Ten Years of the International Parkinson Disease Genomics Consortium: Progress and Next Steps

The endocytic membrane trafficking pathway plays a major role in the risk of Parkinson's disease

(2019) Sara Bandres-Ciga 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

Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts

(2019) Hirotaka Iwaki et al.   MOVEMENT DISORDERS

Coordinating a new approach to basic research into Parkinson’s disease

(2019) Randy Schekman et al.   eLife

ARSA variants in α-synucleinopathies

(2019) Mary B Makarious et al.   BRAIN

The Parkinson's Disease Mendelian Randomization Research Portal

(2019) Alastair J. Noyce et al.   MOVEMENT DISORDERS

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

Mendelian Randomization—A Journey From Obscurity to Center Stage With a Few Potholes Along the Way

(2019) Sara Bandres-Ciga et al.   JAMA Neurology

Genetic modifiers of risk and age at onset in GBA associated Parkinson’s disease and Lewy body dementia

(2019) Cornelis Blauwendraat et al.   BRAIN

Genetic Determinants of Lipids and Cardiovascular Disease Outcomes

(2019) Elias Allara et al.   Circulation-Genomic and Precision Medicine

Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's disease

(2018) Demis A Kia et al.   ANNALS OF NEUROLOGY

Insufficient evidence for pathogenicity of SNCA His50Gln (H50Q) in Parkinson's disease

(2018) Cornelis Blauwendraat et al.   NEUROBIOLOGY OF AGING

Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease

(2018) Cornelis Blauwendraat et al.   JAMA Neurology

LRP10 in α-synucleinopathies

(2018) Demis A Kia et al.   LANCET NEUROLOGY

Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

(2018) Cornelis Blauwendraat et al.   MOVEMENT DISORDERS

Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps

(2018) Anubha Mahajan et al.   NATURE GENETICS

No clear support for a role for vitamin D in Parkinson's disease: A Mendelian randomization study

(2017) Susanna C. Larsson et al.   MOVEMENT DISORDERS

A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci

(2017) Diana Chang et al.   NATURE GENETICS

Lack of evidence for a role of genetic variation in TMEM230 in the risk for Parkinson's disease in the Caucasian population

(2017) Anamika Giri et al.   NEUROBIOLOGY OF AGING

NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseases

(2017) Cornelis Blauwendraat et al.   NEUROBIOLOGY OF AGING

Identification of 64 Novel Genetic Loci Provides an Expanded View on the Genetic Architecture of Coronary Artery Disease

(2017) Pim van der Harst et al.   CIRCULATION RESEARCH

Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy

(2016) Suzanne Lesage et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Deletions at 22q11.2 in idiopathic Parkinson's disease: a combined analysis of genome-wide association data

(2016) Kin Y Mok et al.   LANCET NEUROLOGY

ADORA1mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies

(2016) Cornelis Blauwendraat et al.   MOVEMENT DISORDERS

Is theMC1Rvariant p.R160W associated with Parkinson's?

(2015) Steven J. Lubbe et al.   ANNALS OF NEUROLOGY

CHCHD2 and Parkinson's disease

(2015) Iris E Jansen et al.   LANCET NEUROLOGY

Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study

(2015) Mike A Nalls et al.   LANCET NEUROLOGY

Genetic risk and age in Parkinson's disease: Continuum not stratum

(2015) Mike A. Nalls et al.   MOVEMENT DISORDERS

Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts

(2015) Javier Simón-Sánchez et al.   NEUROBIOLOGY OF AGING

EIF4G1 mutations do not cause Parkinson's disease

(2015) Noah Nichols et al.   NEUROBIOLOGY OF AGING

NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases

(2015) Mike A. Nalls et al.   NEUROBIOLOGY OF AGING

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

(2014) Mike A Nalls et al.   NATURE GENETICS

Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease

(2014) A. Beilina et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

(2012) M. F. Keller et al.   HUMAN MOLECULAR GENETICS

Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database

(2012) Christina M. Lill et al.   PLoS Genetics

Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies

(2011)   LANCET

Genome-wide association study reveals genetic risk underlying Parkinson's disease

(2009) Javier Simón-Sánchez et al.   NATURE GENETICS