The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
Published 2020 View Full Article
- Home
- Publications
- Publication Search
- Publication Details
Title
The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population
Authors
Keywords
-
Journal
BRAIN
Volume 143, Issue 7, Pages 2220-2234
Publisher
Oxford University Press (OUP)
Online
2020-05-06
DOI
10.1093/brain/awaa167
References
Ask authors/readers for more resources
Related references
Note: Only part of the references are listed.- Genetics of Parkinson's disease: An introspection of its journey towards precision medicine
- (2020) Sara Bandres-Ciga et al. NEUROBIOLOGY OF DISEASE
- A Comprehensive Analysis of Population Differences in LRRK2 Variant Distribution in Parkinson's Disease
- (2019) Li Shu et al. Frontiers in Aging Neuroscience
- The distribution and risk effect of GBA variants in a large cohort of PD patients from Colombia and Peru
- (2019) Carlos Velez-Pardo et al. PARKINSONISM & RELATED DISORDERS
- A clinical and genetic study of early-onset and familial parkinsonism in taiwan: An integrated approach combining gene dosage analysis and next-generation sequencing
- (2019) Chin-Hsien Lin et al. MOVEMENT DISORDERS
- Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
- (2019) Cornelis Blauwendraat et al. MOVEMENT DISORDERS
- Genetic analysis of Mendelian mutations in a large UK population-based Parkinson’s disease study
- (2019) Manuela M.X. Tan et al. BRAIN
- Parkinson's disease in the Western Pacific Region
- (2019) Shen-Yang Lim et al. LANCET NEUROLOGY
- Reanalysis of Clinical Exome Sequencing Data
- (2019) Pengfei Liu et al. NEW ENGLAND JOURNAL OF MEDICINE
- Progress in the genetic analysis of Parkinson’s disease
- (2019) Andrew Singleton et al. HUMAN MOLECULAR GENETICS
- The genetic architecture of Parkinson's disease
- (2019) Cornelis Blauwendraat et al. LANCET NEUROLOGY
- The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight
- (2019) Sara Bandres‐Ciga et al. MOVEMENT DISORDERS
- Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia
- (2019) Cornelis Blauwendraat et al. BRAIN
- LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study
- (2018) Marialuisa Quadri et al. LANCET NEUROLOGY
- Genotype-Phenotype Relations for the Parkinson's Disease Genes Parkin , PINK1 , DJ1: MDSGene Systematic Review
- (2018) Meike Kasten et al. MOVEMENT DISORDERS
- OUP accepted manuscript
- (2018) NUCLEIC ACIDS RESEARCH
- Glucocerebrosidase gene variants are accumulated in idiopathic REM sleep behavior disorder
- (2018) Ana Gámez-Valero et al. PARKINSONISM & RELATED DISORDERS
- Assessment of a Targeted Gene Panel for Identification of Genes Associated With Movement Disorders
- (2018) Solveig Montaut et al. JAMA Neurology
- LRP10 in α-synucleinopathies – Authors' reply
- (2018) Marialuisa Quadri et al. LANCET NEUROLOGY
- Genotype-phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review
- (2018) Joanne Trinh et al. MOVEMENT DISORDERS
- Therapeutic strategies for Parkinson disease: beyond dopaminergic drugs
- (2018) Delphine Charvin et al. NATURE REVIEWS DRUG DISCOVERY
- Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease
- (2018) Jinyoung Youn et al. NEUROBIOLOGY OF AGING
- Carriers of both GBA and LRRK2 mutations, compared to carriers of either, in Parkinson's disease: Risk estimates and genotype-phenotype correlations
- (2018) Gilad Yahalom et al. PARKINSONISM & RELATED DISORDERS
- Coding mutations inNUS1contribute to Parkinson’s disease
- (2018) Ji-feng Guo et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Recent Advances in Biomarkers for Parkinson’s Disease
- (2018) Runcheng He et al. Frontiers in Aging Neuroscience
- PLA2G6-Associated Neurodegeneration (PLAN): Review of Clinical Phenotypes and Genotypes
- (2018) Yu-pei Guo et al. Frontiers in Neurology
- Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature
- (2017) Susanne A. Schneider et al. MOVEMENT DISORDERS
- TMEM230 mutation analysis in Parkinson's disease in a Chinese population
- (2017) Weiqian Yan et al. NEUROBIOLOGY OF AGING
- VarCards: an integrated genetic and clinical database for coding variants in the human genome
- (2017) Jinchen Li et al. NUCLEIC ACIDS RESEARCH
- Evidence of mutations inRIC3acetylcholine receptor chaperone as a novel cause of autosomal-dominant Parkinson's disease with non-motor phenotypes
- (2016) Sumedha Sudhaman et al. JOURNAL OF MEDICAL GENETICS
- Identification of TMEM230 mutations in familial Parkinson's disease
- (2016) Han-Xiang Deng et al. NATURE GENETICS
- The Evolution of Genetics: Alzheimer’s and Parkinson’s Diseases
- (2016) Andrew Singleton et al. NEURON
- Autosomal dominant Parkinson's disease caused by SNCA duplications
- (2016) Takuya Konno et al. PARKINSONISM & RELATED DISORDERS
- RAB39B gene mutations are not linked to familial Parkinson’s disease in China
- (2016) Ji-feng Kang et al. Scientific Reports
- Polygenic risk of Parkinson disease is correlated with disease age at onset
- (2015) Valentina Escott-Price et al. ANNALS OF NEUROLOGY
- Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology
- (2015) Sue Richards et al. GENETICS IN MEDICINE
- MDS clinical diagnostic criteria for Parkinson's disease
- (2015) Ronald B. Postuma et al. MOVEMENT DISORDERS
- Genomic variant annotation and prioritization with ANNOVAR and wANNOVAR
- (2015) Hui Yang et al. Nature Protocols
- Mutation analysis of CHCHD2 gene in Chinese familial Parkinson's disease
- (2015) Zhenhua Liu et al. NEUROBIOLOGY OF AGING
- Differential effects of severe vs mild GBA mutations on Parkinson disease
- (2015) Z. Gan-Or et al. NEUROLOGY
- Toward better understanding of artifacts in variant calling from high-coverage samples
- (2014) Heng Li BIOINFORMATICS
- Monogenic Parkinson's disease and parkinsonism: Clinical phenotypes and frequencies of known mutations
- (2013) Andreas Puschmann PARKINSONISM & RELATED DISORDERS
- Genetics of Parkinson's disease – state of the art, 2013
- (2013) Vincenzo Bonifati PARKINSONISM & RELATED DISORDERS
- PLA2G6 gene mutation in autosomal recessive early-onset parkinsonism in a Chinese cohort
- (2011) C.- h. Shi et al. NEUROLOGY
- Predictors of Parkin Mutations in Early-Onset Parkinson Disease
- (2010) Karen S. Marder et al. ARCHIVES OF NEUROLOGY
- Frequency of Known Mutations in Early-Onset Parkinson Disease
- (2010) Roy N. Alcalay et al. ARCHIVES OF NEUROLOGY
- The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data
- (2010) A. McKenna et al. GENOME RESEARCH
- Large-scale screening of the Gaucher's disease-related glucocerebrosidase gene in Europeans with Parkinson's disease
- (2010) Suzanne Lesage et al. HUMAN MOLECULAR GENETICS
- Mutation analysis of Parkin, PINK1 and DJ-1 genes in Chinese patients with sporadic early onset parkinsonism
- (2010) Ji-feng Guo et al. JOURNAL OF NEUROLOGY
- Glucocerebrosidase Gene L444P mutation is a risk factor for Parkinson's disease in Chinese population
- (2010) Qi-Ying Sun et al. MOVEMENT DISORDERS
- Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease
- (2010) Jan O. Aasly et al. MOVEMENT DISORDERS
- ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data
- (2010) K. Wang et al. NUCLEIC ACIDS RESEARCH
- Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: Genetic, clinical, and positron emission tomography findings
- (2009) Jun-Ling Wang et al. MOVEMENT DISORDERS
- Expanding the clinical phenotype of SNCA duplication carriers
- (2009) Kenya Nishioka et al. MOVEMENT DISORDERS
- A novel LRRK2 mutation in a mainland Chinese patient with familial Parkinson's disease
- (2009) Lei Wang et al. NEUROSCIENCE LETTERS
- Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease
- (2009) E. Sidransky et al. NEW ENGLAND JOURNAL OF MEDICINE
- The prevalence of the G2019S and R1441C/G/H mutations in LRRK2 in German patients with Parkinson’s disease
- (2008) J. C. Möller et al. EUROPEAN JOURNAL OF NEUROLOGY
- Mutation analysis ofParkin,PINK1,DJ-1andATP13A2genes in Chinese patients with autosomal recessive early-onset Parkinsonism
- (2008) Ji-Feng Guo et al. MOVEMENT DISORDERS
- Lrrk2 R1441C parkinsonism is clinically similar to sporadic Parkinson disease
- (2008) K. Haugarvoll et al. NEUROLOGY
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreDiscover Peeref hubs
Discuss science. Find collaborators. Network.
Join a conversation