Bryan Traynor
Bryan Traynor
Laboratory of Neurogenetics, National Institute on Aging
Verified email at mail.nih.gov - Homepage
Title
Cited by
Cited by
Year
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
35702011
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, 2009
17612009
State of play in amyotrophic lateral sclerosis genetics
AE Renton, A Chiò, BJ Traynor
Nature neuroscience 17 (1), 17-23, 2014
12472014
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
11752010
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
10962013
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
9912012
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
9192008
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 Genet 6 (5), e1000952, 2010
7912010
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
7842010
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
7782013
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
7472009
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
6552013
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
6472015
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
5402014
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
4972013
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
4692008
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
4682003
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
4502000
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
3782014
Genome-wide meta-analysis identifies new susceptibility loci for migraine
V Anttila, BS Winsvold, P Gormley, T Kurth, F Bettella, G McMahon, ...
Nature genetics 45 (8), 912-917, 2013
3512013
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