Detalhe da pesquisa
1.
SnapShot: Genetics of ALS and FTD.
Cell
; 160(4): 798-798.e1, 2015 Feb 12.
Artigo
Inglês
| MEDLINE | ID: mdl-25679767
2.
Microglia-synapse engulfment via PtdSer-TREM2 ameliorates neuronal hyperactivity in Alzheimer's disease models.
EMBO J
; 42(19): e113246, 2023 Oct 04.
Artigo
Inglês
| MEDLINE | ID: mdl-37575021
3.
MIR-NATs repress MAPT translation and aid proteostasis in neurodegeneration.
Nature
; 594(7861): 117-123, 2021 06.
Artigo
Inglês
| MEDLINE | ID: mdl-34012113
4.
PINK1: From Parkinson's disease to mitophagy and back again.
PLoS Biol
; 21(6): e3002196, 2023 06.
Artigo
Inglês
| MEDLINE | ID: mdl-37384773
5.
eQTL Catalogue 2023: New datasets, X chromosome QTLs, and improved detection and visualisation of transcript-level QTLs.
PLoS Genet
; 19(9): e1010932, 2023 Sep.
Artigo
Inglês
| MEDLINE | ID: mdl-37721944
6.
Towards cascading genetic risk in Alzheimer's disease.
Brain
; 2024 May 31.
Artigo
Inglês
| MEDLINE | ID: mdl-38820112
7.
SnapShot: Genetics of Parkinson's disease.
Cell
; 160(3): 570-570.e1, 2015 Jan 29.
Artigo
Inglês
| MEDLINE | ID: mdl-25635463
8.
Reelin and stk25 have opposing roles in neuronal polarization and dendritic Golgi deployment.
Cell
; 143(5): 826-36, 2010 Nov 24.
Artigo
Inglês
| MEDLINE | ID: mdl-21111240
9.
Genome-Wide Analysis of Structural Variants in Parkinson Disease.
Ann Neurol
; 93(5): 1012-1022, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36695634
10.
Adaptive Long-Read Sequencing Reveals GGC Repeat Expansion in ZFHX3 Associated with Spinocerebellar Ataxia Type 4.
Mov Disord
; 39(3): 486-497, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38197134
11.
Plasma biomarkers and genetics in the diagnosis and prediction of Alzheimer's disease.
Brain
; 146(2): 690-699, 2023 02 13.
Artigo
Inglês
| MEDLINE | ID: mdl-35383826
12.
Association between the LRP1B and APOE loci and the development of Parkinson's disease dementia.
Brain
; 146(5): 1873-1887, 2023 05 02.
Artigo
Inglês
| MEDLINE | ID: mdl-36348503
13.
Functional genomics provide key insights to improve the diagnostic yield of hereditary ataxia.
Brain
; 146(7): 2869-2884, 2023 07 03.
Artigo
Inglês
| MEDLINE | ID: mdl-36624280
14.
Large-scale rare variant burden testing in Parkinson's disease.
Brain
; 146(11): 4622-4632, 2023 11 02.
Artigo
Inglês
| MEDLINE | ID: mdl-37348876
15.
Using blood transcriptome analysis for Alzheimer's disease diagnosis and patient stratification.
Alzheimers Dement
; 20(4): 2469-2484, 2024 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-38323937
16.
A blood-based multi-pathway biomarker assay for early detection and staging of Alzheimer's disease across ethnic groups.
Alzheimers Dement
; 20(3): 2000-2015, 2024 Mar.
Artigo
Inglês
| MEDLINE | ID: mdl-38183344
17.
Human myeloid progenitor glucocorticoid receptor activation causes genomic instability, type 1 IFN- response pathway activation and senescence in differentiated microglia; an early life stress model.
Glia
; 71(4): 1036-1056, 2023 04.
Artigo
Inglês
| MEDLINE | ID: mdl-36571248
18.
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseases.
Neurobiol Dis
; 180: 106082, 2023 05.
Artigo
Inglês
| MEDLINE | ID: mdl-36925053
19.
Defining the Riddle in Order to Solve It: There Is More Than One "Parkinson's Disease".
Mov Disord
; 38(7): 1127-1142, 2023 07.
Artigo
Inglês
| MEDLINE | ID: mdl-37156737
20.
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
Inglês
| MEDLINE | ID: mdl-36074904