<scp> <i>GBA1</i> </scp> Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease Susceptibility

Unknown GBA1 variants may be considered provisionally in clinical trials if also classified as VUS, likely pathogenic, or pathogenic per ACMG criteria. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

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Publication Details

Journal
Movement Disorders
Published
2025-11-15
DOI
https://doi.org/10.1002/mds.70127
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00

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article

GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease Susceptibility

Yoomin Lee, Sitki Cem Parlar, Ziv Gan‐Or
Movement Disorders
Lysosomal Storage Disorders Research
article

GBA1 Variants with Unknown Classification Are Modest Contributors to Parkinson's Disease Susceptibility

Yoomin Lee, Sitki Cem Parlar, Ziv Gan‐Or
article en

Abstract

Unknown GBA1 variants may be considered provisionally in clinical trials if also classified as VUS, likely pathogenic, or pathogenic per ACMG criteria. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Movement DisordersVol. 41(3)
Montreal Neurological Institute and Hospital (CA), McGill University (CA)
Michael J. Fox Foundation for Parkinson's Research, Canadian Institutes of Health Research, Fonds de Recherche du Québec - Santé
Openalex Percentile: Top 57%
Lysosomal Storage Disorders Research
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