A. Richardson

发表

Working memory, attention, and executive function in Alzheimer’s disease and frontotemporal dementia

D. Neary, J. Snowden, C. Stopford, 2012, Cortex.

C9orf72, age at onset, and ancestry help discriminate behavioral from language variants in FTLD cohorts

Demis A. Kia, O. Andreassen, B. Miller, 2020, Neurology.

Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer's disease

D. Hernandez, A. Singleton, J. Hardy, 2018, Neurobiology of Aging.

Classification and pathology of primary progressive aphasia

D. Neary, D. Mann, J. Snowden, 2013, Neurology.

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Frequency and clinical characteristics of progranulin mutation carriers in the Manchester frontotemporal lobar degeneration cohort: comparison with patients with MAPT and no known mutations.

Julie S Snowden, Sara Rollinson, D. Neary, 2008, Brain : a journal of neurology.

Distinct clinical and pathological phenotypes in frontotemporal dementia associated with MAPT, PGRN and C9orf72 mutations

D. Neary, D. Mann, S. Rollinson, 2015, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Frontotemporal dementia with amyotrophic lateral sclerosis: A clinical comparison of patients with and without repeat expansions in C9orf72

D. Neary, D. Mann, S. Rollinson, 2013, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Clinical aspects of hereditary frontotemporal dementia.

D. Neary, A. Richardson, 2008, Handbook of clinical neurology.

Mendelian randomization implies no direct causal association between leukocyte telomere length and amyotrophic lateral sclerosis

Nick C Fox, Alan J. Thomas, D. Hernandez, 2020, Scientific Reports.

TREM2 analysis and increased risk of Alzheimer's disease

D. Mann, S. Rollinson, J. Snowden, 2015, Neurobiology of Aging.

Naming and conceptual understanding in frontotemporal dementia

J. Snowden, J. Thompson, A. Richardson, 2019, Cortex.

Progressive aphasia presenting with deep dyslexia and dysgraphia

D. Neary, J. Snowden, J. Thompson, 2012, Cortex.

Association between semantic dementia and progressive supranuclear palsy

D. Mann, J. Snowden, J. Thompson, 2018, Journal of Neurology, Neurosurgery, and Psychiatry.

p62/SQSTM1 analysis in frontotemporal lobar degeneration

D. Neary, D. Mann, S. Rollinson, 2015, Neurobiology of Aging.

Debrisoquine hydroxylase gene polymorphism (CYP2D6*4) in dementia with Lewy bodies

D. Mann, A. Richardson, S. Pickering-Brown, 2003, Journal of Neurology Neurosurgery & Psychiatry.

Nuclear carrier and RNA‐binding proteins in frontotemporal lobar degeneration associated with fused in sarcoma (FUS) pathological changes

D. Neary, N. Cairns, D. Mann, 2013, Neuropathology and applied neurobiology.

Psychosis, C9ORF72 and dementia with Lewy bodies

D. Neary, D. Mann, S. Rollinson, 2012, Journal of Neurology, Neurosurgery & Psychiatry.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C. Fox, Pietro Pietrini, Alexander Gerhard, 2018, Nature Medicine.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study

Kevin F. Bieniek, C. Geula, M. Mesulam, 2018, The Lancet Neurology.

Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal dementia and GRN mutations: a genome-wide association study

Elizabeth, Sandro, Ying-xue, 2018 .

Semantic dementia, progressive non-fluent aphasia and their association with amyotrophic lateral sclerosis

D. Neary, D. Mann, J. Snowden, 2017, Journal of Neurology, Neurosurgery & Psychiatry.

Neurodegeneration in frontotemporal lobar degeneration and motor neurone disease associated with expansions in C9orf72 is linked to TDP‐43 pathology and not associated with aggregated forms of dipeptide repeat proteins

D. Mann, C. Troakes, S. Rollinson, 2015, Neuropathology and applied neurobiology.

Psychosis associated with expansions in the C9orf72 gene: the influence of a 10 base pair gene deletion

D. Neary, D. Mann, S. Rollinson, 2015, Journal of Neurology, Neurosurgery & Psychiatry.

A small deletion in C9orf72 hides a proportion of expansion carriers in FTLD

Janel O. Johnson, D. Mann, S. Mead, 2015, Neurobiology of Aging.

Sporadic Creutzfeldt-Jakob disease presenting as progressive nonfluent aphasia with speech apraxia.

J. Snowden, J. Thompson, A. Richardson, 2013, Alzheimer disease and associated disorders.

Evidence of a founder effect in families with frontotemporal dementia that harbor the tau +16 splice mutation

J. Trojanowski, J. Hardy, D. Neary, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations.

D. Neary, D. Mann, S. Rollinson, 2012, Brain : a journal of neurology.

Analysis of optineurin in frontotemporal lobar degeneration

D. Neary, S. Rollinson, A. Richardson, 2012, Neurobiology of Aging.

Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17

S. Melquist, D. Neary, B. Boeve, 2006, Nature.

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

D. Neary, D. Mann, J. Snowden, 2013, Neurology.

Functional neuroanatomical associations of working memory in early‐onset Alzheimer's disease

K. Herholz, J. Snowden, C. Stopford, 2018, International journal of geriatric psychiatry.

Gene Expression Imputation Across Multiple Tissue Types Provides Insight Into the Genetic Architecture of Frontotemporal Dementia and Its Clinical Subtypes

Nick C Fox, Alan J. Thomas, D. Hernandez, 2021, Biological Psychiatry.

The most common type of FTLD-FUS (aFTLD-U) is associated with a distinct clinical form of frontotemporal dementia but is not related to mutations in the FUS gene

D. Neary, T. Griffiths, D. Mann, 2011, Acta Neuropathologica.

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

D. Hernandez, A. Singleton, J. Hardy, 2017, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset

D. Hernandez, A. Singleton, D. Neary, 2015 .

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

E. Haan, P. Pietrini, R. Petersen, 2017, Scientific Reports.

D. Hernandez, M. Nalls, L. Ferrucci, 2017, bioRxiv.

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia.

D. Neary, D. Mann, A. Varma, 2006, Brain : a journal of neurology.

Frontotemporal dementia and its subtypes: a genome-wide association study

Alexander Gerhard, Adrian Danek, Luigi Ferrucci, 2014, The Lancet Neurology.

Cognitive Phenotypes in Alzheimer's Disease and Genetic Risk

Julie S. Snowden, D. Neary, D. Mann, 2007, Cortex.

Inferring thought and action in motor neurone disease

D. Neary, F. Happé, J. Snowden, 2007, Neuropsychologia.

Granular expression of prolyl-peptidyl isomerase PIN1 is a constant and specific feature of Alzheimer’s disease pathology and is independent of tau, Aβ and TDP-43 pathology

D. Neary, E. Bigio, D. Mann, 2011, Acta Neuropathologica.

Patterns and severity of vascular amyloid in Alzheimer’s disease associated with duplications and missense mutations in APP gene, Down syndrome and sporadic Alzheimer’s disease

D. Mann, T. Iwatsubo, J. Snowden, 2018, Acta Neuropathologica.

The clinical diagnosis of early-onset dementias: diagnostic accuracy and clinicopathological relationships.

Julie S Snowden, D. Neary, D. Mann, 2011, Brain : a journal of neurology.

Glucocerebrosidase mutations in diffuse Lewy body disease.

M. Farrer, J. Kachergus, D. Neary, 2011, Parkinsonism & related disorders.

Heterogeneous ribonuclear protein E2 (hnRNP E2) is associated with TDP-43-immunoreactive neurites in Semantic Dementia but not with other TDP-43 pathological subtypes of Frontotemporal Lobar Degeneration

S. Rollinson, J. Snowden, A. Richardson, 2017, Acta Neuropathologica Communications.

Heterogeneous ribonuclear protein A3 (hnRNP A3) is present in dipeptide repeat protein containing inclusions in Frontotemporal Lobar Degeneration and Motor Neurone disease associated with expansions in C9orf72 gene

D. Mann, S. Rollinson, J. Snowden, 2017, Acta neuropathologica communications.

Cognition and behaviour in frontotemporal dementia with and without amyotrophic lateral sclerosis

S. Rollinson, J. Snowden, J. Thompson, 2020, Journal of Neurology, Neurosurgery, and Psychiatry.

Do NIA-AA criteria distinguish Alzheimer's disease from frontotemporal dementia?

Julie S. Snowden, D. Neary, D. Mann, 2015, Alzheimer's & Dementia.

Histopathological changes underlying frontotemporal lobar degeneration with clinicopathological correlation

Jing Shi, Julie S. Snowden, David M. A. Mann, 2005, Acta Neuropathologica.

Inherited frontotemporal dementia in nine British families associated with intronic mutations in the tau gene.

J. Hardy, D. Neary, D. Mann, 2002, Brain : a journal of neurology.

Co-Occurrence of Language and Behavioural Change in Frontotemporal Lobar Degeneration

D. Neary, D. Mann, J. Snowden, 2016, Dementia and Geriatric Cognitive Disorders Extra.

Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia.

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Nature Medicine.

Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

S. Rollinson, J. Snowden, A. Richardson, 2016, Acta Neuropathologica Communications.

Semantic dementia and the left and right temporal lobes

Christopher Kobylecki, Julie S. Snowden, D. Neary, 2017, Cortex.

Analysis of the hexanucleotide repeat in C9ORF72 in Alzheimer's disease

D. Neary, S. Rollinson, A. Richardson, 2012, Neurobiology of Aging.

Distinct clinical characteristics in patients with frontotemporal dementia and C9ORF72 mutations: a study of demographics, neurology, behaviour, cognition and histopathology

D. Neary, S. Rollinson, J. Snowden, 2012 .

Pathological correlates of frontotemporal lobar degeneration in the elderly

D. Neary, T. Griffiths, I. McKeith, 2011, Acta Neuropathologica.

Differential diagnosis of Alzheimer’s disease using spectrochemical analysis of blood

Camilo L. M. Morais, D. Mann, J. Snowden, 2017, Proceedings of the National Academy of Sciences.

A C6orf10/LOC101929163 locus is associated with age of onset in C9orf72 carriers

Nick C Fox, Alan J. Thomas, D. Hernandez, 2018, Brain : a journal of neurology.

Behaviour in amyotrophic lateral sclerosis

D. Neary, J. Snowden, A. Richardson, 2008, Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.

18F-Florbetapir PET in Patients with Frontotemporal Dementia and Alzheimer Disease

D. Neary, M. Pontecorvo, K. Herholz, 2015, The Journal of Nuclear Medicine.

The role of lysosomes and autophagosomes in frontotemporal lobar degeneration

D. Mann, S. Rollinson, J. Snowden, 2018, Neuropathology and applied neurobiology.

A UBQLN2 variant of unknown significance in frontotemporal lobar degeneration

D. Mann, S. Rollinson, A. Richardson, 2015, Neurobiology of Aging.

Recent origin and spread of a common Welsh MAPT splice mutation causing frontotemporal lobar degeneration

D. Neary, D. Mann, J. Snowden, 2009, neurogenetics.

Creating the Pick’s disease International Consortium: Association study of MAPT H2 haplotype with risk of Pick’s disease

Derek H. Oakley, A. Singleton, D. Vitale, 2023, medRxiv.

Plasma levels of progranulin and interleukin-6 in frontotemporal lobar degeneration

D. Neary, D. Mann, S. Rollinson, 2015, Neurobiology of Aging.

Susceptible genes and disease mechanisms identified in frontotemporal dementia and frontotemporal dementia with Amyotrophic Lateral Sclerosis by DNA-methylation and GWAS

Nick C Fox, D. Hernandez, M. Nalls, 2017, Scientific Reports.

The Edinburgh Cognitive and Behavioral ALS Screen (ECAS) in frontotemporal dementia

J. Snowden, J. Thompson, A. Richardson, 2020, Amyotrophic lateral sclerosis & frontotemporal degeneration.

Cognitive–behavioural features of progressive supranuclear palsy syndrome overlap with frontotemporal dementia

D. Neary, D. Mann, J. Snowden, 2015, Journal of Neurology.

Examining the language and behavioural profile in FTD and ALS-FTD

D. Neary, D. Mann, J. Snowden, 2017, Journal of Neurology, Neurosurgery, and Psychiatry.

Pathological tau deposition in Motor Neurone Disease and frontotemporal lobar degeneration associated with TDP-43 proteinopathy

D. Mann, S. Rollinson, J. Snowden, 2016, Acta neuropathologica communications.

Frontotemporal lobar degeneration genome wide association study replication confirms a risk locus shared with amyotrophic lateral sclerosis

D. Neary, S. Mead, S. Rollinson, 2011, Neurobiology of Aging.

History of a suspected delirium is more common in dementia with Lewy bodies than Alzheimer's disease: a retrospective study

D. Neary, J. Snowden, A. Richardson, 2014, International journal of geriatric psychiatry.

D. Mann, S. Rollinson, J. Snowden, 2017, Acta neuropathologica communications.

The apolipoprotein E ε4 allele selectively increases the risk of frontotemporal lobar degeneration in males

D. Neary, D. Mann, A. Varma, 2006, Journal of Neurology, Neurosurgery & Psychiatry.

CXCR4 involvement in neurodegenerative diseases

O. Andreassen, G. Schellenberg, A. Dale, 2017, bioRxiv.

Differential diagnosis of Alzheimer’s disease using spectrochemical analysis of blood

Camilo L. M. Morais, D. Mann, J. Snowden, 2017, Proceedings of the National Academy of Sciences.

Lysosomes, autophagosomes and Alzheimer pathology in dementia with Lewy body disease

D. Mann, J. Snowden, A. Richardson, 2018, Neuropathology : official journal of the Japanese Society of Neuropathology.

Genetic variation across RNA metabolism and cell death gene networks is implicated in the semantic variant of primary progressive aphasia

P. Pietrini, R. Desikan, J. Trojanowski, 2019, Scientific Reports.

Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia.

D. Neary, D. Mann, A. Varma, 2006, Brain : a journal of neurology.

Differential diagnosis of Alzheimer’s disease using spectrochemical analysis of blood

Camilo L. M. Morais, D. Mann, J. Snowden, 2017, Proceedings of the National Academy of Sciences.

Naming and conceptual understanding in frontotemporal dementia

J. Snowden, J. Thompson, A. Richardson, 2019, Cortex.

Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

D. Warden, C. Medway, H. Kölsch, 2017, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease

D. Neary, P. Passmore, J. Snowden, 2016, Neurobiology of Aging.

Screening exons 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's

C. Medway, H. Kölsch, A. Richardson, 2015 .

Frontotemporal dementia with amyotrophic lateral sclerosis: A clinical comparison of patients with and without repeat expansions in C9orf72

D. Neary, D. Mann, S. Rollinson, 2013, Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration.

Genome-wide analyses reveal a potential role for the MAPT, MOBP, and APOE loci in sporadic frontotemporal dementia

H. Leonard, D. Knopman, C. van Broeckhoven, 2024, American journal of human genetics.

Sensitivity and specificity of FTDC criteria for behavioral variant frontotemporal dementia

D. Neary, D. Mann, J. Snowden, 2013, Neurology.