Detalhe da pesquisa
1.
MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration.
Nature
; 594(7861): 117-123, 2021 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-34012113
2.
Regulation of mitophagy by the NSL complex underlies genetic risk for Parkinson's disease at 16q11.2 and MAPT H1 loci.
Brain
; 145(12): 4349-4367, 2022 12 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-36074904
3.
The role of body fat in multiple sclerosis susceptibility and severity: A Mendelian randomisation study.
Mult Scler
; 28(11): 1673-1684, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35575213
4.
Mendelian Randomisation Finds No Causal Association between Urate and Parkinson's Disease Progression.
Mov Disord
; 36(9): 2182-2187, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34056740
5.
Genome, transcriptome and proteome: the rise of omics data and their integration in biomedical sciences.
Brief Bioinform
; 19(2): 286-302, 2018 03 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-27881428
6.
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease.
Ann Neurol
; 84(2): 191-199, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30014513
7.
Stratification of candidate genes for Parkinson's disease using weighted protein-protein interaction network analysis.
BMC Genomics
; 19(1): 452, 2018 Jun 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-29898659
8.
Estimating the causal influence of body mass index on risk of Parkinson disease: A Mendelian randomisation study.
PLoS Med
; 14(6): e1002314, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28609445
9.
Age-related telomere attrition in the human putamen.
Aging Cell
; 22(7): e13861, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-37129365
10.
Exploring the Role of Plasma Lipids and Statin Interventions on Multiple Sclerosis Risk and Severity: A Mendelian Randomization Study.
Neurology
; 101(17): e1729-e1740, 2023 10 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-37657941
11.
Finding genetically-supported drug targets for Parkinson's disease using Mendelian randomization of the druggable genome.
Nat Commun
; 12(1): 7342, 2021 12 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-34930919
12.
Identification of Candidate Parkinson Disease Genes by Integrating Genome-Wide Association Study, Expression, and Epigenetic Data Sets.
JAMA Neurol
; 78(4): 464-472, 2021 04 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33523105
13.
Using Mendelian randomization to understand and develop treatments for neurodegenerative disease.
Brain Commun
; 2(1): fcaa031, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32954289
14.
C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts.
Neurology
; 95(24): e3288-e3302, 2020 12 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-32943482
15.
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies.
Lancet Neurol
; 18(12): 1091-1102, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31701892
16.
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease.
JAMA Neurol
; 75(11): 1416-1422, 2018 11 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30039155
17.
Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease.
Neurobiol Aging
; 64: 159.e5-159.e8, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29398121
18.
LRP10 in α-synucleinopathies.
Lancet Neurol
; 17(12): 1032, 2018 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30507383