-
1
-
-
80054928002
-
Genomics and the multifactorial nature of human autoimmune disease
-
Cho, J.H. & Gregersen, P.K. Genomics and the multifactorial nature of human autoimmune disease. N. Engl. J. Med. 365, 1612-1623 (2011).
-
(2011)
N. Engl. J. Med.
, vol.365
, pp. 1612-1623
-
-
Cho, J.H.1
Gregersen, P.K.2
-
2
-
-
16244418695
-
Genetic lesions in T-cell tolerance and thresholds for autoimmunity
-
Liston, A., Lesage, S., Gray, D.H.D., Boyd, R.L. & Goodnow, C.C. Genetic lesions in T-cell tolerance and thresholds for autoimmunity. Immunol. Rev. 204, 87-101 (2005).
-
(2005)
Immunol. Rev.
, vol.204
, pp. 87-101
-
-
Liston, A.1
Lesage, S.2
Gray, D.H.D.3
Boyd, R.L.4
Goodnow, C.C.5
-
3
-
-
40049108936
-
Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX
-
Hom, G. et al. Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. N. Engl. J. Med. 358, 900-909 (2008).
-
(2008)
N. Engl. J. Med.
, vol.358
, pp. 900-909
-
-
Hom, G.1
-
4
-
-
38649108122
-
M encoded by ITGAM) is associated with systemic lupus erythematosus
-
Nath, S.K. et al. A nonsynonymous functional variant in integrin-αM (encoded by ITGAM) is associated with systemic lupus erythematosus. Nat. Genet. 40, 152-154 (2008).
-
(2008)
Nat. Genet.
, vol.40
, pp. 152-154
-
-
Nath, S.K.1
-
5
-
-
46349099824
-
Structural basis for the recognition of c-Src by its inactivator Csk
-
Levinson, N.M., Seeliger, M.A., Cole, P.A. & Kuriyan, J. Structural basis for the recognition of c-Src by its inactivator Csk. Cell 134, 124-134 (2008).
-
(2008)
Cell
, vol.134
, pp. 124-134
-
-
Levinson, N.M.1
Seeliger, M.A.2
Cole, P.A.3
Kuriyan, J.4
-
6
-
-
33745174905
-
PTPN22: Setting thresholds for autoimmunity
-
Gregersen, P.K., Lee, H.-S., Batliwalla, F. & Begovich, A.B. PTPN22: setting thresholds for autoimmunity. Semin. Immunol. 18, 214-223 (2006).
-
(2006)
Semin. Immunol.
, vol.18
, pp. 214-223
-
-
Gregersen, P.K.1
Lee, H.-S.2
Batliwalla, F.3
Begovich, A.B.4
-
7
-
-
82255192188
-
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
-
Trynka, G. et al. Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease. Nat. Genet. 43, 1193-1201 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 1193-1201
-
-
Trynka, G.1
-
8
-
-
84861727232
-
Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up
-
Martin, J.-E. et al. Identification of CSK as a systemic sclerosis genetic risk factor through Genome Wide Association Study follow-up. Hum. Mol. Genet. 21, 2825-2835 (2012).
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 2825-2835
-
-
Martin, J.-E.1
-
9
-
-
11144358198
-
A gene atlas of the mouse and human protein-encoding transcriptomes
-
Su, A.I. et al. A gene atlas of the mouse and human protein-encoding transcriptomes. Proc. Natl. Acad. Sci. USA 101, 6062-6067 (2004).
-
(2004)
Proc. Natl. Acad. Sci. USA
, vol.101
, pp. 6062-6067
-
-
Su, A.I.1
-
10
-
-
77949962019
-
CD45-Csk phosphatase-kinase titration uncouples basal and inducible T cell receptor signaling during thymic development
-
Zikherman, J. et al. CD45-Csk phosphatase-kinase titration uncouples basal and inducible T cell receptor signaling during thymic development. Immunity 32, 342-354 (2010).
-
(2010)
Immunity
, vol.32
, pp. 342-354
-
-
Zikherman, J.1
-
11
-
-
0035451678
-
A CD19-dependent signaling pathway regulates autoimmunity in Lyn-deficient mice
-
Hasegawa, M. et al. A CD19-dependent signaling pathway regulates autoimmunity in Lyn-deficient mice. J. Immunol. 167, 2469-2478 (2001).
-
(2001)
J. Immunol.
, vol.167
, pp. 2469-2478
-
-
Hasegawa, M.1
-
12
-
-
65449176044
-
Cutting edge: The PTPN22 allelic variant associated with autoimmunity impairs B cell signaling
-
Arechiga, A.F. et al. Cutting edge: the PTPN22 allelic variant associated with autoimmunity impairs B cell signaling. J. Immunol. 182, 3343-3347 (2009).
-
(2009)
J. Immunol.
, vol.182
, pp. 3343-3347
-
-
Arechiga, A.F.1
-
13
-
-
64249119896
-
PTPN22 deficiency cooperates with the CD45 E613R allele to break tolerance on a non-autoimmune background
-
Zikherman, J. et al. PTPN22 deficiency cooperates with the CD45 E613R allele to break tolerance on a non-autoimmune background. J. Immunol. 182, 4093-4106 (2009).
-
(2009)
J. Immunol.
, vol.182
, pp. 4093-4106
-
-
Zikherman, J.1
-
14
-
-
80052239824
-
The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness
-
Zhang, J. et al. The autoimmune disease-associated PTPN22 variant promotes calpain-mediated Lyp/Pep degradation associated with lymphocyte and dendritic cell hyperresponsiveness. Nat. Genet. 43, 902-907 (2011).
-
(2011)
Nat. Genet.
, vol.43
, pp. 902-907
-
-
Zhang, J.1
-
15
-
-
80052376347
-
The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans
-
Menard, L. et al. The PTPN22 allele encoding an R620W variant interferes with the removal of developing autoreactive B cells in humans. J. Clin. Invest. 121, 3635-3644 (2011).
-
(2011)
J. Clin. Invest.
, vol.121
, pp. 3635-3644
-
-
Menard, L.1
-
16
-
-
67849097322
-
Genetic associations of LYN with systemic lupus erythematosus
-
Lu, R. et al. Genetic associations of LYN with systemic lupus erythematosus. Genes Immun. 10, 397-403 (2009).
-
(2009)
Genes Immun.
, vol.10
, pp. 397-403
-
-
Lu, R.1
-
17
-
-
84865071401
-
The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development
-
Simpfendorfer, K.R. et al. The autoimmunity-associated BLK haplotype exhibits cis-regulatory effects on mRNA and protein expression that are prominently observed in B cells early in development. Hum. Mol. Genet. 21, 3918-3925 (2012).
-
(2012)
Hum. Mol. Genet.
, vol.21
, pp. 3918-3925
-
-
Simpfendorfer, K.R.1
-
18
-
-
77955894071
-
METAL: Fast and efficient meta-analysis of genomewide association scans
-
Willer, C.J., Li, Y. & Abecasis, G.R. METAL: fast and efficient meta-analysis of genomewide association scans. Bioinformatics 26, 2190-2191 (2010).
-
(2010)
Bioinformatics
, vol.26
, pp. 2190-2191
-
-
Willer, C.J.1
Li, Y.2
Abecasis, G.R.3
-
19
-
-
34249997791
-
Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort
-
Thorburn, C.M. et al. Association of PDCD1 genetic variation with risk and clinical manifestations of systemic lupus erythematosus in a multiethnic cohort. Genes Immun. 8, 279-287 (2007).
-
(2007)
Genes Immun.
, vol.8
, pp. 279-287
-
-
Thorburn, C.M.1
-
20
-
-
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. et al. 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, 561-571 (2005).
-
(2005)
Am. J. Hum. Genet.
, vol.76
, pp. 561-571
-
-
Criswell, L.A.1
-
21
-
-
33646368404
-
A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus
-
Graham, R.R. et al. A common haplotype of interferon regulatory factor 5 (IRF5) regulates splicing and expression and is associated with increased risk of systemic lupus erythematosus. Nat. Genet. 38, 550-555 (2006).
-
(2006)
Nat. Genet.
, vol.38
, pp. 550-555
-
-
Graham, R.R.1
-
22
-
-
80055080962
-
Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus
-
Cunninghame Graham, D.S. et al. Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus. PLoS Genet. 7, e1002341 (2011).
-
(2011)
PLoS Genet.
, vol.7
-
-
Cunninghame Graham, D.S.1
-
23
-
-
34548849168
-
TRAF1-C5 as a risk locus for rheumatoid arthritis - A genomewide study
-
Plenge, R.M. et al. TRAF1-C5 as a risk locus for rheumatoid arthritis-a genomewide study. N. Engl. J. Med. 357, 1199-1209 (2007).
-
(2007)
N. Engl. J. Med.
, vol.357
, pp. 1199-1209
-
-
Plenge, R.M.1
-
24
-
-
67649880295
-
REL, encoding a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis
-
Gregersen, P.K. et al. REL, encoding a member of the NF-κB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis. Nat. Genet. 41, 820-823 (2009).
-
(2009)
Nat. Genet.
, vol.41
, pp. 820-823
-
-
Gregersen, P.K.1
-
25
-
-
34548148686
-
Age-and gender-specific reference values of estimated GFR in Caucasians: The nijmegen biomedical study
-
Wetzels, J.F.M., Kiemeney, L.A.L.M., Swinkels, D.W., Willems, H.L. & Heijer, M.D. Age-and gender-specific reference values of estimated GFR in Caucasians: The Nijmegen Biomedical Study. Kidney Int. 72, 632-637 (2007).
-
(2007)
Kidney Int.
, vol.72
, pp. 632-637
-
-
Wetzels, J.F.M.1
Kiemeney, L.A.L.M.2
Swinkels, D.W.3
Willems, H.L.4
Heijer, M.D.5
-
26
-
-
73249114022
-
European population genetic substructure: Further definition of ancestry informative markers for distinguishing among diverse European ethnic groups
-
Tian, C. et al. European population genetic substructure: further definition of ancestry informative markers for distinguishing among diverse European ethnic groups. Mol. Med. 15, 371-383 (2009).
-
(2009)
Mol. Med.
, vol.15
, pp. 371-383
-
-
Tian, C.1
-
27
-
-
34347344976
-
A new multipoint method for genome-wide association studies by imputation of genotypes
-
Marchini, J., Howie, B., Myers, S., McVean, G. & Donnelly, P. A new multipoint method for genome-wide association studies by imputation of genotypes. Nat. Genet. 39, 906-913 (2007).
-
(2007)
Nat. Genet.
, vol.39
, pp. 906-913
-
-
Marchini, J.1
Howie, B.2
Myers, S.3
McVean, G.4
Donnelly, P.5
-
28
-
-
77449159423
-
Differential expression of CD21 identifies developmentally and functionally distinct subsets of human transitional B cells
-
Suryani, S. et al. Differential expression of CD21 identifies developmentally and functionally distinct subsets of human transitional B cells. Blood 115, 519-529 (2010).
-
(2010)
Blood
, vol.115
, pp. 519-529
-
-
Suryani, S.1
-
29
-
-
0035710746
-
T method
-
Livak, K.J. & Schmittgen, T.D. Analysis of relative gene expression data using real-time quantitative PCR and the 2ΔΔCT method. Methods 25, 402-408 (2001).
-
(2001)
Methods
, vol.25
, pp. 402-408
-
-
Livak, K.J.1
Schmittgen, T.D.2
|