Associated Papers
An update on the monogenic causes of Parkinson's disease: Impact on patient stratification and personalised medicine.
Asmi S et al.
Ageing Research Reviews, 2026
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
31324919 (PubMed )
Supplement: awz191_supplementary_data.pdf
Association analysis of EIF4G1 and Parkinson disease in Xinjiang Uygur and Han nationality.
Ma Y et al.
Medicine, 2018
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
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
Genetics of Parkinson's disease: the yield.
Spatola M et al.
Parkinsonism & Related Disorders, 2014
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
Lesage S et al.
Neurobiology of Aging, 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
Translation initiator EIF4G1 mutations in familial Parkinson disease.
Chartier-Harlin MC et al.
American Journal of Human Genetics, 2011
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