Russell McLaughlin
Russell McLaughlin
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Cited by
Cited by
Genome flux and stasis in a five millennium transect of European prehistory
C Gamba, ER Jones, MD Teasdale, RL McLaughlin, G Gonzalez-Fortes, ...
Nature communications 5 (1), 1-9, 2014
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
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
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
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
Genome-wide association study identifies 19p13. 3 (UNC13A) and 9p21. 2 as susceptibility loci for sporadic amyotrophic lateral sclerosis
MA Van Es, JH Veldink, CGJ Saris, HM Blauw, PWJ van Vught, A Birve, ...
Nature genetics 41 (10), 1083-1087, 2009
Upper Palaeolithic genomes reveal deep roots of modern Eurasians
ER Jones, G Gonzalez-Fortes, S Connell, V Siska, A Eriksson, ...
Nature communications 6 (1), 1-8, 2015
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
Detection of long repeat expansions from PCR-free whole-genome sequence data
E Dolzhenko, JJ Van Vugt, RJ Shaw, MA Bekritsky, M Van Blitterswijk, ...
Genome research 27 (11), 1895-1903, 2017
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
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
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
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
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
Grey matter correlates of clinical variables in amyotrophic lateral sclerosis (ALS): a neuroimaging study of ALS motor phenotype heterogeneity and cortical focality
P Bede, A Bokde, M Elamin, S Byrne, RL McLaughlin, N Jordan, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (7), 766-773, 2013
The multistep hypothesis of ALS revisited: the role of genetic mutations
A Chiò, L Mazzini, S D'Alfonso, L Corrado, A Canosa, C Moglia, U Manera, ...
Neurology 91 (7), e635-e642, 2018
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
A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis
I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ...
Human molecular genetics 23 (8), 2220-2231, 2014
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
RL McLaughlin, D Schijven, W Van Rheenen, KR Van Eijk, M O’Brien, ...
Nature communications 8 (1), 1-12, 2017
The population genomics of archaeological transition in west Iberia: Investigation of ancient substructure using imputation and haplotype-based methods
R Martiniano, LM Cassidy, R Ó'Maoldúin, R McLaughlin, NM Silva, ...
PLoS genetics 13 (7), e1006852, 2017
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