Last Updated: 09/26/2026
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Found 6 publications
A repeat expansion in GOLGA8A is a major risk factor for atypical frontotemporal lobar degeneration with ubiquitin-positive inclusions.
Journal: Nature genetics
Published: February 21, 2025
Deciphering Distinct Genetic Risk Factors for FTLD-TDP Pathological Subtypes via Whole-Genome Sequencing.
Journal: medRxiv : the preprint server for health sciences
Published: July 09, 2024
Deciphering distinct genetic risk factors for FTLD-TDP pathological subtypes via whole-genome sequencing.
Journal: Nature communications
Published: June 05, 2024
MAPT haplotype-stratified GWAS reveals differential association for AD risk variants.
Journal: Alzheimer's & dementia : the journal of the Alzheimer's Association
Published: August 26, 2019
Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD.
Journal: Acta neuropathologica
Published: December 03, 2018
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study.
Journal: The Lancet. Neurology
Published: December 05, 2017
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Last Updated: 09/26/2026