GP2 : The Global Parkinson's Genetics Program

Penetrance of Parkinson's Disease in LRRK2 p.G2019S Carriers Is Modified by a Polygenic Risk Score

(2020) Hirotaka Iwaki et al.   MOVEMENT DISORDERS

Genetic identification of cell types underlying brain complex traits yields insights into the etiology of Parkinson’s disease

(2020) Julien Bryois et al.   NATURE GENETICS

Identification of Risk Loci for Parkinson Disease in Asians and Comparison of Risk Between Asians and Europeans

(2020) Jia Nee Foo et al.   JAMA Neurology

The role of genetics in Parkinson’s disease: a large cohort study in Chinese mainland population

(2020) Yuwen Zhao et al.   BRAIN

Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease Research

(2020) Roopa Rajan et al.   Frontiers in Neurology

Expanding Data Collection for the MDSGene Database: X‐Linked Dystonia‐Parkinsonism as Use Case Example

(2020) Martje G. Pauly et al.   MOVEMENT DISORDERS

A single-cell atlas of the human substantia nigra reveals cell-specific pathways associated with neurological disorders

(2020) Devika Agarwal et al.   Nature Communications

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 hexanucleotide repeat modifies expressivity of X‐linked dystonia parkinsonism

(2019) Ana Westenberger et al.   ANNALS OF NEUROLOGY

Using global team science to identify genetic Parkinson's disease worldwide

(2019) Eva‐Juliane Vollstedt et al.   ANNALS OF NEUROLOGY

Parkinson's disease in the Western Pacific Region

(2019) Shen-Yang Lim et al.   LANCET NEUROLOGY

Imaging gradual neurodegeneration in a basal ganglia model disease

(2019) Henrike Hanssen et al.   ANNALS OF NEUROLOGY

The genetic architecture of Parkinson's disease

(2019) Cornelis Blauwendraat et al.   LANCET NEUROLOGY

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

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

(2019) Cornelis Blauwendraat et al.   BRAIN

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

(2019) Mike A Nalls et al.   LANCET NEUROLOGY

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

(2019)   Journal of Parkinsons Disease

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

(2018) Tatsiana Aneichyk et al.   CELL

LARGE-PD: Examining the genetics of Parkinson's disease in Latin America

(2017) Cyrus P Zabetian et al.   MOVEMENT DISORDERS

Disease onset in X-linked dystonia-parkinsonism correlates with expansion of a hexameric repeat within an SVA retrotransposon inTAF1

(2017) D. Cristopher Bragg et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Neurophysiological fingerprints of X-linked dystonia-parkinsonism: A model basal ganglia disease

(2015) Anne Weissbach et al.   MOVEMENT DISORDERS

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

(2009) Wataru Satake et al.   NATURE GENETICS

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

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

Multicenter Analysis of Glucocerebrosidase Mutations in Parkinson's Disease

(2009) E. Sidransky et al.   NEW ENGLAND JOURNAL OF MEDICINE

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

(2008) Daniel G Healy et al.   LANCET NEUROLOGY