Detalhe da pesquisa
1.
Polymorphism in a lincRNA Associates with a Doubled Risk of Pneumococcal Bacteremia in Kenyan Children.
Am J Hum Genet
; 98(6): 1092-1100, 2016 Jun 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-27236921
2.
Dissection of a Complex Disease Susceptibility Region Using a Bayesian Stochastic Search Approach to Fine Mapping.
PLoS Genet
; 11(6): e1005272, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-26106896
3.
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
4.
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
5.
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
6.
Glucocerebrosidase mutations influence the natural history of Parkinson's disease in a community-based incident cohort.
Brain
; 136(Pt 2): 392-9, 2013 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-23413260
7.
Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Hum Mol Genet
; 20(17): 3517-24, 2011 Sep 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-21653641
8.
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
Hum Mol Genet
; 20(2): 345-53, 2011 Jan 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21044948
9.
Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come.
Am J Hum Genet
; 86(4): 621-5, 2010 Apr 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20362272
10.
CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.
Hum Mol Genet
; 19(11): 2331-40, 2010 Jun 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20211854
11.
Evidence for CRHR1 in multiple sclerosis using supervised machine learning and meta-analysis in 12,566 individuals.
Hum Mol Genet
; 19(21): 4286-95, 2010 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-20699326
12.
Genetic and pathological links between Parkinson's disease and the lysosomal disorder Sanfilippo syndrome.
Mov Disord
; 27(2): 312-5, 2012 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-22102531
13.
Systematic review and UK-based study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease.
Mov Disord
; 27(12): 1522-9, 2012 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22956510
14.
Mapping of multiple susceptibility variants within the MHC region for 7 immune-mediated diseases.
Proc Natl Acad Sci U S A
; 106(44): 18680-5, 2009 Nov 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-19846760
15.
Genetic associations at regulatory phenotypes improve fine-mapping of causal variants for 12 immune-mediated diseases.
Nat Genet
; 54(3): 251-262, 2022 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35288711
16.
Multivariate profile and acute-phase correlates of cognitive deficits in a COVID-19 hospitalised cohort.
EClinicalMedicine
; 47: 101417, 2022 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-35505938
17.
Variation within DNA repair pathway genes and risk of multiple sclerosis.
Am J Epidemiol
; 172(2): 217-24, 2010 Jul 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20522537
18.
Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility.
Hum Genet
; 127(5): 525-35, 2010 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-20112030
19.
Association of the human leucocyte antigen region with susceptibility to Parkinson's disease.
J Neurol Neurosurg Psychiatry
; 81(8): 890-1, 2010 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-20462916
20.
The distinct cognitive syndromes of Parkinson's disease: 5 year follow-up of the CamPaIGN cohort.
Brain
; 132(Pt 11): 2958-69, 2009 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-19812213