Varaico: Literature-Extracted Genetic Variants

Gene:SNCA
Variant:p.G68E
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SNCA

NM_000345.4:p.G68E

Associated Papers

Biobank-scale genetic characterization of Alzheimer's disease and related dementias across diverse ancestries.

Khani M et al.

Nature Communications, 2025

40813364 (PubMed )
Supplement: 41467_2025_62108_MOESM4_ESM.xlsx › Supplementary_Data_2

Biobank-scale characterization of Alzheimer's disease and related dementias identifies potential disease-causing variants, risk factors, and genetic modifiers across diverse ancestries.

Khani M et al.

Medrxiv : the Preprint Server for Health Sciences, 2024

39606324 (PubMed )
Supplement: media-15.xlsx › Supplementary_Table_2

In silico analysis of alpha-synuclein protein variants and posttranslational modifications related to Parkinson's disease.

da Silva ANR et al.

Journal of Cellular Biochemistry, 2024

A population scale analysis of rare SNCA variation in the UK Biobank.

Blauwendraat C et al.

Neurobiology of Disease, 2021

33307186 (PubMed )
Supplement: NIHMS1657197-supplement-mmc4.xls › Sup_Table_1

α-Synucleins from Animal Species Show Low Fibrillation Propensities and Weak Oligomer Membrane Disruption.

Sahin C et al.

Biochemistry, 2018

Analysis of sheep α-synuclein provides a molecular strategy for the reduction of fibrillation.

Bickle L et al.

Biochimica Et Biophysica Acta. Proteins and Proteomics, 2017

The Parkinson Disease gene SNCA: Evolutionary and structural insights with pathological implication.

Siddiqui IJ et al.

Scientific Reports, 2016

Did α-Synuclein and Glucocerebrosidase Coevolve? Implications for Parkinson's Disease.

Gruschus JM

Plos One, 2015

Association of Parkinson's disease with six single nucleotide polymorphisms located in four PARK genes in the northern Han Chinese population.

Zhou Y et al.

Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia, 2012

Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.

Nuytemans K et al.

Human Mutation, 2010

20506312 (PubMed )
Supplement: humu0031-0763-SD1.pdf

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease.

Choi JM et al.

Neurogenetics, 2008

Acceleration of alpha-synuclein aggregation by homologous peptides.

Du HN et al.

Febs Letters, 2006

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Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."