Associated Papers
Population-Specific Differences in Pathogenic Variants of Genes Associated with Monogenic Parkinson's Disease.
Flores-Ocampo V et al.
Genes, 2025
α-Synuclein distribution in olfactory mucosa and skin nerves in Parkinson disease associated with an EIF4G1 gene mutation.
Braccia A et al.
Journal of Neuropathology and Experimental Neurology, 2025
Eukaryotic translation initiation factor EIF4G1 p.Ser637Cys mutation in a family with Parkinson's disease with antecedent essential tremor.
Liu RH et al.
Experimental and Therapeutic Medicine, 2024
Association study of DNAJC13, UCHL1, HTRA2, GIGYF2, and EIF4G1 with Parkinson's disease.
Saini P et al.
Neurobiology of Aging, 2021
Genetics of Parkinson's disease in the Polish population.
Milanowski ŁM et al.
Neurologia I Neurochirurgia Polska, 2021
Genetic architecture of common non-Alzheimer's disease dementias.
Guerreiro R et al.
Neurobiology of Disease, 2020
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease study.
Tan MMX et al.
Brain : a Journal of Neurology, 2019
Association analysis of EIF4G1 and Parkinson disease in Xinjiang Uygur and Han nationality.
Ma Y et al.
Medicine, 2018
Genetic Analysis of FBXO2, FBXO6, FBXO12, and FBXO41 Variants in Han Chinese Patients with Sporadic Parkinson's Disease.
Yuan L et al.
Neuroscience Bulletin, 2017
Systematic analysis of genetic variants in Han Chinese patients with sporadic Parkinson's disease.
Yuan L et al.
Scientific Reports, 2016
Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese.
Weng YC et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi, 2016
SLC6A3 rs28363170 and rs3836790 variants in Han Chinese patients with sporadic Parkinson's disease.
Lu Q et al.
Neuroscience Letters, 2016
Genetic analysis of TREM2 variants in Chinese Han patients with sporadic Parkinson's disease.
Tan T et al.
Neuroscience Letters, 2016
D620N mutation in the VPS35 gene and R1205H mutation in the EIF4G1 gene are uncommon in the Greek population.
Kalinderi K et al.
Neuroscience Letters, 2015
The EIF4G1 gene and Parkinson's disease.
Deng H et al.
Acta Neurologica Scandinavica, 2015
EIF4G1 mutations do not cause Parkinson's disease.
Nichols N et al.
Neurobiology of Aging, 2015
Parkinson disease: α-synuclein mutational screening and new clinical insight into the p.E46K mutation.
Pimentel MM et al.
Parkinsonism & Related Disorders, 2015
EIF4G1 is neither a strong nor a common risk factor for Parkinson's disease: evidence from large European cohorts.
Huttenlocher J et al.
Journal of Medical Genetics, 2015
EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese population.
Nishioka K et al.
Parkinsonism & Related Disorders, 2014
Genetics of Parkinson's disease--state of the art, 2013.
Bonifati V
Parkinsonism & Related Disorders, 2014
Genetics of Parkinson's disease: the yield.
Spatola M et al.
Parkinsonism & Related Disorders, 2014
Genetic analysis of the S100B gene in Chinese patients with Parkinson disease.
Guo Y et al.
Neuroscience Letters, 2013
EIF4G1 Ala502Val and Arg1205His variants in Chinese patients with Parkinson disease.
Yuan L et al.
Neuroscience Letters, 2013
Analysis of EIF4G1 in Parkinson's disease among Asians.
Zhao Y et al.
Neurobiology of Aging, 2013
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
Nuytemans K et al.
Neurology, 2013
Sequence variants in eukaryotic translation initiation factor 4-gamma (eIF4G1) are associated with Lewy body dementia.
Fujioka S et al.
Acta Neuropathologica, 2013
The genetics of Parkinson's disease: progress and therapeutic implications.
Singleton AB et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2013
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
Lesage S et al.
Neurobiology of Aging, 2012
Whole-genome and whole-exome sequencing in neurological diseases.
Foo JN et al.
Nature Reviews. Neurology, 2012
Variants in eukaryotic translation initiation factor 4G1 in sporadic Parkinson's disease.
Schulte EC et al.
Neurogenetics, 2012
Genetics of Parkinson disease and other movement disorders.
Kumar KR et al.
Current Opinion in Neurology, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Tucci A et al.
Neuroscience Letters, 2012
LRRK2 in Transcription and Translation Regulation: Relevance for Parkinson's Disease.
Dorval V et al.
Frontiers in Neurology, 2012
Translation initiator EIF4G1 mutations in familial Parkinson disease.
Chartier-Harlin MC et al.
American Journal of Human Genetics, 2011