Detalhe da pesquisa
1.
ßIV Spectrinopathies Cause Profound Intellectual Disability, Congenital Hypotonia, and Motor Axonal Neuropathy.
Am J Hum Genet
; 102(6): 1158-1168, 2018 06 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-29861105
2.
Genetic fine mapping of systemic lupus erythematosus MHC associations in Europeans and African Americans.
Hum Mol Genet
; 27(21): 3813-3824, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30085094
3.
Identification of a Sjögren's syndrome susceptibility locus at OAS1 that influences isoform switching, protein expression, and responsiveness to type I interferons.
PLoS Genet
; 13(6): e1006820, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28640813
4.
Genetic variants at the 16p13 locus confer risk for eosinophilic esophagitis.
Genes Immun
; 20(4): 281-292, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29904099
5.
Association of Epstein-Barr virus serological reactivation with transitioning to systemic lupus erythematosus in at-risk individuals.
Ann Rheum Dis
; 78(9): 1235-1241, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31217170
6.
Lupus Risk Variant Increases pSTAT1 Binding and Decreases ETS1 Expression.
Am J Hum Genet
; 96(5): 731-9, 2015 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-25865496
7.
ABIN1 Determines Severity of Glomerulonephritis via Activation of Intrinsic Glomerular Inflammation.
Am J Pathol
; 187(12): 2799-2810, 2017 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-28935578
8.
Functional activation of PPARγ in human upper aerodigestive cancer cell lines.
Mol Carcinog
; 56(1): 149-162, 2017 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26999671
9.
Combined role of vitamin D status and CYP24A1 in the transition to systemic lupus erythematosus.
Ann Rheum Dis
; 76(1): 153-158, 2017 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-27283331
10.
Activating mutations in STIM1 and ORAI1 cause overlapping syndromes of tubular myopathy and congenital miosis.
Proc Natl Acad Sci U S A
; 111(11): 4197-202, 2014 Mar 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-24591628
11.
Genetic variants near TNFAIP3 on 6q23 are associated with systemic lupus erythematosus.
Nat Genet
; 40(9): 1059-61, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-19165918
12.
Allelic heterogeneity in NCF2 associated with systemic lupus erythematosus (SLE) susceptibility across four ethnic populations.
Hum Mol Genet
; 23(6): 1656-68, 2014 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-24163247
13.
Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production.
Ann Rheum Dis
; 75(11): 2007-2013, 2016 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26783109
14.
Preferential association of a functional variant in complement receptor 2 with antibodies to double-stranded DNA.
Ann Rheum Dis
; 75(1): 242-52, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-25180293
15.
Forward genetic screening identifies a small molecule that blocks Toxoplasma gondii growth by inhibiting both host- and parasite-encoded kinases.
PLoS Pathog
; 10(6): e1004180, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24945800
16.
Human effector B lymphocytes express ARID3a and secrete interferon alpha.
J Autoimmun
; 75: 130-140, 2016 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-27522115
17.
An enhancer element harboring variants associated with systemic lupus erythematosus engages the TNFAIP3 promoter to influence A20 expression.
PLoS Genet
; 9(9): e1003750, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24039598
18.
Admixture mapping in lupus identifies multiple functional variants within IFIH1 associated with apoptosis, inflammation, and autoantibody production.
PLoS Genet
; 9(2): e1003222, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23441136
19.
Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression.
PLoS Genet
; 9(10): e1003870, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-24130510
20.
Trans-ancestral studies fine map the SLE-susceptibility locus TNFSF4.
PLoS Genet
; 9(7): e1003554, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23874208