Detalhe da pesquisa
1.
Human immune diversity: from evolution to modernity.
Nat Immunol
; 22(12): 1479-1489, 2021 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-34795445
2.
The cellular composition of the human immune system is shaped by age and cohabitation.
Nat Immunol
; 17(4): 461-468, 2016 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-26878114
3.
Author Correction: The cellular composition of the human immune system is shaped by age and cohabitation.
Nat Immunol
; 22(2): 254, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33239822
4.
The origins of diversity in human immunity.
Nat Immunol
; 19(3): 209-210, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29476185
5.
Genetic Variation in WNT9B Increases Relapse Hazard in Multiple Sclerosis.
Ann Neurol
; 89(5): 884-894, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33704824
6.
A robust pipeline with high replication rate for detection of somatic variants in the adaptive immune system as a source of common genetic variation in autoimmune disease.
Hum Mol Genet
; 28(8): 1369-1380, 2019 04 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30541027
7.
CHIT1 at Diagnosis Reflects Long-Term Multiple Sclerosis Disease Activity.
Ann Neurol
; 87(4): 633-645, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31997416
8.
IFN-γ stimulates CpG-induced IL-10 production in B cells via p38 and JNK signalling pathways.
Eur J Immunol
; 48(9): 1506-1521, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-30004580
9.
Machine learning identifies an immunological pattern associated with multiple juvenile idiopathic arthritis subtypes.
Ann Rheum Dis
; 78(5): 617-628, 2019 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-30862608
10.
Multiple sclerosis risk variants alter expression of co-stimulatory genes in B cells.
Brain
; 141(3): 786-796, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29361022
11.
Genetic ablation of IP3 receptor 2 increases cytokines and decreases survival of SOD1G93A mice.
Hum Mol Genet
; 25(16): 3491-3499, 2016 08 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27378687
12.
Genetic basis for relapse rate in multiple sclerosis: Association with LRP2 genetic variation.
Mult Scler
; 24(13): 1773-1775, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-29303040
13.
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis.
Nature
; 476(7359): 214-9, 2011 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-21833088
14.
Power estimation for non-standardized multisite studies.
Neuroimage
; 134: 281-294, 2016 07 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27039700
15.
No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.
Hum Mol Genet
; 23(7): 1916-22, 2014 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-24234648
16.
Genetic variants are major determinants of CSF antibody levels in multiple sclerosis.
Brain
; 138(Pt 3): 632-43, 2015 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-25616667
17.
Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis.
Nat Genet
; 39(9): 1083-91, 2007 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-17660817
18.
Novel COL4A1 mutations cause cerebral small vessel disease by haploinsufficiency.
Hum Mol Genet
; 22(2): 391-7, 2013 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-23065703
19.
Burden of risk variants correlates with phenotype of multiple sclerosis.
Mult Scler
; 21(13): 1670-80, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25948629
20.
Whole-genome sequencing reveals a coding non-pathogenic variant tagging a non-coding pathogenic hexanucleotide repeat expansion in C9orf72 as cause of amyotrophic lateral sclerosis.
Hum Mol Genet
; 21(11): 2412-9, 2012 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22343411