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Promoter methylation analysis of seven clock genes in Parkinson's disease

Neuroscience letters, 2012-01, Vol.507 (2), p.147-150

2012

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Non-Motor Symptoms in Treated and Untreated Chinese Patients with Early Parkinson’s Disease

The Tohoku Journal of Experimental Medicine, 2014, Vol.232(2), pp.129-136

2014

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High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease

NPJ Parkinson's Disease, 2024-07, Vol.10 (1), p.134-14, Article 134

2024

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Education Moderates the Association of Probable REM Sleep Behavior Disorder With Cognitive and Motor Impairments in Community-Dwelling Older People

Frontiers in neurology, 2020-02, Vol.11, p.109-109

2020

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Smoking, genes encoding dopamine pathway and risk for Parkinson's disease

Neuroscience letters, 2010-09, Vol.482 (1), p.31-34

2010

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Validation of the Beijing Version of the REM Sleep Behavior Disorder Questionnaire (RBDQ-Beijing) in a Mainland Chinese Cohort

The Tohoku Journal of Experimental Medicine, 2014, Vol.234(1), pp.7-15

2014

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PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population

Neuroscience letters, 2011-11, Vol.505 (3), p.260-262

2011

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Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population

Neuroscience letters, 2011-07, Vol.498 (2), p.124-126

2011

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Association between postural tremor and risk of disability in community‐dwelling older people

Journal of the American Geriatrics Society (JAGS), 2023-04, Vol.71 (4), p.1220-1227

2023

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Structural and functional brain alterations in patients with idiopathic rapid eye movement sleep behavior disorder

Journal of neuroradiology, 2022-01, Vol.49 (1), p.66-72

2022

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Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese

Scientific reports, 2015-10, Vol.5 (1), p.15891-15891, Article 15891

2015

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Risk factors for possible REM sleep behavior disorders: A community-based study in Beijing

Neurology, 2020-10, Vol.95 (16), p.e2214

2020

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Gender differences on motor and non-motor symptoms of de novo patients with early Parkinson’s disease

Neurological sciences, 2014-12, Vol.35 (12), p.1991-1996

2014

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Validation of a new olfactory test for Chinese Parkinson’s disease patients

Journal of clinical neuroscience, 2020-06, Vol.76, p.31-35

2020

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Postural Tremor Is Associated with Gait and Balance Impairments in Community‐Dwelling Older People

Journal of the American Geriatrics Society (JAGS), 2019-04, Vol.67 (4), p.799-803

2019

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Visual dysfunction in patients with idiopathic rapid eye movement sleep behavior disorder

Neuroscience letters, 2019-09, Vol.709, p.134360-134360, Article 134360

2019

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Decreased Penetrance of Parkinson's Disease in Elderly Carriers of Glucocerebrosidase Gene L444P/R Mutations: A Community‐Based 10‐Year Longitudinal Study

Movement disorders, 2020-04, Vol.35 (4), p.672-678

2020

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Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individuals

Neurobiology of aging, 2014-03, Vol.35 (3), p.725.e1-725.e6

2014

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Association between common genetic risk variants and depression in Parkinson's disease: A dPD study in Chinese

Parkinsonism & related disorders, 2016-12, Vol.33, p.122-126

2016

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Cervical dystonia incidence and diagnostic delay in a multiethnic population

Movement disorders, 2020-03, Vol.35 (3), p.450-456

2020

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Gait Analysis with Wearable Sensors in Isolated REM Sleep Behavior Disorder Associated with Phenoconversion: An Explorative Study

Journal of Parkinson's disease, 2024-01, Vol.14 (5), p.1027-1037

2024

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Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease

Neurobiology of aging, 2013-11, Vol.34 (11), p.2695.e9-2695.e10

2013

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Validation of the utility of the Brief Smell Identification Test in Chinese patients with Parkinson’s disease

Journal of clinical neuroscience, 2019-02, Vol.60, p.68-72

2019

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Stereopsis impairment is associated with decreased color perception and worse motor performance in Parkinson's disease

European journal of medical research, 2014-05, Vol.19 (1), p.29-29, Article 29

2014

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Clinical Manifestation of Parkinson's Disease in Association with Rapid Eye Movement Sleep Behavior Disorder Onset

European neurology, 2016-01, Vol.76 (3-4), p.154-160

2016

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Promoter methylation analysis of seven clock genes in Parkinson's disease

Non-Motor Symptoms in Treated and Untreated Chinese Patients with Early Parkinson’s Disease

High-depth whole-genome sequencing identifies structure variants, copy number variants and short tandem repeats associated with Parkinson’s disease

Education Moderates the Association of Probable REM Sleep Behavior Disorder With Cognitive and Motor Impairments in Community-Dwelling Older People

Smoking, genes encoding dopamine pathway and risk for Parkinson's disease

Validation of the Beijing Version of the REM Sleep Behavior Disorder Questionnaire (RBDQ-Beijing) in a Mainland Chinese Cohort

PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population

Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population

Association between postural tremor and risk of disability in community‐dwelling older people

Structural and functional brain alterations in patients with idiopathic rapid eye movement sleep behavior disorder

Association of ARNTL and PER1 genes with Parkinson's disease: a case-control study of Han Chinese

Risk factors for possible REM sleep behavior disorders: A community-based study in Beijing

Gender differences on motor and non-motor symptoms of de novo patients with early Parkinson’s disease

Validation of a new olfactory test for Chinese Parkinson’s disease patients

Postural Tremor Is Associated with Gait and Balance Impairments in Community‐Dwelling Older People

Visual dysfunction in patients with idiopathic rapid eye movement sleep behavior disorder

Decreased Penetrance of Parkinson's Disease in Elderly Carriers of Glucocerebrosidase Gene L444P/R Mutations: A Community‐Based 10‐Year Longitudinal Study

Clinical profiles of Parkinson's disease associated with common leucine-rich repeat kinase 2 and glucocerebrosidase genetic variants in Chinese individuals

Association between common genetic risk variants and depression in Parkinson's disease: A dPD study in Chinese

Cervical dystonia incidence and diagnostic delay in a multiethnic population

Gait Analysis with Wearable Sensors in Isolated REM Sleep Behavior Disorder Associated with Phenoconversion: An Explorative Study

Exonic sequencing revealed no causative mutation in the BST1 gene in patients with Parkinson's disease

Validation of the utility of the Brief Smell Identification Test in Chinese patients with Parkinson’s disease

Stereopsis impairment is associated with decreased color perception and worse motor performance in Parkinson's disease

Clinical Manifestation of Parkinson's Disease in Association with Rapid Eye Movement Sleep Behavior Disorder Onset

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