Bryan Traynor
Bryan Traynor
Laboratory of Neurogenetics, National Institute on Aging
Verified email at - Homepage
Cited by
Cited by
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, 2011
Genome-wide association study reveals genetic risk underlying Parkinson's disease
J Simon-Sanchez, C Schulte, JM Bras, M Sharma, JR Gibbs, D Berg, ...
Nature genetics 41 (12), 1308-1312, 2009
State of play in amyotrophic lateral sclerosis genetics
AE Renton, A Chiò, BJ Traynor
Nature neuroscience 17 (1), 17-23, 2014
Exome sequencing reveals VCP mutations as a cause of familial ALS
JO Johnson, J Mandrioli, M Benatar, Y Abramzon, VM Van Deerlin, ...
Neuron 68 (5), 857-864, 2010
Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS
HJ Kim, NC Kim, YD Wang, EA Scarborough, J Moore, Z Diaz, ...
Nature 495 (7442), 467-473, 2013
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
Genotype, haplotype and copy-number variation in worldwide human populations
M Jakobsson, SW Scholz, P Scheet, JR Gibbs, JM VanLiere, HC Fung, ...
Nature 451 (7181), 998-1003, 2008
Prognostic factors in ALS: a critical review
A Chio, G Logroscino, O Hardiman, R Swingler, D Mitchell, E Beghi, ...
Amyotrophic lateral sclerosis 10 (5-6), 310-323, 2009
Incidence of amyotrophic lateral sclerosis in Europe
G Logroscino, BJ Traynor, O Hardiman, A Chiò, D Mitchell, RJ Swingler, ...
Journal of Neurology, Neurosurgery & Psychiatry 81 (4), 385-390, 2010
RNA toxicity from the ALS/FTD C9ORF72 expansion is mitigated by antisense intervention
CJ Donnelly, PW Zhang, JT Pham, AR Haeusler, NA Mistry, S Vidensky, ...
Neuron 80 (2), 415-428, 2013
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
JR Gibbs, MP Van Der Brug, DG Hernandez, BJ Traynor, MA Nalls, SL Lai, ...
PLoS genetics 6 (5), e1000952, 2010
Global epidemiology of amyotrophic lateral sclerosis: a systematic review of the published literature
A Chiò, G Logroscino, BJ Traynor, J Collins, JC Simeone, LA Goldstein, ...
Neuroepidemiology 41 (2), 118-130, 2013
Common genetic variants influence human subcortical brain structures
DP Hibar, JL Stein, ME Renteria, A Arias-Vasquez, S Desrivières, ...
Nature 520 (7546), 224-229, 2015
Genetic variability in the regulation of gene expression in ten regions of the human brain
A Ramasamy, D Trabzuni, S Guelfi, V Varghese, C Smith, R Walker, T De, ...
Nature neuroscience 17 (10), 1418-1428, 2014
Controversies and priorities in amyotrophic lateral sclerosis
MR Turner, O Hardiman, M Benatar, BR Brooks, A Chio, M De Carvalho, ...
The Lancet Neurology 12 (3), 310-322, 2013
Descriptive epidemiology of amyotrophic lateral sclerosis: new evidence and unsolved issues
G Logroscino, BJ Traynor, O Hardiman, P Couratier, JD Mitchell, ...
Journal of Neurology, Neurosurgery & Psychiatry 79 (1), 6-11, 2008
Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000
BJ Traynor, M Alexander, B Corr, E Frost, O Hardiman
Journal of Neurology, Neurosurgery & Psychiatry 74 (9), 1258-1261, 2003
Clinical features of amyotrophic lateral sclerosis according to the El Escorial and Airlie House diagnostic criteria: A population-based study
BJ Traynor, MB Codd, B Corr, C Forde, E Frost, OM Hardiman
Archives of neurology 57 (8), 1171-1176, 2000
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), 664-666, 2014
The transcriptional landscape of age in human peripheral blood
MJ Peters, R Joehanes, LC Pilling, C Schurmann, KN Conneely, J Powell, ...
Nature communications 6 (1), 1-14, 2015
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