-
1
-
-
33646196946
-
Regulation of Th2 differentiation and Il4 locus accessibility
-
10.1146/annurev.immunol.23.021704.115821 1:CAS:528:DC%2BD28XkvFSqtLY%3D 16551261
-
KM Ansel, et al. 2006 Regulation of Th2 differentiation and Il4 locus accessibility Annu Rev Immunol 24 607 656 10.1146/annurev.immunol.23.021704. 115821 1:CAS:528:DC%2BD28XkvFSqtLY%3D 16551261
-
(2006)
Annu Rev Immunol
, vol.24
, pp. 607-656
-
-
Ansel, K.M.1
-
2
-
-
67649881102
-
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosome 12 and 20
-
Australia and New Zealand Multiple Sclerosis Genetics Consortium. 10.1038/ng.396
-
Australia and New Zealand Multiple Sclerosis Genetics Consortium 2009 Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosome 12 and 20 Nat Genet 41 7 824 828 10.1038/ng.396
-
(2009)
Nat Genet
, vol.41
, Issue.7
, pp. 824-828
-
-
-
3
-
-
70349629969
-
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
-
10.1038/ejhg.2009.41 1:CAS:528:DC%2BD1MXhtFKnsLbP 19293837
-
M Ban, et al. 2009 Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor Eur J Hum Genet 17 10 1309 1313 10.1038/ejhg.2009.41 1:CAS:528:DC%2BD1MXhtFKnsLbP 19293837
-
(2009)
Eur J Hum Genet
, vol.17
, Issue.10
, pp. 1309-1313
-
-
Ban, M.1
-
4
-
-
65549084289
-
Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
-
10.1093/hmg/ddp120 1:CAS:528:DC%2BD1MXlslWqtrw%3D 19286671
-
SE Baranzini, et al. 2009 Pathway and network-based analysis of genome-wide association studies in multiple sclerosis Hum Mol Genet 18 11 2078 2090 10.1093/hmg/ddp120 1:CAS:528:DC%2BD1MXlslWqtrw%3D 19286671
-
(2009)
Hum Mol Genet
, vol.18
, Issue.11
, pp. 2078-2090
-
-
Baranzini, S.E.1
-
5
-
-
58949099391
-
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
-
10.1093/hmg/ddn388 1:CAS:528:DC%2BD1MXhtVWjsb0%3D 19010793
-
SE Baranzini J Wang RA Gibson 2009 Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis Hum Mol Genet 18 4 767 778 10.1093/hmg/ddn388 1:CAS:528:DC%2BD1MXhtVWjsb0%3D 19010793
-
(2009)
Hum Mol Genet
, vol.18
, Issue.4
, pp. 767-778
-
-
Baranzini, S.E.1
Wang, J.2
Gibson, R.A.3
-
6
-
-
13444269543
-
Haploview: Analysis and visualization of LD and haplotype maps
-
DOI 10.1093/bioinformatics/bth457
-
JC Barrett, et al. 2005 Haploview: analysis and visualization of LD and haplotype maps Bioinformatics 21 2 263 265 10.1093/bioinformatics/bth457 1:CAS:528:DC%2BD2MXkt1WitQ%3D%3D 15297300 (Pubitemid 40202029)
-
(2005)
Bioinformatics
, vol.21
, Issue.2
, pp. 263-265
-
-
Barrett, J.C.1
Fry, B.2
Maller, J.3
Daly, M.J.4
-
7
-
-
0015252399
-
HL-A antigen frequencies in multiple sclerosis. Significant increase of HL-A3, HL-A10 and W5, and decrease of HL-A12
-
J Bertrams E Kuwert 1972 HL-A antigen frequencies in multiple sclerosis. Significant increase of HL-A3, HL-A10 and W5, and decrease of HL-A12 Eur J Neurol 7 74 78
-
(1972)
Eur J Neurol
, vol.7
, Issue.74
, pp. 78
-
-
Bertrams, J.1
Kuwert, E.2
-
8
-
-
0037029424
-
Multiple sclerosis
-
DOI 10.1016/S0140-6736(02)08220-X
-
A Compston A Coles 2002 Multiple sclerosis Lancet 359 9313 1221 1231 10.1016/S0140-6736(02)08220-X 11955556 (Pubitemid 34304266)
-
(2002)
Lancet
, vol.359
, Issue.9313
, pp. 1221-1231
-
-
Compston, A.1
Coles, A.2
-
9
-
-
67649876123
-
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
-
10.1038/ng.401 19525953
-
PL De Jager, et al. 2009 Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci Nat Genet 41 7 776 782 10.1038/ng.401 19525953
-
(2009)
Nat Genet
, vol.41
, Issue.7
, pp. 776-782
-
-
De Jager, P.L.1
-
10
-
-
0029121088
-
A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group [see comments]
-
10.1038/377150a0 1:CAS:528:DyaK2MXotVOhtLw%3D 7675080
-
GC Ebers AD Sadovnick NJ Risch 1995 A genetic basis for familial aggregation in multiple sclerosis. Canadian Collaborative Study Group [see comments] Nature 377 6545 150 151 10.1038/377150a0 1:CAS:528:DyaK2MXotVOhtLw%3D 7675080
-
(1995)
Nature
, vol.377
, Issue.6545
, pp. 150-151
-
-
Ebers, G.C.1
Sadovnick, A.D.2
Risch, N.J.3
-
11
-
-
15844366743
-
A full genome search in multiple sclerosis
-
DOI 10.1038/ng0896-472
-
GC Ebers, et al. 1996 A full genome search in multiple sclerosis Nat Genet 13 4 472 476 10.1038/ng0896-472 1:CAS:528:DyaK28XkslOnu7Y%3D 8696345 (Pubitemid 26256624)
-
(1996)
Nature Genetics
, vol.13
, Issue.4
, pp. 472-476
-
-
Ebers, G.C.1
Kukay, K.2
Bulman, D.E.3
Sadovnick, A.D.4
Rice, G.5
Anderson, C.6
Armstrong, H.7
Cousin, K.8
Bell, R.B.9
Hader, W.10
Paty, D.W.11
Hashimoto, S.12
Oger, J.13
Duquette, P.14
Warren, S.15
Gray, T.16
O'Connor, P.17
Nath, A.18
Auty, A.19
-
12
-
-
18944379196
-
The many faces of IL-7: From lymphopoiesis to peripheral T cell maintenance
-
1:CAS:528:DC%2BD2MXkt1Oms7c%3D 15905493
-
TJ Fry CL Mackall 2005 The many faces of IL-7: from lymphopoiesis to peripheral T cell maintenance J Immunol 174 11 6571 6576 1:CAS:528: DC%2BD2MXkt1Oms7c%3D 15905493
-
(2005)
J Immunol
, vol.174
, Issue.11
, pp. 6571-6576
-
-
Fry, T.J.1
MacKall, C.L.2
-
13
-
-
59649090821
-
SNP genotyping using the Sequenom MassARRAY iPLEX platform
-
Chapter 2:Unit
-
Gabriel S, Ziaugra L, Tabbaa D (2009) SNP genotyping using the Sequenom MassARRAY iPLEX platform. Curr Protoc Hum Genet, Chapter 2:Unit
-
(2009)
Curr Protoc Hum Genet
-
-
Gabriel, S.1
Ziaugra, L.2
Tabbaa, D.3
-
14
-
-
67349216357
-
Autoimmune T cell responses in the central nervous system
-
10.1038/nri2550 1:CAS:528:DC%2BD1MXlvFShs7c%3D 19444307
-
J Goverman 2009 Autoimmune T cell responses in the central nervous system Nat Rev Immunol 9 6 393 407 10.1038/nri2550 1:CAS:528:DC%2BD1MXlvFShs7c%3D 19444307
-
(2009)
Nat Rev Immunol
, vol.9
, Issue.6
, pp. 393-407
-
-
Goverman, J.1
-
15
-
-
34548351247
-
Interleukin 7 receptor α chain (IL7R) shows allelic and functional association with multiple sclerosis
-
DOI 10.1038/ng2103, PII NG2103
-
SG Gregory, et al. 2007 Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis Nat Genet 39 9 1083 1091 10.1038/ng2103 1:CAS:528:DC%2BD2sXps12gtb8%3D 17660817 (Pubitemid 47340652)
-
(2007)
Nature Genetics
, vol.39
, Issue.9
, pp. 1083-1091
-
-
Gregory, S.G.1
Schmidt, S.2
Seth, P.3
Oksenberg, J.R.4
Hart, J.5
Prokop, A.6
Caillier, S.J.7
Ban, M.8
Goris, A.9
Barcellos, L.F.10
Lincoln, R.11
McCauley, J.L.12
Sawcer, S.J.13
Compston, D.A.S.14
Dubois, B.15
Hauser, S.L.16
Garcia-Blanco, M.A.17
Pericak-Vance, M.A.18
Haines, J.L.19
-
16
-
-
0009573338
-
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatibility complex
-
DOI 10.1038/ng0896-469
-
JL Haines, et al. 1996 A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex. The Multiple Sclerosis Genetics Group Nat Genet 13 4 469 471 10.1038/ng0896-469 1:CAS:528:DyaK28XkslOnu7k%3D 8696344 (Pubitemid 26256623)
-
(1996)
Nature Genetics
, vol.13
, Issue.4
, pp. 469-471
-
-
Haines, J.L.1
Ter-Minassian, M.2
Bazyk, A.3
Gusella, J.F.4
Kim, D.J.5
Terwedow, H.6
Pericak-Vance, M.A.7
Rimmler, J.B.8
Haynes, C.S.9
Roses, A.D.10
Lee, A.11
Shaner, B.12
Menold, M.13
Seboun, E.14
Fitoussi, R.-P.15
Gartioux, C.16
Reyes, C.17
Ribierre, F.18
Gyapay, G.19
-
17
-
-
0002063324
-
Multiple sclerosis and other demyelinating diseases
-
A.D. Fauci (eds) et al. McGraw Hill New York
-
Hauser SL, Goodkin DE (1998) Multiple sclerosis and other demyelinating diseases. In: Fauci AD et al (eds) Harrison's principle of internal medicine. McGraw Hill, New York, pp 2409-2419
-
(1998)
Harrison's Principle of Internal Medicine
, pp. 2409-2419
-
-
Hauser, S.L.1
Goodkin, D.E.2
-
18
-
-
0037444214
-
Genomic convergence: Identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage
-
DOI 10.1093/hmg/12.6.671
-
MA Hauser, et al. 2003 Genomic convergence: identifying candidate genes for Parkinson's disease by combining serial analysis of gene expression and genetic linkage Hum Mol Genet 12 6 671 677 10.1093/hmg/12.6.671 1:CAS:528:DC%2BD3sXjt1Slsbo%3D 12620972 (Pubitemid 36372493)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.6
, pp. 671-677
-
-
Hauser, M.A.1
Li, Y.-J.2
Takeuchi, S.3
Walters, R.4
Noureddine, M.5
Maready, M.6
Darden, T.7
Hulette, C.8
Martin, E.9
Hauser, E.10
Xu, H.11
Schmechel, D.12
Stenger, J.E.13
Dietrich, F.14
Vance, J.15
-
19
-
-
34047152928
-
Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1
-
DOI 10.1093/hmg/ddl462
-
W Hennah, et al. 2007 Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1 Hum Mol Genet 16 5 453 462 10.1093/hmg/ddl462 1:CAS:528: DC%2BD2sXjslers7c%3D 17185386 (Pubitemid 46522609)
-
(2007)
Human Molecular Genetics
, vol.16
, Issue.5
, pp. 453-462
-
-
Hennah, W.1
Tomppo, L.2
Hiekkalinna, T.3
Palo, O.M.4
Kilpinen, H.5
Ekelund, J.6
Tuulio-Henriksson, A.7
Silander, K.8
Partonen, T.9
Paunio, T.10
Terwilliger, J.D.11
Lonnqvist, J.12
Peltonen, L.13
-
20
-
-
0036517472
-
A comprehensive review of genetic association studies
-
DOI 10.1097/00125817-200203000-00002
-
JN Hirschhorn, et al. 2002 A comprehensive review of genetic association studies Genet Med 4 2 45 61 10.1097/00125817-200203000-00002 1:CAS:528:DC%2BD38XjtFSru7w%3D 11882781 (Pubitemid 44698579)
-
(2002)
Genetics in Medicine
, vol.4
, Issue.2
, pp. 45-61
-
-
Hirschhorn, J.N.1
Lohmueller, K.2
Byrne, E.3
Hirschhorn, K.4
-
21
-
-
0033103099
-
Interleukin-7: Physiological roles and mechanisms of action
-
DOI 10.1016/S1359-6101(98)00025-2, PII S1359610198000252
-
R Hofmeister, et al. 1999 Interleukin-7: physiological roles and mechanisms of action Cytokine Growth Factor Rev 10 1 41 60 10.1016/S1359- 6101(98)00025-2 1:CAS:528:DyaK1MXjsVOkt7w%3D 10379911 (Pubitemid 29230851)
-
(1999)
Cytokine and Growth Factor Reviews
, vol.10
, Issue.1
, pp. 41-60
-
-
Hofmeister, R.1
Khaled, A.R.2
Benbernou, N.3
Rajnavolgyi, E.4
Muegge, K.5
Durum, S.K.6
-
22
-
-
23944499790
-
A high-density screen for linkage in multiple sclerosis
-
DOI 10.1086/444547
-
International Multiple Sclerosis Genetics Consortium 2005 A high-density screen for linkage in multiple sclerosis Am J Hum Genet 77 454 467 10.1086/444547 (Pubitemid 41192651)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.3
, pp. 454-467
-
-
Sawcer, S.1
-
23
-
-
34548299105
-
Risk alleles for multiple sclerosis identified by a genomewide study
-
DOI 10.1056/NEJMoa073493
-
International Multiple Sclerosis Genetics Consortium 2007 Risk alleles for multiple sclerosis identified by a genomewide study N Engl J Med 357 9 851 862 10.1056/NEJMoa073493 (Pubitemid 47347319)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.9
, pp. 851-862
-
-
Hafler, D.A.1
Compston, A.2
Sawcer, S.3
Lander, E.S.4
Daly, M.J.5
De Jager, P.L.6
De Bakker, P.I.W.7
Gabriel, S.B.8
Mirel, D.B.9
Ivinson, A.J.10
Pericak-Vance, M.A.11
Gregory, S.G.12
Rioux, J.D.13
McCauley, J.L.14
Haines, J.L.15
Barcellos, L.F.16
Cree, B.17
Oksenberg, J.R.18
Hauser, S.L.19
-
24
-
-
59149093148
-
The expanding genetic overlap between multiple sclerosis and type i diabetes
-
International Multiple Sclerosis Genetics Consortium. 10.1038/gene.2008.83
-
International Multiple Sclerosis Genetics Consortium 2009 The expanding genetic overlap between multiple sclerosis and type I diabetes Genes Immun 10 1 11 14 10.1038/gene.2008.83
-
(2009)
Genes Immun
, vol.10
, Issue.1
, pp. 11-14
-
-
-
25
-
-
77952094786
-
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 [Epub ahead of print]
-
International Multiple Sclerosis Genetics Consortium (2009b) Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. Hum Mol Genet [Epub ahead of print]
-
(2009)
Hum Mol Genet
-
-
-
26
-
-
3042716781
-
Distinct regions of the interleukin-7 receptor regulate different Bcl2 family members
-
DOI 10.1128/MCB.24.14.6501-6513.2004
-
Q Jiang, et al. 2004 Distinct regions of the interleukin-7 receptor regulate different Bcl2 family members Mol Cell Biol 24 14 6501 6513 10.1128/MCB.24.14.6501-6513.2004 1:CAS:528:DC%2BD2cXlslentrc%3D 15226449 (Pubitemid 38891148)
-
(2004)
Molecular and Cellular Biology
, vol.24
, Issue.14
, pp. 6501-6513
-
-
Jiang, Q.1
Li, W.Q.2
Hofmeister, R.R.3
Young, H.A.4
Hodge, D.R.5
Keller, J.R.6
Khaled, A.R.7
Durum, S.K.8
-
27
-
-
22544452762
-
Cell biology of IL-7, a key lymphotrophin
-
DOI 10.1016/j.cytogfr.2005.05.004, PII S1359610105000626
-
Q Jiang, et al. 2005 Cell biology of IL-7, a key lymphotrophin Cytokine Growth Factor Rev 16 4-5 513 533 10.1016/j.cytogfr.2005.05.004 1:CAS:528:DC%2BD2MXmvVCnu7Y%3D 15996891 (Pubitemid 41022015)
-
(2005)
Cytokine and Growth Factor Reviews
, vol.16
, Issue.4-5
, pp. 513-533
-
-
Jiang, Q.1
Wen, Q.L.2
Aiello, F.B.3
Mazzucchelli, R.4
Asefa, B.5
Khaled, A.R.6
Durum, S.K.7
-
28
-
-
0037138370
-
Signaling through the JAK/STAT pathway, recent advances and future challenges
-
DOI 10.1016/S0378-1119(02)00398-0, PII S0378111902003980
-
T Kisseleva, et al. 2002 Signaling through the JAK/STAT pathway, recent advances and future challenges Gene 285 1-2 1 24 10.1016/S0378-1119(02)00398-0 1:CAS:528:DC%2BD38XitlWmsbg%3D 12039028 (Pubitemid 34246317)
-
(2002)
Gene
, vol.285
, Issue.1-2
, pp. 1-24
-
-
Kisseleva, T.1
Bhattacharya, S.2
Braunstein, J.3
Schindler, C.W.4
-
29
-
-
41549156916
-
TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome
-
DOI 10.1212/01.wnl.0000296279.98236.8a, PII 0000611420080325100005
-
T Kumpfel, et al. 2008 Multiple sclerosis and the TNFRSF1A R92Q mutation: clinical characteristics of 21 cases Neurology 71 22 1812 1820 10.1212/01.wnl.0000335930.18776.47 1:STN:280:DC%2BD1cjmtFKgtA%3D%3D 19029521 (Pubitemid 351464752)
-
(2008)
Neurology
, vol.70
, Issue.13 PART 2
, pp. 1155-1156
-
-
Hoffmann, L.A.1
Lohse, P.2
Konig, F.B.3
Feneberg, W.4
Hohlfeld, R.5
Kumpfel, T.6
-
30
-
-
17344367913
-
Genomewide scan of multiple sclerosis in Finnish multiplex families
-
DOI 10.1086/301637
-
S Kuokkanen, et al. 1997 Genomewide scan of multiple sclerosis in Finnish multiplex families Am J Hum Genet 61 1379 1387 10.1086/301637 1:CAS:528:DyaK1cXntVKkuw%3D%3D 9399895 (Pubitemid 28046915)
-
(1997)
American Journal of Human Genetics
, vol.61
, Issue.6
, pp. 1379-1387
-
-
Kuokkanen, S.1
Gschwend, M.2
Rioux, J.D.3
Daly, M.J.4
Terwilliger, J.D.5
Tienari, P.J.6
Wikstrom, J.7
Palo, J.8
Stein, L.D.9
Hudson, T.J.10
Lander, E.S.11
Peltonen, L.12
-
31
-
-
34548368541
-
Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis
-
DOI 10.1038/ng2106, PII NG2106
-
F Lundmark 2007 Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis Nat Genet 39 9 1108 1113 10.1038/ng2106 1:CAS:528:DC%2BD2sXps12gtb0%3D 17660816 (Pubitemid 47340654)
-
(2007)
Nature Genetics
, vol.39
, Issue.9
, pp. 1108-1113
-
-
Lundmark, F.1
Duvefelt, K.2
Iacobaeus, E.3
Kockum, I.4
Wallstrom, E.5
Khademi, M.6
Oturai, A.7
Ryder, L.P.8
Saarela, J.9
Harbo, H.F.10
Celius, E.G.11
Salter, H.12
Olsson, T.13
Hillert, J.14
-
32
-
-
0034955141
-
Recommended diagnostic criteria for multiple sclerosis: Guidelines from the International Panel on the Diagnosis of Multiple Sclerosis
-
DOI 10.1002/ana.1032
-
WI McDonald, et al. 2001 Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis Ann Neurol 50 1 121 127 10.1002/ana.1032 1:STN:280: DC%2BD38%2FitFOhug%3D%3D 11456302 (Pubitemid 32591472)
-
(2001)
Annals of Neurology
, vol.50
, Issue.1
, pp. 121-127
-
-
Buckley, C.1
Douek, D.2
Newsom-Davis, J.3
Vincent, A.4
Willcox, N.5
-
33
-
-
67650255063
-
Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease
-
10.1002/ibd.20855 19235914
-
DP McGovern, et al. 2009 Genetic epistasis of IL23/IL17 pathway genes in Crohn's disease Inflamm Bowel Dis 15 6 883 889 10.1002/ibd.20855 19235914
-
(2009)
Inflamm Bowel Dis
, vol.15
, Issue.6
, pp. 883-889
-
-
McGovern, D.P.1
-
34
-
-
33845669548
-
Complex gene-gene interactions in multiple sclerosis: A multifactorial approach reveals associations with inflammatory genes
-
DOI 10.1007/s10048-006-0058-9
-
AA Motsinger, et al. 2007 Complex gene-gene interactions in multiple sclerosis: a multifactorial approach reveals associations with inflammatory genes Neurogenetics 8 1 11 20 10.1007/s10048-006-0058-9 1:CAS:528: DC%2BD28XhtlShsL7M 17024427 (Pubitemid 44951514)
-
(2007)
Neurogenetics
, vol.8
, Issue.1
, pp. 11-20
-
-
Motsinger, A.A.1
Brassat, D.2
Caillier, S.J.3
Erlich, H.A.4
Walker, K.5
Steiner, L.L.6
Barcellos, L.F.7
Pericak-Vance, M.A.8
Schmidt, S.9
Gregory, S.10
Hauser, S.L.11
Haines, J.L.12
Oksenberg, J.R.13
Ritchie, M.D.14
-
35
-
-
0028128084
-
The British Isles survey of multiple sclerosis in twins
-
GL Mumford, et al. 1994 The British Isles survey of multiple sclerosis in twins Neurology 44 11 15
-
(1994)
Neurology
, vol.44
, Issue.11
, pp. 15
-
-
Mumford, G.L.1
-
36
-
-
0015273990
-
Multiple sclerosis: Association with HL-A3
-
1:STN:280:DyaE3s%2FitVOmsg%3D%3D 5077731
-
S Naito, et al. 1972 Multiple sclerosis: association with HL-A3 Tissue Antigens 2 1 1 4 1:STN:280:DyaE3s%2FitVOmsg%3D%3D 5077731
-
(1972)
Tissue Antigens
, vol.2
, Issue.1
, pp. 1-4
-
-
Naito, S.1
-
37
-
-
7044272247
-
Targeting the Jak/STAT pathway for immunosuppression
-
DOI 10.1136/ard.2004.028290
-
JJ O'Shea 2004 Targeting the Jak/STAT pathway for immunosuppression Ann Rheum Dis 63 Suppl 2 ii67 ii71 10.1136/ard.2004.028290 15479876 (Pubitemid 39424662)
-
(2004)
Annals of the Rheumatic Diseases
, vol.63
, Issue.SUPPL. 2
-
-
O'Shea, J.J.1
-
38
-
-
0034973569
-
Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer
-
DOI 10.1086/321276
-
MD Ritchie, et al. 2001 Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer Am J Hum Genet 69 1 138 147 10.1086/321276 1:CAS:528:DC%2BD3MXls1emt7k%3D 11404819 (Pubitemid 32614026)
-
(2001)
American Journal of Human Genetics
, vol.69
, Issue.1
, pp. 138-147
-
-
Ritchie, M.D.1
Hahn, L.W.2
Roodi, N.3
Bailey, L.R.4
Dupont, W.D.5
Parl, F.F.6
Moore, J.H.7
-
39
-
-
0029874022
-
Age-adjusted recurrence risks for relatives of patients with multiple sclerosis
-
10.1093/brain/119.2.449 8800940
-
NP Robertson, et al. 1996 Age-adjusted recurrence risks for relatives of patients with multiple sclerosis Brain 119 Pt 2 449 455 10.1093/brain/119.2.449 8800940
-
(1996)
Brain
, vol.119
, Issue.PT 2
, pp. 449-455
-
-
Robertson, N.P.1
-
40
-
-
0028898566
-
Genetics of multiple sclerosis
-
1:STN:280:DyaK2M3lsl2jsQ%3D%3D 7739507
-
AD Sadovnick GC Ebers 1995 Genetics of multiple sclerosis Neurol Clin 13 99 118 1:STN:280:DyaK2M3lsl2jsQ%3D%3D 7739507
-
(1995)
Neurol Clin
, vol.13
, pp. 99-118
-
-
Sadovnick, A.D.1
Ebers, G.C.2
-
41
-
-
0027537583
-
A population-based study of multiple sclerosis in twins: Update
-
AD Sadovnick, et al. 1993 A population-based study of multiple sclerosis in twins: update Annal Neurol 33 281 285 10.1002/ana.410330309 1:STN:280:DyaK3s3ntVChtA%3D%3D 8498811 (Pubitemid 23081159)
-
(1993)
Annals of Neurology
, vol.33
, Issue.3
, pp. 281-285
-
-
Sadovnick, A.D.1
Armstrong, H.2
Rice, G.P.A.3
Bulman, D.4
Hashimoto, L.5
Paty, D.W.6
Hashimoto, S.A.7
Warren, S.8
Hader, W.9
Murray, T.J.10
Seland, T.P.11
Metz, L.12
Bell, R.13
Duquette, P.14
Gray, T.15
Nelson, R.16
Weinshenker, B.17
Brunet, D.18
Ebers, G.C.19
-
42
-
-
0030007661
-
Evidence for genetic basis of multiple sclerosis
-
AD Sadovnick, et al. 1996 Evidence for genetic basis of multiple sclerosis Lancet 347 1728 1730
-
(1996)
Lancet
, vol.347
, Issue.1728
, pp. 1730
-
-
Sadovnick, A.D.1
-
43
-
-
45549092100
-
The genetics of multiple sclerosis: SNPs to pathways to pathogenesis
-
DOI 10.1038/nrg2395, PII NRG2395
-
S Sawcer 2008 The complex genetics of multiple sclerosis: pitfalls and prospects Brain 131 Pt 12 3118 3131 10.1093/brain/awn081 18490360 (Pubitemid 351861542)
-
(2008)
Nature Reviews Genetics
, vol.9
, Issue.7
, pp. 516-526
-
-
Oksenberg, J.R.1
Baranzini, S.E.2
Sawcer, S.3
Hauser, S.L.4
-
44
-
-
15844368830
-
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22
-
DOI 10.1038/ng0896-464
-
S Sawcer, et al. 1996 A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22 Nat Genet 13 464 468 10.1038/ng0896-464 1:CAS:528:DyaK28XkslOnu7g%3D 8696343 (Pubitemid 26256622)
-
(1996)
Nature Genetics
, vol.13
, Issue.4
, pp. 464-468
-
-
Sawcer, S.1
Jones, H.B.2
Feakes, R.3
Gray, J.4
Smaldon, N.5
Chataway, J.6
Robertson, N.7
Clayton, D.8
Goodfellow, P.N.9
Compston, A.10
-
45
-
-
77952092658
-
The Whole-genome Association Study Pipeline (WASP): A comprehensive tool for large-scale association studies
-
DP Sexton, et al. 2007 The Whole-genome Association Study Pipeline (WASP): a comprehensive tool for large-scale association studies Am J Hum Genet 57 413S
-
(2007)
Am J Hum Genet
, vol.57
-
-
Sexton, D.P.1
-
46
-
-
48249144457
-
Protein kinase Cepsilon: Function in neurons
-
10.1111/j.1742-4658.2008.06556.x 1:CAS:528:DC%2BD1cXhtVCltr7L 18637121
-
Y Shirai N Adachi N Saito 2008 Protein kinase Cepsilon: function in neurons FEBS J. 275 16 3988 3994 10.1111/j.1742-4658.2008.06556.x 1:CAS:528:DC%2BD1cXhtVCltr7L 18637121
-
(2008)
FEBS J.
, vol.275
, Issue.16
, pp. 3988-3994
-
-
Shirai, Y.1
Adachi, N.2
Saito, N.3
-
47
-
-
31344476038
-
Whole-genome genotyping with the single-base extension assay
-
DOI 10.1038/nmeth842, PII N842
-
FJ Steemers, et al. 2006 Whole-genome genotyping with the single-base extension assay Nat. Methods 3 1 31 33 10.1038/nmeth842 1:CAS:528: DC%2BD2MXhtlagurrI 16369550 (Pubitemid 43135346)
-
(2006)
Nature Methods
, vol.3
, Issue.1
, pp. 31-33
-
-
Steemers, F.J.1
Chang, W.2
Lee, G.3
Barker, D.L.4
Shen, R.5
Gunderson, K.L.6
-
48
-
-
17744398193
-
A meta-analysis of genomic screens in multiple sclerosis
-
DOI 10.1191/135245801669625359
-
Transatlantic Multiple Sclerosis Genetics Cooperative 2001 A meta-analysis of genomic screens in multiple sclerosis Mult Scler 7 1 3 11 10.1191/135245801669625359 (Pubitemid 32396572)
-
(2001)
Multiple Sclerosis
, vol.7
, Issue.1
, pp. 3-11
-
-
Pericak-Vance, M.A.1
Rimmler, J.B.2
Saunders, A.M.3
Martin, E.R.4
Haines, J.L.5
Garcia, M.E.6
Oksenberg, J.R.7
Barcellos, L.F.8
Lincoln, R.9
Goodkin, D.E.10
Hauser, S.L.11
Compston, D.A.S.12
Sawcer, S.J.13
Clayton, D.14
Jones, H.B.15
Walker, N.16
Goodfellow, P.N.17
Bulman, D.18
Sadovnick, D.19
Ebers, G.C.20
Dyment, D.21
Willer, C.22
Risch, N.23
more..
-
49
-
-
13144265739
-
Genome-wide association studies: Theoretical and practical concerns
-
DOI 10.1038/nrg1522
-
WY Wang, et al. 2005 Genome-wide association studies: theoretical and practical concerns Nat Rev Genet 6 2 109 118 10.1038/nrg1522 1:CAS:528:DC%2BD2MXhtFyjsrw%3D 15716907 (Pubitemid 40179533)
-
(2005)
Nature Reviews Genetics
, vol.6
, Issue.2
, pp. 109-118
-
-
Wang, W.Y.S.1
Barratt, B.J.2
Clayton, D.G.3
Todd, J.A.4
-
50
-
-
84969213492
-
Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls
-
DOI 10.1038/nature05911, PII NATURE05911
-
Wellcome Trust Case Control Consortium 2007 Genome-wide association study of 14, 000 cases of seven common diseases and 3, 000 shared controls Nature 447 7145 661 678 10.1038/nature05911 (Pubitemid 46889737)
-
(2007)
Nature
, vol.447
, Issue.7145
, pp. 661-678
-
-
Burton, P.R.1
Clayton, D.G.2
Cardon, L.R.3
Craddock, N.4
Deloukas, P.5
Duncanson, A.6
Kwiatkowski, D.P.7
McCarthy, M.I.8
Ouwehand, W.H.9
Samani, N.J.10
Todd, J.A.11
Donnelly, P.12
Barrett, J.C.13
Davison, D.14
Easton, D.15
Evans, D.16
Leung, H.-T.17
Marchini, J.L.18
Morris, A.P.19
Spencer, C.C.A.20
Tobin, M.D.21
more..
|