Detalhe da pesquisa
1.
Polygenic risk score association with multiple sclerosis susceptibility and phenotype in Europeans.
Brain
; 146(2): 645-656, 2023 02 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-35253861
2.
Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics.
Am J Hum Genet
; 107(1): 46-59, 2020 07 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-32470373
3.
The CYP24A1 gene variant rs2762943 is associated with low serum 1,25-dihydroxyvitamin D levels in multiple sclerosis patients.
Eur J Neurol
; 30(8): 2401-2410, 2023 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-37183562
4.
Genetic and epigenetic fine mapping of causal autoimmune disease variants.
Nature
; 518(7539): 337-43, 2015 Feb 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-25363779
5.
Mother-child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers.
Genes Immun
; 21(1): 27-36, 2020 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30635658
6.
Genetic and gene expression signatures in multiple sclerosis.
Mult Scler
; 26(5): 576-581, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31965883
7.
Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.
Am J Hum Genet
; 97(4): 576-92, 2015 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-26430803
8.
A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome.
Hum Mol Genet
; 24(24): 7151-8, 2015 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-26433934
9.
Increased risk of rheumatoid arthritis among mothers with children who carry DRB1 risk-associated alleles.
Ann Rheum Dis
; 76(8): 1405-1410, 2017 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-28391248
10.
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
11.
Functional variations modulating PRKCA expression and alternative splicing predispose to multiple sclerosis.
Hum Mol Genet
; 23(25): 6746-61, 2014 Dec 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-25080502
12.
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
13.
A Child's HLA-DRB1 genotype increases maternal risk of systemic lupus erythematosus.
J Autoimmun
; 74: 201-207, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-27388144
14.
A pharmacogenetic study implicates SLC9a9 in multiple sclerosis disease activity.
Ann Neurol
; 78(1): 115-27, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25914168
15.
Genetic loci for Epstein-Barr virus nuclear antigen-1 are associated with risk of multiple sclerosis.
Mult Scler
; 22(13): 1655-1664, 2016 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-26819262
16.
Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects.
PLoS Genet
; 9(11): e1003926, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24278027
17.
Use of a multiethnic approach to identify rheumatoid- arthritis-susceptibility loci, 1p36 and 17q12.
Am J Hum Genet
; 90(3): 524-32, 2012 Mar 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-22365150
18.
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
19.
Fine-mapping classical HLA variation associated with durable host control of HIV-1 infection in African Americans.
Hum Mol Genet
; 21(19): 4334-47, 2012 Oct 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-22718199
20.
Immediate-release methylphenidate for attention deficit hyperactivity disorder (ADHD) in adults.
Cochrane Database Syst Rev
; (9): CD005041, 2014 Sep 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-25230710