-
1
-
-
0036866635
-
Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design
-
Barratt B.J., Payne F., Rance H.E., Nutland S., Todd J.A., and Clayton D.G. Identification of the sources of error in allele frequency estimations from pooled DNA indicates an optimal experimental design. Ann. Hum. Genet. 66 (2002) 393-405
-
(2002)
Ann. Hum. Genet.
, vol.66
, pp. 393-405
-
-
Barratt, B.J.1
Payne, F.2
Rance, H.E.3
Nutland, S.4
Todd, J.A.5
Clayton, D.G.6
-
2
-
-
11144292728
-
The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis
-
Begovich A.B., Caillier S.J., Alexander H.C., Penko J.M., Hauser S.L., Barcellos L.F., and Oksenberg J.R. The R620W polymorphism of the protein tyrosine phosphatase PTPN22 is not associated with multiple sclerosis. Am. J. Hum. Genet. 76 (2005) 184-187
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 184-187
-
-
Begovich, A.B.1
Caillier, S.J.2
Alexander, H.C.3
Penko, J.M.4
Hauser, S.L.5
Barcellos, L.F.6
Oksenberg, J.R.7
-
3
-
-
7044264955
-
How to track and assess genotyping errors in population genetics studies
-
Bonin A., Bellemain E., Bronken E.P., Pompanon F., Brochmann C., and Taberlet P. How to track and assess genotyping errors in population genetics studies. Mol. Ecol. 13 (2004) 3261-3273
-
(2004)
Mol. Ecol.
, vol.13
, pp. 3261-3273
-
-
Bonin, A.1
Bellemain, E.2
Bronken, E.P.3
Pompanon, F.4
Brochmann, C.5
Taberlet, P.6
-
4
-
-
12144291502
-
A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes
-
Bottini N., Musumeci L., Alonso A., Rahmouni S., Nika K., Rostamkhani M., MacMurray J., Meloni G.F., Lucarelli P., Pellecchia M., Eisenbarth G.S., Comings D., and Mustelin T. A functional variant of lymphoid tyrosine phosphatase is associated with type I diabetes. Nat. Genet. 36 (2004) 337-338
-
(2004)
Nat. Genet.
, vol.36
, pp. 337-338
-
-
Bottini, N.1
Musumeci, L.2
Alonso, A.3
Rahmouni, S.4
Nika, K.5
Rostamkhani, M.6
MacMurray, J.7
Meloni, G.F.8
Lucarelli, P.9
Pellecchia, M.10
Eisenbarth, G.S.11
Comings, D.12
Mustelin, T.13
-
5
-
-
0027514896
-
Molecular and statistical approaches to the detection and correction of errors in genotype databases
-
Brzustowicz L.M., Merette C., Xie X., Townsend L., Gilliam T.C., and Ott J. Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am. J. Hum. Genet. 53 (1993) 1137-1145
-
(1993)
Am. J. Hum. Genet.
, vol.53
, pp. 1137-1145
-
-
Brzustowicz, L.M.1
Merette, C.2
Xie, X.3
Townsend, L.4
Gilliam, T.C.5
Ott, J.6
-
6
-
-
0037029424
-
Multiple sclerosis
-
Compston A., and Coles A. Multiple sclerosis. Lancet 359 (2002) 1221-1231
-
(2002)
Lancet
, vol.359
, pp. 1221-1231
-
-
Compston, A.1
Coles, A.2
-
7
-
-
0017109389
-
B-lymphocyte alloantigens associated with multiple sclerosis
-
Compston D.A., Batchelor J.R., and McDonald W.I. B-lymphocyte alloantigens associated with multiple sclerosis. Lancet 2 (1976) 1261-1265
-
(1976)
Lancet
, vol.2
, pp. 1261-1265
-
-
Compston, D.A.1
Batchelor, J.R.2
McDonald, W.I.3
-
8
-
-
20144387851
-
Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes
-
Criswell L.A., Pfeiffer K.A., Lum R.F., Gonzales B., Novitzke J., Kern M., Moser K.L., Begovich A.B., Carlton V.E., Li W., Lee A.T., Ortmann W., Behrens T.W., and Gregersen P.K. Analysis of families in the multiple autoimmune disease genetics consortium (MADGC) collection: the PTPN22 620W allele associates with multiple autoimmune phenotypes. Am. J. Hum. Genet. 76 (2005) 561-571
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 561-571
-
-
Criswell, L.A.1
Pfeiffer, K.A.2
Lum, R.F.3
Gonzales, B.4
Novitzke, J.5
Kern, M.6
Moser, K.L.7
Begovich, A.B.8
Carlton, V.E.9
Li, W.10
Lee, A.T.11
Ortmann, W.12
Behrens, T.W.13
Gregersen, P.K.14
-
9
-
-
18044401969
-
The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis
-
Dai K.Z., Harbo H.F., Celius E.G., Oturai A., Sorensen P.S., Ryder L.P., Datta P., Svejgaard A., Hillert J., Fredrikson S., Sandberg-Wollheim M., Laaksonen M., Myhr K.M., Nyland H., Vartdal F., and Spurkland A. The T cell regulator gene SH2D2A contributes to the genetic susceptibility of multiple sclerosis. Genes Immun. 2 (2001) 263-268
-
(2001)
Genes Immun.
, vol.2
, pp. 263-268
-
-
Dai, K.Z.1
Harbo, H.F.2
Celius, E.G.3
Oturai, A.4
Sorensen, P.S.5
Ryder, L.P.6
Datta, P.7
Svejgaard, A.8
Hillert, J.9
Fredrikson, S.10
Sandberg-Wollheim, M.11
Laaksonen, M.12
Myhr, K.M.13
Nyland, H.14
Vartdal, F.15
Spurkland, A.16
-
10
-
-
12344265251
-
Comparison of two screening methods for in-house genotyping in clinical pharmacology units
-
Darimont J., Grosch S., Skarke C., Geisslinger G., and Lotsch J. Comparison of two screening methods for in-house genotyping in clinical pharmacology units. Int. J. Clin. Pharmacol. Ther. 43 (2005) 17-22
-
(2005)
Int. J. Clin. Pharmacol. Ther.
, vol.43
, pp. 17-22
-
-
Darimont, J.1
Grosch, S.2
Skarke, C.3
Geisslinger, G.4
Lotsch, J.5
-
11
-
-
0036184219
-
No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study
-
Dyment D.A., Steckley J.L., Willer C.J., Armstrong H., Sadovnick A.D., Risch N., and Ebers G.C. No evidence to support CTLA-4 as a susceptibility gene in MS families: the Canadian Collaborative Study. J. Neuroimmunol. 123 (2002) 193-198
-
(2002)
J. Neuroimmunol.
, vol.123
, pp. 193-198
-
-
Dyment, D.A.1
Steckley, J.L.2
Willer, C.J.3
Armstrong, H.4
Sadovnick, A.D.5
Risch, N.6
Ebers, G.C.7
-
13
-
-
4344622641
-
TCR beta polymorphisms and multiple sclerosis
-
Dyment D.A., Steckley J.L., Morrison K., Willer C.J., Cader M.Z., DeLuca G.C., Sadovnick A.D., Risch N., and Ebers G.C. TCR beta polymorphisms and multiple sclerosis. Genes Immun. 5 (2004) 337-342
-
(2004)
Genes Immun.
, vol.5
, pp. 337-342
-
-
Dyment, D.A.1
Steckley, J.L.2
Morrison, K.3
Willer, C.J.4
Cader, M.Z.5
DeLuca, G.C.6
Sadovnick, A.D.7
Risch, N.8
Ebers, G.C.9
-
14
-
-
26444469579
-
Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance
-
Dyment D.A., Herrera B.M., Cader M.Z., Willer C.J., Lincoln M.R., Sadovnick A.D., Risch N., and Ebers G.C. Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance. Hum. Mol. Genet. 14 (2005) 2019-2026
-
(2005)
Hum. Mol. Genet.
, vol.14
, pp. 2019-2026
-
-
Dyment, D.A.1
Herrera, B.M.2
Cader, M.Z.3
Willer, C.J.4
Lincoln, M.R.5
Sadovnick, A.D.6
Risch, N.7
Ebers, G.C.8
-
15
-
-
0041468563
-
Population screening of single-nucleotide polymorphisms exemplified by analysis of 8000 alleles
-
Ekstrom P.O., Bjorheim J., Gaudernack G., and Giercksky K.E. Population screening of single-nucleotide polymorphisms exemplified by analysis of 8000 alleles. J. Biomol. Screen. 7 (2002) 501-506
-
(2002)
J. Biomol. Screen.
, vol.7
, pp. 501-506
-
-
Ekstrom, P.O.1
Bjorheim, J.2
Gaudernack, G.3
Giercksky, K.E.4
-
16
-
-
0001430252
-
DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory
-
Fischer S.G., and Lerman L.S. DNA fragments differing by single base-pair substitutions are separated in denaturing gradient gels: correspondence with melting theory. Proc. Natl. Acad. Sci. U. S. A. 80 (1983) 1579-1583
-
(1983)
Proc. Natl. Acad. Sci. U. S. A.
, vol.80
, pp. 1579-1583
-
-
Fischer, S.G.1
Lerman, L.S.2
-
18
-
-
0015492877
-
HL-A antigens and multiple sclerosis
-
Jersild C., Svejgaard A., and Fog T. HL-A antigens and multiple sclerosis. Lancet 1 (1972) 1240-1241
-
(1972)
Lancet
, vol.1
, pp. 1240-1241
-
-
Jersild, C.1
Svejgaard, A.2
Fog, T.3
-
19
-
-
15044364239
-
Regulatory polymorphisms underlying complex disease traits
-
Knight J.C. Regulatory polymorphisms underlying complex disease traits. J. Mol. Med. 83 (2005) 97-109
-
(2005)
J. Mol. Med.
, vol.83
, pp. 97-109
-
-
Knight, J.C.1
-
20
-
-
0347093674
-
DNA variants in the ATM gene are not associated with sporadic rectal cancer in a Norwegian population-based study
-
Kristensen A.T., Bjorheim J., Wiig J., Giercksky K.E., and Ekstrom P.O. DNA variants in the ATM gene are not associated with sporadic rectal cancer in a Norwegian population-based study. Int. J. Colorectal Dis. 19 (2004) 49-54
-
(2004)
Int. J. Colorectal Dis.
, vol.19
, pp. 49-54
-
-
Kristensen, A.T.1
Bjorheim, J.2
Wiig, J.3
Giercksky, K.E.4
Ekstrom, P.O.5
-
21
-
-
0034139830
-
CTLA-4 in autoimmune diseases-a general susceptibility gene to autoimmunity?
-
Kristiansen O.P., Larsen Z.M., and Pociot F. CTLA-4 in autoimmune diseases-a general susceptibility gene to autoimmunity?. Genes Immun. 1 (2000) 170-184
-
(2000)
Genes Immun.
, vol.1
, pp. 170-184
-
-
Kristiansen, O.P.1
Larsen, Z.M.2
Pociot, F.3
-
22
-
-
4143105691
-
Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE
-
Kyogoku C., Langefeld C.D., Ortmann W.A., Lee A., Selby S., Carlton V.E., Chang M., Ramos P., Baechler E.C., Batliwalla F.M., Novitzke J., Williams A.H., Gillett C., Rodine P., Graham R.R., Ardlie K.G., Gaffney P.M., Moser K.L., Petri M., Begovich A.B., Gregersen P.K., and Behrens T.W. Genetic association of the R620W polymorphism of protein tyrosine phosphatase PTPN22 with human SLE. Am. J. Hum. Genet. 75 (2004) 504-507
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 504-507
-
-
Kyogoku, C.1
Langefeld, C.D.2
Ortmann, W.A.3
Lee, A.4
Selby, S.5
Carlton, V.E.6
Chang, M.7
Ramos, P.8
Baechler, E.C.9
Batliwalla, F.M.10
Novitzke, J.11
Williams, A.H.12
Gillett, C.13
Rodine, P.14
Graham, R.R.15
Ardlie, K.G.16
Gaffney, P.M.17
Moser, K.L.18
Petri, M.19
Begovich, A.B.20
Gregersen, P.K.21
Behrens, T.W.22
more..
-
23
-
-
23044468792
-
Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients
-
Lorentzen A.R., Celius E.G., Ekstrom P.O., Wiencke K., Lie B.A., Myhr K.M., Ling V., Thorsby E., Vartdal F., Spurkland A., and Harbo H.F. Lack of association with the CD28/CTLA4/ICOS gene region among Norwegian multiple sclerosis patients. J. Neuroimmunol. 166 (2005) 197-201
-
(2005)
J. Neuroimmunol.
, vol.166
, pp. 197-201
-
-
Lorentzen, A.R.1
Celius, E.G.2
Ekstrom, P.O.3
Wiencke, K.4
Lie, B.A.5
Myhr, K.M.6
Ling, V.7
Thorsby, E.8
Vartdal, F.9
Spurkland, A.10
Harbo, H.F.11
-
24
-
-
23844551123
-
Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis
-
Matesanz F., Rueda B., Orozco G., Fernandez O., Leyva L., Alcina A., and Martin J. Protein tyrosine phosphatase gene (PTPN22) polymorphism in multiple sclerosis. J. Neurol. (2005)
-
(2005)
J. Neurol.
-
-
Matesanz, F.1
Rueda, B.2
Orozco, G.3
Fernandez, O.4
Leyva, L.5
Alcina, A.6
Martin, J.7
-
25
-
-
28444460187
-
Multiple sclerosis genetics: leaving no stone unturned
-
Oksenberg J.R., and Barcellos L.F. Multiple sclerosis genetics: leaving no stone unturned. Genes Immun. 6 (2005) 375-387
-
(2005)
Genes Immun.
, vol.6
, pp. 375-387
-
-
Oksenberg, J.R.1
Barcellos, L.F.2
-
26
-
-
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., and Tourtellotte W.W. New diagnostic criteria for multiple sclerosis: guidelines for research protocols. Intern. Med. J. 13 (1983) 227-231
-
(1983)
Intern. Med. J.
, 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
-
27
-
-
29244433178
-
No evidence of a significant role for CTLA-4 in multiple sclerosis
-
Roxburgh R.H., Sawcer S., Maranian M., Seaman S., Hensiek A., Yeo T., Deans J., and Compston A. No evidence of a significant role for CTLA-4 in multiple sclerosis. J. Neuroimmunol. 171 (2006) 193-197
-
(2006)
J. Neuroimmunol.
, vol.171
, pp. 193-197
-
-
Roxburgh, R.H.1
Sawcer, S.2
Maranian, M.3
Seaman, S.4
Hensiek, A.5
Yeo, T.6
Deans, J.7
Compston, A.8
-
28
-
-
0345414139
-
Altered thymic T-cell selection due to a mutation of the ZAP-70 gene causes autoimmune arthritis in mice
-
Sakaguchi N., Takahashi T., Hata H., Nomura T., Tagami T., Yamazaki S., Sakihama T., Matsutani T., Negishi I., Nakatsuru S., and Sakaguchi S. Altered thymic T-cell selection due to a mutation of the ZAP-70 gene causes autoimmune arthritis in mice. Nature 426 (2003) 454-460
-
(2003)
Nature
, vol.426
, pp. 454-460
-
-
Sakaguchi, N.1
Takahashi, T.2
Hata, H.3
Nomura, T.4
Tagami, T.5
Yamazaki, S.6
Sakihama, T.7
Matsutani, T.8
Negishi, I.9
Nakatsuru, S.10
Sakaguchi, S.11
-
29
-
-
0142248427
-
The genetic analysis of multiple sclerosis in Europeans: concepts and design
-
Sawcer S., and Compston A. The genetic analysis of multiple sclerosis in Europeans: concepts and design. J. Neuroimmunol. 143 (2003) 13-16
-
(2003)
J. Neuroimmunol.
, vol.143
, pp. 13-16
-
-
Sawcer, S.1
Compston, A.2
-
30
-
-
0024406282
-
A susceptibility locus for multiple sclerosis is linked to the T cell receptor beta chain complex
-
Seboun E., Robinson M.A., Doolittle T.H., Ciulla T.A., Kindt T.J., and Hauser S.L. A susceptibility locus for multiple sclerosis is linked to the T cell receptor beta chain complex. Cell 57 (1989) 1095-1100
-
(1989)
Cell
, vol.57
, pp. 1095-1100
-
-
Seboun, E.1
Robinson, M.A.2
Doolittle, T.H.3
Ciulla, T.A.4
Kindt, T.J.5
Hauser, S.L.6
-
31
-
-
0142186257
-
Statistical analysis of the GAMES studies
-
Setakis E. Statistical analysis of the GAMES studies. J. Neuroimmunol. 143 (2003) 47-52
-
(2003)
J. Neuroimmunol.
, vol.143
, pp. 47-52
-
-
Setakis, E.1
-
32
-
-
3242682494
-
Genetic association between juvenile rheumatoid arthritis and polymorphism in the SH2D2A gene
-
Smerdel A., Dai K.Z., Lorentzen A.R., Flato B., Maslinski S., Thorsby E., Forre O., and Spurkland A. Genetic association between juvenile rheumatoid arthritis and polymorphism in the SH2D2A gene. Genes Immun. 5 (2004) 310-312
-
(2004)
Genes Immun.
, vol.5
, pp. 310-312
-
-
Smerdel, A.1
Dai, K.Z.2
Lorentzen, A.R.3
Flato, B.4
Maslinski, S.5
Thorsby, E.6
Forre, O.7
Spurkland, A.8
-
34
-
-
1242295125
-
Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients
-
Teutsch S.M., Booth D.R., Bennetts B.H., Heard R.N., and Stewart G.J. Association of common T cell activation gene polymorphisms with multiple sclerosis in Australian patients. J. Neuroimmunol. 148 (2004) 218-230
-
(2004)
J. Neuroimmunol.
, vol.148
, pp. 218-230
-
-
Teutsch, S.M.1
Booth, D.R.2
Bennetts, B.H.3
Heard, R.N.4
Stewart, G.J.5
-
37
-
-
20844452226
-
Association analysis of the 1858C > T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases
-
Viken M.K., Amundsen S.S., Kvien T.K., Boberg K.M., Gilboe I.M., Lilleby V., Sollid L.M., Forre O.T., Thorsby E., Smerdel A., and Lie B.A. Association analysis of the 1858C > T polymorphism in the PTPN22 gene in juvenile idiopathic arthritis and other autoimmune diseases. Genes Immun. 6 (2005) 271-273
-
(2005)
Genes Immun.
, vol.6
, pp. 271-273
-
-
Viken, M.K.1
Amundsen, S.S.2
Kvien, T.K.3
Boberg, K.M.4
Gilboe, I.M.5
Lilleby, V.6
Sollid, L.M.7
Forre, O.T.8
Thorsby, E.9
Smerdel, A.10
Lie, B.A.11
-
38
-
-
0016752595
-
B-cell alloantigen Ag 7a in multiple sclerosis
-
Winchester R., Ebers G., Fu S.M., Espinosa L., Zabriskie J., and Kunkel H.G. B-cell alloantigen Ag 7a in multiple sclerosis. Lancet 2 (1975) 814
-
(1975)
Lancet
, vol.2
, pp. 814
-
-
Winchester, R.1
Ebers, G.2
Fu, S.M.3
Espinosa, L.4
Zabriskie, J.5
Kunkel, H.G.6
-
39
-
-
0036699521
-
Cblb is a major susceptibility gene for rat type 1 diabetes mellitus
-
Yokoi N., Komeda K., Wang H.Y., Yano H., Kitada K., Saitoh Y., Seino Y., Yasuda K., Serikawa T., and Seino S. Cblb is a major susceptibility gene for rat type 1 diabetes mellitus. Nat. Genet. 31 (2002) 391-394
-
(2002)
Nat. Genet.
, vol.31
, pp. 391-394
-
-
Yokoi, N.1
Komeda, K.2
Wang, H.Y.3
Yano, H.4
Kitada, K.5
Saitoh, Y.6
Seino, Y.7
Yasuda, K.8
Serikawa, T.9
Seino, S.10
|