Detalhe da pesquisa
1.
omicSynth: An open multi-omic community resource for identifying druggable targets across neurodegenerative diseases.
Am J Hum Genet
; 111(1): 150-164, 2024 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-38181731
2.
Towards a Global View of Parkinson's Disease Genetics.
Ann Neurol
; 95(5): 831-842, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38557965
3.
Genome-Wide Analysis of Structural Variants in Parkinson Disease.
Ann Neurol
; 93(5): 1012-1022, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36695634
4.
GBA1 rs3115534 Is Associated with REM Sleep Behavior Disorder in Parkinson's Disease in Nigerians.
Mov Disord
; 39(4): 728-733, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38390630
5.
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
em Inglês
| MEDLINE | ID: mdl-38197134
6.
Multi-ancestry meta-analysis and fine-mapping in Alzheimer's disease.
Mol Psychiatry
; 28(7): 3121-3132, 2023 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-37198259
7.
Genome-wide contribution of common short-tandem repeats to Parkinson's disease genetic risk.
Brain
; 146(1): 65-74, 2023 01 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36347471
8.
Genetic risk factor clustering within and across neurodegenerative diseases.
Brain
; 146(11): 4486-4494, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37192343
9.
Large-scale rare variant burden testing in Parkinson's disease.
Brain
; 146(11): 4622-4632, 2023 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-37348876
10.
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
11.
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
12.
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk Factors.
Ann Neurol
; 92(2): 270-278, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35599344
13.
Genome-Wide Meta-Analysis of Cerebrospinal Fluid Biomarkers in Alzheimer's Disease and Parkinson's Disease Cohorts.
Mov Disord
; 38(9): 1697-1705, 2023 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-37539664
14.
Investigation of Shared Genetic Risk Factors Between Parkinson's Disease and Cancers.
Mov Disord
; 38(4): 604-615, 2023 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-36788297
15.
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease.
Brain
; 145(6): 2077-2091, 2022 06 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-35640906
16.
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
17.
Artificial intelligence for dementia genetics and omics.
Alzheimers Dement
; 19(12): 5905-5921, 2023 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-37606627
18.
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation.
Am J Hum Genet
; 104(5): 925-935, 2019 05 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-30982609
19.
Investigation of Autosomal Genetic Sex Differences in Parkinson's Disease.
Ann Neurol
; 90(1): 35-42, 2021 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-33901317
20.
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease Risk.
Mov Disord
; 37(1): 95-105, 2022 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34542912