Browse by UCL Departments and Centres
Group by: Author | Type
Number of items: 54.
A
Avet-Rochex, A;
Kaul, AK;
Gatt, AP;
McNeill, H;
Bateman, JM;
(2012)
Concerted control of gliogenesis by InR/TOR and FGF signalling in the Drosophila post-embryonic brain.
Development
, 139
(15)
pp. 2763-2772.
10.1242/dev.074179.
|
B
Beall, C;
Hamilton, DL;
Gallagher, J;
Logie, L;
Wright, K;
Soutar, MP;
Dadak, S;
... Ashford, MLJ; + view all
(2012)
Mouse hypothalamic GT1-7 cells demonstrate AMPK-dependent intrinsic glucose-sensing behaviour.
Diabetologia
, 55
(9)
pp. 2432-2444.
10.1007/s00125-012-2617-y.
|
Bendlin, BB;
Carlsson, CM;
Johnson, SC;
Zetterberg, H;
Blennow, K;
Willette, AA;
Okonkwo, OC;
... Sager, MA; + view all
(2012)
CSF T-Tau/Aβ42 predicts white matter microstructure in healthy adults at risk for Alzheimer's disease.
PLoS One
, 7
(6)
, Article e37720. 10.1371/journal.pone.0037720.
|
Boccardi, Marina;
Bocchetta, Martina;
Apostolova, Liana;
Barnes, Josephine;
Bartzokis, George;
Corbetta, Gabriele;
DeCarli, Charles;
... Frisoni, Giovanni; + view all
(2012)
IC‐P‐034: Definition of harmonized protocol for hippocampal segmentation.
Presented at: AAIC 2012, Vancouver, Canada.
|
Boccardi, Marina;
Bocchetta, Martina;
Apostolova, Liana;
Barnes, Josephine;
Bartzokis, George;
Corbetta, Gabriele;
DeCarli, Charles;
... Frisoni, Giovanni; + view all
(2012)
O2‐11‐02: Definition of harmonized protocol for hippocampal segmentation.
Presented at: AAIC 2012, Vancouver, Canada.
|
Bras, J;
Verloes, A;
Schneider, SA;
Mole, SE;
Guerreiro, RJ;
(2012)
Mutation of the parkinsonism gene ATP13A2 causes neuronal ceroid-lipofuscinosis.
Human Molecular Genetics
, 21
(12)
2646 - 2650.
10.1093/hmg/dds089.
|
C
Casas, JP;
Hingorani, AD;
(2012)
The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis.
Lancet
, 379
(9822)
1214 - 1224.
10.1016/S0140-6736(12)60110-X.
|
Castro-Seoane, R;
Hummerich, H;
Sweeting, T;
Tattum, MH;
Linehan, JM;
Fernandez de Marco, M;
Brandner, S;
... Klöhn, PC; + view all
(2012)
Plasmacytoid dendritic cells sequester high prion titres at early stages of prion infection.
PLoS Pathogens
, 8
(2)
, Article e1002538. 10.1371/journal.ppat.1002538.
|
Charlesworth, G;
Plagnol, V;
Holmström, KM;
Bras, J;
Sheerin, UM;
Preza, E;
Rubio-Agusti, I;
... Wood, NW; + view all
(2012)
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesis.
The American Journal of Human Genetics
, 91
(6)
1041 - 1050.
10.1016/j.ajhg.2012.10.024.
|
Chu, EM;
Kolappan, M;
Barnes, TR;
Joyce, EM;
Ron, MA;
(2012)
A window into the brain: an in vivo study of the retina in schizophrenia using optical coherence tomography.
Psychiatry Research: Neuroimaging
, 203
(1)
89 - 94.
10.1016/j.pscychresns.2011.08.011.
|
Cooper-Knock, J;
Hewitt, C;
Highley, JR;
Brockington, A;
Milano, A;
Man, S;
Martindale, J;
... Shaw, PJ; + view all
(2012)
Clinico-pathological features in amyotrophic lateral sclerosis with expansions in C9ORF72.
Brain
, 135
(3)
751 - 764.
10.1093/brain/awr365.
|
Corrêa, SAL;
Hunter, CJ;
Palygin, O;
Wauters, SC;
Martin, KJ;
McKenzie, C;
McKelvey, K;
... Frenguelli, BG; + view all
(2012)
MSK1 regulates homeostatic and experience-dependent synaptic plasticity.
Journal of Neuroscience
, 32
(38)
pp. 13039-13051.
10.1523/JNEUROSCI.0930-12.2012.
|
Crutch, SJ;
Lehmann, M;
Schott, JM;
Rabinovici, GD;
Rossor, MN;
Fox, NC;
(2012)
Posterior cortical atrophy.
Lancet Neurology
, 11
(2)
170 - 178.
10.1016/S1474-4422(11)70289-7.
|
D
Devine, MJ;
Kaganovich, A;
Ryten, M;
Mamais, A;
Trabzuni, D;
Manzoni, C;
McGoldrick, P;
... Lewis, PA; + view all
(2012)
Correction: Pathogenic LRRK2 Mutations Do Not Alter Gene Expression in Cell Model Systems or Human Brain Tissue.
PLOS ONE
, 7
(1)
, Article e22489. 10.1371/annotation/c12e4f9e-5aae-424b-a69f-fddf16976dc5.
|
F
Fratta, P;
Mizielinska, S;
Nicoll, AJ;
Zloh, M;
Fisher, EM;
Parkinson, G;
Isaacs, AM;
(2012)
C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes.
Scientific Reports
, 2
, Article 1016. 10.1038/srep01016.
|
G
Guerreiro, RJ;
Gustafson, DR;
Hardy, J;
(2012)
The genetic architecture of Alzheimer's disease: beyond APP, PSENs and APOE.
Neurobiology of Disease
, 33
(3)
437 - 456.
10.1016/j.neurobiolaging.2010.03.025.
|
H
Hailstone, JC;
Ridgway, GR;
Bartlett, JW;
Goll, JC;
Crutch, SJ;
Warren, JD;
(2012)
Accent processing in dementia.
Neuropsychologia
, 50
(9)
pp. 2233-2244.
10.1016/j.neuropsychologia.2012.05.027.
|
Hernandez, DG;
Nalls, MA;
Moore, M;
Chong, S;
Dillman, A;
Trabzuni, D;
Gibbs, JR;
... Cookson, MR; + view all
(2012)
Integration of GWAS SNPs and tissue specific expression profiling reveal discrete eQTLs for human traits in blood and brain.
Neurobiology of Disease
, 47
(1)
20 - 28.
10.1016/j.nbd.2012.03.020.
|
Hernandez, DG;
Nalls, MA;
Ylikotila, P;
Keller, M;
Hardy, JA;
Majamaa, K;
Singleton, AB;
(2012)
Genome Wide Assessment of Young Onset Parkinson's Disease from Finland.
PLOS ONE
, 7
(7)
, Article e41859. 10.1371/journal.pone.0041859.
|
Hölttä, M;
Zetterberg, H;
Mirgorodskaya, E;
Mattsson, N;
Blennow, K;
Gobom, J;
(2012)
Peptidome analysis of cerebrospinal fluid by LC-MALDI MS.
PLoS One
, 7
(8)
, Article e42555. 10.1371/journal.pone.0042555.
|
K
Kara, E;
Ling, H;
Pittman, AM;
Shaw, K;
de Silva, R;
Simone, R;
Holton, JL;
... Revesz, T; + view all
(2012)
The MAPT p.A152T variant is a risk factor associated with tauopathies with atypical clinical and neuropathological features.
Neurobioly of Aging
, 33
(9)
2231.e7 - 2231.e14.
10.1016/j.neurobiolaging.2012.04.006.
|
Keihaninejad, S;
Ryan, NS;
Malone, IB;
Modat, M;
Cash, D;
Ridgway, GR;
Zhang, H;
... Ourselin, S; + view all
(2012)
The importance of group-wise registration in tract based spatial statistics study of neurodegeneration: a simulation study in Alzheimer's disease.
PLOS One
, 7
(11)
, Article e45996. 10.1371/journal.pone.0045996.
|
Kojovic, M;
Sheerin, UM;
Rubio-Agusti, I;
Saha, A;
Bras, J;
Gibbons, V;
Palmer, R;
... Bhatia, KP; + view all
(2012)
Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.
Mov Disord
, 27
(14)
pp. 1829-1830.
10.1002/mds.25199.
|
L
Labbadia, J;
Novoselov, SS;
Bett, JS;
Weiss, A;
Paganetti, P;
Bates, GP;
Cheetham, ME;
(2012)
Suppression of protein aggregation by chaperone modification of high molecular weight complexes.
Brain
, 135
(4)
1180 -1196.
10.1093/brain/aws022.
|
Lehmann, M;
Barnes, J;
Ridgway, GR;
Ryan, NS;
Warrington, EK;
Crutch, SJ;
Fox, NC;
(2012)
Global gray matter changes in posterior cortical atrophy: a serial imaging study.
Alzheimer's & Dementia
, 8
(6)
502 - 512.
10.1016/j.jalz.2011.09.225.
|
Lehmann, M;
Koedam, EL;
Barnes, J;
Bartlett, JW;
Ryan, NS;
Pijnenburg, YA;
Barkhof, F;
... Fox, NC; + view all
(2012)
Posterior cerebral atrophy in the absence of medial temporal lobe atrophy in pathologically-confirmed Alzheimer's disease.
Neurobiology of Disease
, 33
(3)
627.e1 - 627.e12.
10.1016/j.neurobiolaging.2011.04.003.
|
Lescai, F;
Bonfiglio, S;
Bacchelli, C;
Chanudet, E;
Waters, A;
Sisodiya, SM;
Kasperavičiūtė, D;
... Stupka, E; + view all
(2012)
Characterisation and validation of insertions and deletions in 173 patient exomes.
PLoS One
, 7
(12)
, Article e51292. 10.1371/journal.pone.0051292.
|
Lill, CM;
Roehr, JT;
McQueen, MB;
Kavvoura, FK;
Bagade, S;
Schjeide, B-MM;
Schjeide, LM;
... WTCCC2; + view all
(2012)
Comprehensive Research Synopsis and Systematic Meta-Analyses in Parkinson's Disease Genetics: The PDGene Database.
PLOS GENETICS
, 8
(3)
, Article e1002548. 10.1371/journal.pgen.1002548.
|
M
Mahoney, CJ;
Beck, J;
Rohrer, JD;
Lashley, T;
Mok, K;
Shakespeare, T;
Yeatman, T;
... Warren, JD; + view all
(2012)
Frontotemporal dementia with the C9ORF72 hexanucleotide repeat expansion: clinical, neuroanatomical and neuropathological features.
Brain
, 135
(3)
736 - 750.
10.1093/brain/awr361.
|
Majounie, E;
Renton, AE;
Mok, K;
Dopper, EG;
Waite, A;
Rollinson, S;
Chiò, A;
... Traynor, BJ; + view all
(2012)
Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.
Lancet Neurology
, 11
(4)
323 - 330.
10.1016/S1474-4422(12)70043-1.
|
Matsuki, T;
Zaka, M;
Guerreiro, R;
van der Brug, MP;
Cooper, JA;
Cookson, MR;
Hardy, JA;
(2012)
Identification of Stk25 as a genetic modifier of Tau phosphorylation in Dab1-mutant mice.
PLoS One
, 7
(2)
, Article e31152. 10.1371/journal.pone.0031152.
|
Mattsson, N;
Rajendran, L;
Zetterberg, H;
Gustavsson, M;
Andreasson, U;
Olsson, M;
Brinkmalm, G;
... Portelius, E; + view all
(2012)
BACE1 inhibition induces a specific cerebrospinal fluid β-amyloid pattern that identifies drug effects in the central nervous system.
PLoS One
, 7
(2)
, Article e31084. 10.1371/journal.pone.0031084.
|
McNaughton, D;
Knight, W;
Guerreiro, R;
Ryan, N;
Lowe, J;
Poulter, M;
Nicholl, DJ;
... Mead, S; + view all
(2012)
Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series.
Neurobioly of Aging
, 33
(2)
426.e13 - 426.e21.
10.1016/j.neurobiolaging.2010.10.010.
|
Modat, M;
Leung, KK;
Cardoso, MJ;
Fox, NC;
(2012)
Atrophy Measurement Based on Segmentation Propagation and the Boundary Shift Integral Technique.
In: Wang, L and Yushkevich, P and Ourselin, S, (eds.)
NIBAD'12: MICCAI 2012 Workshop on Novel Imaging Biomarkers for Alzheimer's Disease and Related Disorders, October 5, 2012, Acropolis Convention Center, Nice, France.
(pp. 266 - 274).
CreateSpace Independent Publishing Platform
|
Mok, K;
Traynor, BJ;
Schymick, J;
Tienari, PJ;
Laaksovirta, H;
Peuralinna, T;
Myllykangas, L;
... Hardy, J; + view all
(2012)
Chromosome 9 ALS and FTD locus is probably derived from a single founder.
Neurobiology of Disease
, 33
(1)
209.e3 - 209.e8.
10.1016/j.neurobiolaging.2011.08.005.
|
Mok, KY;
Koutsis, G;
Schottlaender, LV;
Polke, J;
Panas, M;
Houlden, H;
(2012)
High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients.
Neurobioly of Aging
, 33
(8)
1851.e1 - 1851.e5.
10.1016/j.neurobiolaging.2012.02.021.
|
N
Neselius, S;
Brisby, H;
Theodorsson, A;
Blennow, K;
Zetterberg, H;
Marcusson, J;
(2012)
CSF-biomarkers in Olympic boxing: diagnosis and effects of repetitive head trauma.
PLoS One
, 7
(4)
, Article e33606. 10.1371/journal.pone.0033606.
|
P
Palmqvist, S;
Hertze, J;
Minthon, L;
Wattmo, C;
Zetterberg, H;
Blennow, K;
Londos, E;
(2012)
Comparison of brief cognitive tests and CSF biomarkers in predicting Alzheimer's disease in mild cognitive impairment: six-year follow-up study.
PLoS One
, 7
(6)
, Article e38639. 10.1371/journal.pone.0038639.
|
Petkova, VI;
Zetterberg, H;
Ehrsson, HH;
(2012)
Rubber hands feel touch, but not in blind individuals.
PLoS One
, 7
(4)
, Article e35912. 10.1371/journal.pone.0035912.
|
Pievani, Michela;
Bocchetta, Martina;
Boccardi, Marina;
Galluzzi, Samantha;
Bonetti, Matteo;
Thompson, Paul;
Frisoni, Giovanni;
(2012)
IC‐P‐037: Morphological differences in the striatum in early‐ and late‐onset Alzheimer's disease.
Presented at: AAIC 2012, Vancouver, Canada.
|
Pievani, Michela;
Bocchetta, Martina;
Boccardi, Marina;
Galluzzi, Samantha;
Bonetti, Matteo;
Thompson, Paul;
Frisoni, Giovanni;
(2012)
O5‐04‐05: Morphological differences in the striatum in early and late‐onset Alzheimer's disease.
Presented at: AAIC 2012, Vancouver, Canada.
|
Pillai, A;
Bruno, D;
Sarreal, AS;
Hernando, RT;
Saint-Louis, LA;
Nierenberg, J;
Ginsberg, SD;
... Buckley, PF; + view all
(2012)
Plasma BDNF levels vary in relation to body weight in females.
PLoS One
, 7
(7)
, Article e39358. 10.1371/journal.pone.0039358.
|
Plagnol, V;
Curtis, J;
Epstein, M;
Mok, KY;
Stebbings, E;
Grigoriadou, S;
Wood, NW;
... Nejentsev, S; + view all
(2012)
A robust model for read count data in exome sequencing experiments and implications for copy number variant calling.
Bioinformatics
, 28
(21)
2747 - 2754.
10.1093/bioinformatics/bts526.
|
Plun-Favreau, H;
Burchell, VS;
Holmström, KM;
Yao, Z;
Deas, E;
Cain, K;
Fedele, V;
... Abramov, AY; + view all
(2012)
HtrA2 deficiency causes mitochondrial uncoupling through the F₁F₀-ATP synthase and consequent ATP depletion.
Cell Death and Disease
, 3
, Article e335. 10.1038/cddis.2012.77.
|
R
Rogers, I;
Kerr, F;
Martinez, P;
Hardy, J;
Lovestone, S;
Partridge, L;
(2012)
Ageing increases vulnerability to aβ42 toxicity in Drosophila.
PLOS One
, 7
(7)
, Article e40569. 10.1371/journal.pone.0040569.
|
S
Scahill, RI;
Wild, EJ;
Tabrizi, SJ;
(2012)
Biomarkers for Huntington's disease: an update.
Expert Opinion on Medical Diagnostics
, 6
(5)
371 - 375.
10.1517/17530059.2012.701205.
|
Simon-Sanchez, J;
Kilarski, LL;
Nalls, MA;
Martinez, M;
Schulte, C;
Holmans, P;
Gasser, T;
... Consor, WTCC; + view all
(2012)
Cooperative Genome-Wide Analysis Shows Increased Homozygosity in Early Onset Parkinson's Disease.
PLOS ONE
, 7
(3)
, Article e28787. 10.1371/journal.pone.0028787.
|
Swaminathan, S;
Huentelman, MJ;
Corneveaux, JJ;
Myers, AJ;
Faber, KM;
Foroud, T;
Mayeux, R;
... Grp, NIA-LOADNCRADFS; + view all
(2012)
Analysis of Copy Number Variation in Alzheimer's Disease in a Cohort of Clinically Characterized and Neuropathologically Verified Individuals.
PLOS ONE
, 7
(12)
, Article e50640. 10.1371/journal.pone.0050640.
|
T
Trabzuni, D;
Wray, S;
Vandrovcova, J;
Ramasamy, A;
Walker, R;
Smith, C;
Luk, C;
... Ryten, M; + view all
(2012)
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies.
Human Molecular Genetics
, 21
(18)
4094 -4103.
10.1093/hmg/dds238.
|
Tucci, A;
Charlesworth, G;
Sheerin, UM;
Plagnol, V;
Wood, NW;
Hardy, J;
(2012)
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Neurosci Lett
, 518
(1)
19 - 22.
10.1016/j.neulet.2012.04.033.
|
W
Weiss, A;
Träger, U;
Wild, EJ;
Grueninger, S;
Farmer, R;
Landles, C;
Scahill, RI;
... Tabrizi, SJ; + view all
(2012)
Mutant huntingtin fragmentation in immune cells tracks Huntington's disease progression.
Journal of Clinical Investigation
, 122
(10)
3731 - 3736.
10.1172/JCI64565.
|
Wild, EJ;
Carroll, JB;
(2012)
HDBuzz: empowering patients through accessible education.
Trends in Molecular Medicine
, 18
(1)
1 - 3.
10.1016/j.molmed.2011.09.003.
|
Wray, S;
Self, M;
NINDS Parkinson's Disease iPSC Consortium;
NINDS Huntington's Disease iPSC Consortium;
NINDS ALS iPSC Consortium;
Lewis, PA;
Taanman, JW;
... Hardy, J; + view all
(2012)
Creation of an open-access, mutation-defined fibroblast resource for neurological disease research.
PLOS One
, 7
(8)
, Article e43099. 10.1371/journal.pone.0043099.
|
Writer, MJ;
Kyrtatos, PG;
Bienemann, AS;
Pugh, JA;
Lowe, AS;
Villegas-Llerena, C;
Kenny, GD;
... Hart, SL; + view all
(2012)
Lipid peptide nanocomplexes for gene delivery and magnetic resonance imaging in the brain.
Journal of Controlled Release
, 162
(2)
340 - 348.
10.1016/j.jconrel.2012.07.002.
|