-
1
-
-
0025360899
-
Criteria for diagnosis of Behcet's disease
-
International Study Group for Behcet's Disease
-
(1990) Criteria for diagnosis of Behcet's disease. International Study Group for Behcet's Disease. Lancet 335:1078-1080
-
(1990)
Lancet
, vol.335
, pp. 1078-1080
-
-
-
2
-
-
0018657559
-
Behcet's syndrome: A family study and the elucidation of a genetic role
-
443880 10.1136/ard.38.2.118 1:STN:280:DyaE1M7os1eisQ%3D%3D
-
Berman L, Trappler B, Jenkins T (1979) Behcet's syndrome: a family study and the elucidation of a genetic role. Ann Rheum Dis 38:118-121
-
(1979)
Ann Rheum Dis
, vol.38
, pp. 118-121
-
-
Berman, L.1
Trappler, B.2
Jenkins, T.3
-
3
-
-
0018173593
-
A family study of Behcet's syndrome
-
718279 10.1136/ard.37.5.459 1:STN:280:DyaE1M%2FmtFWntA%3D%3D
-
Chamberlain MA (1978) A family study of Behcet's syndrome. Ann Rheum Dis 37:459-465
-
(1978)
Ann Rheum Dis
, vol.37
, pp. 459-465
-
-
Chamberlain, M.A.1
-
4
-
-
84855161941
-
CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population
-
10.1093/rheumatology/ker345 1:CAS:528:DC%2BC3MXhs12htLfN
-
Chen F, Hou S, Jiang Z, Chen Y, Kijlstra A, Rosenbaum JT, Yang P (2012a) CD40 gene polymorphisms confer risk of Behcet's disease but not of Vogt-Koyanagi-Harada syndrome in a Han Chinese population. Rheumatology (Oxford) 51:47-51
-
(2012)
Rheumatology (Oxford)
, vol.51
, pp. 47-51
-
-
Chen, F.1
Hou, S.2
Jiang, Z.3
Chen, Y.4
Kijlstra, A.5
Rosenbaum, J.T.6
Yang, P.7
-
5
-
-
84867496591
-
JAK1 gene polymorphisms are associated with the outcomes of hepatitis B virus infection, but not with alpha interferon therapy response in a Han Chinese population
-
22901011 10.1089/gtmb.2012.0141
-
Chen K, Min H, Wu X, Zhu X, Li Z, Li H, Liu Y (2012b) JAK1 gene polymorphisms are associated with the outcomes of hepatitis B virus infection, but not with alpha interferon therapy response in a Han Chinese population. Genet Test Mol Biomarkers 16:1206-1210
-
(2012)
Genet Test Mol Biomarkers
, vol.16
, pp. 1206-1210
-
-
Chen, K.1
Min, H.2
Wu, X.3
Zhu, X.4
Li, Z.5
Li, H.6
Liu, Y.7
-
6
-
-
70349768117
-
HLA-B51/B5 and the risk of Behcet's disease: A systematic review and meta-analysis of case-control genetic association studies
-
19790126 10.1002/art.24642
-
de Menthon M, Lavalley MP, Maldini C, Guillevin L, Mahr A (2009) HLA-B51/B5 and the risk of Behcet's disease: a systematic review and meta-analysis of case-control genetic association studies. Arthritis Rheum 61:1287-1296
-
(2009)
Arthritis Rheum
, vol.61
, pp. 1287-1296
-
-
De Menthon, M.1
Lavalley, M.P.2
Maldini, C.3
Guillevin, L.4
Mahr, A.5
-
7
-
-
70350141054
-
Cytokine gene polymorphisms in Behcet's disease and their association with clinical and laboratory findings
-
19796538 1:STN:280:DC%2BD1MjlslChsQ%3D%3D
-
Dilek K, Ozcimen AA, Saricaoglu H, Saba D, Yucel A, Yurtkuran M, Yurtkuran M, Oral HB (2009) Cytokine gene polymorphisms in Behcet's disease and their association with clinical and laboratory findings. Clin Exp Rheumatol 27:S73-S78
-
(2009)
Clin Exp Rheumatol
, vol.27
-
-
Dilek, K.1
Ozcimen, A.A.2
Saricaoglu, H.3
Saba, D.4
Yucel, A.5
Yurtkuran, M.6
Yurtkuran, M.7
Oral, H.B.8
-
8
-
-
33751435160
-
Autoimmunity vs autoinflammation in Behcet's disease: Do we oversimplify a complex disorder?
-
10.1093/rheumatology/kel329 1:STN:280:DC%2BD28notlGjug%3D%3D
-
Direskeneli H (2006) Autoimmunity vs autoinflammation in Behcet's disease: do we oversimplify a complex disorder? Rheumatology (Oxford) 45:1461-1465
-
(2006)
Rheumatology (Oxford)
, vol.45
, pp. 1461-1465
-
-
Direskeneli, H.1
-
9
-
-
0036133044
-
AliBaba2: Context specific identification of transcription factor binding sites
-
11808873
-
Grabe N (2002) AliBaba2: context specific identification of transcription factor binding sites. In Silico Biol 2:S1-S15
-
(2002)
In Silico Biol
, vol.2
-
-
Grabe, N.1
-
10
-
-
0033623688
-
Familial aggregation of Behcet's disease in Turkey
-
10913059 10.1136/ard.59.8.622 1:STN:280:DC%2BD3cvjt1amuw%3D%3D
-
Gul A, Inanc M, Ocal L, Aral O, Konice M (2000) Familial aggregation of Behcet's disease in Turkey. Ann Rheum Dis 59:622-625
-
(2000)
Ann Rheum Dis
, vol.59
, pp. 622-625
-
-
Gul, A.1
Inanc, M.2
Ocal, L.3
Aral, O.4
Konice, M.5
-
11
-
-
0035147053
-
Evidence for linkage of the HLA-B locus in Behcet's disease, obtained using the transmission disequilibrium test
-
11212166 10.1002/1529-0131(200101)44:1<239: AID-ANR31>3.0.CO;2-X 1:CAS:528:DC%2BD3MXht1yhsr8%3D
-
Gul A, Hajeer AH, Worthington J, Barrett JH, Ollier WE, Silman AJ (2001) Evidence for linkage of the HLA-B locus in Behcet's disease, obtained using the transmission disequilibrium test. Arthritis Rheum 44:239-240
-
(2001)
Arthritis Rheum
, vol.44
, pp. 239-240
-
-
Gul, A.1
Hajeer, A.H.2
Worthington, J.3
Barrett, J.H.4
Ollier, W.E.5
Silman, A.J.6
-
12
-
-
84887403196
-
Identification of JAK1 as a candidate inflammatory signalling pathway by genome-wide expression profiling in monocytes from patients with Behcet's disease
-
Haner D, Joseph JB, Filiz TO, Vuslat Y, Emel E-D, Dorian H, Güher S-D (2010) Identification of JAK1 as a candidate inflammatory signalling pathway by genome-wide expression profiling in monocytes from patients with Behcet's disease. Clin Exp Rheumatol 28:S108-S108
-
(2010)
Clin Exp Rheumatol
, vol.28
-
-
Haner, D.1
Joseph, J.B.2
Filiz, T.O.3
Vuslat, Y.4
Emel, E.-D.5
Dorian, H.6
Güher, S.-D.7
-
13
-
-
0345659216
-
A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis
-
14608357 10.1038/ng1268 1:CAS:528:DC%2BD3sXpt1Ciu70%3D
-
Helms C, Cao L, Krueger JG, Wijsman EM, Chamian F, Gordon D, Heffernan M, Daw JA, Robarge J, Ott J, Kwok PY, Menter A, Bowcock AM (2003) A putative RUNX1 binding site variant between SLC9A3R1 and NAT9 is associated with susceptibility to psoriasis. Nat Genet 35:349-356
-
(2003)
Nat Genet
, vol.35
, pp. 349-356
-
-
Helms, C.1
Cao, L.2
Krueger, J.G.3
Wijsman, E.M.4
Chamian, F.5
Gordon, D.6
Heffernan, M.7
Daw, J.A.8
Robarge, J.9
Ott, J.10
Kwok, P.Y.11
Menter, A.12
Bowcock, A.M.13
-
14
-
-
51249087940
-
SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease
-
18657476 10.1016/j.clim.2008.06.006 1:CAS:528:DC%2BD1cXhtFansLzO
-
Hou S, Yang P, Du L, Zhou H, Lin X, Liu X, Kijlstra A (2008) SUMO4 gene polymorphisms in Chinese Han patients with Behcet's disease. Clin Immunol 129:170-175
-
(2008)
Clin Immunol
, vol.129
, pp. 170-175
-
-
Hou, S.1
Yang, P.2
Du, L.3
Zhou, H.4
Lin, X.5
Liu, X.6
Kijlstra, A.7
-
15
-
-
84858993405
-
Replication study confirms the association between UBAC2 and Behcet's disease in two independent Chinese sets of patients and controls
-
22455605 10.1186/ar3789 1:CAS:528:DC%2BC38XnvFWktL4%3D
-
Hou S, Shu Q, Jiang Z, Chen Y, Li F, Chen F, Kijlstra A, Yang P (2012a) Replication study confirms the association between UBAC2 and Behcet's disease in two independent Chinese sets of patients and controls. Arthritis Res Ther 14:R70
-
(2012)
Arthritis Res Ther
, vol.14
, pp. 70
-
-
Hou, S.1
Shu, Q.2
Jiang, Z.3
Chen, Y.4
Li, F.5
Chen, F.6
Kijlstra, A.7
Yang, P.8
-
16
-
-
84871027597
-
Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behcet's disease susceptibility
-
Hou S, Xiao X, Li F, Jiang Z, Kijlstra A, Yang P (2012b) Two-stage association study in Chinese Han identifies two independent associations in CCR1/CCR3 locus as candidate for Behcet's disease susceptibility. Hum Genet 131:1841-1850
-
(2012)
Hum Genet
, vol.131
, pp. 1841-1850
-
-
Hou, S.1
Xiao, X.2
Li, F.3
Jiang, Z.4
Kijlstra, A.5
Yang, P.6
-
17
-
-
84871620678
-
Genetic variant on PDGFRL associated with Behcet's disease in Chinese Han populations
-
Hou S, Xiao X, Zhou Y, Zhu X, Li F, Kijlstra A, Yang P (2012c) Genetic variant on PDGFRL associated with Behcet's disease in Chinese Han populations. Hum Mutat 34:74-78
-
(2012)
Hum Mutat
, vol.34
, pp. 74-78
-
-
Hou, S.1
Xiao, X.2
Zhou, Y.3
Zhu, X.4
Li, F.5
Kijlstra, A.6
Yang, P.7
-
18
-
-
84870326659
-
Genome-wide association study identifies susceptible locus in STAT4 for Behcet's disease in Han Chinese
-
Hou S, Yang Z, Du L, Jiang Z, Shu Q, Chen Y, Li F, Zhou Q, Ohno S, Chen R, Kijlstra A, Rosenbaum JT, Yang P (2012d) Genome-wide association study identifies susceptible locus in STAT4 for Behcet's disease in Han Chinese. Arthritis Rheum 64:4104-4113
-
(2012)
Arthritis Rheum
, vol.64
, pp. 4104-4113
-
-
Hou, S.1
Yang, Z.2
Du, L.3
Jiang, Z.4
Shu, Q.5
Chen, Y.6
Li, F.7
Zhou, Q.8
Ohno, S.9
Chen, R.10
Kijlstra, A.11
Rosenbaum, J.T.12
Yang, P.13
-
19
-
-
79958778683
-
Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population
-
21674708 10.1002/ibd.21532
-
Hradsky O, Dusatkova P, Lenicek M, Bronsky J, Duricova D, Nevoral J, Vitek L, Lukas M, Cinek O (2011) Two independent genetic factors responsible for the associations of the IBD5 locus with Crohn's disease in the Czech population. Inflamm Bowel Dis 17:1523-1529
-
(2011)
Inflamm Bowel Dis
, vol.17
, pp. 1523-1529
-
-
Hradsky, O.1
Dusatkova, P.2
Lenicek, M.3
Bronsky, J.4
Duricova, D.5
Nevoral, J.6
Vitek, L.7
Lukas, M.8
Cinek, O.9
-
20
-
-
84055193697
-
JAK-1 rs2780895 C-related genotype and allele but not JAK-1 rs10789166, rs4916008, rs2780885, rs17127114, and rs3806277 are associated with higher susceptibility to asthma
-
21827323 10.1089/gtmb.2011.0002 1:CAS:528:DC%2BC3MXhs1Gru7rN
-
Hsieh YY, Chang CC, Hsu CM, Wan L, Chen SY, Lin WH, Tsai FJ (2011) JAK-1 rs2780895 C-related genotype and allele but not JAK-1 rs10789166, rs4916008, rs2780885, rs17127114, and rs3806277 are associated with higher susceptibility to asthma. Genet Test Mol Biomarkers 15:841-847
-
(2011)
Genet Test Mol Biomarkers
, vol.15
, pp. 841-847
-
-
Hsieh, Y.Y.1
Chang, C.C.2
Hsu, C.M.3
Wan, L.4
Chen, S.Y.5
Lin, W.H.6
Tsai, F.J.7
-
21
-
-
77953913256
-
STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behcet's disease
-
20438790 10.1016/j.humimm.2010.04.007 1:CAS:528:DC%2BC3cXnvVeltLY%3D
-
Hu K, Yang P, Jiang Z, Hou S, Du L, Li F (2010) STAT4 polymorphism in a Chinese Han population with Vogt-Koyanagi-Harada syndrome and Behcet's disease. Hum Immunol 71:723-726
-
(2010)
Hum Immunol
, vol.71
, pp. 723-726
-
-
Hu, K.1
Yang, P.2
Jiang, Z.3
Hou, S.4
Du, L.5
Li, F.6
-
22
-
-
77954984271
-
IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population
-
20375120 10.1136/ard.2009.119420 1:CAS:528:DC%2BC3cXhtVSltbfE
-
Jiang Z, Yang P, Hou S, Du L, Xie L, Zhou H, Kijlstra A (2010) IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population. Ann Rheum Dis 69:1325-1328
-
(2010)
Ann Rheum Dis
, vol.69
, pp. 1325-1328
-
-
Jiang, Z.1
Yang, P.2
Hou, S.3
Du, L.4
Xie, L.5
Zhou, H.6
Kijlstra, A.7
-
23
-
-
84867076238
-
Epidemiology of Behcet disease
-
23030353 10.3109/09273948.2012.723112 1:CAS:528:DC%2BC38XhsVKls7fJ
-
Khairallah M, Accorinti M, Muccioli C, Kahloun R, Kempen JH (2012) Epidemiology of Behcet disease. Ocul Immunol Inflamm 20:324-335
-
(2012)
Ocul Immunol Inflamm
, vol.20
, pp. 324-335
-
-
Khairallah, M.1
Accorinti, M.2
Muccioli, C.3
Kahloun, R.4
Kempen, J.H.5
-
24
-
-
0033238059
-
Familial aggregation in Behcet's disease: High frequency in siblings and parents of pediatric probands
-
10393610 10.1016/S0022-3476(99)70333-1 1:STN:280:DyaK1Mzit1SnsA%3D%3D
-
Kone-Paut I, Geisler I, Wechsler B, Ozen S, Ozdogan H, Rozenbaum M, Touitou I (1999) Familial aggregation in Behcet's disease: high frequency in siblings and parents of pediatric probands. J Pediatr 135:89-93
-
(1999)
J Pediatr
, vol.135
, pp. 89-93
-
-
Kone-Paut, I.1
Geisler, I.2
Wechsler, B.3
Ozen, S.4
Ozdogan, H.5
Rozenbaum, M.6
Touitou, I.7
-
25
-
-
65949093502
-
Ocular involvement is associated with HLA-B51 in Adamantiades-Behcet's disease
-
10.1038/eye.2008.177 1:CAS:528:DC%2BD1MXlvVGrs7k%3D
-
Krause L, Kohler AK, Altenburg A, Papoutsis N, Zouboulis CC, Pleyer U, Stroux A, Foerster MH (2009) Ocular involvement is associated with HLA-B51 in Adamantiades-Behcet's disease. Eye (Lond) 23:1182-1186
-
(2009)
Eye (Lond)
, vol.23
, pp. 1182-1186
-
-
Krause, L.1
Kohler, A.K.2
Altenburg, A.3
Papoutsis, N.4
Zouboulis, C.C.5
Pleyer, U.6
Stroux, A.7
Foerster, M.H.8
-
26
-
-
63649092983
-
IGR2096a-1 T and IGR2198a-1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients
-
19214536 10.1007/s00384-009-0670-x
-
Lakner L, Csongei V, Sarlos P, Jaromi L, Safrany E, Varga M, Orosz P, Magyari L, Bene J, Miheller P, Tulassay Z, Melegh B (2009) IGR2096a-1 T and IGR2198a-1 C alleles on IBD5 locus of chromosome 5q31 region confer risk for Crohn's disease in Hungarian patients. Int J Colorectal Dis 24:503-507
-
(2009)
Int J Colorectal Dis
, vol.24
, pp. 503-507
-
-
Lakner, L.1
Csongei, V.2
Sarlos, P.3
Jaromi, L.4
Safrany, E.5
Varga, M.6
Orosz, P.7
Magyari, L.8
Bene, J.9
Miheller, P.10
Tulassay, Z.11
Melegh, B.12
-
27
-
-
52949124119
-
The 5q31 variants associated with psoriasis and Crohn's disease are distinct
-
18614543 10.1093/hmg/ddn196 1:CAS:528:DC%2BD1cXhtFCisL3E
-
Li Y, Chang M, Schrodi SJ, Callis-Duffin KP, Matsunami N, Civello D, Bui N, Catanese JJ, Leppert MF, Krueger GG, Begovich AB (2008) The 5q31 variants associated with psoriasis and Crohn's disease are distinct. Hum Mol Genet 17:2978-2985
-
(2008)
Hum Mol Genet
, vol.17
, pp. 2978-2985
-
-
Li, Y.1
Chang, M.2
Schrodi, S.J.3
Callis-Duffin, K.P.4
Matsunami, N.5
Civello, D.6
Bui, N.7
Catanese, J.J.8
Leppert, M.F.9
Krueger, G.G.10
Begovich, A.B.11
-
28
-
-
34250821108
-
A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence
-
17503330 10.1086/518312 1:CAS:528:DC%2BD2sXmtFGmsbk%3D
-
Lou XY, Chen GB, Yan L, Ma JZ, Zhu J, Elston RC, Li MD (2007) A generalized combinatorial approach for detecting gene-by-gene and gene-by-environment interactions with application to nicotine dependence. Am J Hum Genet 80:1125-1137
-
(2007)
Am J Hum Genet
, vol.80
, pp. 1125-1137
-
-
Lou, X.Y.1
Chen, G.B.2
Yan, L.3
Ma, J.Z.4
Zhu, J.5
Elston, R.C.6
Li, M.D.7
-
29
-
-
84860231111
-
Relationships of HLA-B51 or B5 genotype with Behcet's disease clinical characteristics: Systematic review and meta-analyses of observational studies
-
10.1093/rheumatology/ker428
-
Maldini C, Lavalley MP, Cheminant M, de Menthon M, Mahr A (2012) Relationships of HLA-B51 or B5 genotype with Behcet's disease clinical characteristics: systematic review and meta-analyses of observational studies. Rheumatology (Oxford) 51:887-900
-
(2012)
Rheumatology (Oxford)
, vol.51
, pp. 887-900
-
-
Maldini, C.1
Lavalley, M.P.2
Cheminant, M.3
De Menthon, M.4
Mahr, A.5
-
30
-
-
67349196503
-
Behcet's disease - A contemporary review
-
19324519 10.1016/j.jaut.2009.02.011 1:CAS:528:DC%2BD1MXls12qs7c%3D
-
Mendes D, Correia M, Barbedo M, Vaio T, Mota M, Goncalves O, Valente J (2009) Behcet's disease - a contemporary review. J Autoimmun 32:178-188
-
(2009)
J Autoimmun
, vol.32
, pp. 178-188
-
-
Mendes, D.1
Correia, M.2
Barbedo, M.3
Vaio, T.4
Mota, M.5
Goncalves, O.6
Valente, J.7
-
31
-
-
0027339163
-
Behcet's disease associated with one of the HLA-B51 subantigens, HLA-B5101
-
8213969 1:STN:280:DyaK2c%2Fislahsw%3D%3D
-
Mizuki N, Inoko H, Ando H, Nakamura S, Kashiwase K, Akaza T, Fujino Y, Masuda K, Takiguchi M, Ohno S (1993) Behcet's disease associated with one of the HLA-B51 subantigens, HLA-B5101. Am J Ophthalmol 116:406-409
-
(1993)
Am J Ophthalmol
, vol.116
, pp. 406-409
-
-
Mizuki, N.1
Inoko, H.2
Ando, H.3
Nakamura, S.4
Kashiwase, K.5
Akaza, T.6
Fujino, Y.7
Masuda, K.8
Takiguchi, M.9
Ohno, S.10
-
32
-
-
0030998631
-
Pathogenic gene responsible for the predisposition of Behcet's disease
-
9203025 10.3109/08830189709116843 1:STN:280:DyaK2szks1Kjug%3D%3D
-
Mizuki N, Inoko H, Ohno S (1997) Pathogenic gene responsible for the predisposition of Behcet's disease. Int Rev Immunol 14:33-48
-
(1997)
Int Rev Immunol
, vol.14
, pp. 33-48
-
-
Mizuki, N.1
Inoko, H.2
Ohno, S.3
-
33
-
-
17444443156
-
Association analysis between the MIC-A and HLA-B alleles in Japanese patients with Behcet's disease
-
10513813 10.1002/1529-0131(199909)42:9<1961: AID-ANR23>3.0.CO;2-7 1:STN:280:DyaK1MvktF2ksw%3D%3D
-
Mizuki N, Ota M, Katsuyama Y, Yabuki K, Ando H, Goto K, Nakamura S, Bahram S, Ohno S, Inoko H (1999) Association analysis between the MIC-A and HLA-B alleles in Japanese patients with Behcet's disease. Arthritis Rheum 42:1961-1966
-
(1999)
Arthritis Rheum
, vol.42
, pp. 1961-1966
-
-
Mizuki, N.1
Ota, M.2
Katsuyama, Y.3
Yabuki, K.4
Ando, H.5
Goto, K.6
Nakamura, S.7
Bahram, S.8
Ohno, S.9
Inoko, H.10
-
34
-
-
0033747061
-
Localization of the pathogenic gene of Behcet's disease by microsatellite analysis of three different populations
-
11053265 1:STN:280:DC%2BD3M%2FisFSiug%3D%3D
-
Mizuki N, Ota M, Yabuki K, Katsuyama Y, Ando H, Palimeris GD, Kaklamani E, Accorinti M, Pivetti-Pezzi P, Ohno S, Inoko H (2000) Localization of the pathogenic gene of Behcet's disease by microsatellite analysis of three different populations. Invest Ophthalmol Vis Sci 41:3702-3708
-
(2000)
Invest Ophthalmol Vis Sci
, vol.41
, pp. 3702-3708
-
-
Mizuki, N.1
Ota, M.2
Yabuki, K.3
Katsuyama, Y.4
Ando, H.5
Palimeris, G.D.6
Kaklamani, E.7
Accorinti, M.8
Pivetti-Pezzi, P.9
Ohno, S.10
Inoko, H.11
-
35
-
-
77955091234
-
Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci
-
20622879 10.1038/ng.624 1:CAS:528:DC%2BC3cXos1ahsLw%3D
-
Mizuki N, Meguro A, Ota M, Ohno S, Shiota T, Kawagoe T, Ito N, Kera J, Okada E, Yatsu K, Song YW, Lee EB, Kitaichi N, Namba K, Horie Y, Takeno M, Sugita S, Mochizuki M, Bahram S, Ishigatsubo Y, Inoko H (2010) Genome-wide association studies identify IL23R-IL12RB2 and IL10 as Behcet's disease susceptibility loci. Nat Genet 42:703-706
-
(2010)
Nat Genet
, vol.42
, pp. 703-706
-
-
Mizuki, N.1
Meguro, A.2
Ota, M.3
Ohno, S.4
Shiota, T.5
Kawagoe, T.6
Ito, N.7
Kera, J.8
Okada, E.9
Yatsu, K.10
Song, Y.W.11
Lee, E.B.12
Kitaichi, N.13
Namba, K.14
Horie, Y.15
Takeno, M.16
Sugita, S.17
Mochizuki, M.18
Bahram, S.19
Ishigatsubo, Y.20
Inoko, H.21
more..
-
36
-
-
0027979817
-
Thalidomide neuropathy incidence and clinico-electrophysiologic findings in 42 patients
-
8285742 10.1001/archderm.1994.01690010070009 1:STN:280: DyaK2c7htlOrsA%3D%3D
-
Ochonisky S, Verroust J, Bastuji-Garin S, Gherardi R, Revuz J (1994) Thalidomide neuropathy incidence and clinico-electrophysiologic findings in 42 patients. Arch Dermatol 130:66-69
-
(1994)
Arch Dermatol
, vol.130
, pp. 66-69
-
-
Ochonisky, S.1
Verroust, J.2
Bastuji-Garin, S.3
Gherardi, R.4
Revuz, J.5
-
37
-
-
0026691249
-
HLA-DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours: An alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation
-
1357775 10.1111/j.1399-0039.1992.tb01940.x 1:CAS:528:DyaK3sXhsVSktbo%3D
-
Olerup O, Zetterquist H (1992) HLA-DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation. Tissue Antigens 39:225-235
-
(1992)
Tissue Antigens
, vol.39
, pp. 225-235
-
-
Olerup, O.1
Zetterquist, H.2
-
38
-
-
78751694700
-
Genetic susceptibility to Behcet's disease: Role of genes belonging to the MHC region
-
10.1093/rheumatology/keq331 1:CAS:528:DC%2BC3MXhtVehtb8%3D
-
Piga M, Mathieu A (2011) Genetic susceptibility to Behcet's disease: role of genes belonging to the MHC region. Rheumatology (Oxford) 50:299-310
-
(2011)
Rheumatology (Oxford)
, vol.50
, pp. 299-310
-
-
Piga, M.1
Mathieu, A.2
-
39
-
-
13244277850
-
A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans
-
12402038 10.1038/ng1020 1:CAS:528:DC%2BD38XptVShtbg%3D
-
Prokunina L, Castillejo-Lopez C, Oberg F, Gunnarsson I, Berg L, Magnusson V, Brookes AJ, Tentler D, Kristjansdottir H, Grondal G, Bolstad AI, Svenungsson E, Lundberg I, Sturfelt G, Jonssen A, Truedsson L, Lima G, Alcocer-Varela J, Jonsson R, Gyllensten UB, Harley JB, Alarcon-Segovia D, Steinsson K, Alarcon-Riquelme ME (2002) A regulatory polymorphism in PDCD1 is associated with susceptibility to systemic lupus erythematosus in humans. Nat Genet 32:666-669
-
(2002)
Nat Genet
, vol.32
, pp. 666-669
-
-
Prokunina, L.1
Castillejo-Lopez, C.2
Oberg, F.3
Gunnarsson, I.4
Berg, L.5
Magnusson, V.6
Brookes, A.J.7
Tentler, D.8
Kristjansdottir, H.9
Grondal, G.10
Bolstad, A.I.11
Svenungsson, E.12
Lundberg, I.13
Sturfelt, G.14
Jonssen, A.15
Truedsson, L.16
Lima, G.17
Alcocer-Varela, J.18
Jonsson, R.19
Gyllensten, U.B.20
Harley, J.B.21
Alarcon-Segovia, D.22
Steinsson, K.23
Alarcon-Riquelme, M.E.24
more..
-
40
-
-
84855257058
-
A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap
-
22174698 10.1371/journal.pgen.1002406 1:CAS:528:DC%2BC3MXhs1OhtL%2FE
-
Ramos PS, Criswell LA, Moser KL, Comeau ME, Williams AH, Pajewski NM, Chung SA, Graham RR, Zidovetzki R, Kelly JA, Kaufman KM, Jacob CO, Vyse TJ, Tsao BP, Kimberly RP, Gaffney PM, Alarcon-Riquelme ME, Harley JB, Langefeld CD (2011) A comprehensive analysis of shared loci between systemic lupus erythematosus (SLE) and sixteen autoimmune diseases reveals limited genetic overlap. PLoS Genet 7:e1002406
-
(2011)
PLoS Genet
, vol.7
, pp. 1002406
-
-
Ramos, P.S.1
Criswell, L.A.2
Moser, K.L.3
Comeau, M.E.4
Williams, A.H.5
Pajewski, N.M.6
Chung, S.A.7
Graham, R.R.8
Zidovetzki, R.9
Kelly, J.A.10
Kaufman, K.M.11
Jacob, C.O.12
Vyse, T.J.13
Tsao, B.P.14
Kimberly, R.P.15
Gaffney, P.M.16
Alarcon-Riquelme, M.E.17
Harley, J.B.18
Langefeld, C.D.19
-
41
-
-
77955087288
-
Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease
-
20622878 10.1038/ng.625 1:CAS:528:DC%2BC3cXos1aisbY%3D
-
Remmers EF, Cosan F, Kirino Y, Ombrello MJ, Abaci N, Satorius C, Le JM, Yang B, Korman BD, Cakiris A, Aglar O, Emrence Z, Azakli H, Ustek D, Tugal-Tutkun I, Akman-Demir G, Chen W, Amos CI, Dizon MB, Kose AA, Azizlerli G, Erer B, Brand OJ, Kaklamani VG, Kaklamanis P, Ben-Chetrit E, Stanford M, Fortune F, Ghabra M, Ollier WE, Cho YH, Bang D, O'Shea J, Wallace GR, Gadina M, Kastner DL, Gul A (2010) Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behcet's disease. Nat Genet 42:698-702
-
(2010)
Nat Genet
, vol.42
, pp. 698-702
-
-
Remmers, E.F.1
Cosan, F.2
Kirino, Y.3
Ombrello, M.J.4
Abaci, N.5
Satorius, C.6
Le, J.M.7
Yang, B.8
Korman, B.D.9
Cakiris, A.10
Aglar, O.11
Emrence, Z.12
Azakli, H.13
Ustek, D.14
Tugal-Tutkun, I.15
Akman-Demir, G.16
Chen, W.17
Amos, C.I.18
Dizon, M.B.19
Kose, A.A.20
Azizlerli, G.21
Erer, B.22
Brand, O.J.23
Kaklamani, V.G.24
Kaklamanis, P.25
Ben-Chetrit, E.26
Stanford, M.27
Fortune, F.28
Ghabra, M.29
Ollier, W.E.30
Cho, Y.H.31
Bang, D.32
O'Shea, J.33
Wallace, G.R.34
Gadina, M.35
Kastner, D.L.36
Gul, A.37
more..
-
42
-
-
0033592467
-
Behcet's disease
-
10528040 10.1056/NEJM199910213411707 1:STN:280:DyaK1Mvkt1aktg%3D%3D
-
Sakane T, Takeno M, Suzuki N, Inaba G (1999) Behcet's disease. N Engl J Med 341:1284-1291
-
(1999)
N Engl J Med
, vol.341
, pp. 1284-1291
-
-
Sakane, T.1
Takeno, M.2
Suzuki, N.3
Inaba, G.4
-
43
-
-
84868530288
-
Defining a tissue stem cell-driven Runx1/Stat3 signalling axis in epithelial cancer
-
23034403 10.1038/emboj.2012.270 1:CAS:528:DC%2BC38XhsVGjsbnM
-
Scheitz CJ, Lee TS, McDermitt DJ, Tumbar T (2012) Defining a tissue stem cell-driven Runx1/Stat3 signalling axis in epithelial cancer. EMBO J 31:4124-4139
-
(2012)
EMBO J
, vol.31
, pp. 4124-4139
-
-
Scheitz, C.J.1
Lee, T.S.2
McDermitt, D.J.3
Tumbar, T.4
-
44
-
-
77958483927
-
Dengue hemorrhagic fever is associated with polymorphisms in JAK1
-
20588308 10.1038/ejhg.2010.98 1:CAS:528:DC%2BC3cXhtlWmurzJ
-
Silva LK, Blanton RE, Parrado AR, Melo PS, Morato VG, Reis EA, Dias JP, Castro JM, Vasconcelos PF, Goddard KA, Barreto ML, Reis MG, Teixeira MG (2010) Dengue hemorrhagic fever is associated with polymorphisms in JAK1. Eur J Hum Genet 18:1221-1227
-
(2010)
Eur J Hum Genet
, vol.18
, pp. 1221-1227
-
-
Silva, L.K.1
Blanton, R.E.2
Parrado, A.R.3
Melo, P.S.4
Morato, V.G.5
Reis, E.A.6
Dias, J.P.7
Castro, J.M.8
Vasconcelos, P.F.9
Goddard, K.A.10
Barreto, M.L.11
Reis, M.G.12
Teixeira, M.G.13
-
45
-
-
79956146788
-
AAV2-mediated subretinal gene transfer of hIFN-alpha attenuates experimental autoimmune uveoretinitis in mice
-
21611186 10.1371/journal.pone.0019542 1:CAS:528:DC%2BC3MXmsFGqsLo%3D
-
Tian L, Yang P, Lei B, Shao J, Wang C, Xiang Q, Wei L, Peng Z, Kijlstra A (2011) AAV2-mediated subretinal gene transfer of hIFN-alpha attenuates experimental autoimmune uveoretinitis in mice. PLoS ONE 6:e19542
-
(2011)
PLoS ONE
, vol.6
, pp. 19542
-
-
Tian, L.1
Yang, P.2
Lei, B.3
Shao, J.4
Wang, C.5
Xiang, Q.6
Wei, L.7
Peng, Z.8
Kijlstra, A.9
-
46
-
-
84862017173
-
AAV2-mediated combined subretinal delivery of IFN-alpha and IL-4 reduces the severity of experimental autoimmune uveoretinitis
-
22685550 10.1371/journal.pone.0037995 1:CAS:528:DC%2BC38XptlWjsLs%3D
-
Tian L, Lei B, Shao J, Wei L, Kijlstra A, Yang P (2012) AAV2-mediated combined subretinal delivery of IFN-alpha and IL-4 reduces the severity of experimental autoimmune uveoretinitis. PLoS ONE 7:e37995
-
(2012)
PLoS ONE
, vol.7
, pp. 37995
-
-
Tian, L.1
Lei, B.2
Shao, J.3
Wei, L.4
Kijlstra, A.5
Yang, P.6
-
47
-
-
0344364566
-
An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis
-
14608356 10.1038/ng1267 1:CAS:528:DC%2BD3sXpt1Ciu7w%3D
-
Tokuhiro S, Yamada R, Chang X, Suzuki A, Kochi Y, Sawada T, Suzuki M, Nagasaki M, Ohtsuki M, Ono M, Furukawa H, Nagashima M, Yoshino S, Mabuchi A, Sekine A, Saito S, Takahashi A, Tsunoda T, Nakamura Y, Yamamoto K (2003) An intronic SNP in a RUNX1 binding site of SLC22A4, encoding an organic cation transporter, is associated with rheumatoid arthritis. Nat Genet 35:341-348
-
(2003)
Nat Genet
, vol.35
, pp. 341-348
-
-
Tokuhiro, S.1
Yamada, R.2
Chang, X.3
Suzuki, A.4
Kochi, Y.5
Sawada, T.6
Suzuki, M.7
Nagasaki, M.8
Ohtsuki, M.9
Ono, M.10
Furukawa, H.11
Nagashima, M.12
Yoshino, S.13
Mabuchi, A.14
Sekine, A.15
Saito, S.16
Takahashi, A.17
Tsunoda, T.18
Nakamura, Y.19
Yamamoto, K.20
more..
-
48
-
-
77954428013
-
Clinical characteristics of Behcet's disease in China
-
19777242 10.1007/s00296-009-1127-9 1:CAS:528:DC%2BC3cXhtlyiu7fI
-
Wang LY, Zhao DB, Gu J, Dai SM (2010) Clinical characteristics of Behcet's disease in China. Rheumatol Int 30:1191-1196
-
(2010)
Rheumatol Int
, vol.30
, pp. 1191-1196
-
-
Wang, L.Y.1
Zhao, D.B.2
Gu, J.3
Dai, S.M.4
-
49
-
-
65649096940
-
Mutational analysis of JAK1 gene in human hepatocellular carcinoma
-
19239328 10.4149/neo-2009-02-136 1:CAS:528:DC%2BD1MXjs12qtLw%3D
-
Xie HJ, Bae HJ, Noh JH, Eun JW, Kim JK, Jung KH, Ryu JC, Ahn YM, Kim SY, Lee SH, Yoo NJ, Lee JY, Park WS, Nam SW (2009) Mutational analysis of JAK1 gene in human hepatocellular carcinoma. Neoplasma 56:136-140
-
(2009)
Neoplasma
, vol.56
, pp. 136-140
-
-
Xie, H.J.1
Bae, H.J.2
Noh, J.H.3
Eun, J.W.4
Kim, J.K.5
Jung, K.H.6
Ryu, J.C.7
Ahn, Y.M.8
Kim, S.Y.9
Lee, S.H.10
Yoo, N.J.11
Lee, J.Y.12
Park, W.S.13
Nam, S.W.14
-
50
-
-
84857039485
-
Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: A meta-analysis
-
21706137 10.1007/s00384-011-1265-x
-
Xuan C, Zhang BB, Yang T, Deng KF, Li M, Tian RJ (2012) Association between OCTN1/2 gene polymorphisms (1672C-T, 207G-C) and susceptibility of Crohn's disease: a meta-analysis. Int J Colorectal Dis 27:11-19
-
(2012)
Int J Colorectal Dis
, vol.27
, pp. 11-19
-
-
Xuan, C.1
Zhang, B.B.2
Yang, T.3
Deng, K.F.4
Li, M.5
Tian, R.J.6
-
51
-
-
0032828180
-
HLA class i and II typing of the patients with Behcet's disease in Saudi Arabia
-
10519364 10.1034/j.1399-0039.1999.540308.x 1:CAS:528:DyaK1MXms1yltbs%3D
-
Yabuki K, Ohno S, Mizuki N, Ando H, Tabbara KF, Goto K, Nomura E, Nakamura S, Ito N, Ota M, Katsuyama Y, Inoko H (1999) HLA class I and II typing of the patients with Behcet's disease in Saudi Arabia. Tissue Antigens 54:273-277
-
(1999)
Tissue Antigens
, vol.54
, pp. 273-277
-
-
Yabuki, K.1
Ohno, S.2
Mizuki, N.3
Ando, H.4
Tabbara, K.F.5
Goto, K.6
Nomura, E.7
Nakamura, S.8
Ito, N.9
Ota, M.10
Katsuyama, Y.11
Inoko, H.12
-
52
-
-
4744342646
-
SLC22A4 and RUNX1: Identification of RA susceptible genes
-
1:CAS:528:DC%2BD2cXntlWmsL4%3D
-
Yamada R, Tokuhiro S, Chang X, Yamamoto K (2004) SLC22A4 and RUNX1: identification of RA susceptible genes. J Mol Med (Berl) 82:558-564
-
(2004)
J Mol Med (Berl)
, vol.82
, pp. 558-564
-
-
Yamada, R.1
Tokuhiro, S.2
Chang, X.3
Yamamoto, K.4
|