Articles with public access mandates - Jason HehirLearn more
Available somewhere: 6
Ambroxol for the Treatment of Patients With Parkinson Disease With and Without Glucocerebrosidase Gene Mutations: A Nonrandomized, Noncontrolled Trial
S Mullin, L Smith, K Lee, G D’Souza, P Woodgate, J Elflein, J Hällqvist, ...
JAMA neurology, 2020
Mandates: US National Science Foundation, Swedish Research Council, UK Medical …
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies
DJH Moss, M Poulter, J Beck, J Hehir, JM Polke, T Campbell, G Adamson, ...
Neurology 82 (4), 292-299, 2014
Mandates: UK Biotechnology and Biological Sciences Research Council, UK Medical …
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson’s disease study
MMX Tan, N Malek, MA Lawton, L Hubbard, AM Pittman, T Joseph, ...
Brain 142 (9), 2828-2844, 2019
Mandates: UK Medical Research Council, National Institute for Health Research, UK …
A 6.4 Mb Duplication of the α-Synuclein Locus Causing Frontotemporal Dementia and Parkinsonism: Phenotype-Genotype Correlations.
E Kara, AP Kiely, C Proukakis, N Giffin, S Love, J Hehir, K Rantell, ...
JAMA neurology 71 (9), 1162-1171, 2014
Mandates: US National Institutes of Health, UK Medical Research Council, National …
Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk
SJ Lubbe, BI Bustos, J Hu, D Krainc, T Joseph, J Hehir, M Tan, W Zhang, ...
Human molecular genetics 30 (1), 78-86, 2021
Mandates: UK Medical Research Council, Parkinson's UK, Wellcome Trust
Analysis of the genetic variability in Parkinson's disease from Southern Spain
S Bandrés-Ciga, NE Mencacci, R Durán, FJ Barrero, F Escamilla-Sevilla, ...
Neurobiology of aging 37, 210. e1-210. e5, 2016
Mandates: UK Medical Research Council, Wellcome Trust, Government of Spain
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