-
1
-
-
67649881102
-
Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20
-
ANZgene
-
ANZgene Genome-wide association study identifies new multiple sclerosis susceptibility loci on chromosomes 12 and 20. Nat. Genet. 2009, 41:824-828.
-
(2009)
Nat. Genet.
, vol.41
, pp. 824-828
-
-
-
2
-
-
70349629969
-
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor
-
Ban M., Goris A., Lorentzen A.R., Baker A., Mihalova T., Ingram G., Booth D.R., Heard R.N., Stewart G.J., Bogaert E., Dubois B., Harbo H.F., Celius E.G., Spurkland A., Strange R., Hawkins C., Robertson N.P., Dudbridge F., Wason J., De Jager P.L., Hafler D., Rioux J.D., Ivinson A.J., McCauley J.L., Pericak-Vance M., Oksenberg J.R., Hauser S.L., Sexton D., Haines J., Sawcer S. Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. Eur. J. Hum. Genet. 2009, 17:1309-1313.
-
(2009)
Eur. J. Hum. Genet.
, vol.17
, pp. 1309-1313
-
-
Ban, M.1
Goris, A.2
Lorentzen, A.R.3
Baker, A.4
Mihalova, T.5
Ingram, G.6
Booth, D.R.7
Heard, R.N.8
Stewart, G.J.9
Bogaert, E.10
Dubois, B.11
Harbo, H.F.12
Celius, E.G.13
Spurkland, A.14
Strange, R.15
Hawkins, C.16
Robertson, N.P.17
Dudbridge, F.18
Wason, J.19
De Jager, P.L.20
Hafler, D.21
Rioux, J.D.22
Ivinson, A.J.23
McCauley, J.L.24
Pericak-Vance, M.25
Oksenberg, J.R.26
Hauser, S.L.27
Sexton, D.28
Haines, J.29
Sawcer, S.30
more..
-
3
-
-
58949099391
-
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis
-
Baranzini S.E., Wang J., Gibson R.A., Galwey N., Naegelin Y., Barkhof F., Radue E.W., Lindberg R.L., Uitdehaag B.M., Johnson M.R., Angelakopoulou A., Hall L., Richardson J.C., Prinjha R.K., Gass A., Geurts J.J., Kragt J., Sombekke M., Vrenken H., Qualley P., Lincoln R.R., Gomez R., Caillier S.J., George M.F., Mousavi H., Guerrero R., Okuda D.T., Cree B.A., Green A.J., Waubant E., Goodin D.S., Pelletier D., Matthews P.M., Hauser S.L., Kappos L., Polman C.H., Oksenberg J.R. 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
Galwey, N.4
Naegelin, Y.5
Barkhof, F.6
Radue, E.W.7
Lindberg, R.L.8
Uitdehaag, B.M.9
Johnson, M.R.10
Angelakopoulou, A.11
Hall, L.12
Richardson, J.C.13
Prinjha, R.K.14
Gass, A.15
Geurts, J.J.16
Kragt, J.17
Sombekke, M.18
Vrenken, H.19
Qualley, P.20
Lincoln, R.R.21
Gomez, R.22
Caillier, S.J.23
George, M.F.24
Mousavi, H.25
Guerrero, R.26
Okuda, D.T.27
Cree, B.A.28
Green, A.J.29
Waubant, E.30
Goodin, D.S.31
Pelletier, D.32
Matthews, P.M.33
Hauser, S.L.34
Kappos, L.35
Polman, C.H.36
Oksenberg, J.R.37
more..
-
4
-
-
33646712168
-
APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers
-
Burwick R.M., Ramsay P.P., Haines J.L., Hauser S.L., Oksenberg J.R., Pericak-Vance M.A., Schmidt S., Compston A., Sawcer S., Cittadella R., Savettieri G., Quattrone A., Polman C.H., Uitdehaag B.M., Zwemmer J.N., Hawkins C.P., Ollier W.E., Weatherby S., Enzinger C., Fazekas F., Schmidt H., Schmidt R., Hillert J., Masterman T., Hogh P., Niino M., Kikuchi S., Maciel P., Santos M., Rio M.E., Kwiecinski H., Zakrzewska-Pniewska B., Evangelou N., Palace J., Barcellos L.F. APOE epsilon variation in multiple sclerosis susceptibility and disease severity: some answers. Neurology 2006, 66:1373-1383.
-
(2006)
Neurology
, vol.66
, pp. 1373-1383
-
-
Burwick, R.M.1
Ramsay, P.P.2
Haines, J.L.3
Hauser, S.L.4
Oksenberg, J.R.5
Pericak-Vance, M.A.6
Schmidt, S.7
Compston, A.8
Sawcer, S.9
Cittadella, R.10
Savettieri, G.11
Quattrone, A.12
Polman, C.H.13
Uitdehaag, B.M.14
Zwemmer, J.N.15
Hawkins, C.P.16
Ollier, W.E.17
Weatherby, S.18
Enzinger, C.19
Fazekas, F.20
Schmidt, H.21
Schmidt, R.22
Hillert, J.23
Masterman, T.24
Hogh, P.25
Niino, M.26
Kikuchi, S.27
Maciel, P.28
Santos, M.29
Rio, M.E.30
Kwiecinski, H.31
Zakrzewska-Pniewska, B.32
Evangelou, N.33
Palace, J.34
Barcellos, L.F.35
more..
-
5
-
-
77951498680
-
STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility
-
Cenit M.C., Alcina A., Marquez A., Mendoza J.L., Diaz-Rubio M., de las Heras V., Izquierdo G., Arroyo R., Fernandez O., de la Concha E.G., Matesanz F., Urcelay E. STAT3 locus in inflammatory bowel disease and multiple sclerosis susceptibility. Genes Immun. 2010, 11:264-268.
-
(2010)
Genes Immun.
, vol.11
, pp. 264-268
-
-
Cenit, M.C.1
Alcina, A.2
Marquez, A.3
Mendoza, J.L.4
Diaz-Rubio, M.5
de las Heras, V.6
Izquierdo, G.7
Arroyo, R.8
Fernandez, O.9
de la Concha, E.G.10
Matesanz, F.11
Urcelay, E.12
-
6
-
-
3242780090
-
Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis
-
Cournu-Rebeix I., Genin E., Lesca G., Azoulay-Cayla A., Tubridy N., Noe E., Clanet M., Edan G., Clerget-Darpoux F., Semana G., Fontaine B. Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis. Genes Immun. 2003, 4:518-523.
-
(2003)
Genes Immun.
, vol.4
, pp. 518-523
-
-
Cournu-Rebeix, I.1
Genin, E.2
Lesca, G.3
Azoulay-Cayla, A.4
Tubridy, N.5
Noe, E.6
Clanet, M.7
Edan, G.8
Clerget-Darpoux, F.9
Semana, G.10
Fontaine, B.11
-
7
-
-
65249155425
-
The role of the CD58 locus in multiple sclerosis
-
De Jager P.L., Baecher-Allan C., Maier L.M., Arthur A.T., Ottoboni L., Barcellos L., McCauley J.L., Sawcer S., Goris A., Saarela J., Yelensky R., Price A., Leppa V., Patterson N., de Bakker P.I., Tran D., Aubin C., Pobywajlo S., Rossin E., Hu X., Ashley C.W., Choy E., Rioux J.D., Pericak-Vance M.A., Ivinson A., Booth D.R., Stewart G.J., Palotie A., Peltonen L., Dubois B., Haines J.L., Weiner H.L., Compston A., Hauser S.L., Daly M.J., Reich D., Oksenberg J.R., Hafler D.A. The role of the CD58 locus in multiple sclerosis. Proc. Natl. Acad. Sci. U. S. A. 2009, 106:5264-5269.
-
(2009)
Proc. Natl. Acad. Sci. U. S. A.
, vol.106
, pp. 5264-5269
-
-
De Jager, P.L.1
Baecher-Allan, C.2
Maier, L.M.3
Arthur, A.T.4
Ottoboni, L.5
Barcellos, L.6
McCauley, J.L.7
Sawcer, S.8
Goris, A.9
Saarela, J.10
Yelensky, R.11
Price, A.12
Leppa, V.13
Patterson, N.14
de Bakker, P.I.15
Tran, D.16
Aubin, C.17
Pobywajlo, S.18
Rossin, E.19
Hu, X.20
Ashley, C.W.21
Choy, E.22
Rioux, J.D.23
Pericak-Vance, M.A.24
Ivinson, A.25
Booth, D.R.26
Stewart, G.J.27
Palotie, A.28
Peltonen, L.29
Dubois, B.30
Haines, J.L.31
Weiner, H.L.32
Compston, A.33
Hauser, S.L.34
Daly, M.J.35
Reich, D.36
Oksenberg, J.R.37
Hafler, D.A.38
more..
-
8
-
-
84866053994
-
Exome sequencing identifies a novel multiple sclerosis susceptibility variant in the TYK2 gene
-
Dyment D.A., Cader M.Z., Chao M.J., Lincoln M.R., Morrison K.M., Disanto G., Morahan J.M., De Luca G.C., Sadovnick A.D., Lepage P., Montpetit A., Ebers G.C., Ramagopalan S.V. 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
Lincoln, M.R.4
Morrison, K.M.5
Disanto, G.6
Morahan, J.M.7
De Luca, G.C.8
Sadovnick, A.D.9
Lepage, P.10
Montpetit, A.11
Ebers, G.C.12
Ramagopalan, S.V.13
-
9
-
-
79959660678
-
Interleukin-7 receptor alpha gene polymorphism influences multiple sclerosis risk in Asians
-
Fang L., Isobe N., Yoshimura S., Yonekawa T., Matsushita T., Masaki K., Doi H., Ochi K., Miyamoto K., Kawano Y., Kira J. Interleukin-7 receptor alpha gene polymorphism influences multiple sclerosis risk in Asians. Neurology 2011, 76:2125-2127.
-
(2011)
Neurology
, vol.76
, pp. 2125-2127
-
-
Fang, L.1
Isobe, N.2
Yoshimura, S.3
Yonekawa, T.4
Matsushita, T.5
Masaki, K.6
Doi, H.7
Ochi, K.8
Miyamoto, K.9
Kawano, Y.10
Kira, J.11
-
10
-
-
34548351247
-
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis
-
Gregory S.G., Schmidt S., Seth P., Oksenberg J.R., Hart J., Prokop A., Caillier S.J., Ban M., Goris A., Barcellos L.F., Lincoln R., McCauley J.L., Sawcer S.J., Compston D.A., Dubois B., Hauser S.L., Garcia-Blanco M.A., Pericak-Vance M.A., Haines J.L. Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis. Nat. Genet. 2007, 39:1083-1091.
-
(2007)
Nat. Genet.
, vol.39
, 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.14
Dubois, B.15
Hauser, S.L.16
Garcia-Blanco, M.A.17
Pericak-Vance, M.A.18
Haines, J.L.19
-
11
-
-
34548299105
-
Risk alleles for multiple sclerosis identified by a genomewide study
-
Hafler D.A., Compston A., Sawcer S., Lander E.S., Daly M.J., De Jager P.L., de Bakker P.I., Gabriel S.B., Mirel D.B., Ivinson A.J., Pericak-Vance M.A., Gregory S.G., Rioux J.D., McCauley J.L., Haines J.L., Barcellos L.F., Cree B., Oksenberg J.R., Hauser S.L. Risk alleles for multiple sclerosis identified by a genomewide study. N. Engl. J. Med. 2007, 357:851-862.
-
(2007)
N. Engl. J. Med.
, vol.357
, 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.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
-
12
-
-
74049085453
-
Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis
-
Hoppenbrouwers I.A., Aulchenko Y.S., Janssens A.C., Ramagopalan S.V., Broer L., Kayser M., Ebers G.C., Oostra B.A., van Duijn C.M., Hintzen R.Q. Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis. J. Hum. Genet. 2009, 54:676-680.
-
(2009)
J. Hum. Genet.
, vol.54
, pp. 676-680
-
-
Hoppenbrouwers, I.A.1
Aulchenko, Y.S.2
Janssens, A.C.3
Ramagopalan, S.V.4
Broer, L.5
Kayser, M.6
Ebers, G.C.7
Oostra, B.A.8
van Duijn, C.M.9
Hintzen, R.Q.10
-
13
-
-
4143091289
-
Apolipoprotein E: diversity of cellular origins, structural and biophysical properties, and effects in Alzheimer's disease
-
Huang Y., Weisgraber K.H., Mucke L., Mahley R.W. Apolipoprotein E: diversity of cellular origins, structural and biophysical properties, and effects in Alzheimer's disease. J. Mol. Neurosci. 2004, 23:189-204.
-
(2004)
J. Mol. Neurosci.
, vol.23
, pp. 189-204
-
-
Huang, Y.1
Weisgraber, K.H.2
Mucke, L.3
Mahley, R.W.4
-
14
-
-
49849091315
-
Refining genetic associations in multiple sclerosis
-
IMSGC
-
IMSGC Refining genetic associations in multiple sclerosis. Lancet Neurol. 2008, 7:567-569.
-
(2008)
Lancet Neurol.
, vol.7
, pp. 567-569
-
-
-
15
-
-
59149093148
-
The expanding genetic overlap between multiple sclerosis and type I diabetes
-
IMSGC
-
IMSGC The expanding genetic overlap between multiple sclerosis and type I diabetes. Genes Immun. 2009, 10:11-14.
-
(2009)
Genes Immun.
, vol.10
, pp. 11-14
-
-
-
16
-
-
84860488313
-
HLA-DRB1*15:01 and multiple sclerosis: a female association?
-
Irizar H., Munoz-Culla M., Zuriarrain O., Goyenechea E., Castillo-Trivino T., Prada A., Saenz-Cuesta M., De Juan D., Lopez de Munain A., Olascoaga J., Otaegui D. HLA-DRB1*15:01 and multiple sclerosis: a female association?. Mult. Scler. 2011, 18:569-577.
-
(2011)
Mult. Scler.
, vol.18
, pp. 569-577
-
-
Irizar, H.1
Munoz-Culla, M.2
Zuriarrain, O.3
Goyenechea, E.4
Castillo-Trivino, T.5
Prada, A.6
Saenz-Cuesta, M.7
De Juan, D.8
Lopez de Munain, A.9
Olascoaga, J.10
Otaegui, D.11
-
17
-
-
76049083598
-
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 gene
-
Jakkula E., Leppa V., Sulonen A.M., Varilo T., Kallio S., Kemppinen A., Purcell S., Koivisto K., Tienari P., Sumelahti M.L., Elovaara I., Pirttila T., Reunanen M., Aromaa A., Oturai A.B., Sondergaard H.B., Harbo H.F., Mero I.L., Gabriel S.B., Mirel D.B., Hauser S.L., Kappos L., Polman C., De Jager P.L., Hafler D.A., Daly M.J., Palotie A., Saarela J., Peltonen L. 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
Leppa, V.2
Sulonen, A.M.3
Varilo, T.4
Kallio, S.5
Kemppinen, A.6
Purcell, S.7
Koivisto, K.8
Tienari, P.9
Sumelahti, M.L.10
Elovaara, I.11
Pirttila, T.12
Reunanen, M.13
Aromaa, A.14
Oturai, A.B.15
Sondergaard, H.B.16
Harbo, H.F.17
Mero, I.L.18
Gabriel, S.B.19
Mirel, D.B.20
Hauser, S.L.21
Kappos, L.22
Polman, C.23
De Jager, P.L.24
Hafler, D.A.25
Daly, M.J.26
Palotie, A.27
Saarela, J.28
Peltonen, L.29
more..
-
18
-
-
45249112573
-
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations
-
Kristjansdottir G., Sandling J.K., Bonetti A., Roos I.M., Milani L., Wang C., Gustafsdottir S.M., Sigurdsson S., Lundmark A., Tienari P.J., Koivisto K., Elovaara I., Pirttila T., Reunanen M., Peltonen L., Saarela J., Hillert J., Olsson T., Landegren U., Alcina A., Fernandez O., Leyva L., Guerrero M., Lucas M., Izquierdo G., Matesanz F., Syvanen A.C. Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations. J. Med. Genet. 2008, 45:362-369.
-
(2008)
J. Med. Genet.
, vol.45
, pp. 362-369
-
-
Kristjansdottir, G.1
Sandling, J.K.2
Bonetti, A.3
Roos, I.M.4
Milani, L.5
Wang, C.6
Gustafsdottir, S.M.7
Sigurdsson, S.8
Lundmark, A.9
Tienari, P.J.10
Koivisto, K.11
Elovaara, I.12
Pirttila, T.13
Reunanen, M.14
Peltonen, L.15
Saarela, J.16
Hillert, J.17
Olsson, T.18
Landegren, U.19
Alcina, A.20
Fernandez, O.21
Leyva, L.22
Guerrero, M.23
Lucas, M.24
Izquierdo, G.25
Matesanz, F.26
Syvanen, A.C.27
more..
-
19
-
-
84870262595
-
Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects
-
Lill C.M., Liu T., Schjeide B.M., Roehr J.T., Akkad D.A., Damotte V., Alcina A., Ortiz M.A., Arroyo R., Lopez de Lapuente A., Blaschke P., Winkelmann A., Gerdes L.A., Luessi F., Fernadez O., Izquierdo G., Antiguedad A., Hoffjan S., Cournu-Rebeix I., Gromoller S., Faber H., Liebsch M., Meissner E., Chanvillard C., Touze E., Pico F., Corcia P., Dorner T., Steinhagen-Thiessen E., Baeckman L., Heekeren H.R., Li S.C., Lindenberger U., Chan A., Hartung H.P., Aktas O., Lohse P., Kumpfel T., Kubisch C., Epplen J.T., Zettl U.K., Fontaine B., Vandenbroeck K., Matesanz F., Urcelay E., Bertram L., Zipp F. Closing the case of APOE in multiple sclerosis: no association with disease risk in over 29 000 subjects. J. Med. Genet. 2012, 49:558-562.
-
(2012)
J. Med. Genet.
, vol.49
, pp. 558-562
-
-
Lill, C.M.1
Liu, T.2
Schjeide, B.M.3
Roehr, J.T.4
Akkad, D.A.5
Damotte, V.6
Alcina, A.7
Ortiz, M.A.8
Arroyo, R.9
Lopez de Lapuente, A.10
Blaschke, P.11
Winkelmann, A.12
Gerdes, L.A.13
Luessi, F.14
Fernadez, O.15
Izquierdo, G.16
Antiguedad, A.17
Hoffjan, S.18
Cournu-Rebeix, I.19
Gromoller, S.20
Faber, H.21
Liebsch, M.22
Meissner, E.23
Chanvillard, C.24
Touze, E.25
Pico, F.26
Corcia, P.27
Dorner, T.28
Steinhagen-Thiessen, E.29
Baeckman, L.30
Heekeren, H.R.31
Li, S.C.32
Lindenberger, U.33
Chan, A.34
Hartung, H.P.35
Aktas, O.36
Lohse, P.37
Kumpfel, T.38
Kubisch, C.39
Epplen, J.T.40
Zettl, U.K.41
Fontaine, B.42
Vandenbroeck, K.43
Matesanz, F.44
Urcelay, E.45
Bertram, L.46
Zipp, F.47
more..
-
20
-
-
44449136105
-
+ T cells prevents development of experimental autoimmune diseases
-
+ T cells prevents development of experimental autoimmune diseases. J. Immunol. 2008, 180:6070-6076.
-
(2008)
J. Immunol.
, vol.180
, pp. 6070-6076
-
-
Liu, X.1
Lee, Y.S.2
Yu, C.R.3
Egwuagu, C.E.4
-
21
-
-
34548368541
-
Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis
-
Lundmark F., Duvefelt K., Iacobaeus E., Kockum I., Wallstrom E., Khademi M., Oturai A., Ryder L.P., Saarela J., Harbo H.F., Celius E.G., Salter H., Olsson T., Hillert J. Variation in interleukin 7 receptor alpha chain (IL7R) influences risk of multiple sclerosis. Nat. Genet. 2007, 39:1108-1113.
-
(2007)
Nat. Genet.
, vol.39
, 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
-
22
-
-
66349085616
-
Apolipoprotein E: structure determines function, from atherosclerosis to Alzheimer's disease to AIDS
-
(Suppl.)
-
Mahley R.W., Weisgraber K.H., Huang Y. Apolipoprotein E: structure determines function, from atherosclerosis to Alzheimer's disease to AIDS. J. Lipid Res. 2009, 50:S183-S188. (Suppl.).
-
(2009)
J. Lipid Res.
, vol.50
-
-
Mahley, R.W.1
Weisgraber, K.H.2
Huang, Y.3
-
23
-
-
0033029507
-
The role of CTLA-4 in the regulation of T cell immune responses
-
McCoy K.D., Le Gros G. The role of CTLA-4 in the regulation of T cell immune responses. Immunol. Cell Biol. 1999, 77:1-10.
-
(1999)
Immunol. Cell Biol.
, vol.77
, pp. 1-10
-
-
McCoy, K.D.1
Le Gros, G.2
-
24
-
-
0034955141
-
Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis
-
McDonald W.I., Compston A., Edan G., Goodkin D., Hartung H.P., Lublin F.D., McFarland H.F., Paty D.W., Polman C.H., Reingold S.C., Sandberg-Wollheim M., Sibley W., Thompson A., van den Noort S., Weinshenker B.Y., Wolinsky J.S. Recommended diagnostic criteria for multiple sclerosis: guidelines from the International Panel on the diagnosis of multiple sclerosis. Ann. Neurol. 2001, 50:121-127.
-
(2001)
Ann. Neurol.
, vol.50
, pp. 121-127
-
-
McDonald, W.I.1
Compston, A.2
Edan, G.3
Goodkin, D.4
Hartung, H.P.5
Lublin, F.D.6
McFarland, H.F.7
Paty, D.W.8
Polman, C.H.9
Reingold, S.C.10
Sandberg-Wollheim, M.11
Sibley, W.12
Thompson, A.13
van den Noort, S.14
Weinshenker, B.Y.15
Wolinsky, J.S.16
-
25
-
-
77949658437
-
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis
-
Mero I.L., Lorentzen A.R., Ban M., Smestad C., Celius E.G., Aarseth J.H., Myhr K.M., Link J., Hillert J., Olsson T., Kockum I., Masterman T., Oturai A.B., Sondergaard H.B., Sellebjerg F., Saarela J., Kemppinen A., Elovaara I., Spurkland A., Dudbridge F., Lie B.A., Harbo H.F. A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. Eur. J. Hum. Genet. 2010, 18:502-504.
-
(2010)
Eur. J. Hum. Genet.
, vol.18
, pp. 502-504
-
-
Mero, I.L.1
Lorentzen, A.R.2
Ban, M.3
Smestad, C.4
Celius, E.G.5
Aarseth, J.H.6
Myhr, K.M.7
Link, J.8
Hillert, J.9
Olsson, T.10
Kockum, I.11
Masterman, T.12
Oturai, A.B.13
Sondergaard, H.B.14
Sellebjerg, F.15
Saarela, J.16
Kemppinen, A.17
Elovaara, I.18
Spurkland, A.19
Dudbridge, F.20
Lie, B.A.21
Harbo, H.F.22
more..
-
26
-
-
0031947049
-
Multiple sclerosis: the increased frequency of the ICAM-1 exon 6 gene point mutation genetic type K469
-
Mycko M.P., Kwinkowski M., Tronczynska E., Szymanska B., Selmaj K.W. Multiple sclerosis: the increased frequency of the ICAM-1 exon 6 gene point mutation genetic type K469. Ann. Neurol. 1998, 44:70-75.
-
(1998)
Ann. Neurol.
, vol.44
, pp. 70-75
-
-
Mycko, M.P.1
Kwinkowski, M.2
Tronczynska, E.3
Szymanska, B.4
Selmaj, K.W.5
-
27
-
-
20244388365
-
Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis
-
Nejentsev S., Laaksonen M., Tienari P.J., Fernandez O., Cordell H., Ruutiainen J., Wikstrom J., Pastinen T., Kuokkanen S., Hillert J., Ilonen J. Intercellular adhesion molecule-1 K469E polymorphism: study of association with multiple sclerosis. Hum. Immunol. 2003, 64:345-349.
-
(2003)
Hum. Immunol.
, vol.64
, pp. 345-349
-
-
Nejentsev, S.1
Laaksonen, M.2
Tienari, P.J.3
Fernandez, O.4
Cordell, H.5
Ruutiainen, J.6
Wikstrom, J.7
Pastinen, T.8
Kuokkanen, S.9
Hillert, J.10
Ilonen, J.11
-
28
-
-
39049159767
-
IL7RA polymorphisms and susceptibility to multiple sclerosis
-
O'Doherty C., Kantarci O., Vandenbroeck K. IL7RA polymorphisms and susceptibility to multiple sclerosis. N. Engl. J. Med. 2008, 358:753-754.
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 753-754
-
-
O'Doherty, C.1
Kantarci, O.2
Vandenbroeck, K.3
-
29
-
-
79951523735
-
Evaluation of the established non-MHC multiple sclerosis loci in an Indian population
-
Pandit L., Ban M., Sawcer S., Singhal B., Nair S., Radhakrishnan K., Shetty R., Misri Z., Hegde S., Bhat I.G. Evaluation of the established non-MHC multiple sclerosis loci in an Indian population. Mult. Scler. 2011, 17:139-143.
-
(2011)
Mult. Scler.
, vol.17
, pp. 139-143
-
-
Pandit, L.1
Ban, M.2
Sawcer, S.3
Singhal, B.4
Nair, S.5
Radhakrishnan, K.6
Shetty, R.7
Misri, Z.8
Hegde, S.9
Bhat, I.G.10
-
30
-
-
67349258910
-
Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus
-
Perera D., Stankovich J., Butzkueven H., Taylor B.V., Foote S.J., Kilpatrick T.J., Rubio J.P. Fine mapping of multiple sclerosis susceptibility genes provides evidence of allelic heterogeneity at the IL2RA locus. J. Neuroimmunol. 2009, 211:105-109.
-
(2009)
J. Neuroimmunol.
, vol.211
, pp. 105-109
-
-
Perera, D.1
Stankovich, J.2
Butzkueven, H.3
Taylor, B.V.4
Foote, S.J.5
Kilpatrick, T.J.6
Rubio, J.P.7
-
31
-
-
0020686503
-
New diagnostic criteria for multiple sclerosis: guidelines for research protocols
-
Poser C.M., Paty D.W., Scheinberg L., McDonald W.I., Davis F.A., Ebers G.C., Johnson K.P., Sibley W.A., Silberberg D.H., Tourtellotte W.W. New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Ann. Neurol. 1983, 13:227-231.
-
(1983)
Ann. Neurol.
, vol.13
, pp. 227-231
-
-
Poser, C.M.1
Paty, D.W.2
Scheinberg, L.3
McDonald, W.I.4
Davis, F.A.5
Ebers, G.C.6
Johnson, K.P.7
Sibley, W.A.8
Silberberg, D.H.9
Tourtellotte, W.W.10
-
32
-
-
67651152724
-
Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians
-
Rubio J.P., Stankovich J., Field J., Tubridy N., Marriott M., Chapman C., Bahlo M., Perera D., Johnson L.J., Tait B.D., Varney M.D., Speed T.P., Taylor B.V., Foote S.J., Butzkueven H., Kilpatrick T.J. Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians. Genes Immun. 2008, 9:624-630.
-
(2008)
Genes Immun.
, vol.9
, pp. 624-630
-
-
Rubio, J.P.1
Stankovich, J.2
Field, J.3
Tubridy, N.4
Marriott, M.5
Chapman, C.6
Bahlo, M.7
Perera, D.8
Johnson, L.J.9
Tait, B.D.10
Varney, M.D.11
Speed, T.P.12
Taylor, B.V.13
Foote, S.J.14
Butzkueven, H.15
Kilpatrick, T.J.16
-
33
-
-
0035130704
-
HLA-DRB1 DNA sequencing based typing: an approach suitable for high throughput typing including unrelated bone marrow registry donors
-
Sayer D., Whidborne R., Brestovac B., Trimboli F., Witt C., Christiansen F. HLA-DRB1 DNA sequencing based typing: an approach suitable for high throughput typing including unrelated bone marrow registry donors. Tissue Antigens 2001, 57:46-54.
-
(2001)
Tissue Antigens
, vol.57
, pp. 46-54
-
-
Sayer, D.1
Whidborne, R.2
Brestovac, B.3
Trimboli, F.4
Witt, C.5
Christiansen, F.6
-
34
-
-
78049504134
-
Differential roles for endothelial ICAM-1, ICAM-2, and VCAM-1 in shear-resistant T cell arrest, polarization, and directed crawling on blood-brain barrier endothelium
-
Steiner O., Coisne C., Cecchelli R., Boscacci R., Deutsch U., Engelhardt B., Lyck R. Differential roles for endothelial ICAM-1, ICAM-2, and VCAM-1 in shear-resistant T cell arrest, polarization, and directed crawling on blood-brain barrier endothelium. J. Immunol. 2010, 185:4846-4855.
-
(2010)
J. Immunol.
, vol.185
, pp. 4846-4855
-
-
Steiner, O.1
Coisne, C.2
Cecchelli, R.3
Boscacci, R.4
Deutsch, U.5
Engelhardt, B.6
Lyck, R.7
-
35
-
-
70349673166
-
Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy
-
van der Walt A., Stankovich J., Bahlo M., Taylor B.V., van der Mei I.A., Foote S.J., Kilpatrick T.J., Rubio J.P., Butzkueven H. Apolipoprotein genotype does not influence MS severity, cognition, or brain atrophy. Neurology 2009, 73:1018-1025.
-
(2009)
Neurology
, vol.73
, pp. 1018-1025
-
-
van der Walt, A.1
Stankovich, J.2
Bahlo, M.3
Taylor, B.V.4
van der Mei, I.A.5
Foote, S.J.6
Kilpatrick, T.J.7
Rubio, J.P.8
Butzkueven, H.9
-
36
-
-
79951713725
-
Apolipoprotein E in Alzheimer's disease and other neurological disorders
-
Verghese P.B., Castellano J.M., Holtzman D.M. Apolipoprotein E in Alzheimer's disease and other neurological disorders. Lancet Neurol. 2011, 10:241-252.
-
(2011)
Lancet Neurol.
, vol.10
, pp. 241-252
-
-
Verghese, P.B.1
Castellano, J.M.2
Holtzman, D.M.3
-
37
-
-
80051684615
-
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
-
WTCCC
-
WTCCC Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. Nature 2011, 476:214-219.
-
(2011)
Nature
, vol.476
, pp. 214-219
-
-
-
38
-
-
77249176523
-
HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in Western Australia
-
Wu J.S., James I., Qiu W., Castley A., Christiansen F.T., Carroll W.M., Mastaglia F.L., Kermode A.G. HLA-DRB1 allele heterogeneity influences multiple sclerosis severity as well as risk in Western Australia. J. Neuroimmunol. 2010, 219:109-113.
-
(2010)
J. Neuroimmunol.
, vol.219
, pp. 109-113
-
-
Wu, J.S.1
James, I.2
Qiu, W.3
Castley, A.4
Christiansen, F.T.5
Carroll, W.M.6
Mastaglia, F.L.7
Kermode, A.G.8
-
39
-
-
20144388185
-
Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis
-
Zhang Z., Duvefelt K., Svensson F., Masterman T., Jonasdottir G., Salter H., Emahazion T., Hellgren D., Falk G., Olsson T., Hillert J., Anvret M. Two genes encoding immune-regulatory molecules (LAG3 and IL7R) confer susceptibility to multiple sclerosis. Genes Immun. 2005, 6:145-152.
-
(2005)
Genes Immun.
, vol.6
, pp. 145-152
-
-
Zhang, Z.1
Duvefelt, K.2
Svensson, F.3
Masterman, T.4
Jonasdottir, G.5
Salter, H.6
Emahazion, T.7
Hellgren, D.8
Falk, G.9
Olsson, T.10
Hillert, J.11
Anvret, M.12
|