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.
Reelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deployment.
Cell
; 143(5): 826-36, 2010 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21111240
3.
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia.
Brain
; 146(7): 2869-2884, 2023 07 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-36624280
4.
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.
Neurobiol Dis
; 180: 106082, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36925053
5.
Dissecting the Phenotype and Genotype of PLA2G6-Related Parkinsonism.
Mov Disord
; 37(1): 148-161, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34622992
6.
The human brainome: network analysis identifies HSPA2 as a novel Alzheimer’s disease target.
Brain
; 141(9): 2721-2739, 2018 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30137212
7.
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies.
Neurobiol Dis
; 94: 55-62, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27312774
8.
First effects of rising amyloid-ß in transgenic mouse brain: synaptic transmission and gene expression.
Brain
; 138(Pt 7): 1992-2004, 2015 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-25981962
9.
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
PLoS Genet
; 8(3): e1002548, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22438815
10.
A coding variant in CR1 interacts with APOE-ε4 to influence cognitive decline.
Hum Mol Genet
; 21(10): 2377-88, 2012 May 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-22343410
11.
Genotype, haplotype and copy-number variation in worldwide human populations.
Nature
; 451(7181): 998-1003, 2008 Feb 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-18288195
12.
Genome-wide structural variant analysis identifies risk loci for non-Alzheimer's dementias.
Cell Genom
; 3(6): 100316, 2023 Jun 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-37388914
13.
Genotype-imputation accuracy across worldwide human populations.
Am J Hum Genet
; 84(2): 235-50, 2009 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19215730
14.
CR1 is associated with amyloid plaque burden and age-related cognitive decline.
Ann Neurol
; 69(3): 560-9, 2011 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21391232
15.
Multi-modality machine learning predicting Parkinson's disease.
NPJ Parkinsons Dis
; 8(1): 35, 2022 Apr 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-35365675
16.
Comparing spatial maps of human population-genetic variation using Procrustes analysis.
Stat Appl Genet Mol Biol
; 9: Article 13, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-20196748
17.
Abrogation of LRRK2 dependent Rab10 phosphorylation with TLR4 activation and alterations in evoked cytokine release in immune cells.
Neurochem Int
; 147: 105070, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-34004238
18.
Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.
Neuron
; 109(3): 448-460.e4, 2021 02 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33242422
19.
SNCA variants are associated with increased risk for multiple system atrophy.
Ann Neurol
; 65(5): 610-4, 2009 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-19475667
20.
Sequencing analysis of the ITPR1 gene in a pure autosomal dominant spinocerebellar ataxia series.
Mov Disord
; 25(6): 771-3, 2010 Apr 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-20437544