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Human Molecular Genetics|November 11, 2008
Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degenerationClaire L Simpson, Robin Lemmens, Katarzyna Miskiewicz, et al.
The Lancet. Neurology|June 20, 2025
Diagnostic and prognostic value of α-synuclein seed amplification assay kinetic measures in Parkinson's disease: a longitudinal cohort studyChristina D Orrú, David P Vaughan, Nirosen Vijiaratnam, et al.
JAMA Neurology|December 21, 2019
Diagnosis Across the Spectrum of Progressive Supranuclear Palsy and Corticobasal SyndromeEdwin Jabbari, Negin Holland, Viorica Chelban, et al.
Annals of Neurology|June 17, 2014
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisFrank P Diekstra, Vivianna M Van Deerlin, John C van Swieten, et al.
The Lancet. Neurology|August 31, 2010
Chromosome 9p21 in sporadic amyotrophic lateral sclerosis in the UK and seven other countries: a genome-wide association studyAleksey Shatunov, Kin Mok, Stephen Newhouse, et al.
Brain : a Journal of Neurology|July 29, 2022
Neurofilament light levels predict clinical progression and death in multiple system atrophyViorica Chelban, Elham Nikram, Alexandra Perez-Soriano, et al.
Brain : a Journal of Neurology|April 16, 2025
Intronic FGF14 GAA repeat expansions impact progression and survival in multiple system atrophyViorica Chelban, David Pellerin, Nirosen Vijiaratnam, et al.
JAMA Neurology|June 1, 2016
Association of a Locus in the CAMTA1 Gene With Survival in Patients With Sporadic Amyotrophic Lateral SclerosisIsabella Fogh, Kuang Lin, Cinzia Tiloca, et al.
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