Detalhe da pesquisa
1.
Activation of naïve CD4+ T cells re-tunes STAT1 signaling to deliver unique cytokine responses in memory CD4+ T cells.
Nat Immunol
; 20(4): 458-470, 2019 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-30890796
2.
Th1 Cells Alter the Inflammatory Signature of IL-6 by Channeling STAT Transcription Factors to Alu-like Retroelements.
J Immunol
; 211(2): 274-286, 2023 07 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-37272871
3.
Rare coding variants as risk modifiers of the 22q11.2 deletion implicate postnatal cortical development in syndromic schizophrenia.
Mol Psychiatry
; 28(5): 2071-2080, 2023 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-36869225
4.
Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.
Hum Mol Genet
; 30(1): 78-86, 2021 03 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-33448283
5.
Induced pluripotent stem cells derived from the developing striatum as a potential donor source for cell replacement therapy for Huntington disease.
Cytotherapy
; 23(2): 111-118, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33246883
6.
Genome-Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease.
Mov Disord
; 36(2): 424-433, 2021 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33111402
7.
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Brain
; 142(9): 2828-2844, 2019 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31324919
8.
The genetic and clinico-pathological profile of early-onset progressive supranuclear palsy.
Mov Disord
; 34(9): 1307-1314, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31299107
9.
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance.
Hum Mol Genet
; 25(24): 5483-5489, 2016 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-27798102
10.
Identification of loci associated with schizophrenia by genome-wide association and follow-up.
Nat Genet
; 40(9): 1053-5, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18677311
11.
Polygenic risk of Parkinson disease is correlated with disease age at onset.
Ann Neurol
; 77(4): 582-91, 2015 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-25773351
12.
Vascular disease and vascular risk factors in relation to motor features and cognition in early Parkinson's disease.
Mov Disord
; 31(10): 1518-1526, 2016 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-27324570
13.
A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease.
Hum Mol Genet
; 22(5): 1039-49, 2013 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23223016
14.
Genetic risk and age in Parkinson's disease: Continuum not stratum.
Mov Disord
; 30(6): 850-4, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25778492
15.
Genome-Wide Association Study of Pain in Parkinson's Disease Implicates TRPM8 as a Risk Factor.
Mov Disord
; 35(4): 705-707, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-32078185
16.
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease.
medRxiv
; 2023 May 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-37425912
17.
Genetic meta-analysis of levodopa induced dyskinesia in Parkinson's disease.
NPJ Parkinsons Dis
; 9(1): 128, 2023 Aug 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-37652906
18.
Is the MC1R variant p.R160W associated with Parkinson's?
Ann Neurol
; 79(1): 159-61, 2016 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-26389967
19.
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
20.
Recent advances in the genetics of the ALS-FTLD complex.
Curr Neurol Neurosci Rep
; 12(3): 243-50, 2012 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-22477152