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Associations between gut microbiota and Parkinson disease: A bidirectional Mendelian randomization analysis

European journal of neurology, 2023-11, Vol.30 (11), p.3471-3477

2023

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Impaired meningeal lymphatic drainage in patients with idiopathic Parkinson’s disease

Nature medicine, 2021-03, Vol.27 (3), p.411-418

2021

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The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review

Molecular neurobiology, 2022-01, Vol.59 (1), p.523-534

2022

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Research advances on neurite outgrowth inhibitor B receptor

Journal of cellular and molecular medicine, 2020-07, Vol.24 (14), p.7697-7705

2020

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Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

American journal of human genetics, 2019-07, Vol.105 (1), p.166-176

2019

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PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

Frontiers in neurology, 2018-12, Vol.9, p.1100-1100

2018

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Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

Movement disorders, 2018-03, Vol.33 (3), p.459-467

2018

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Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy

Nature communications, 2020-02, Vol.11 (1), p.934-934, Article 934

2020

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Association between inflammatory bowel disease and Alzheimer’s disease: multivariable and bidirectional Mendelian randomisation analyses

Gut, 2023-09, Vol.72 (9), p.1797-1799

2023

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Microglial Activation in the Pathogenesis of Huntington's Disease

Frontiers in aging neuroscience, 2017-06, Vol.9, p.193-193

2017

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Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Journal of medical genetics, 2019-04, Vol.56 (4), p.265-270

2019

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Analysis of Salivary Microbiome in Patients with Alzheimer’s Disease

Journal of Alzheimer's disease, 2019-01, Vol.72 (2), p.633-640

2019

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Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project

Nature communications, 2022-05, Vol.13 (1), p.2939-15, Article 2939

2022

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Lack of bidirectional association between age‐related macular degeneration and Alzheimer's disease: A Mendelian randomization study

Alzheimer's & dementia, 2022-12, Vol.18 (12), p.2725-2729

2022

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Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study

Frontiers in genetics, 2022-05, Vol.13, p.805903-805903

2022

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Examining the causal role of leptin in bone mineral density: A Mendelian randomization study

Bone (New York, N.Y.), 2019-08, Vol.125, p.25-29

2019

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VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

Molecular brain, 2015-10, Vol.8 (1), p.70-70, Article 70

2015

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Different iron deposition patterns in akinetic/rigid-dominant and tremor-dominant Parkinson's disease

Clinical neurology and neurosurgery, 2020-11, Vol.198, p.106181-106181, Article 106181

2020

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Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants

Chinese medical journal, 2016-05, Vol.129 (9), p.1009-1010

Tang, Bei-Sha

2016

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Polygenic determinants of Parkinson's disease in a Chinese population

Neurobiology of aging, 2015-04, Vol.36 (4), p.1765.e1-1765.e6

2015

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Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in China

Chinese medical journal, 2020-11, Vol.133 (21), p.2616-2618

2020

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Simvastatin Induces Neuroprotection in 6‐OHDA‐Lesioned PC12 via the PI3K/AKT/Caspase 3 Pathway and Anti‐Inflammatory Responses

CNS neuroscience & therapeutics, 2013-03, Vol.19 (3), p.170-177

2013

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Parkinson's Disease and Cognitive Impairment

Parkinson's disease, 2016-01, Vol.2016 (2016), p.402-409

2016

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Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

Brain (London, England : 1878), 2019-08, Vol.142 (8), p.2215-2229

2019

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Central motor conduction time in spinocerebellar ataxia: a meta-analysis

Aging (Albany, NY.), 2020-11, Vol.12 (24), p.25718-25729

2020

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Associations between gut microbiota and Parkinson disease: A bidirectional Mendelian randomization analysis

Impaired meningeal lymphatic drainage in patients with idiopathic Parkinson’s disease

The Phenotypes and Mechanisms of NOTCH2NLC-Related GGC Repeat Expansion Disorders: a Comprehensive Review

Research advances on neurite outgrowth inhibitor B receptor

Expansion of Human-Specific GGC Repeat in Neuronal Intranuclear Inclusion Disease-Related Disorders

PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes

Proline‐rich transmembrane protein 2–negative paroxysmal kinesigenic dyskinesia: Clinical and genetic analyses of 163 patients

Autonomic ganglionic injection of α-synuclein fibrils as a model of pure autonomic failure α-synucleinopathy

Association between inflammatory bowel disease and Alzheimer’s disease: multivariable and bidirectional Mendelian randomisation analyses

Microglial Activation in the Pathogenesis of Huntington's Disease

Long-read sequencing identified intronic repeat expansions in SAMD12 from Chinese pedigrees affected with familial cortical myoclonic tremor with epilepsy

Analysis of Salivary Microbiome in Patients with Alzheimer’s Disease

Genomic analyses of 10,376 individuals in the Westlake BioBank for Chinese (WBBC) pilot project

Lack of bidirectional association between age‐related macular degeneration and Alzheimer's disease: A Mendelian randomization study

Telomere Length and COVID-19 Outcomes: A Two-Sample Bidirectional Mendelian Randomization Study

Examining the causal role of leptin in bone mineral density: A Mendelian randomization study

VPS35-deficiency results in an impaired AMPA receptor trafficking and decreased dendritic spine maturation

Different iron deposition patterns in akinetic/rigid-dominant and tremor-dominant Parkinson's disease

Attention Should be Drawn to Rare Diseases and Interpretation of Sequence Variants

Polygenic determinants of Parkinson's disease in a Chinese population

Clinical and genetic features of transthyretin-related familial amyloid polyneuropathy in China

Simvastatin Induces Neuroprotection in 6‐OHDA‐Lesioned PC12 via the PI3K/AKT/Caspase 3 Pathway and Anti‐Inflammatory Responses

Parkinson's Disease and Cognitive Impairment

Mutations in C1orf194, encoding a calcium regulator, cause dominant Charcot-Marie-Tooth disease

Central motor conduction time in spinocerebellar ataxia: a meta-analysis

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