-
1
-
-
12144275864
-
Type 1 diabetes mellitus of man: Genetic susceptibility and resistance
-
A. Pugliese, and G.S. Eisenbarth Type 1 diabetes mellitus of man: genetic susceptibility and resistance Adv. Exp. Med. Biol. 552 2004 170 203
-
(2004)
Adv. Exp. Med. Biol.
, vol.552
, pp. 170-203
-
-
Pugliese, A.1
Eisenbarth, G.S.2
-
2
-
-
0035212224
-
A genome-wide scan for type 1 diabetes susceptibility genes in Scandinavian families. Identification of new loci with evidence of interactions
-
European Consortium for IDDM Genome Studies, A genome-wide scan for type 1 diabetes susceptibility genes in Scandinavian families. Identification of new loci with evidence of interactions, Am. J. Hum. Genet. 69 (2001) 1301-1313.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1301-1313
-
-
-
3
-
-
0034821661
-
Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families
-
N.J. Cox, B. Wapelhorst, V.A. Morrison, L. Johnson, L. Pinchuk, R.S. Spielman, J.A. Todd, and P. Concannon Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families Am. J. Hum. Genet. 69 2001 820 830
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 820-830
-
-
Cox, N.J.1
Wapelhorst, B.2
Morrison, V.A.3
Johnson, L.4
Pinchuk, L.5
Spielman, R.S.6
Todd, J.A.7
Concannon, P.8
-
4
-
-
0032544004
-
Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases
-
K.G. Becker, R.M. Simon, J.E. Bailey-Wilson, B. Freidlin, W.E. Biddison, H.F. McFarland, and J.M. Trent Clustering of non-major histocompatibility complex susceptibility candidate loci in human autoimmune diseases Proc. Natl. Acad. Sci. USA 95 1998 9979 9984
-
(1998)
Proc. Natl. Acad. Sci. USA
, vol.95
, pp. 9979-9984
-
-
Becker, K.G.1
Simon, R.M.2
Bailey-Wilson, J.E.3
Freidlin, B.4
Biddison, W.E.5
McFarland, H.F.6
Trent, J.M.7
-
5
-
-
0035555022
-
The genetics of complex autoimmune diseases: Non-MHC susceptibility genes
-
A. Wandstrat, and E. Wakeland The genetics of complex autoimmune diseases: non-MHC susceptibility genes Nat. Immunol. 2 2001 802 809
-
(2001)
Nat. Immunol.
, vol.2
, pp. 802-809
-
-
Wandstrat, A.1
Wakeland, E.2
-
6
-
-
0035004413
-
International collaboration provides convincing linkage replication in complex disease through analysis of a large pooled data set: Crohn disease and chromosome 16
-
J. Cavanaugh 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 2001 1165 1671
-
(2001)
Am. J. Hum. Genet.
, vol.68
, pp. 1165-1671
-
-
Cavanaugh, J.1
-
7
-
-
0035978651
-
Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease
-
J.P. Hugot, M. Chamaillard, H. Zouali, S. Lesage, J.P. Cezard, J. Belaiche, S. Almer, C. Tysk, C.A. O'Morain, M. Gassull, V. Binder, Y. Finkel, A. Cortot, R. Modigliani, P. Laurent-Puig, C. Gower-Rousseau, J. Macry, J.F. Colombel, M. Sahbatou, and G. Thomas Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease Nature 411 2001 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
Binder, V.11
Finkel, Y.12
Cortot, A.13
Modigliani, R.14
Laurent-Puig, P.15
Gower-Rousseau, C.16
MacRy, J.17
Colombel, J.F.18
Sahbatou, M.19
Thomas, G.20
more..
-
8
-
-
0035978533
-
A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
-
Y. Ogura, D.K. Bonen, N. Inohara, D.L. Nicolae, F.F. Chen, R. Ramos, H. Britton, T. Moran, R. Karaliuskas, R.H. Duerr, J.P. Achkar, S.R. Brant, T.M. Bayless, B.S. Kirschner, S.B. Hanauer, G. Nunez, and J.H. Cho A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease Nature 411 2001 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
Achkar, J.P.11
Brant, S.R.12
Bayless, T.M.13
Kirschner, B.S.14
Hanauer, S.B.15
Nunez, G.16
Cho, J.H.17
-
10
-
-
0041885442
-
CARD15: A pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis
-
P. Rahman, S. Bartlett, F. Siannis, F.J. Pellett, V.T. Farewell, L. Peddle, C.T. Schentag, C.A. Alderdice, S. Hamilton, M. Khraishi, Y. Tobin, D. Hefferton, and D.D. Gladman CARD15: a pleiotropic autoimmune gene that confers susceptibility to psoriatic arthritis Am. J. Hum. Genet. 73 2003 677 681
-
(2003)
Am. J. Hum. Genet.
, vol.73
, pp. 677-681
-
-
Rahman, P.1
Bartlett, S.2
Siannis, F.3
Pellett, F.J.4
Farewell, V.T.5
Peddle, L.6
Schentag, C.T.7
Alderdice, C.A.8
Hamilton, S.9
Khraishi, M.10
Tobin, Y.11
Hefferton, D.12
Gladman, D.D.13
-
11
-
-
0037393553
-
Association between polymorphisms in caspase recruitment domain containing protein 15 and allergy in two German populations
-
M. Kabesch, W. Peters, D. Carr, W. Leupold, S.K. Weiland, and E. von Mutius Association between polymorphisms in caspase recruitment domain containing protein 15 and allergy in two German populations J. Allergy Clin. Immunol. 111 2003 813 817
-
(2003)
J. Allergy Clin. Immunol.
, vol.111
, pp. 813-817
-
-
Kabesch, M.1
Peters, W.2
Carr, D.3
Leupold, W.4
Weiland, S.K.5
Von Mutius, E.6
-
12
-
-
4444253690
-
NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses
-
T. Watanabe, A. Kitani, P.J. Murray, and W. Strober NOD2 is a negative regulator of Toll-like receptor 2-mediated T helper type 1 responses Nat. Immunol. 5 2004 800 808
-
(2004)
Nat. Immunol.
, vol.5
, pp. 800-808
-
-
Watanabe, T.1
Kitani, A.2
Murray, P.J.3
Strober, W.4
-
13
-
-
13244277880
-
Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing
-
S. Maeda, L.C. Hsu, H. Liu, L.A. Bankston, M. Iimura, M.F. Kagnoff, L. Eckmann, and M. Karin Nod2 mutation in Crohn's disease potentiates NF-kappaB activity and IL-1beta processing Science 307 2005 734 738
-
(2005)
Science
, vol.307
, pp. 734-738
-
-
Maeda, S.1
Hsu, L.C.2
Liu, H.3
Bankston, L.A.4
Iimura, M.5
Kagnoff, M.F.6
Eckmann, L.7
Karin, M.8
-
14
-
-
1442332521
-
Mycobacteria and other environmental organisms as immunomodulators for immunoregulatory disorders
-
G.A. Rook, V. Adams, J. Hunt, R. Palmer, R. Martinelli, and L.R. Brunet Mycobacteria and other environmental organisms as immunomodulators for immunoregulatory disorders Springer Semin. Immunopathol. 25 2004 237 255
-
(2004)
Springer Semin. Immunopathol.
, vol.25
, pp. 237-255
-
-
Rook, G.A.1
Adams, V.2
Hunt, J.3
Palmer, R.4
Martinelli, R.5
Brunet, L.R.6
-
15
-
-
0026494911
-
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations
-
J.D. Terwilliger, and J. Ott A haplotype-based 'haplotype relative risk' approach to detecting allelic associations Hum. Hered. 42 1992 337 346
-
(1992)
Hum. Hered.
, vol.42
, pp. 337-346
-
-
Terwilliger, J.D.1
Ott, J.2
-
16
-
-
17944372335
-
CARD15 mutations in Blau syndrome
-
C. Miceli-Richard, S. Lesage, M. Rybojad, A.M. Prieur, S. Manouvrier-Hanu, R. Hafner, M. Chamaillard, H. Zouali, G. Thomas, and J.P. Hugot CARD15 mutations in Blau syndrome Nat. Genet. 29 2001 19 20
-
(2001)
Nat. Genet.
, vol.29
, pp. 19-20
-
-
Miceli-Richard, C.1
Lesage, S.2
Rybojad, M.3
Prieur, A.M.4
Manouvrier-Hanu, S.5
Hafner, R.6
Chamaillard, M.7
Zouali, H.8
Thomas, G.9
Hugot, J.P.10
-
17
-
-
19944431022
-
Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: Common genetic etiology with Blau syndrome
-
N. Kanazawa, I. Okafuji, N. Kambe, R. Nishikomori, M. Nakata-Hizume, S. Nagai, A. Fuji, T. Yuasa, A. Manki, Y. Sakurai, M. Nakajima, H. Kobayashi, I. Fujiwara, H. Tsutsumi, A. Utani, C. Nishigori, T. Heike, T. Nakahata, and Y. Miyachi Early-onset sarcoidosis and CARD15 mutations with constitutive nuclear factor-kappaB activation: common genetic etiology with Blau syndrome Blood 105 2005 1195 1197
-
(2005)
Blood
, vol.105
, pp. 1195-1197
-
-
Kanazawa, N.1
Okafuji, I.2
Kambe, N.3
Nishikomori, R.4
Nakata-Hizume, M.5
Nagai, S.6
Fuji, A.7
Yuasa, T.8
Manki, A.9
Sakurai, Y.10
Nakajima, M.11
Kobayashi, H.12
Fujiwara, I.13
Tsutsumi, H.14
Utani, A.15
Nishigori, C.16
Heike, T.17
Nakahata, T.18
Miyachi, Y.19
-
18
-
-
0345700824
-
The three most common CARD15 mutations associated with Crohn's disease and the chromosome 16 susceptibility locus for systemic lupus erythematosus
-
I. Ferreiros-Vidal, J. Garcia-Meijide, P. Carreira, F. Barros, A. Carracedo, J.J. Gomez-Reino, and A. Gonzalez The three most common CARD15 mutations associated with Crohn's disease and the chromosome 16 susceptibility locus for systemic lupus erythematosus Rheumatology (Oxford) 42 2003 570 574
-
(2003)
Rheumatology (Oxford)
, vol.42
, pp. 570-574
-
-
Ferreiros-Vidal, I.1
Garcia-Meijide, J.2
Carreira, P.3
Barros, F.4
Carracedo, A.5
Gomez-Reino, J.J.6
Gonzalez, A.7
-
19
-
-
0344406270
-
Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15
-
S. Steer, S.A. Fisher, M. Fife, A. Cuthbert, J. Newton, P. Wordsworth, C.M. Lewis, C.G. Mathew, and J.S. Lanchbury Development of rheumatoid arthritis is not associated with two polymorphisms in the Crohn's disease gene CARD15 Rheumatology (Oxford) 42 2003 304 307
-
(2003)
Rheumatology (Oxford)
, vol.42
, pp. 304-307
-
-
Steer, S.1
Fisher, S.A.2
Fife, M.3
Cuthbert, A.4
Newton, J.5
Wordsworth, P.6
Lewis, C.M.7
Mathew, C.G.8
Lanchbury, J.S.9
-
20
-
-
0036095952
-
CARD15/NOD2 analyses in spondylarthropathy
-
C. Miceli-Richard, H. Zouali, S. Lesage, G. Thomas, J.P. Hugot, R. Said-Nahal, and M. Breban CARD15/NOD2 analyses in spondylarthropathy Arthritis Rheum. 46 2002 1405 1406
-
(2002)
Arthritis Rheum.
, vol.46
, pp. 1405-1406
-
-
Miceli-Richard, C.1
Zouali, H.2
Lesage, S.3
Thomas, G.4
Hugot, J.P.5
Said-Nahal, R.6
Breban, M.7
-
21
-
-
0037227353
-
Lack of association of ankylosing spondylitis with the most common NOD2 susceptibility alleles to Crohn's disease
-
I. Ferreiros-Vidal, J. Amarelo, F. Barros, A. Carracedo, J.J. Gomez-Reino, and A. Gonzalez Lack of association of ankylosing spondylitis with the most common NOD2 susceptibility alleles to Crohn's disease J. Rheumatol. 30 2003 102 104
-
(2003)
J. Rheumatol.
, vol.30
, pp. 102-104
-
-
Ferreiros-Vidal, I.1
Amarelo, J.2
Barros, F.3
Carracedo, A.4
Gomez-Reino, J.J.5
Gonzalez, A.6
-
22
-
-
0041704527
-
Crohn's associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis
-
S. Sawcer, M. Maranian, A. Hensiek, R. Roxburgh, J. Gray, and A. Compston Crohn's associated NOD2 gene variants are not involved in determining susceptibility to multiple sclerosis J. Neurol. Neurosurg. Psychiatry 74 2003 1157
-
(2003)
J. Neurol. Neurosurg. Psychiatry
, vol.74
, pp. 1157
-
-
Sawcer, S.1
Maranian, M.2
Hensiek, A.3
Roxburgh, R.4
Gray, J.5
Compston, A.6
-
23
-
-
0036861693
-
Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population
-
P. Borgiani, L. Vallo, M.R. D'Apice, E. Giardina, S. Pucci, F. Capon, S. Nistico, S. Chimenti, F. Pallone, and G. Novelli Exclusion of CARD15/NOD2 as a candidate susceptibility gene to psoriasis in the Italian population Eur. J. Dermatol. 12 2002 540 542
-
(2002)
Eur. J. Dermatol.
, vol.12
, pp. 540-542
-
-
Borgiani, P.1
Vallo, L.2
D'Apice, M.R.3
Giardina, E.4
Pucci, S.5
Capon, F.6
Nistico, S.7
Chimenti, S.8
Pallone, F.9
Novelli, G.10
-
24
-
-
2442516014
-
Psoriatic arthritis and CARD15 gene polymorphisms: No evidence for association in the Italian population
-
E. Giardina, G. Novelli, A. Costanzo, S. Nistico, C. Bulli, C. Sinibaldi, M.L. Sorgi, S. Chimenti, F. Pallone, E. Taccari, and P. Borgiani Psoriatic arthritis and CARD15 gene polymorphisms: no evidence for association in the Italian population J. Invest. Dermatol. 122 2004 1106 1107
-
(2004)
J. Invest. Dermatol.
, vol.122
, pp. 1106-1107
-
-
Giardina, E.1
Novelli, G.2
Costanzo, A.3
Nistico, S.4
Bulli, C.5
Sinibaldi, C.6
Sorgi, M.L.7
Chimenti, S.8
Pallone, F.9
Taccari, E.10
Borgiani, P.11
-
25
-
-
21144457073
-
Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohort
-
J. Lascorz, H. Burkhardt, U. Huffmeier, B. Bohm, F. Schurmeyer-Horst, J. Lohmann, M. Stander, J. Wendler, R. Kelsch, C. Baumann, W. Kuster, H. Traupe, and A. Reis Lack of genetic association of the three more common polymorphisms of CARD15 with psoriatic arthritis and psoriasis in a German cohort Ann. Rheum. Dis. 64 2005 951 954
-
(2005)
Ann. Rheum. Dis.
, vol.64
, pp. 951-954
-
-
Lascorz, J.1
Burkhardt, H.2
Huffmeier, U.3
Bohm, B.4
Schurmeyer-Horst, F.5
Lohmann, J.6
Stander, M.7
Wendler, J.8
Kelsch, R.9
Baumann, C.10
Kuster, W.11
Traupe, H.12
Reis, A.13
-
26
-
-
18244375904
-
Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p
-
J. Hampe, H. Frenzel, M.M. Mirza, P.J. Croucher, A. Cuthbert, S. Mascheretti, K. Huse, M. Platzer, S. Bridger, B. Meyer, P. Nurnberg, P. Stokkers, M. Krawczak, C.G. Mathew, M. Curran, and S. Schreiber Evidence for a NOD2-independent susceptibility locus for inflammatory bowel disease on chromosome 16p Proc. Natl. Acad. Sci. USA 99 2002 321 326
-
(2002)
Proc. Natl. Acad. Sci. USA
, vol.99
, pp. 321-326
-
-
Hampe, J.1
Frenzel, H.2
Mirza, M.M.3
Croucher, P.J.4
Cuthbert, A.5
Mascheretti, S.6
Huse, K.7
Platzer, M.8
Bridger, S.9
Meyer, B.10
Nurnberg, P.11
Stokkers, P.12
Krawczak, M.13
Mathew, C.G.14
Curran, M.15
Schreiber, S.16
|