PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease
@article{Beecham2015PARK10IA, title={PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease}, author={G. Beecham and D. Dickson and W. Scott and E. Martin and G. Schellenberg and K. Nuytemans and E. Larson and J. Buxbaum and J. Trojanowski and V. V. Van Deerlin and H. Hurtig and D. Mash and T. Beach and J. Troncoso and O. Pletnikov{\'a} and M. Frosch and B. Ghetti and T. Foroud and L. Honig and K. Marder and J. Vonsattel and S. Goldman and H. Vinters and O. Ross and Z. Wszolek and L. Wang and D. Dykxhoorn and M. Pericak-Vance and T. Montine and J. Leverenz and T. Dawson and J. Vance}, journal={Neurology}, year={2015}, volume={84}, pages={972 - 980} }
Objective: To minimize pathologic heterogeneity in genetic studies of Parkinson disease (PD), the Autopsy-Confirmed Parkinson Disease Genetics Consortium conducted a genome-wide association study using both patients with neuropathologically confirmed PD and controls. Methods: Four hundred eighty-four cases and 1,145 controls met neuropathologic diagnostic criteria, were genotyped, and then imputed to 3,922,209 variants for genome-wide association study analysis. Results: A small region on… CONTINUE READING
37 Citations
Is PARK10 a Locus for Familial PD? Yes or No?
- Medicine
- Movement disorders : official journal of the Movement Disorder Society
- 2016
- Highly Influenced
Parkinson's disease susceptibility variants and severity of Lewy body pathology.
- Medicine
- Parkinsonism & related disorders
- 2017
- 7
Variation in PARK10 is not associated with risk and age at onset of Parkinson's disease in large clinical cohorts
- Biology, Medicine
- Neurobiology of Aging
- 2015
- 6
Neuropathology of genetic synucleinopathies with parkinsonism: Review of the literature
- Medicine
- Movement disorders : official journal of the Movement Disorder Society
- 2017
- 98
TCEANC2 rs10788972 and rs12046178 variants in the PARK10 region in Chinese Han patients with sporadic Parkinson's disease
- Biology, Medicine
- Neurobiology of Aging
- 2015
- 10
Assessment of risk factor variants of LRRK2, MAPT, SNCA and TCEANC2 genes in Hungarian sporadic Parkinson’s disease patients
- Biology, Medicine
- Neuroscience Letters
- 2019
- PDF
Advances in understanding genomic markers and pharmacogenetics of Parkinson’s disease
- Medicine
- Expert opinion on drug metabolism & toxicology
- 2016
- 22
References
SHOWING 1-10 OF 34 REFERENCES
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson’s disease
- Biology, Medicine
- Nature Genetics
- 2010
- 576
- PDF
Genome-Wide Association Study reveals genetic risk underlying Parkinson’s disease
- Biology, Medicine
- Nature Genetics
- 2009
- 1,526
- PDF
A susceptibility gene for late‐onset idiopathic Parkinson's disease
- Medicine
- Annals of neurology
- 2002
- 202
Genomic convergence to identify candidate genes for Parkinson disease: SAGE analysis of the substantia nigra
- Biology, Medicine
- Movement disorders : official journal of the Movement Disorder Society
- 2005
- 48
Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.
- Biology, Medicine
- American journal of human genetics
- 2005
- 66
Age at onset in two common neurodegenerative diseases is genetically controlled.
- Biology, Medicine
- American journal of human genetics
- 2002
- 317
- PDF
A Two-Stage Meta-Analysis Identifies Several New Loci for Parkinson's Disease
- Biology, Medicine
- PLoS genetics
- 2011
- 223
- PDF
Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson’s disease
- Biology, Medicine
- Nature Genetics
- 2014
- 1,208
- PDF
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
- Medicine, Biology
- The Lancet
- 2011
- 770
- PDF
Genome‐Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
- Biology, Medicine
- Annals of human genetics
- 2010
- 403
- PDF