertson, N.P.1
Fraser, M.2
Deans, J.3
Clayton, D.4
Walker, N.5
Compston, D.A.6
-
5
-
-
84866347085
-
Modelling genetic susceptibility to multiple sclerosis with family data
-
O'Gorman C, Lin R, Stankovich J, Broadley SA Modelling genetic susceptibility to multiple sclerosis with family data. Neuroepidemiology 2013, 40:1-12.
-
(2013)
Neuroepidemiology
, vol.40
, pp. 1-12
-
-
O'Gorman, C.1
Lin, R.2
Stankovich, J.3
Broadley, S.A.4
-
6
-
-
80052610245
-
Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis
-
Simpson S, Blizzard L, Otahal P, Van der Mei I, Taylor B Latitude is significantly associated with the prevalence of multiple sclerosis: a meta-analysis. J Neurol Neurosurg Psychiatry 2011, 82:1132-1141.
-
(2011)
J Neurol Neurosurg Psychiatry
, vol.82
, pp. 1132-1141
-
-
Simpson, S.1
Blizzard, L.2
Otahal, P.3
Van der Mei, I.4
Taylor, B.5
-
7
-
-
80051985156
-
High nationwide prevalence of multiple sclerosis in Sweden
-
Ahlgren C, Odén A, Lycke J High nationwide prevalence of multiple sclerosis in Sweden. Mult Scler 2011, 17:901-908.
-
(2011)
Mult Scler
, vol.17
, pp. 901-908
-
-
Ahlgren, C.1
Odén, A.2
Lycke, J.3
-
8
-
-
0242268416
-
Twin concordance and sibling recurrence rates in multiple sclerosis
-
the Canadian Collaborative Study
-
Willer CJ, Dyment DA, Risch NJ, Sadovnick AD, Ebers GC Twin concordance and sibling recurrence rates in multiple sclerosis. Proc Natl Acad Sci USA 2003, 100:12877-12882. the Canadian Collaborative Study.
-
(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
-
9
-
-
0029121088
-
A genetic basis for familial aggregation in multiple sclerosis
-
the Canadian Collaborative Study
-
Ebers GC, Sadovnick AD, Risch NJ A genetic basis for familial aggregation in multiple sclerosis. Nature 1995, 377:150-151. the Canadian Collaborative Study.
-
(1995)
Nature
, vol.377
, pp. 150-151
-
-
Ebers, G.C.1
Sadovnick, A.D.2
Risch, N.J.3
-
10
-
-
0033674248
-
Conjugal multiple sclerosis: population-based prevalence and recurrence risks in offspring
-
the Canadian Collaborative Study
-
Ebers GC, Yee IM, Sadovnick AD, Duquette P Conjugal multiple sclerosis: population-based prevalence and recurrence risks in offspring. Ann Neurol 2000, 48:927-931. the Canadian Collaborative Study.
-
(2000)
Ann Neurol
, vol.48
, pp. 927-931
-
-
Ebers, G.C.1
Yee, I.M.2
Sadovnick, A.D.3
Duquette, P.4
-
11
-
-
0017259265
-
Multiple sclerosis among immigrants in Greater London
-
Dean G, McLoughlin H, Brady R, Adelstein AM, Tallett-Williams J Multiple sclerosis among immigrants in Greater London. BMJ 1976, 1:861-864.
-
(1976)
BMJ
, vol.1
, pp. 861-864
-
-
Dean, G.1
McLoughlin, H.2
Brady, R.3
Adelstein, A.M.4
Tallett-Williams, J.5
-
12
-
-
32344446192
-
Multiple sclerosis in stepsiblings: recurrence risk and ascertainment
-
the Canadian Collaborative Study
-
Dyment DA, Yee IM, Ebers GC, Sadovnick AD Multiple sclerosis in stepsiblings: recurrence risk and ascertainment. J Neurol Neurosurg Psychiatry 2006, 77:258-259. the Canadian Collaborative Study.
-
(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
-
13
-
-
37849008962
-
HLA-DRB1 and multiple sclerosis in Malta
-
Dean G, Yeo TW, Goris A, et al. HLA-DRB1 and multiple sclerosis in Malta. Neurology 2008, 70:101-105.
-
(2008)
Neurology
, vol.70
, pp. 101-105
-
-
Dean, G.1
Yeo, T.W.2
Goris, A.3
-
14
-
-
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 2010, 67:3-10.
-
(2010)
Ann Neurol
, vol.67
, pp. 3-10
-
-
Sawcer, S.1
Ban, M.2
Wason, J.3
Dudbridge, F.4
-
15
-
-
0032231780
-
Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting
-
Guo SW Inflation of sibling recurrence-risk ratio, due to ascertainment bias and/or overreporting. Am J Hum Genet 1998, 63:252-258.
-
(1998)
Am J Hum Genet
, vol.63
, pp. 252-258
-
-
Guo, S.W.1
-
17
-
-
0041660848
-
Risk for relatives of patients with multiple sclerosis in central Sardinia, Italy
-
Prokopenko I, Montomoli C, Ferrai R, et al. Risk for relatives of patients with multiple sclerosis in central Sardinia, Italy. Neuroepidemiology 2003, 22:290-296.
-
(2003)
Neuroepidemiology
, vol.22
, pp. 290-296
-
-
Prokopenko, I.1
Montomoli, C.2
Ferrai, R.3
-
18
-
-
84856405512
-
The mystery of missing heritability: Genetic interactions create phantom heritability
-
Zuk O, Hechter E, Sunyaev SR, Lander ES The mystery of missing heritability: Genetic interactions create phantom heritability. Proc Natl Acad Sci USA 2012, 109:1193-1198.
-
(2012)
Proc Natl Acad Sci USA
, vol.109
, pp. 1193-1198
-
-
Zuk, O.1
Hechter, E.2
Sunyaev, S.R.3
Lander, E.S.4
-
19
-
-
80051586618
-
Modelling the effects of penetrance and family size on rates of sporadic and familial disease
-
Al-Chalabi A, Lewis CM Modelling the effects of penetrance and family size on rates of sporadic and familial disease. Hum Hered 2011, 71:281-288.
-
(2011)
Hum Hered
, vol.71
, pp. 281-288
-
-
Al-Chalabi, A.1
Lewis, C.M.2
-
20
-
-
13144265739
-
Genome-wide association studies: theoretical and practical concerns
-
Wang WY, Barratt BJ, Clayton DG, Todd JA Genome-wide association studies: theoretical and practical concerns. Nat Rev Genet 2005, 6:109-118.
-
(2005)
Nat Rev Genet
, vol.6
, pp. 109-118
-
-
Wang, W.Y.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
21
-
-
0029741063
-
The future of genetic studies of complex human diseases
-
Risch N, Merikangas K The future of genetic studies of complex human diseases. Science 1996, 273:1516-1517.
-
(1996)
Science
, vol.273
, pp. 1516-1517
-
-
Risch, N.1
Merikangas, K.2
-
22
-
-
36448943599
-
A genome-wide scan in forty large pedigrees with multiple sclerosis
-
Willer CJ, Dyment DA, Cherny S, et al. A genome-wide scan in forty large pedigrees with multiple sclerosis. J Hum Genet 2007, 52:955-962.
-
(2007)
J Hum Genet
, vol.52
, pp. 955-962
-
-
Willer, C.J.1
Dyment, D.A.2
Cherny, S.3
-
23
-
-
0037356710
-
Genome-wide linkage screen of a consanguineous multiple sclerosis kinship
-
Modin H, Masterman T, Thorlacius T, et al. Genome-wide linkage screen of a consanguineous multiple sclerosis kinship. Mult Scler 2003, 9:128-134.
-
(2003)
Mult Scler
, vol.9
, pp. 128-134
-
-
Modin, H.1
Masterman, T.2
Thorlacius, T.3
-
24
-
-
33846322954
-
A linkage study in two families with multiple sclerosis and healthy members with oligoclonal CSF immunopathy
-
Haghighi S, Andersen O, Nilsson S, Rydberg L, Wahlström J A linkage study in two families with multiple sclerosis and healthy members with oligoclonal CSF immunopathy. Mult Scler 2006, 12:723-730.
-
(2006)
Mult Scler
, vol.12
, pp. 723-730
-
-
Haghighi, S.1
Andersen, O.2
Nilsson, S.3
Rydberg, L.4
Wahlström, J.5
-
25
-
-
38849112760
-
A genome scan in a single pedigree with a high prevalence of multiple sclerosis
-
Dyment DA, Cader MZ, Herrera BM, et al. A genome scan in a single pedigree with a high prevalence of multiple sclerosis. J Neurol Neurosurg Psychiatry 2008, 79:158-162.
-
(2008)
J Neurol Neurosurg Psychiatry
, vol.79
, pp. 158-162
-
-
Dyment, D.A.1
Cader, M.Z.2
Herrera, B.M.3
-
26
-
-
0025767289
-
HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation
-
Olerup O, Hillert J HLA class II-associated genetic susceptibility in multiple sclerosis: a critical evaluation. Tissue Antigens 1991, 38:1-15.
-
(1991)
Tissue Antigens
, vol.38
, pp. 1-15
-
-
Olerup, O.1
Hillert, J.2
-
27
-
-
80051684615
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
-
The International Multiple Sclerosis Genetics, the Wellcome Trust Case Control Consortium 2the Wellcome Trust Case Control Consortium 2
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011, 476:214-219. The International Multiple Sclerosis Genetics, the Wellcome Trust Case Control Consortium 2the Wellcome Trust Case Control Consortium 2.
-
(2011)
Nature
, vol.476
, pp. 214-219
-
-
-
28
-
-
23944499790
-
A high-density screen for linkage in multiple sclerosis
-
The International Multiple Sclerosis Genetics
-
A high-density screen for linkage in multiple sclerosis. Am J Hum Genet 2005, 77:454-467. The International Multiple Sclerosis Genetics.
-
(2005)
Am J Hum Genet
, vol.77
, pp. 454-467
-
-
-
29
-
-
0015273990
-
Multiple sclerosis: association with HL-A3
-
Naito S, Namerow N, Mickey MR, Terasaki PI Multiple sclerosis: association with HL-A3. Tissue Antigens 1972, 2:1-4.
-
(1972)
Tissue Antigens
, vol.2
, pp. 1-4
-
-
Naito, S.1
Namerow, N.2
Mickey, M.R.3
Terasaki, P.I.4
-
30
-
-
0015733713
-
Histocompatibility determinants in multiple sclerosis, with special reference to clinical course
-
Jersild C, Hansen GS, Svejgaard A, Fog T, Thomsen M, Dupont B Histocompatibility determinants in multiple sclerosis, with special reference to clinical course. Lancet 1973, 302:1221-1225.
-
(1973)
Lancet
, vol.302
, pp. 1221-1225
-
-
Jersild, C.1
Hansen, G.S.2
Svejgaard, A.3
Fog, T.4
Thomsen, M.5
Dupont, B.6
-
31
-
-
38349100266
-
Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project
-
Horton R, Gibson R, Coggill P, et al. Variation analysis and gene annotation of eight MHC haplotypes: the MHC Haplotype Project. Immunogenetics 2008, 60:1-18.
-
(2008)
Immunogenetics
, vol.60
, pp. 1-18
-
-
Horton, R.1
Gibson, R.2
Coggill, P.3
-
32
-
-
33749137515
-
A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC
-
de Bakker PI, McVean G, Sabeti PC, et al. A high-resolution HLA and SNP haplotype map for disease association studies in the extended human MHC. Nat Genet 2006, 38:1166-1172.
-
(2006)
Nat Genet
, vol.38
, pp. 1166-1172
-
-
de Bakker, P.I.1
McVean, G.2
Sabeti, P.C.3
-
33
-
-
79953314023
-
HLA*IMP-an integrated framework for imputing classical HLA alleles from SNP genotypes
-
Dilthey AT, Moutsianas L, Leslie S, McVean G HLA*IMP-an integrated framework for imputing classical HLA alleles from SNP genotypes. Bioinformatics 2011, 27:968-972.
-
(2011)
Bioinformatics
, vol.27
, pp. 968-972
-
-
Dilthey, A.T.1
Moutsianas, L.2
Leslie, S.3
McVean, G.4
-
34
-
-
38749115455
-
A statistical method for predicting classical HLA alleles from SNP data
-
Leslie S, Donnelly P, McVean G A statistical method for predicting classical HLA alleles from SNP data. Am J Hum Genet 2008, 82:48-56.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 48-56
-
-
Leslie, S.1
Donnelly, P.2
McVean, G.3
-
35
-
-
84888231843
-
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects
-
the IMSGC and the
-
Patsopoulos NA, Barcellos LF, Hintzen RQ, et al. Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects. PLoS Genet 2013, 9:e1003926. the IMSGC and the.
-
(2013)
PLoS Genet
, vol.9
-
-
Patsopoulos, N.A.1
Barcellos, L.F.2
Hintzen, R.Q.3
-
36
-
-
18344385134
-
Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis
-
Rubio JP, Bahlo M, Butzkueven H, et al. Genetic dissection of the human leukocyte antigen region by use of haplotypes of Tasmanians with multiple sclerosis. Am J Hum Genet 2002, 70:1125-1137.
-
(2002)
Am J Hum Genet
, vol.70
, pp. 1125-1137
-
-
Rubio, J.P.1
Bahlo, M.2
Butzkueven, H.3
-
37
-
-
10744231677
-
Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis
-
Harbo HF, Lie BA, Sawcer S, et al. Genes in the HLA class I region may contribute to the HLA class II-associated genetic susceptibility to multiple sclerosis. Tissue Antigens 2004, 63:237-247.
-
(2004)
Tissue Antigens
, vol.63
, pp. 237-247
-
-
Harbo, H.F.1
Lie, B.A.2
Sawcer, S.3
-
38
-
-
34147167634
-
A second major histocompatibility complex susceptibility locus for multiple sclerosis
-
the International Multiple Sclerosis Genetics Consortium (IMSGC)
-
Yeo TW, De Jager PL, Gregory SG, et al. A second major histocompatibility complex susceptibility locus for multiple sclerosis. Ann Neurol 2007, 61:228-236. the International Multiple Sclerosis Genetics Consortium (IMSGC).
-
(2007)
Ann Neurol
, vol.61
, pp. 228-236
-
-
Yeo, T.W.1
De Jager, P.L.2
Gregory, S.G.3
-
39
-
-
67649876123
-
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
-
the International MS Genetics
-
De Jager PL, Jia X, Wang J, et al. Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci. Nat Genet 2009, 41:776-782. the International MS Genetics.
-
(2009)
Nat Genet
, vol.41
, pp. 776-782
-
-
De Jager, P.L.1
Jia, X.2
Wang, J.3
-
40
-
-
18244367163
-
Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia
-
Marrosu MG, Murru R, Murru MR, et al. Dissection of the HLA association with multiple sclerosis in the founder isolated population of Sardinia. Hum Mol Genet 2001, 10:2907-2916.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 2907-2916
-
-
Marrosu, M.G.1
Murru, R.2
Murru, M.R.3
-
41
-
-
26444469579
-
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
-
Dyment DA, Herrera BM, Cader MZ, et al. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. Hum Mol Genet 2005, 14:2019-2026.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 2019-2026
-
-
Dyment, D.A.1
Herrera, B.M.2
Cader, M.Z.3
-
42
-
-
33748740746
-
Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis
-
Barcellos LF, Sawcer S, Ramsay PP, et al. Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis. Hum Mol Genet 2006, 15:2813-2824.
-
(2006)
Hum Mol Genet
, vol.15
, pp. 2813-2824
-
-
Barcellos, L.F.1
Sawcer, S.2
Ramsay, P.P.3
-
43
-
-
66149110388
-
Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility
-
Lincoln MR, Ramagopalan SV, Chao MJ, et al. Epistasis among HLA-DRB1, HLA-DQA1, and HLA-DQB1 loci determines multiple sclerosis susceptibility. Proc Natl Acad Sci USA 2009, 106:7542-7547.
-
(2009)
Proc Natl Acad Sci USA
, vol.106
, pp. 7542-7547
-
-
Lincoln, M.R.1
Ramagopalan, S.V.2
Chao, M.J.3
-
44
-
-
78149463010
-
A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis
-
the Australia and New Zealand Multiple Sclerosis Genetics
-
Field J, Browning SR, Johnson LJ, et al. A polymorphism in the HLA-DPB1 gene is associated with susceptibility to multiple sclerosis. PLoS One 2010, 5:e13454. the Australia and New Zealand Multiple Sclerosis Genetics.
-
(2010)
PLoS One
, vol.5
-
-
Field, J.1
Browning, S.R.2
Johnson, L.J.3
-
45
-
-
0037444214
-
Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage
-
Hauser MA, Li YJ, Takeuchi S, et al. Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage. Hum Mol Genet 2003, 12:671-677.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 671-677
-
-
Hauser, M.A.1
Li, Y.J.2
Takeuchi, S.3
-
46
-
-
34548351247
-
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis
-
the Multiple Sclerosis Genetics
-
Gregory SG, Schmidt S, Seth P, et al. Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nat Genet 2007, 39:1083-1091. the Multiple Sclerosis Genetics.
-
(2007)
Nat Genet
, vol.39
, pp. 1083-1091
-
-
Gregory, S.G.1
Schmidt, S.2
Seth, P.3
-
47
-
-
34548299105
-
Risk alleles for multiple sclerosis identified by a genomewide study
-
The International Multiple Sclerosis Genetics
-
Risk alleles for multiple sclerosis identified by a genomewide study. N Engl J Med 2007, 357:851-862. The International Multiple Sclerosis Genetics.
-
(2007)
N Engl J Med
, vol.357
, pp. 851-862
-
-
-
48
-
-
35748981184
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants
-
The Wellcome Trust Case Control, the Australo-Anglo-American Spondylitis Consortium (TASC)the Australo-Anglo-American Spondylitis Consortium (TASC), the Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steeringthe Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering, the Breast Cancer Susceptibility Collaboration (UK)the Breast Cancer Susceptibility Collaboration (UK)
-
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants. Nat Genet 2007, 39:1329-1337. The Wellcome Trust Case Control, the Australo-Anglo-American Spondylitis Consortium (TASC)the Australo-Anglo-American Spondylitis Consortium (TASC), the Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steeringthe Biologics in RA Genetics and Genomics Study Syndicate (BRAGGS) Steering, the Breast Cancer Susceptibility Collaboration (UK)the Breast Cancer Susceptibility Collaboration (UK).
-
(2007)
Nat Genet
, vol.39
, pp. 1329-1337
-
-
-
49
-
-
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
-
the BiomarkerMS Study
-
Comabella M, Craig DW, Camiña-Tato 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 2008, 3:e3490. the BiomarkerMS Study.
-
(2008)
PLoS One
, vol.3
-
-
Comabella, M.1
Craig, D.W.2
Camiña-Tato, M.3
-
50
-
-
56749098072
-
Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis
-
Aulchenko YS, Hoppenbrouwers IA, Ramagopalan SV, et al. Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis. Nat Genet 2008, 40:1402-1403.
-
(2008)
Nat Genet
, vol.40
, pp. 1402-1403
-
-
Aulchenko, Y.S.1
Hoppenbrouwers, I.A.2
Ramagopalan, S.V.3
-
51
-
-
58949099391
-
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
-
Baranzini SE, Wang J, Gibson RA, et al. Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis. Hum Mol Genet 2009, 18:767-778.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 767-778
-
-
Baranzini, S.E.1
Wang, J.2
Gibson, R.A.3
-
52
-
-
67649881102
-
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
-
the Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene)
-
Bahlo M, Booth D, Broadley S, et al. Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nat Genet 2009, 41:824-828. the Australia and New Zealand Multiple Sclerosis Genetics Consortium (ANZgene).
-
(2009)
Nat Genet
, vol.41
, pp. 824-828
-
-
Bahlo, M.1
Booth, D.2
Broadley, S.3
-
53
-
-
77952884985
-
Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis
-
Sanna S, Pitzalis M, Zoledziewska M, et al. Variants within the immunoregulatory CBLB gene are associated with multiple sclerosis. Nat Genet 2010, 42:495-497.
-
(2010)
Nat Genet
, vol.42
, pp. 495-497
-
-
Sanna, S.1
Pitzalis, M.2
Zoledziewska, M.3
-
54
-
-
77956649792
-
Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis
-
Nischwitz S, Cepok S, Kroner A, et al. Evidence for VAV2 and ZNF433 as susceptibility genes for multiple sclerosis. J Neuroimmunol 2010, 227:162-166.
-
(2010)
J Neuroimmunol
, vol.227
, pp. 162-166
-
-
Nischwitz, S.1
Cepok, S.2
Kroner, A.3
-
55
-
-
76049083598
-
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
-
Jakkula E, Leppä V, Sulonen AM, et al. Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene. Am J Hum Genet 2010, 86:285-291.
-
(2010)
Am J Hum Genet
, vol.86
, pp. 285-291
-
-
Jakkula, E.1
Leppä, V.2
Sulonen, A.M.3
-
56
-
-
84255194782
-
Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci
-
the Bayer Pharma MS Genetics Working, the Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonistthe Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonist, the ANZgenethe ANZgene, thethe, the International Multiple Sclerosis Geneticsthe International Multiple Sclerosis Genetics
-
Patsopoulos NA, Esposito F, Reischl J, et al. Genome-wide meta-analysis identifies novel multiple sclerosis susceptibility loci. Ann Neurol 2011, 70:897-912. the Bayer Pharma MS Genetics Working, the Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonistthe Steering Committees of Studies Evaluating IFNβ-1b and a CCR1-Antagonist, the ANZgenethe ANZgene, thethe, the International Multiple Sclerosis Geneticsthe International Multiple Sclerosis Genetics.
-
(2011)
Ann Neurol
, vol.70
, pp. 897-912
-
-
Patsopoulos, N.A.1
Esposito, F.2
Reischl, J.3
-
57
-
-
84860524935
-
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1
-
Matesanz F, González-Pérez A, Lucas M, et al. Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1. PLoS One 2012, 7:e36140.
-
(2012)
PLoS One
, vol.7
-
-
Matesanz, F.1
González-Pérez, A.2
Lucas, M.3
-
58
-
-
84867011935
-
A genome-wide association study in progressive multiple sclerosis
-
Martinelli-Boneschi F, Esposito F, Brambilla P, et al. A genome-wide association study in progressive multiple sclerosis. Mult Scler 2012, 18:1384-1394.
-
(2012)
Mult Scler
, vol.18
, pp. 1384-1394
-
-
Martinelli-Boneschi, F.1
Esposito, F.2
Brambilla, P.3
-
59
-
-
84878863691
-
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis
-
The International Multiple Sclerosis Genetics
-
MANBA, CXCR5, SOX8, RPS6KB1 and ZBTB46 are genetic risk loci for multiple sclerosis. Brain 2013, 136:1778-1782. The International Multiple Sclerosis Genetics.
-
(2013)
Brain
, vol.136
, pp. 1778-1782
-
-
-
60
-
-
84874779411
-
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk
-
Lill CM, Schjeide BM, Graetz C, et al. Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. J Med Genet 2013, 50:140-143.
-
(2013)
J Med Genet
, vol.50
, pp. 140-143
-
-
Lill, C.M.1
Schjeide, B.M.2
Graetz, C.3
-
61
-
-
42349112088
-
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
-
McCarthy MI, Abecasis GR, Cardon LR, et al. Genome-wide association studies for complex traits: consensus, uncertainty and challenges. Nat Rev Genet 2008, 9:356-369.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 356-369
-
-
McCarthy, M.I.1
Abecasis, G.R.2
Cardon, L.R.3
-
62
-
-
80052325959
-
Pervasive sharing of genetic effects in autoimmune disease
-
the FOCiS Network of
-
Cotsapas C, Voight BF, Rossin E, et al. Pervasive sharing of genetic effects in autoimmune disease. PLoS Genet 2011, 7:e1002254. the FOCiS Network of.
-
(2011)
PLoS Genet
, vol.7
-
-
Cotsapas, C.1
Voight, B.F.2
Rossin, E.3
-
63
-
-
79960279940
-
Promise and pitfalls of the Immunochip
-
Cortes A, Brown MA Promise and pitfalls of the Immunochip. Arthritis Res Ther 2011, 13:101.
-
(2011)
Arthritis Res Ther
, vol.13
, pp. 101
-
-
Cortes, A.1
Brown, M.A.2
-
64
-
-
84887058596
-
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
-
The International Multiple Sclerosis Genetics Consortium (IMSGC)
-
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. Nat Genet 2013, 45:1353-1360. The International Multiple Sclerosis Genetics Consortium (IMSGC).
-
(2013)
Nat Genet
, vol.45
, pp. 1353-1360
-
-
-
65
-
-
84865790047
-
An integrated encyclopedia of DNA elements in the human genome
-
the ENCODE Project
-
Bernstein BE, Birney E, Dunham I, Green ED, Gunter C, Snyder M An integrated encyclopedia of DNA elements in the human genome. Nature 2012, 489:57-74. the ENCODE Project.
-
(2012)
Nature
, vol.489
, pp. 57-74
-
-
Bernstein, B.E.1
Birney, E.2
Dunham, I.3
Green, E.D.4
Gunter, C.5
Snyder, M.6
-
66
-
-
84870502629
-
Bayesian refinement of association signals for 14 loci in 3 common diseases
-
the Wellcome Trust Case Control
-
Maller JB, McVean G, Byrnes J, et al. Bayesian refinement of association signals for 14 loci in 3 common diseases. Nat Genet 2012, 44:1294-1301. the Wellcome Trust Case Control.
-
(2012)
Nat Genet
, vol.44
, pp. 1294-1301
-
-
Maller, J.B.1
McVean, G.2
Byrnes, J.3
-
67
-
-
49849091315
-
Refining genetic associations in multiple sclerosis
-
International Multiple Sclerosis Genetics Consortium (IMSGC)
-
Refining genetic associations in multiple sclerosis. Lancet Neurol 2008, 7:567-569. International Multiple Sclerosis Genetics Consortium (IMSGC).
-
(2008)
Lancet Neurol
, vol.7
, pp. 567-569
-
-
-
68
-
-
58149122959
-
The complex genetics of multiple sclerosis: pitfalls and prospects
-
Sawcer S The complex genetics of multiple sclerosis: pitfalls and prospects. Brain 2008, 131:3118-3131.
-
(2008)
Brain
, vol.131
, pp. 3118-3131
-
-
Sawcer, S.1
-
69
-
-
77954140531
-
Common SNPs explain a large proportion of the heritability for human height
-
Yang J, Benyamin B, McEvoy BP, et al. Common SNPs explain a large proportion of the heritability for human height. Nat Genet 2010, 42:565-569.
-
(2010)
Nat Genet
, vol.42
, pp. 565-569
-
-
Yang, J.1
Benyamin, B.2
McEvoy, B.P.3
-
70
-
-
77950329947
-
Evidence for polygenic susceptibility to multiple sclerosis-the shape of things to come
-
The International Multiple Sclerosis Genetics Consortium (IMSGC)
-
Evidence for polygenic susceptibility to multiple sclerosis-the shape of things to come. Am J Hum Genet 2010, 86:621-625. The International Multiple Sclerosis Genetics Consortium (IMSGC).
-
(2010)
Am J Hum Genet
, vol.86
, pp. 621-625
-
-
-
71
-
-
77955405475
-
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
-
McLaren W, Pritchard B, Rios D, Chen Y, Flicek P, Cunningham F Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor. Bioinformatics 2010, 26:2069-2070.
-
(2010)
Bioinformatics
, vol.26
, pp. 2069-2070
-
-
McLaren, W.1
Pritchard, B.2
Rios, D.3
Chen, Y.4
Flicek, P.5
Cunningham, F.6
-
72
-
-
77951640946
-
A method and server for predicting damaging missense mutations
-
Adzhubei IA, Schmidt S, Peshkin L, et al. A method and server for predicting damaging missense mutations. Nat Methods 2010, 7:248-249.
-
(2010)
Nat Methods
, vol.7
, pp. 248-249
-
-
Adzhubei, I.A.1
Schmidt, S.2
Peshkin, L.3
-
73
-
-
84867301515
-
Predicting the functional effect of amino acid substitutions and indels
-
Choi Y, Sims GE, Murphy S, Miller JR, Chan AP Predicting the functional effect of amino acid substitutions and indels. PLoS One 2012, 7:e46688.
-
(2012)
PLoS One
, vol.7
-
-
Choi, Y.1
Sims, G.E.2
Murphy, S.3
Miller, J.R.4
Chan, A.P.5
-
74
-
-
84858779229
-
HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants
-
Ward LD, Kellis M HaploReg: a resource for exploring chromatin states, conservation, and regulatory motif alterations within sets of genetically linked variants. Nucleic Acids Res 2012, 40:D930-D934.
-
(2012)
Nucleic Acids Res
, vol.40
-
-
Ward, L.D.1
Kellis, M.2
-
75
-
-
84873086126
-
Chromatin marks identify critical cell types for fine mapping complex trait variants
-
Trynka G, Sandor C, Han B, et al. Chromatin marks identify critical cell types for fine mapping complex trait variants. Nat Genet 2013, 45:124-130.
-
(2013)
Nat Genet
, vol.45
, pp. 124-130
-
-
Trynka, G.1
Sandor, C.2
Han, B.3
-
76
-
-
77249134594
-
Rare variants create synthetic genome-wide associations
-
Dickson SP, Wang K, Krantz I, Hakonarson H, Goldstein DB Rare variants create synthetic genome-wide associations. PLoS Biol 2010, 8:e1000294.
-
(2010)
PLoS Biol
, vol.8
-
-
Dickson, S.P.1
Wang, K.2
Krantz, I.3
Hakonarson, H.4
Goldstein, D.B.5
-
77
-
-
79851468862
-
Synthetic associations are unlikely to account for many common disease genome-wide association signals
-
Anderson CA, Soranzo N, Zeggini E, Barrett JC Synthetic associations are unlikely to account for many common disease genome-wide association signals. PLoS Biol 2011, 9:e1000580.
-
(2011)
PLoS Biol
, vol.9
-
-
Anderson, C.A.1
Soranzo, N.2
Zeggini, E.3
Barrett, J.C.4
-
79
-
-
31844443695
-
The Environment and Disease: association or Causation?
-
Hill AB The Environment and Disease: association or Causation?. Proc R Soc Med 1965, 58:295-300.
-
(1965)
Proc R Soc Med
, vol.58
, pp. 295-300
-
-
Hill, A.B.1
-
80
-
-
84862909349
-
Five years of GWAS discovery
-
Visscher PM, Brown MA, McCarthy MI, Yang J Five years of GWAS discovery. Am J Hum Genet 2012, 90:7-24.
-
(2012)
Am J Hum Genet
, vol.90
, pp. 7-24
-
-
Visscher, P.M.1
Brown, M.A.2
McCarthy, M.I.3
Yang, J.4
-
81
-
-
34247554965
-
Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis
-
Rioux JD, Xavier RJ, Taylor KD, et al. Genome-wide association study identifies new susceptibility loci for Crohn disease and implicates autophagy in disease pathogenesis. Nat Genet 2007, 39:596-604.
-
(2007)
Nat Genet
, vol.39
, pp. 596-604
-
-
Rioux, J.D.1
Xavier, R.J.2
Taylor, K.D.3
-
82
-
-
63149109244
-
Soluble IL-2RA levels in multiple sclerosis subjects and the effect of soluble IL-2RA on immune responses
-
Maier LM, Anderson DE, Severson CA, et al. Soluble IL-2RA levels in multiple sclerosis subjects and the effect of soluble IL-2RA on immune responses. J Immunol 2009, 182:1541-1547.
-
(2009)
J Immunol
, vol.182
, pp. 1541-1547
-
-
Maier, L.M.1
Anderson, D.E.2
Severson, C.A.3
-
83
-
-
84865261493
-
TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis
-
Gregory AP, Dendrou CA, Attfield KE, et al. TNF receptor 1 genetic risk mirrors outcome of anti-TNF therapy in multiple sclerosis. Nature 2012, 488:508-511.
-
(2012)
Nature
, vol.488
, pp. 508-511
-
-
Gregory, A.P.1
Dendrou, C.A.2
Attfield, K.E.3
-
85
-
-
79952158486
-
Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility
-
Couturier N, Bucciarelli F, Nurtdinov RN, et al. Tyrosine kinase 2 variant influences T lymphocyte polarization and multiple sclerosis susceptibility. Brain 2011, 134:693-703.
-
(2011)
Brain
, vol.134
, pp. 693-703
-
-
Couturier, N.1
Bucciarelli, F.2
Nurtdinov, R.N.3
-
86
-
-
33846566857
-
Familial effects on the clinical course of multiple sclerosis
-
Hensiek AE, Seaman SR, Barcellos LF, et al. Familial effects on the clinical course of multiple sclerosis. Neurology 2007, 68:376-383.
-
(2007)
Neurology
, vol.68
, pp. 376-383
-
-
Hensiek, A.E.1
Seaman, S.R.2
Barcellos, L.F.3
-
87
-
-
77649189376
-
MGAT5 alters the severity of multiple sclerosis
-
Brynedal B, Wojcik J, Esposito F, et al. MGAT5 alters the severity of multiple sclerosis. J Neuroimmunol 2010, 220:120-124.
-
(2010)
J Neuroimmunol
, vol.220
, pp. 120-124
-
-
Brynedal, B.1
Wojcik, J.2
Esposito, F.3
-
88
-
-
82555174406
-
Genome-wide association study of severity in multiple sclerosis
-
International Multiple Sclerosis Genetics
-
Genome-wide association study of severity in multiple sclerosis. Genes Immun 2011, 12:615-625. International Multiple Sclerosis Genetics.
-
(2011)
Genes Immun
, vol.12
, pp. 615-625
-
-
-
89
-
-
77956369535
-
Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis
-
Baranzini SE, Srinivasan R, Khankhanian P, et al. Genetic variation influences glutamate concentrations in brains of patients with multiple sclerosis. Brain 2010, 133:2603-2611.
-
(2010)
Brain
, vol.133
, pp. 2603-2611
-
-
Baranzini, S.E.1
Srinivasan, R.2
Khankhanian, P.3
-
90
-
-
20144387016
-
Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity
-
Roxburgh RH, Seaman SR, Masterman T, et al. Multiple Sclerosis Severity Score: using disability and disease duration to rate disease severity. Neurology 2005, 64:1144-1151.
-
(2005)
Neurology
, vol.64
, pp. 1144-1151
-
-
Roxburgh, R.H.1
Seaman, S.R.2
Masterman, T.3
-
91
-
-
84873379575
-
Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis
-
the International Multiple Sclerosis Genetics Consortium and the Wellcome Trust Case Control
-
Buck D, Albrecht E, Aslam M, et al. Genetic variants in the immunoglobulin heavy chain locus are associated with the IgG index in multiple sclerosis. Ann Neurol 2013, 73:86-94. the International Multiple Sclerosis Genetics Consortium and the Wellcome Trust Case Control.
-
(2013)
Ann Neurol
, vol.73
, pp. 86-94
-
-
Buck, D.1
Albrecht, E.2
Aslam, M.3
-
92
-
-
84902540564
-
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis
-
The International Multiple Sclerosis Genetics Consortium and the The Australia and New Zealand MS Genetics, published online Nov 13.
-
Goris A, van Setten J, Diekstra F, et al. No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis. Hum Mol Genet 2013, The International Multiple Sclerosis Genetics Consortium and the The Australia and New Zealand MS Genetics, published online Nov 13. 10.1093/hmg/ddt574.
-
(2013)
Hum Mol Genet
-
-
Goris, A.1
van Setten, J.2
Diekstra, F.3
-
93
-
-
84874604770
-
Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles
-
the International Multiple Sclerosis Genetics
-
Mero IL, Gustavsen MW, Sæther HS, et al. Oligoclonal band status in Scandinavian multiple sclerosis patients is associated with specific genetic risk alleles. PLoS One 2013, 8:e58352. the International Multiple Sclerosis Genetics.
-
(2013)
PLoS One
, vol.8
-
-
Mero, I.L.1
Gustavsen, M.W.2
Sæther, H.S.3
-
94
-
-
84879052306
-
Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients
-
the International Multiple Sclerosis Genetics, the Wellcome Trust Case Control Consortium 2the Wellcome Trust Case Control Consortium 2, the PROGEMUSthe PROGEMUS, the PROGRESSOthe PROGRESSO
-
Leone MA, Barizzone N, Esposito F, et al. Association of genetic markers with CSF oligoclonal bands in multiple sclerosis patients. PLoS One 2013, 8:e64408. the International Multiple Sclerosis Genetics, the Wellcome Trust Case Control Consortium 2the Wellcome Trust Case Control Consortium 2, the PROGEMUSthe PROGEMUS, the PROGRESSOthe PROGRESSO.
-
(2013)
PLoS One
, vol.8
-
-
Leone, M.A.1
Barizzone, N.2
Esposito, F.3
-
95
-
-
84876016091
-
A genome-wide association study of brain lesion distribution in multiple sclerosis
-
Gourraud PA, Sdika M, Khankhanian P, et al. A genome-wide association study of brain lesion distribution in multiple sclerosis. Brain 2013, 136:1012-1024.
-
(2013)
Brain
, vol.136
, pp. 1012-1024
-
-
Gourraud, P.A.1
Sdika, M.2
Khankhanian, P.3
-
96
-
-
84871781182
-
Sustained activation of ERK1/2 MAPK in oligodendrocytes and schwann cells enhances myelin growth and stimulates oligodendrocyte progenitor expansion
-
Ishii A, Furusho M, Bansal R Sustained activation of ERK1/2 MAPK in oligodendrocytes and schwann cells enhances myelin growth and stimulates oligodendrocyte progenitor expansion. J Neurosci 2013, 33:175-186.
-
(2013)
J Neurosci
, vol.33
, pp. 175-186
-
-
Ishii, A.1
Furusho, M.2
Bansal, R.3
-
97
-
-
33748143936
-
Inflammation stimulates myelination by transplanted oligodendrocyte precursor cells
-
Setzu A, Lathia JD, Zhao C, et al. Inflammation stimulates myelination by transplanted oligodendrocyte precursor cells. Glia 2006, 54:297-303.
-
(2006)
Glia
, vol.54
, pp. 297-303
-
-
Setzu, A.1
Lathia, J.D.2
Zhao, C.3
-
98
-
-
77954543178
-
Functionally defective germline variants of sialic acid acetylesterase in autoimmunity
-
Surolia I, Pirnie SP, Chellappa V, et al. Functionally defective germline variants of sialic acid acetylesterase in autoimmunity. Nature 2010, 466:243-247.
-
(2010)
Nature
, vol.466
, pp. 243-247
-
-
Surolia, I.1
Pirnie, S.P.2
Chellappa, V.3
-
99
-
-
84555191729
-
Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
-
the Type 1 Diabetes Genetics, the UK Inflammatory Bowel Disease (IBD) Geneticsthe UK Inflammatory Bowel Disease (IBD) Genetics, the Wellcome Trust Case Controlthe Wellcome Trust Case Control
-
Hunt KA, Smyth DJ, Balschun T, et al. Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry. Nat Genet 2012, 44:3-5. the Type 1 Diabetes Genetics, the UK Inflammatory Bowel Disease (IBD) Geneticsthe UK Inflammatory Bowel Disease (IBD) Genetics, the Wellcome Trust Case Controlthe Wellcome Trust Case Control.
-
(2012)
Nat Genet
, vol.44
, pp. 3-5
-
-
Hunt, K.A.1
Smyth, D.J.2
Balschun, T.3
-
100
-
-
84975742565
-
A map of human genome variation from population-scale sequencing
-
the 1000 Genomes Project
-
Abecasis GR, Altshuler D, Auton A, et al. A map of human genome variation from population-scale sequencing. Nature 2010, 467:1061-1073. the 1000 Genomes Project.
-
(2010)
Nature
, vol.467
, pp. 1061-1073
-
-
Abecasis, G.R.1
Altshuler, D.2
Auton, A.3
-
101
-
-
84255175933
-
Rare variants in the CYP27B1 gene are associated with multiple sclerosis
-
Ramagopalan SV, Dyment DA, Cader MZ, et al. Rare variants in the CYP27B1 gene are associated with multiple sclerosis. Ann Neurol 2011, 70:881-886.
-
(2011)
Ann Neurol
, vol.70
, pp. 881-886
-
-
Ramagopalan, S.V.1
Dyment, D.A.2
Cader, M.Z.3
-
102
-
-
84877898509
-
Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes
-
the ANZgene
-
Cortes A, Field J, Glazov EA, Hadler J, Stankovich J, Brown MA Resequencing and fine-mapping of the chromosome 12q13-14 locus associated with multiple sclerosis refines the number of implicated genes. Hum Mol Genet 2013, 22:2283-2292. the ANZgene.
-
(2013)
Hum Mol Genet
, vol.22
, pp. 2283-2292
-
-
Cortes, A.1
Field, J.2
Glazov, E.A.3
Hadler, J.4
Stankovich, J.5
Brown, M.A.6
-
103
-
-
84876483525
-
No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis
-
Ban M, Caillier S, Mero IL, et al. No evidence of association between mutant alleles of the CYP27B1 gene and multiple sclerosis. Ann Neurol 2013, 73:430-432.
-
(2013)
Ann Neurol
, vol.73
, pp. 430-432
-
-
Ban, M.1
Caillier, S.2
Mero, I.L.3
-
104
-
-
84876492894
-
No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis
-
Barizzone N, Pauwels I, Luciano B, et al. No evidence for a role of rare CYP27B1 functional variations in multiple sclerosis. Ann Neurol 2013, 73:433-437.
-
(2013)
Ann Neurol
, vol.73
, pp. 433-437
-
-
Barizzone, N.1
Pauwels, I.2
Luciano, B.3
-
105
-
-
84866053994
-
Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene
-
Dyment DA, Cader MZ, Chao MJ, et al. Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene. Neurology 2012, 79:406-411.
-
(2012)
Neurology
, vol.79
, pp. 406-411
-
-
Dyment, D.A.1
Cader, M.Z.2
Chao, M.J.3
-
106
-
-
84878994629
-
Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
-
Hunt KA, Mistry V, Bockett NA, et al. Negligible impact of rare autoimmune-locus coding-region variants on missing heritability. Nature 2013, 498:232-235.
-
(2013)
Nature
, vol.498
, pp. 232-235
-
-
Hunt, K.A.1
Mistry, V.2
Bockett, N.A.3
-
107
-
-
68249108329
-
Prediction and interaction in complex disease genetics: experience in type 1 diabetes
-
Clayton DG Prediction and interaction in complex disease genetics: experience in type 1 diabetes. PLoS Genet 2009, 5:e1000540.
-
(2009)
PLoS Genet
, vol.5
-
-
Clayton, D.G.1
-
108
-
-
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 2009, 10:5-11.
-
(2009)
Neurogenetics
, vol.10
, pp. 5-11
-
-
Hemminki, K.1
Li, X.2
Sundquist, J.3
Hillert, J.4
Sundquist, K.5
-
109
-
-
84868212192
-
Risk in complex genetics: "all models are wrong but some are useful"
-
Sawcer S, Wason J Risk in complex genetics: "all models are wrong but some are useful". Ann Neurol 2012, 72:502-509.
-
(2012)
Ann Neurol
, vol.72
, pp. 502-509
-
-
Sawcer, S.1
Wason, J.2
-
110
-
-
0021983786
-
Sick individuals and sick populations
-
Rose G Sick individuals and sick populations. Int J Epidemiol 1985, 14:32-38.
-
(1985)
Int J Epidemiol
, vol.14
, pp. 32-38
-
-
Rose, G.1
-
111
-
-
27144472560
-
A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility
-
Reich D, Patterson N, De Jager PL, et al. A whole-genome admixture scan finds a candidate locus for multiple sclerosis susceptibility. Nat Genet 2005, 37:1113-1118.
-
(2005)
Nat Genet
, vol.37
, pp. 1113-1118
-
-
Reich, D.1
Patterson, N.2
De Jager, P.L.3
-
112
-
-
84874636721
-
Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis
-
the ANZgene
-
Lin R, Charlesworth J, Stankovich J, Perreau VM, Brown MA, Taylor BV Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis. PLoS One 2013, 8:e56379. the ANZgene.
-
(2013)
PLoS One
, vol.8
-
-
Lin, R.1
Charlesworth, J.2
Stankovich, J.3
Perreau, V.M.4
Brown, M.A.5
Taylor, B.V.6
-
113
-
-
2342597140
-
A high-density admixture map for disease gene discovery in African Americans
-
Smith MW, Patterson N, Lautenberger JA, et al. A high-density admixture map for disease gene discovery in African Americans. Am J Hum Genet 2004, 74:1001-1013.
-
(2004)
Am J Hum Genet
, vol.74
, pp. 1001-1013
-
-
Smith, M.W.1
Patterson, N.2
Lautenberger, J.A.3
|