Artikkelit, joihin on yleisen käytön mandaatti - Russell McLaughlinLisätietoja
Ei saatavilla missään: 13
Arvostele
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
Mandaatit: Motor Neurone Disease Association, UK
Arvostele
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
Mandaatit: Science Foundation Ireland
Arvostele
Connectivity-based characterisation of subcortical grey matter pathology in frontotemporal dementia and ALS: a multimodal neuroimaging study
P Bede, T Omer, E Finegan, RH Chipika, PM Iyer, MA Doherty, A Vajda, ...
Brain imaging and behavior 12, 1696-1707, 2018
Mandaatit: Health Research Board, Ireland, Motor Neurone Disease Association, UK
Arvostele
Neuroimaging patterns along the ALS-FTD spectrum: a multiparametric imaging study
T Omer, E Finegan, S Hutchinson, M Doherty, A Vajda, RL McLaughlin, ...
Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 18 (7-8), 611-623, 2017
Mandaatit: Health Research Board, Ireland
Arvostele
The clinical and radiological profile of primary lateral sclerosis: a population-based study
E Finegan, RH Chipika, S Li Hi Shing, MA Doherty, JC Hengeveld, ...
Journal of neurology 266, 2718-2733, 2019
Mandaatit: Health Research Board, Ireland, Science Foundation Ireland, Motor Neurone …
Arvostele
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
Mandaatit: Health Research Board, Ireland
Arvostele
Heritability of amyotrophic lateral sclerosis: insights from disparate numbers
RL McLaughlin, A Vajda, O Hardiman
JAMA neurology 72 (8), 857-858, 2015
Mandaatit: Health Research Board, Ireland
Arvostele
Extra-motor cerebral changes and manifestations in primary lateral sclerosis
E Finegan, SLH Shing, RH Chipika, KM Chang, MC McKenna, ...
Brain Imaging and Behavior 15, 2283-2296, 2021
Mandaatit: Health Research Board, Ireland, Science Foundation Ireland, Motor Neurone …
Arvostele
Spatial cluster analysis of population amyotrophic lateral sclerosis risk in Ireland
J Rooney, A Vajda, M Heverin, M Elamin, A Crampsie, R McLaughlin, ...
Neurology 84 (15), 1537-1544, 2015
Mandaatit: Health Research Board, Ireland, Motor Neurone Disease Association, UK
Arvostele
No association between soil constituents and amyotrophic lateral sclerosis relative risk in Ireland
J Rooney, A Vajda, M Heverin, A Crampsie, K Tobin, R McLaughlin, ...
Environmental Research 147, 102-107, 2016
Mandaatit: Health Research Board, Ireland, Motor Neurone Disease Association, UK
Arvostele
Social deprivation and population density are not associated with small area risk of amyotrophic lateral sclerosis
JPK Rooney, K Tobin, A Crampsie, A Vajda, M Heverin, R McLaughlin, ...
Environmental Research 142, 141-147, 2015
Mandaatit: Health Research Board, Ireland
Arvostele
A second-generation Irish genome-wide association study for amyotrophic lateral sclerosis
RL McLaughlin, KP Kenna, A Vajda, P Bede, M Elamin, S Cronin, ...
Neurobiology of aging 36 (2), 1221. e7-1221. e13, 2015
Mandaatit: Health Research Board, Ireland
Arvostele
Language deficits in primary lateral sclerosis: Cortical atrophy, white matter degeneration and functional disconnection between cerebral regions
EL Tan, M Tahedl, J Lope, JC Hengeveld, MA Doherty, RL McLaughlin, ...
Journal of Neurology 271 (1), 431-445, 2024
Mandaatit: Health Research Board, Ireland, Science Foundation Ireland, European Commission
Saatavilla jossain: 92
Arvostele
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), 5257, 2014
Mandaatit: Science Foundation Ireland, UK Natural Environment Research Council …
Arvostele
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), 1267-1288, 2018
Mandaatit: US National Institutes of Health, US Department of Veterans Affairs, Howard …
Arvostele
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
Mandaatit: US National Institutes of Health, UK Economic and Social Research Council …
Arvostele
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
Mandaatit: Motor Neurone Disease Association, UK
Arvostele
Upper Palaeolithic genomes reveal deep roots of modern Eurasians
ER Jones, G Gonzalez-Fortes, S Connell, V Siska, A Eriksson, ...
Nature communications 6 (1), 8912, 2015
Mandaatit: Swiss National Science Foundation, Bill & Melinda Gates Foundation, UK …
Arvostele
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
Mandaatit: US National Institutes of Health
Arvostele
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
Mandaatit: US National Institutes of Health, National Health and Medical Research …
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