Associated Papers
Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS.
Abner E et al.
Nature Communications, 2025
41062462 (PubMed )
Supplement: 41467_2025_64006_MOESM6_ESM.xlsx › Figure1a
Biochemical Characteristics of iPSC-Derived Dopaminergic Neurons from N370S GBA Variant Carriers with and without Parkinson's Disease.
Grigor'eva EV et al.
International Journal of Molecular Sciences, 2023
36901867 (PubMed )
Supplement: ijms-24-04437-s001.zip › ijms-2163006-supplementary.pdf
Validating Amino Acid Variants in Proteogenomics Using Sequence Coverage by Multiple Reads.
Levitsky LI et al.
Journal of Proteome Research, 2022
35536917 (PubMed )
Supplement: pr2c00033_si_002.pdf
Mitochondrial Serine Protease HTRA2 p.G399S in a Female with Di George Syndrome and Parkinson's Disease.
Gambardella S et al.
Parkinson's Disease, 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
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
Whole exome sequencing of rare variants in EIF4G1 and VPS35 in Parkinson disease.
Nuytemans K et al.
Neurology, 2013
EIF4G1 in familial Parkinson's disease: pathogenic mutations or rare benign variants?
Lesage S et al.
Neurobiology of Aging, 2012
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Tucci A et al.
Neuroscience Letters, 2012
Select a paper to view details