Követés
Kevin Kenna
Kevin Kenna
UNIVERSITY MEDICAL CENTER UTRECHT
E-mail megerősítve itt: tcd.ie
Cím
Hivatkozott rá
Hivatkozott rá
Év
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
5772018
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
4742011
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
1892013
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
1832013
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
1502017
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
1402013
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
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
732022
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
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
702015
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
682019
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