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Kevin Kenna
Kevin Kenna
UNIVERSITY MEDICAL CENTER UTRECHT
Verified email at tcd.ie
Title
Cited by
Cited by
Year
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
ET Cirulli, BN Lasseigne, S Petrovski, PC Sapp, PA Dion, CS Leblond, ...
Science 347 (6229), 1436-1441, 2015
9872015
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
5882016
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
5762018
Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study
S Byrne, M Elamin, P Bede, A Shatunov, C Walsh, B Corr, M Heverin, ...
The Lancet Neurology 11 (3), 232-240, 2012
5572012
Rate of familial amyotrophic lateral sclerosis: a systematic review and meta-analysis
S Byrne, C Walsh, C Lynch, P Bede, M Elamin, K Kenna, R McLaughlin, ...
Journal of Neurology, Neurosurgery & Psychiatry 82 (6), 623-627, 2011
4732011
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
4112014
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
2822016
Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology
W Van Rheenen, RAA Van Der Spek, MK Bakker, JJFA Van Vugt, PJ Hop, ...
Nature genetics 53 (12), 1636-1648, 2021
2752021
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencing
KP Kenna, RL McLaughlin, S Byrne, M Elamin, M Heverin, EM Kenny, ...
Journal of medical genetics 50 (11), 776-783, 2013
1982013
Multiparametric MRI study of ALS stratified for the C9orf72 genotype
P Bede, ALW Bokde, S Byrne, M Elamin, RL McLaughlin, K Kenna, ...
Neurology 81 (4), 361-369, 2013
1882013
Basal ganglia involvement in amyotrophic lateral sclerosis
P Bede, M Elamin, S Byrne, RL McLaughlin, K Kenna, A Vajda, N Pender, ...
Neurology 81 (24), 2107-2115, 2013
1822013
Proposed criteria for familial amyotrophic lateral sclerosis
S Byrne, P Bede, M Elamin, K Kenna, C Lynch, R McLaughlin, ...
Amyotrophic Lateral Sclerosis 12 (3), 157-159, 2011
1662011
Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis
BN Smith, SD Topp, C Fallini, H Shibata, HJ Chen, C Troakes, A King, ...
Science translational medicine 9 (388), eaad9157, 2017
1482017
Aggregation of neurologic and neuropsychiatric disease in amyotrophic lateral sclerosis kindreds: A population‐based case–control cohort study of familial and sporadic …
S Byrne, M Heverin, M Elamin, P Bede, C Lynch, K Kenna, ...
Annals of neurology 74 (5), 699-708, 2013
1392013
Project MinE: study design and pilot analyses of a large-scale whole-genome sequencing study in amyotrophic lateral sclerosis
European Journal of Human Genetics 26 (10), 1537-1546, 2018
1322018
ALS-associated missense and nonsense TBK1 mutations can both cause loss of kinase function
M de Majo, SD Topp, BN Smith, AL Nishimura, HJ Chen, AS Gkazi, ...
Neurobiology of aging 71, 266. e1-266. e10, 2018
752018
The selective anatomical vulnerability of ALS:‘disease-defining’and ‘disease-defying’brain regions
P Bede, PM Iyer, C Schuster, M Elamin, RL Mclaughlin, K Kenna, ...
Amyotrophic lateral sclerosis and frontotemporal degeneration 17 (7-8), 561-570, 2016
732016
Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis
S Zhang, J Cooper-Knock, AK Weimer, M Shi, T Moll, JNG Marshall, ...
Neuron 110 (6), 992-1008. e11, 2022
722022
Patterns of cerebral and cerebellar white matter degeneration in ALS
P Bede, M Elamin, S Byrne, RL McLaughlin, K Kenna, A Vajda, A Fagan, ...
Journal of Neurology, Neurosurgery & Psychiatry 86 (4), 468-470, 2015
692015
The project MinE databrowser: bringing large-scale whole-genome sequencing in ALS to researchers and the public
RAA van der Spek, W van Rheenen, SL Pulit, KP Kenna, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 20 (5-6), 432-440, 2019
672019
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