Detalhe da pesquisa
1.
Effect Modification between Genes and Environment and Parkinson's Disease Risk.
Ann Neurol
; 92(5): 715-724, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35913124
2.
Mendelian Randomisation Confirms the Role of Y-Chromosome Loss in Alzheimer's Disease Aetiopathogenesis in Men.
Int J Mol Sci
; 24(2)2023 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36674414
3.
Intermediate and Expanded HTT Alleles and the Risk for α-Synucleinopathies.
Mov Disord
; 37(9): 1841-1849, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35852957
4.
Association of PICALM with Cognitive Impairment in Parkinson's Disease.
Mov Disord
; 36(1): 118-123, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32914893
5.
Mutational spectrum of GNAL, THAP1 and TOR1A genes in isolated dystonia: study in a population from Spain and systematic literature review.
Eur J Neurol
; 28(4): 1188-1197, 2021 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-33175450
6.
The Parkinson's Disease Genome-Wide Association Study Locus Browser.
Mov Disord
; 35(11): 2056-2067, 2020 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-32864809
7.
PTPA variants and the risk for Parkinson's disease in diverse ancestry populations.
Brain
; 146(12): e120-e124, 2023 12 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37467482
8.
The Glycoprotein GPNMB: A Secret Ingredient for Understanding Parkinson's Disease Etiology?
Mov Disord
; 37(12): 2342, 2022 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-36321268
9.
Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations.
Mov Disord
; 37(1): 225-227, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34859503
10.
Reply to: "Increased Stroke Risk in Patients with Parkinson's Disease with LRRK2 Mutations".
Mov Disord
; 37(5): 1119-1120, 2022 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-35587631
11.
AccessPD as a next generation registry to accelerate Parkinson's disease research.
NPJ Parkinsons Dis
; 10(1): 66, 2024 Mar 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-38503768
12.
Role of ATP10B in Parkinson disease in a cohort from southern Spain.
Parkinsonism Relat Disord
; 124: 106989, 2024 May 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38754220
13.
RAB32 Ser71Arg in autosomal dominant Parkinson's disease: linkage, association, and functional analyses.
Lancet Neurol
; 23(6): 603-614, 2024 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-38614108
14.
Genome sequence analyses identify novel risk loci for multiple system atrophy.
Neuron
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38701790
15.
Homocysteine levels, genetic background, and cognitive impairment in Parkinson's disease.
J Neurol
; 270(1): 477-485, 2023 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-36169739
16.
Peripheral inflammatory immune response differs among sporadic and familial Parkinson's disease.
NPJ Parkinsons Dis
; 9(1): 12, 2023 Jan 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-36720879
17.
Evaluating the performance of polygenic risk profiling across diverse ancestry populations in Parkinson's disease.
medRxiv
; 2023 Nov 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-38076954
18.
Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(4): e200079, 2023 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-37293291
19.
Erratum: Cumulative Genetic Score and C9orf72 Repeat Status Independently Contribute to Amyotrophic Lateral Sclerosis Risk in 2 Case-Control Studies.
Neurol Genet
; 9(5): e200095, 2023 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-37521204
20.
The IPDGC/GP2 Hackathon - an open science event for training in data science, genomics, and collaboration using Parkinson's disease data.
NPJ Parkinsons Dis
; 9(1): 33, 2023 Mar 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36871034