Detalhe da pesquisa
1.
Identification and single-base gene-editing functional validation of a cis-EPO variant as a genetic predictor for EPO-increasing therapies.
Am J Hum Genet
; 109(9): 1638-1652, 2022 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36055212
2.
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
3.
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
4.
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
5.
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
6.
Dairy Intake and Parkinson's Disease: A Mendelian Randomization Study.
Mov Disord
; 37(4): 857-864, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-34997937
7.
The Interaction between HLA-DRB1 and Smoking in Parkinson's Disease Revisited.
Mov Disord
; 37(9): 1929-1937, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35810454
8.
The Parkinson's Disease DNA Variant Browser.
Mov Disord
; 36(5): 1250-1258, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33497488
9.
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource.
Mov Disord
; 36(8): 1795-1804, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33960523
10.
Differences in the Presentation and Progression of Parkinson's Disease by Sex.
Mov Disord
; 36(1): 106-117, 2021 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33002231
11.
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia.
Brain
; 143(1): 234-248, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31755958
12.
Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease.
Circulation
; 140(8): 645-657, 2019 08 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-31424985
13.
Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score.
Mov Disord
; 35(5): 774-780, 2020 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31958187
14.
Genome-wide meta-analysis of macronutrient intake of 91,114 European ancestry participants from the cohorts for heart and aging research in genomic epidemiology consortium.
Mol Psychiatry
; 24(12): 1920-1932, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29988085
15.
Rare coding variants in the phospholipase D3 gene confer risk for Alzheimer's disease.
Nature
; 505(7484): 550-554, 2014 Jan 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-24336208
16.
A SINE-VNTR-Alu in the LRIG2 Promoter Is Associated with Gene Expression at the Locus.
Int J Mol Sci
; 21(22)2020 Nov 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-33187279
17.
Assessment of APOE in atypical parkinsonism syndromes.
Neurobiol Dis
; 127: 142-146, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30798004
18.
Heritability and genetic variance of dementia with Lewy bodies.
Neurobiol Dis
; 127: 492-501, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-30953760
19.
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy.
Am J Hum Genet
; 98(3): 500-513, 2016 Mar 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26942284
20.
Parkinson's disease age at onset genome-wide association study: Defining heritability, genetic loci, and α-synuclein mechanisms.
Mov Disord
; 34(6): 866-875, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30957308