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Number of items: 36.
A
Asante, EA;
Linehan, JM;
Tomlinson, AD;
Jakubcova, T;
Hamdan, S;
Grimshaw, A;
Smidak, M;
... Collinge, J; + view all
(2020)
Spontaneous generation of prions and transmissible PrP amyloid in a humanised transgenic mouse model of A117V GSS.
PLOS Biology
, 18
(6)
, Article e3000725. 10.1371/journal.pbio.3000725.
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B
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Benilova, I;
Reilly, M;
Terry, C;
Wenborn, A;
Schmidt, C;
Marinho, AT;
Risse, E;
... Collinge, J; + view all
(2020)
Highly infectious prions are not directly neurotoxic.
Proceeding of the National Academy of Sciences of the United States of America
10.1073/pnas.2007406117.
(In press).
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Bettencourt, C;
Foti, SC;
Miki, Y;
Botia, J;
Chatterjee, A;
Warner, TT;
Revesz, T;
... Holton, JL; + view all
(2020)
White matter DNA methylation profiling reveals deregulation of HIP1, LMAN2, MOBP, and other loci in multiple system atrophy.
Acta Neuropathologica
, 139
pp. 135-156.
10.1007/s00401-019-02074-0.
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Bettencourt, C;
Piras, IS;
Foti, SC;
Talboom, J;
Miki, Y;
Lashley, T;
Balazs, R;
... Holton, JL; + view all
(2020)
Epigenomics and transcriptomics analyses of multiple system atrophy brain tissue supports a role for inflammatory processes in disease pathogenesis.
Acta Neuropathologica Communications
, 8
, Article 71. 10.1186/s40478-020-00946-1.
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C
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C Dabin, L;
Guntoro, F;
Campbell, T;
Bélicard, T;
Smith, AR;
Smith, RG;
Raybould, R;
... Viré, E; + view all
(2020)
Altered DNA methylation profiles in blood from patients with sporadic Creutzfeldt–Jakob disease.
Acta Neuropathologica
10.1007/s00401-020-02224-9.
(In press).
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Cerofolini, L;
Ravera, E;
Bologna, S;
Wiglenda, T;
Böddrich, A;
Purfürst, B;
Benilova, I;
... Luchinat, C; + view all
(2020)
Mixing Aβ(1–40) and Aβ(1–42) peptides generates unique amyloid fibrils.
Chemical Communications
10.1039/d0cc02463e.
(In press).
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D
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De Bruijn, SE;
Fiorentino, A;
Ottaviani, D;
Fanucchi, S;
Melo, US;
Corral-Serrano, JC;
Mulders, T;
... Hardcastle, AJ; + view all
(2020)
Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa.
American Journal of Human Genetics
10.1016/j.ajhg.2020.09.002.
(In press).
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Dylewski, JF;
Wilson, N;
Lu, S;
Jat, P;
Weiser-Evans, M;
Panzer, SE;
Blaine, J;
(2020)
Isolation, purification, and conditional immortalization of murine glomerular endothelial cells of microvascular phenotype.
MethodsX
, 7
, Article 101048. 10.1016/j.mex.2020.101048.
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F
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Fassad, MR;
Shoman, WI;
Morsy, H;
Patel, MP;
Radwan, N;
Jenkins, L;
Cullup, T;
... Fasseeh, N; + view all
(2020)
Clinical and genetic spectrum in 33 Egyptian families with suspected primary ciliary dyskinesia.
Clinical Genetics
, 97
(3)
pp. 509-515.
10.1111/cge.13661.
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G
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Gao, Y;
Wang, T;
Yu, X;
International FTD-Genomics Consortium (IFGC);
Zhao, H;
Zeng, P;
(2020)
Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis.
Scientific Reports
, 10
, Article 12184. 10.1038/s41598-020-68848-9.
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Gill, ON;
Spencer, Y;
Richard-Loendt, A;
Kelly, C;
Brown, D;
Sinka, K;
Andrews, N;
... Brandner, S; + view all
(2020)
Prevalence in Britain of abnormal prion protein in human appendices before and after exposure to the cattle BSE epizootic.
Acta Neuropathologica
10.1007/s00401-020-02153-7.
(In press).
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H
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Heller, C;
Foiani, MS;
Moore, K;
Convery, R;
Bocchetta, M;
Neason, M;
Cash, DM;
... GENFI; + view all
(2020)
Plasma glial fibrillary acidic protein is raised in progranulin-associated frontotemporal dementia.
Journal of Neurology, Neurosurgery and Psychiatry
10.1136/jnnp-2019-321954.
(In press).
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Hosszu, LLP;
Conners, R;
Sangar, D;
Batchelor, M;
Sawyer, EB;
Fisher, S;
Cliff, MJ;
... Collinge, J; + view all
(2020)
Structural effects of the highly protective V127 polymorphism on human prion protein.
Communications Biology
, 3
(1)
, Article 402. 10.1038/s42003-020-01126-6.
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Hyare, H;
De Vita, E;
Porter, M-C;
Simpson, I;
Ridgway, G;
Lowe, J;
Thompson, A;
... Thornton, JS; + view all
(2020)
Putaminal diffusion tensor imaging measures predict disease severity across human prion diseases.
Brain Communications
, 2
(1)
, Article fcaa032. 10.1093/braincomms/fcaa032.
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J
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Jones, E;
Hummerich, H;
Viré, E;
Uphill, J;
Dimitriadis, A;
Speedy, H;
Campbell, T;
... Mead, S; + view all
(2020)
Identification of novel risk loci and causal insights for sporadic Creutzfeldt-Jakob disease: a genome-wide association study.
The Lancet Neurology
, 19
(10)
pp. 840-848.
10.1016/S1474-4422(20)30273-8.
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Jones, E;
Mead, S;
(2020)
Genetic risk factors for Creutzfeldt-Jakob disease.
Neurobiology of Disease
, 142
, Article 104973. 10.1016/j.nbd.2020.104973.
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K
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Koriath, Carolin Anna Maria;
(2020)
Next‐generation sequencing in the diagnosis of Dementia and Huntington’s disease Phenocopy Syndromes.
Doctoral thesis (Ph.D), UCL (University College London).
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L
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Lauwers, E;
Lalli, G;
Brandner, S;
Collinge, J;
Compernolle, V;
Duyckaerts, C;
Edgren, G;
... De Strooper, B; + view all
(2020)
Potential human transmission of amyloid β pathology: surveillance and risks.
The Lancet Neurology
, 19
(10)
pp. 872-878.
10.1016/S1474-4422(20)30238-6.
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M
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Manka, SW;
Brew, K;
(2020)
Thermodynamic and Mechanistic Insights into Coupled Binding and Unwinding of Collagen by Matrix Metalloproteinase 1.
Journal of Molecular Biology
, 432
(22)
pp. 5985-5993.
10.1016/j.jmb.2020.10.003.
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Manka, SW;
Moores, CA;
(2020)
Pseudo-repeats in doublecortin make distinct mechanistic contributions to microtubule regulation.
EMBO Reports
, Article e51534. 10.15252/embr.202051534.
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Mead, S;
(2020)
Marked abnormalities of plasma protein biomarkers in Creutzfeldt-Jakob disease (CJD).
Journal of Neurology, Neurosurgery and Psychiatry
10.1136/jnnp-2020-324307.
(In press).
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Mok, TH;
Mead, S;
(2020)
Preclinical biomarkers of prion infection and neurodegeneration.
Current Opinion in Neurobiology
, 61
pp. 82-88.
10.1016/j.conb.2020.01.009.
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Mole, J;
Mead, S;
Rudge, P;
Nihat, A;
Tzehow, M;
Collinge, J;
Caine, D;
(2020)
Cognitive decline heralds onset of symptomatic inherited prion disease.
MedRxiv: Cold Spring Harbor, NY, USA.
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Moore, K;
Convery, R;
Bocchetta, M;
Neason, M;
Cash, DM;
Greaves, C;
Russell, LL;
... Anderl-Straub, S; + view all
(2020)
A modified Camel and Cactus Test detects presymptomatic semantic impairment in genetic frontotemporal dementia within the GENFI cohort.
Applied Neuropsychology: Adult
10.1080/23279095.2020.1716357.
(In press).
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N
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Norsworthy, PJ;
Thompson, AGB;
Mok, TH;
Guntoro, F;
Dabin, LC;
Nihat, A;
Paterson, RW;
... Viré, EA; + view all
(2020)
A blood miRNA signature associates with sporadic Creutzfeldt-Jakob disease diagnosis.
Nature Communications
, 11
(1)
, Article 3960. 10.1038/s41467-020-17655-x.
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O
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O'Connor, A;
Karikari, TK;
Poole, T;
Ashton, NJ;
Rodriguez, JL;
Khatun, A;
Swift, I;
... Fox, NC; + view all
(2020)
Plasma phospho-tau181 in presymptomatic and symptomatic familial Alzheimer's disease: a longitudinal cohort study.
Molecular Psychiatry
10.1038/s41380-020-0838-x.
(In press).
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Orme, T;
Hernandez, D;
Ross, OA;
Kun-Rodrigues, C;
Darwent, L;
Shepherd, CE;
Parkkinen, L;
... Bras, J; + view all
(2020)
Analysis of neurodegenerative disease-causing genes in dementia with Lewy bodies.
Acta Neuropathologica Communications
, 8
(1)
, Article 5. 10.1186/s40478-020-0879-z.
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R
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Robson, EA;
Dixon, L;
Causon, L;
Dawes, W;
Benenati, M;
Fassad, M;
Hirst, RA;
... O'Callaghan, C; + view all
(2020)
Hydrocephalus and diffuse choroid plexus hyperplasia in primary ciliary dyskinesia-related MCIDAS mutation.
Neurology: Genetics
, 6
(4)
, Article e482. 10.1212/NXG.0000000000000482.
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Russell, LL;
Greaves, CV;
Bocchetta, M;
Nicholas, J;
Convery, RS;
Moore, K;
Cash, DM;
... Anderl-Straub, S; + view all
(2020)
Social cognition impairment in genetic frontotemporal dementia within the GENFI cohort.
Cortex
10.1016/j.cortex.2020.08.023.
(In press).
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S
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Sampson, EL;
Anderson, J;
Candy, B;
Davies, N;
Ellis-Smith, C;
Gola, A;
Harding, R;
... Evans, CJ; + view all
(2020)
Empowering Better End‐of‐Life Dementia Care (EMBED‐Care): A mixed methods protocol to achieve integrated person‐centred care across settings.
International Journal of Geriatric Psychiatry
10.1002/gps.5251.
(In press).
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Shoemark, A;
Pinto, AL;
Patel, MP;
Daudvohra, F;
Hogg, C;
Mitchison, HM;
Burgoyne, T;
(2020)
PCD Detect: enhancing ciliary features through image averaging and classification.
American Journal of Physiology: Lung Cellular and Molecular Physiology
, 319
(6)
L1048-L1060.
10.1152/ajplung.00264.2020.
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Smethurst, P;
Risse, E;
Tyzack, GE;
Mitchell, JS;
Taha, DM;
Chen, Y-R;
Newcombe, J;
... Patani, R; + view all
(2020)
Distinct responses of neurons and astrocytes to TDP-43 proteinopathy in amyotrophic lateral sclerosis.
Brain
, 143
(2)
pp. 430-440.
10.1093/brain/awz419.
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T
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Thomas, DX;
Bajaj, S;
McRae-McKee, K;
Hadjichrysanthou, C;
Anderson, RM;
Collinge, J;
(2020)
Association ofTDP‑43
proteinopathy, cerebral
amyloid angiopathy, and Lewy
bodies with cognitive
impairment in individuals
with or withoutAlzheimer’s disease
neuropathology.
Scientific Reports
, 10
(1)
, Article 14579. 10.1038/s41598-020-71305-2.
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Tsvetanov, KA;
Gazzina, S;
Jones, PS;
van Swieten, J;
Borroni, B;
Sanchez-Valle, R;
Moreno, F;
... Genetic FTD Initiative, GENFI; + view all
(2020)
Brain functional network integrity sustains cognitive function despite atrophy in presymptomatic genetic frontotemporal dementia.
Alzheimer's & Dementia
10.1002/alz.12209.
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V
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van der Lee, SJ;
Conway, OJ;
Jansen, I;
Carrasquillo, MM;
Kleineidam, L;
van den Akker, E;
Hernández, I;
... Holstege, H; + view all
(2020)
Correction to: A nonsynonymous mutation in PLCG2 reduces the risk of Alzheimer's disease, dementia with Lewy bodies and frontotemporal dementia, and increases the likelihood of longevity.
[Corrigendum].
Acta Neuropathologica
10.1007/s00401-019-02107-8.
(In press).
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Verzini, Silvia;
Shah, Maliha;
Theillet, Francois-Xavier;
Belsom, Adam;
Bieschke, Jan;
Wanker, Erich E;
Rappsilber, Juri;
... Selenko, Philipp; + view all
(2020)
Megadalton-sized Dityrosine Aggregates of α-Synuclein Retain High Degrees of Structural Disorder and Internal Dynamics.
Journal of Molecular Biology (JMB)
, 432
(24)
, Article 166689. 10.1016/j.jmb.2020.10.023.
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