Alan Renton
Alan Renton
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TitleCited byYear
A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
AE Renton, E Majounie, A Waite, J Simón-Sánchez, S Rollinson, ...
Neuron 72 (2), 257-268, 2011
State of play in amyotrophic lateral sclerosis genetics
AE Renton, A Chị, BJ Traynor
Nature neuroscience 17 (1), 17, 2014
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study
E Majounie, AE Renton, K Mok, EGP Dopper, A Waite, S Rollinson, ...
The Lancet Neurology 11 (4), 323-330, 2012
PINK1 cleavage at position A103 by the mitochondrial protease PARL
E Deas, H Plun-Favreau, S Gandhi, H Desmond, S Kjaer, SHY Loh, ...
Human molecular genetics 20 (5), 867-879, 2010
Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis
JO Johnson, EP Pioro, A Boehringer, R Chia, H Feit, AE Renton, ...
Nature neuroscience 17 (5), 664, 2014
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chị, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
Repeat Expansion in C9ORF72 in Alzheimer's Disease
E Majounie, Y Abramzon, AE Renton, R Perry, SS Bassett, O Pletnikova, ...
New England Journal of Medicine 366 (3), 283-284, 2012
Mitochondrial dysfunction triggered by loss of HtrA2 results in the activation of a brain-specific transcriptional stress response
N Moisoi, K Klupsch, V Fedele, P East, S Sharma, A Renton, ...
Cell death and differentiation 16 (3), 449, 2009
Genetic variants of the α-synuclein gene SNCA are associated with multiple system atrophy
A Al-Chalabi, A Dürr, NW Wood, MH Parkinson, A Camuzat, JS Hulot, ...
PloS one 4 (9), e7114, 2009
Extensive genetics of ALS: a population-based study in Italy
A Chị, A Calvo, L Mazzini, R Cantello, G Mora, C Moglia, L Corrado, ...
Neurology 79 (19), 1983-1989, 2012
A common haplotype lowers PU. 1 expression in myeloid cells and delays onset of Alzheimer's disease
K Huang, E Marcora, AA Pimenova, AF Di Narzo, M Kapoor, SC Jin, ...
Nature neuroscience 20 (8), 1052, 2017
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
A genome-wide association study of myasthenia gravis
AE Renton, HA Pliner, C Provenzano, A Evoli, R Ricciardi, MA Nalls, ...
JAMA neurology 72 (4), 396-404, 2015
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population
M Sabatelli, FL Conforti, M Zollino, G Mora, MR Monsurṛ, P Volanti, ...
Neurobiology of aging 33 (8), 1848. e15-1848. e20, 2012
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases
MA Nalls, J Bras, DG Hernandez, MF Keller, E Majounie, AE Renton, ...
Neurobiology of aging 36 (3), 1605. e7-1605. e12, 2015
GroupICA dual regression analysis of resting state networks in a behavioral variant of frontotemporal dementia
R Rytty, J Nikkinen, L Paavola, A Abou Elseoud, V Moilanen, A Visuri, ...
Frontiers in human neuroscience 7, 461, 2013
Simó n-Sá nchez
AE Renton, E Majounie, A Waite
J., Rollinson, S., Gibbs, JR, Schymick, JC, Laaksovirta, H., van Swieten, JC …, 2011
The RNA-binding motif 45 (RBM45) protein accumulates in inclusion bodies in amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration with TDP-43 inclusions …
M Collins, D Riascos, T Kovalik, J An, K Krupa, K Krupa, BL Hood, ...
Acta neuropathologica 124 (5), 717-732, 2012
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations
A Chị, G Restagno, M Brunetti, I Ossola, A Calvo, A Canosa, C Moglia, ...
J Neurol Neurosurg Psychiatry 83 (7), 730-733, 2012
Large C9orf72 repeat expansions are not a common cause of Parkinson's disease
E Majounie, Y Abramzon, AE Renton, MF Keller, BJ Traynor, AB Singleton
Neurobiology of aging 33 (10), 2527. e1-2527. e2, 2012
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