Progress in unraveling the genetic etiology of Parkinson disease in a genomic era
- 1 March 2015
- journal article
- review article
- Published by Elsevier BV in Trends in Genetics
- Vol. 31 (3), 140-149
- https://doi.org/10.1016/j.tig.2015.01.004
Abstract
No abstract availableKeywords
This publication has 120 references indexed in Scilit:
- A Multicenter Study of Glucocerebrosidase Mutations in Dementia With Lewy BodiesJAMA Neurology, 2013
- Meta‐analysis of Parkinson's Disease: Identification of a novel locus, RIT2Annals of Neurology, 2011
- Translation Initiator EIF4G1 Mutations in Familial Parkinson DiseaseAmerican Journal of Human Genetics, 2011
- A Mutation in VPS35, Encoding a Subunit of the Retromer Complex, Causes Late-Onset Parkinson DiseaseAmerican Journal of Human Genetics, 2011
- VPS35 Mutations in Parkinson DiseaseAmerican Journal of Human Genetics, 2011
- Gaucher Disease Glucocerebrosidase and α-Synuclein Form a Bidirectional Pathogenic Loop in SynucleinopathiesCell, 2011
- Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation updateHuman Mutation, 2010
- SNCA variants are associated with increased risk for multiple system atrophyAnnals of Neurology, 2009
- Role of the Tau Gene Region Chromosome Inversion in Progressive Supranuclear Palsy, Corticobasal Degeneration, and Related DisordersArchives of Neurology, 2008
- Genome-wide Linkage Analysis of a Parkinsonian-Pyramidal Syndrome Pedigree by 500 K SNP ArraysAmerican Journal of Human Genetics, 2008