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The Lancet. Neurology|September 11, 2007
ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association studyMichael A van Es, Paul W Van Vught, Hylke M Blauw, et al.
Iscience|May 1, 2026
Small RNA sequencing identifies serum tDR-1:34-Gly-GCC tiRNA levels as a biomarker for survival in amyotrophic lateral sclerosisKoen C Demaegd, Lindy Kool, Sharada Baindoor, et al.
The Lancet. Neurology|October 11, 2014
Analysis of amyotrophic lateral sclerosis as a multistep process: a population-based modelling studyAmmar Al-Chalabi, Andrea Calvo, Adriano Chio, et al.
Annals of Neurology|April 11, 2025
UNC13A Polymorphism Influences Survival in Patients with Frontotemporal DementiaLianne M Reus, Sean W Willemse, Sterre C M de Boer, et al.
Journal of Neurology|December 12, 2024
Diagnosing primary lateral sclerosis: a clinico-pathological studyEva M J de Boer, Bálint S de Vries, Wim Van Hecke, et al.
Neurobiology of Disease|March 16, 2023
The contribution of Neanderthal introgression and natural selection to neurodegenerative diseasesZhongbo Chen, Regina H Reynolds, Antonio F Pardiñas, et al.
Heliyon|February 6, 2024
Rare and common genetic determinants of mitochondrial function determine severity but not risk of amyotrophic lateral sclerosisCalum Harvey, Marcel Weinreich, James A K Lee, et al.
Nature Genetics|December 18, 2007
Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosisMichael A van Es, Paul W J van Vught, Hylke M Blauw, et al.
Neurology|October 4, 2019
Prospective natural history study of C9orf72 ALS clinical characteristics and biomarkersAlexander J Cammack, Nazem Atassi, Theodore Hyman, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 6, 2025
Examining changing working status and caregiver assistance in amyotrophic lateral sclerosis (ALS) using large-scale European databases as part of PRECISION-ALSHarry McDonough, Robert McFarlane, Alejandro Caravaca Puchades, et al.
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