-
1
-
-
0034660559
-
Searching for genetic determinants in the new millennium
-
Risch, N.J. (2000) Searching for genetic determinants in the new millennium. Nature, 405, 847-856.
-
(2000)
Nature
, vol.405
, pp. 847-856
-
-
Risch, N.J.1
-
2
-
-
15844368830
-
A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22
-
Sawcer, S., Jones, H.B., Feakes, R., Gray, J., Smaldon, N., Chataway, J., Robertson, N., Clayton, D., Goodfellow, P.N. and Compston, A. (1996) A genome screen in multiple sclerosis reveals susceptibility loci on chromosome 6p21 and 17q22. Nat. Genet., 13, 464-468.
-
(1996)
Nat. Genet.
, vol.13
, 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
-
3
-
-
0009573338
-
A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex
-
The Multiple Sclerosis Genetics Group
-
Haines, J.L., Ter Minassian, M., Bazyk, A., Gusella, J.F., Kim, D.J., Terwedow, H., Pericak-Vance, M.A., Rimmler, J.B., Haynes, C.S., Roses, A.D. 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, 469-471.
-
(1996)
Nat. Genet.
, vol.13
, 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
-
4
-
-
15844366743
-
A full genome search in multiple sclerosis
-
Ebers, G.C., Kukay, K., Bulman, D.E., Sadovnick, A.D., Rice, G., Anderson, C., Armstrong, H., Cousin, K., Bell, R.B., Hader, W. et al. (1996) A full genome search in multiple sclerosis. Nat. Genet., 13, 472-476.
-
(1996)
Nat. Genet.
, vol.13
, 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
-
5
-
-
17344367913
-
Genomewide scan of multiple sclerosis in Finnish multiplex families
-
Kuokkanen, S., Gschwend, M., Rioux, J.D., Daly, M.J., Terwilliger, J.D., Tienari, P.J., Wikstrom, J., Palo, J., Stein, L.D., Hudson, T.J. et al. (1997) Genomewide scan of multiple sclerosis in Finnish multiplex families. Am. J. Hum. Genet., 61, 1379-1387.
-
(1997)
Am. J. Hum. Genet.
, vol.61
, 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
-
6
-
-
18044401149
-
A genome screen for multiple sclerosis in Italian families
-
Broadley, S., Sawcer, S., D'Alfonso, S., Hensiek, A., Coraddu, F., Gray, J., Roxburgh, R., Clayton, D., Buttinelli, C., Quattrone, A. et al. (2001) A genome screen for multiple sclerosis in Italian families. Genes Immun., 2, 205-210.
-
(2001)
Genes Immun.
, vol.2
, pp. 205-210
-
-
Broadley, S.1
Sawcer, S.2
D'Alfonso, S.3
Hensiek, A.4
Coraddu, F.5
Gray, J.6
Roxburgh, R.7
Clayton, D.8
Buttinelli, C.9
Quattrone, A.10
-
7
-
-
17944373274
-
A genome screen for multiple sclerosis in Sardinian multiplex families
-
Coraddu, F., Sawcer, S., D'Alfonso, S., Lai, M., Hensiek, A., Solla, E., Broadley, S., Mancosu, C., Pugliatti, M., Marrosu, M.G. and Compston, A. (2001) A genome screen for multiple sclerosis in Sardinian multiplex families. Eur. J. Hum. Genet., 9, 621-626.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 621-626
-
-
Coraddu, F.1
Sawcer, S.2
D'Alfonso, S.3
Lai, M.4
Hensiek, A.5
Solla, E.6
Broadley, S.7
Mancosu, C.8
Pugliatti, M.9
Marrosu, M.G.10
Compston, A.11
-
8
-
-
0036691491
-
A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis
-
Akesson, E., Oturai, A., Berg, J., Fredrikson, S., Andersen, O., Harbo, H.F., Laaksonen, M., Myhr, K.M., Nyland, H.I., Ryder, L.P. et al. (2002) A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis. Genes Immun., 3, 279-285.
-
(2002)
Genes Immun.
, vol.3
, pp. 279-285
-
-
Akesson, E.1
Oturai, A.2
Berg, J.3
Fredrikson, S.4
Andersen, O.5
Harbo, H.F.6
Laaksonen, M.7
Myhr, K.M.8
Nyland, H.I.9
Ryder, L.P.10
-
9
-
-
0042914324
-
A genome screen for linkage in Australian sibling-pairs with multiple sclerosis
-
Ban, M., Stewart, G.J., Bennetts, B.H., Heard, R., Simmons, R., Maranian, M., Compston, A. and Sawcer, S.J. (2002) A genome screen for linkage in Australian sibling-pairs with multiple sclerosis. Genes Immun., 3, 464-469.
-
(2002)
Genes Immun.
, vol.3
, pp. 464-469
-
-
Ban, M.1
Stewart, G.J.2
Bennetts, B.H.3
Heard, R.4
Simmons, R.5
Maranian, M.6
Compston, A.7
Sawcer, S.J.8
-
10
-
-
10744229264
-
A whole genome screen for linkage in Turkish multiple sclerosis
-
Eraksoy, M., Kurtuncu, M., Akman-Demir, G., Kilinc, M., Gedizlioglu, M., Mirza, M., Anlar, O., Kutlu, C., Demirkiran, M., Idrisoglu, H.A. et al. (2003) A whole genome screen for linkage in Turkish multiple sclerosis. J. Neuroimmunol., 143, 17-24.
-
(2003)
J. Neuroimmunol.
, vol.143
, pp. 17-24
-
-
Eraksoy, M.1
Kurtuncu, M.2
Akman-Demir, G.3
Kilinc, M.4
Gedizlioglu, M.5
Mirza, M.6
Anlar, O.7
Kutlu, C.8
Demirkiran, M.9
Idrisoglu, H.A.10
-
11
-
-
0142155199
-
Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis
-
Hensiek, A.E., Roxburgh, R., Smilie, B., Coraddu, F., Akesson, E., Holmans, P., Sawcer, S.J. and Compston, D.A. (2003) Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis. J. Neuroimmunol., 143, 25-30.
-
(2003)
J. Neuroimmunol.
, vol.143
, pp. 25-30
-
-
Hensiek, A.E.1
Roxburgh, R.2
Smilie, B.3
Coraddu, F.4
Akesson, E.5
Holmans, P.6
Sawcer, S.J.7
Compston, D.A.8
-
12
-
-
0142186253
-
GAMES and the Transatlantic Multiple Sclerosis Cooperative. A meta-analysis of whole genome linkage screens in multiple sclerosis
-
GAMES and the Transatlantic Multiple Sclerosis Cooperative (2003) A meta-analysis of whole genome linkage screens in multiple sclerosis. J. Neuroimmunol., 143, 39-46.
-
(2003)
J. Neuroimmunol.
, vol.143
, pp. 39-46
-
-
-
13
-
-
0033975139
-
Multiple sclerosis: A modifying influence of HLA class I genes in an HLA class II associated autoimmune disease
-
Fogdell-Hahn, A., Ligers, A., Gronning, M., Hillert, J. and Olerup, O. (2000) Multiple sclerosis: a modifying influence of HLA class I genes in an HLA class II associated autoimmune disease. Tissue Antigens, 55, 140-148.
-
(2000)
Tissue Antigens
, vol.55
, pp. 140-148
-
-
Fogdell-Hahn, A.1
Ligers, A.2
Gronning, M.3
Hillert, J.4
Olerup, O.5
-
14
-
-
0029996490
-
Affected-sib-pair interval mapping and exclusion for complex genetic traits: Sampling considerations
-
Hauser, E.R., Boehnke, M., Guo, S.W. and Risch, N. (1996) Affected-sib-pair interval mapping and exclusion for complex genetic traits: sampling considerations. Genet. Epidemiol., 13, 117-137.
-
(1996)
Genet. Epidemiol.
, vol.13
, pp. 117-137
-
-
Hauser, E.R.1
Boehnke, M.2
Guo, S.W.3
Risch, N.4
-
15
-
-
18544381909
-
A high-resolution recombination map of the human genome
-
Kong, A., Gudbjartsson, D.F., Sainz, J., Jonsdottir, G.M., Gudjonsson, S.A., Richardsson, B., Sigurdardottir, S., Barnard, J., Hallbeck, B., Masson, G. et al. (2002) A high-resolution recombination map of the human genome. Nat. Genet., 31, 241-247.
-
(2002)
Nat. Genet.
, vol.31
, pp. 241-247
-
-
Kong, A.1
Gudbjartsson, D.F.2
Sainz, J.3
Jonsdottir, G.M.4
Gudjonsson, S.A.5
Richardsson, B.6
Sigurdardottir, S.7
Barnard, J.8
Hallbeck, B.9
Masson, G.10
-
16
-
-
0020532390
-
Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping
-
Lathrop, G.M., Hooper, A.B., Huntsman, J.W. and Ward, R.H. (1983) Evaluating pedigree data. I. The estimation of pedigree error in the presence of marker mistyping. Am. J. Hum. Genet., 35, 241-262.
-
(1983)
Am. J. Hum. Genet.
, vol.35
, pp. 241-262
-
-
Lathrop, G.M.1
Hooper, A.B.2
Huntsman, J.W.3
Ward, R.H.4
-
17
-
-
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. (1993) Molecular and statistical approaches to the detection and correction of errors in genotype databases. Am. J. Hum. Genet., 53, 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
-
18
-
-
0035131982
-
The impact of genotyping error on family-based analysis of quantitative traits
-
Abecasis, G.R., Cherny, S.S. and Cardon, L.R. (2001) The impact of genotyping error on family-based analysis of quantitative traits. Eur. J. Hum. Genet., 9, 130-134.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 130-134
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cardon, L.R.3
-
19
-
-
0036338150
-
Merlin - Rapid analysis of dense genetic maps using sparse gene flow trees
-
Abecasis, G.R., Cherny, S.S., Cookson, W.O. and Cardon, L.R. (2002) Merlin - rapid analysis of dense genetic maps using sparse gene flow trees. Nat. Genet., 30, 97-101.
-
(2002)
Nat. Genet.
, vol.30
, pp. 97-101
-
-
Abecasis, G.R.1
Cherny, S.S.2
Cookson, W.O.3
Cardon, L.R.4
-
20
-
-
0025019555
-
Linkage strategies for genetically complex traits. I. Multilocus models
-
Risch, N. (1990) Linkage strategies for genetically complex traits. I. Multilocus models. Am. J. Hum. Genet., 46, 222-228.
-
(1990)
Am. J. Hum. Genet.
, vol.46
, pp. 222-228
-
-
Risch, N.1
-
21
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
Cavanaugh, J. (2001) International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16. Am. J. Hum. Genet., 68, 1165-1171.
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1165-1171
-
-
Cavanaugh, J.1
-
22
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
Hugot, J.P., Chamaillard, M., Zouali, H., Lesage, S., Cezard, J.P., Belaiche, J., Almer, S., Tysk, C., O'Morain, C.A., Gassull, M. et al. (2001) Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease. Nature, 411, 599-603.
-
(2001)
Nature
, vol.411
, pp. 599-603
-
-
Hugot, J.P.1
Chamaillard, M.2
Zouali, H.3
Lesage, S.4
Cezard, J.P.5
Belaiche, J.6
Almer, S.7
Tysk, C.8
O'Morain, C.A.9
Gassull, M.10
-
23
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Ogura, Y., Bonen, D.K., Inohara, N., Nicolae, D.L., Chen, F.F., Ramos, R., Britton, H., Moran, T., Karaliuskas, R., Duerr, R.H. et al. (2001) A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature, 411, 603-606.
-
(2001)
Nature
, vol.411
, pp. 603-606
-
-
Ogura, Y.1
Bonen, D.K.2
Inohara, N.3
Nicolae, D.L.4
Chen, F.F.5
Ramos, R.6
Britton, H.7
Moran, T.8
Karaliuskas, R.9
Duerr, R.H.10
-
24
-
-
4544237553
-
Replication of linkage on 2p for chronic mucocutaneous candidiasis and thyroid disease using two different high-density SNP genome scan technologies
-
(Suppl. poster) 1911
-
Tsai, Y.Y., Pugh, E.W., Boyce, P., Doheny, K.F., Fan, Y.T., Scott, A.F., St Hansen, M., Oliphant, A., Loi, H., Mei, R. and Puck, J.M. (2003) Replication of linkage on 2p for chronic mucocutaneous candidiasis and thyroid disease using two different high-density SNP genome scan technologies. Am. J. Hum. Genet., 73 (suppl. poster) 1911, 495.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 495
-
-
Tsai, Y.Y.1
Pugh, E.W.2
Boyce, P.3
Doheny, K.F.4
Fan, Y.T.5
Scott, A.F.6
St Hansen, M.7
Oliphant, A.8
Loi, H.9
Mei, R.10
Puck, J.M.11
-
25
-
-
2342635193
-
Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: A comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22
-
Middleton, F.A., Pato, M.T., Gentile, K.L., Morley, C.P., Zhao, X., Eisener, A.F., Brown, A., Petryshen, T.L., Kirby, A.N., Medeiros, H. et al. (2004) Genomewide linkage analysis of bipolar disorder by use of a high-density single-nucleotide-polymorphism (SNP) genotyping assay: a comparison with microsatellite marker assays and finding of significant linkage to chromosome 6q22. Am. J. Hum. Genet., 74, 886-897.
-
(2004)
Am. J. Hum. Genet.
, vol.74
, pp. 886-897
-
-
Middleton, F.A.1
Pato, M.T.2
Gentile, K.L.3
Morley, C.P.4
Zhao, X.5
Eisener, A.F.6
Brown, A.7
Petryshen, T.L.8
Kirby, A.N.9
Medeiros, H.10
-
26
-
-
3042548992
-
Whole-genome scan, in a complex disease, using 11 245 single-nucleotide polymorphisms: Comparison with microsatellites
-
John, S., Shephard, N., Liu, G., Zeggini, E., Cao, M., Chen, W., Vasavda, N., Mills, T., Barton, A., Hinks, A. et al. (2004) Whole-genome scan, in a complex disease, using 11 245 single-nucleotide polymorphisms: comparison with microsatellites. Am. J. Hum. Genet., 75, 54-64.
-
(2004)
Am. J. Hum. Genet.
, vol.75
, pp. 54-64
-
-
John, S.1
Shephard, N.2
Liu, G.3
Zeggini, E.4
Cao, M.5
Chen, W.6
Vasavda, N.7
Mills, T.8
Barton, A.9
Hinks, A.10
-
27
-
-
4544334546
-
High density SNP linkage panel for human genetic studies
-
(suppl. poster) 1813
-
Shaw, S. (2003) High density SNP linkage panel for human genetic studies. Am. J. Hum. Genet., 73 (suppl. poster) 1813, 479.
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 479
-
-
Shaw, S.1
-
28
-
-
0036263896
-
A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility
-
Sawcer, S., Maranian, M., Setakis, E., Curwen, V., Akesson, E., Hensiek, A., Coraddu, F., Roxburgh, R., Sawcer, D., Gray, J. et al. (2002) A whole genome screen for linkage disequilibrium in multiple sclerosis confirms disease associations with regions previously linked to susceptibility. Brain, 125, 1337-1347.
-
(2002)
Brain
, vol.125
, pp. 1337-1347
-
-
Sawcer, S.1
Maranian, M.2
Setakis, E.3
Curwen, V.4
Akesson, E.5
Hensiek, A.6
Coraddu, F.7
Roxburgh, R.8
Sawcer, D.9
Gray, J.10
-
29
-
-
0029886532
-
Parametric and nonparametric linkage analysis: A unified multipoint approach
-
Kruglyak, L., Daly, M.J., Reeve-Daly, M.P. and Lander, E.S. (1996) Parametric and nonparametric linkage analysis: a unified multipoint approach. Am. J. Hum. Genet., 58, 1347-1363.
-
(1996)
Am. J. Hum. Genet.
, vol.58
, pp. 1347-1363
-
-
Kruglyak, L.1
Daly, M.J.2
Reeve-Daly, M.P.3
Lander, E.S.4
-
30
-
-
17444436401
-
The genetics of multiple sclerosis: Principles, background and updated results of the United Kingdom systematic genome screen
-
Chataway, J., Feakes, R., Coraddu, F., Gray, J., Deans, J., Fraser, M., Robertson, N., Broadley, S., Jones, H., Clayton, D. et al. (1998) The genetics of multiple sclerosis: principles, background and updated results of the United Kingdom systematic genome screen. Brain, 121, 1869-1887.
-
(1998)
Brain
, vol.121
, pp. 1869-1887
-
-
Chataway, J.1
Feakes, R.2
Coraddu, F.3
Gray, J.4
Deans, J.5
Fraser, M.6
Robertson, N.7
Broadley, S.8
Jones, H.9
Clayton, D.10
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