SNCA rs3910105 Is Associated With Development of Rapid Eye Movement Sleep Behavior Disorder in Parkinson's Disease.
PMID:35310107
Parkinson Disease and Subthalamic Nucleus Deep Brain Stimulation: Cognitive Effects in GBA Mutation Carriers.
PMID:34984729
Development and Validation of a Prognostic Model for Cognitive Impairment in Parkinson's Disease With REM Sleep Behavior Disorder.
PMID:34322014
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource.
PMID:33960523
Association of Dual LRRK2 G2019S and GBA Variations With Parkinson Disease Progression.
PMID:33881531
Polygenic Score Models for Alzheimer's Disease: From Research to Clinical Applications.
PMID:33854414
Common X-Chromosome Variants Are Associated with Parkinson Disease Risk.
PMID:33583074
Network Protein Interaction in Parkinson's Disease and Periodontitis Interplay: A Preliminary Bioinformatic Analysis.
PMID:33238395
Longitudinal Measurements of Glucocerebrosidase activity in Parkinson's patients.
PMID:32888397
Excess of singleton loss-of-function variants in Parkinson's disease contributes to genetic risk.
PMID:32054687
Parkinson's disease prognostic scores for progression of cognitive decline.
PMID:31767922
Longitudinal analyses of cerebrospinal fluid α-Synuclein in prodromal and early Parkinson's disease.
PMID:31361367
The Personalized Parkinson Project: examining disease progression through broad biomarkers in early Parkinson's disease.
PMID:31315608
TMEM106B Effect on cognition in Parkinson disease and frontotemporal dementia.
PMID:30973966
An increased rate of longitudinal cognitive decline is observed in Parkinson's disease patients with low CSF Aß42 and an APOE ε4 allele.
PMID:30826425
Selecting variants of unknown significance through network-based gene-association significantly improves risk prediction for disease-control cohorts.
PMID:30824863
Effectiveness of imaging genetics analysis to explain degree of depression in Parkinson's disease.
PMID:30742647
A paradoxical relationship between family history, onset age, and genetic risk in Parkinson's disease.
PMID:30484896
Risk factors of levodopa-induced dyskinesia in Parkinson's disease: results from the PPMI cohort.
PMID:30480086
No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease.
PMID:30340792
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson disease.
PMID:30146727
Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases.
PMID:30089514
Parkinson disease polygenic risk score is associated with Parkinson disease status and age at onset but not with alpha-synuclein cerebrospinal fluid levels.
PMID:29141588
Longitudinal CSF biomarkers in patients with early Parkinson disease and healthy controls.
PMID:29030452
Predicting progression in patients with Parkinson's disease.
PMID:28958800
Latent Cognitive Phenotypes in De Novo Parkinson's Disease: A Person-Centered Approach.
PMID:28651678
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases.
PMID:28602509
Multiple modality biomarker prediction of cognitive impairment in prospectively followed de novo Parkinson disease.
PMID:28520803
Predictive Big Data Analytics: A Study of Parkinson's Disease Using Large, Complex, Heterogeneous, Incongruent, Multi-Source and Incomplete Observations.
PMID:27494614
The BioFIND study: Characteristics of a clinically typical Parkinson's disease biomarker cohort.
PMID:27113479