×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
24511991
2014
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
22451204
2012
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
22438815
2012
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Web-based genome-wide association study identifies two novel loci and a substantial genetic component for Parkinson's disease.
21738487
2011
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.
21084426
2011
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Dissection of the genetics of Parkinson's disease identifies an additional association 5' of SNCA and multiple associated haplotypes at 17q21.
21044948
2011
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies.
21292315
2011
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Common genetic variation in the HLA region is associated with late-onset sporadic Parkinson's disease.
20711177
2010
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease.
20070850
2010
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
By comparing results of a GWAS performed on individuals of European ancestry, we identified PARK16, SNCA and LRRK2 as shared risk loci for PD and BST1 and MAPT as loci showing population differences.
19915576
2009
×
Entrez Id:
6622
Gene Symbol:
SNCA
SNCA
Parkinson Disease
0.700
GeneticVariation
GWASDB
Association to PD at SNCA was replicated in the Japanese GWAS, confirming this as a major risk locus across populations.
19915575
2009