A. King

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Mutations in the vesicular trafficking protein annexin A11 are associated with amyotrophic lateral sclerosis

Robert H. Brown, M. Weale, F. Baas, 2017, Science Translational Medicine.

Diabetes, aging, and the brain: A comparative test of brain amylin in diabetics with late-onset Alzheimer's disease versus non-diabetics with late-onset Alzheimer's disease or early-onset Alzheimer's disease

C. Troakes, S. Al-Sarraj, P. Nelson, 2015, Alzheimer's & Dementia.

RRM adjacent TARDBP mutations disrupt RNA binding and enhance TDP-43 proteinopathy

C. Shaw, C. Troakes, Bradley N Smith, 2019, Brain : a journal of neurology.

An MND/ALS phenotype associated with C9orf72 repeat expansion: Abundant p62‐positive, TDP‐43‐negative inclusions in cerebral cortex, hippocampus and cerebellum but without associated cognitive decline

T. Hortobágyi, A. Al-Chalabi, C. Shaw, 2012, Neuropathology : official journal of the Japanese Society of Neuropathology.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Annelot M. Dekker, Robert H. Brown, F. Baas, 2016, Nature Genetics.

Striking phenotypic variation in a family with the P506S UBQLN2 mutation including amyotrophic lateral sclerosis, spastic paraplegia, and frontotemporal dementia

A. Al-Chalabi, C. Shaw, C. Troakes, 2019, Neurobiology of Aging.

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

Kevin F. Bieniek, B. Miller, C. Geula, 2019, Acta Neuropathologica.

Assessment of beta-amyloid deposits in human brain: a study of the BrainNet Europe Consortium.

Andrew King, Nikolaos Kavantzas, Istvan Bodi, 2009, Acta neuropathologica.

Multisite Assessment of Aging-Related Tau Astrogliopathy (ARTAG)

John L. Robinson, Kevin F. Bieniek, Janna H. Neltner, 2017, Journal of neuropathology and experimental neurology.

Neuropathological assessments of the pathology in frontotemporal lobar degeneration with TDP43-positive inclusions: an inter-laboratory study by the BrainNet Europe consortium

T. Hortobágyi, I. Ferrer, S. Al-Sarraj, 2014, Journal of Neural Transmission.

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis

Timothy A. Miller, Jennifer E. Phillips-Cremins, Lilah M. Besser, 2020, Neuron.

Frontotemporal lobar degeneration with FUS-positive inclusions

Aj Lees, Jason D. Warren, Andrew King, 2010 .

APOE ε4 is also required in TREM2 R47H variant carriers for Alzheimer's disease to develop

C. Troakes, A. Hodges, A. King, 2019, Neuropathology and applied neurobiology.

Novel mutations support a role for Profilin 1 in the pathogenesis of ALS

Robert H. Brown, A. Al-Chalabi, C. Shaw, 2015, Neurobiology of Aging.

Expression of the chondroitin sulphate proteoglycan, NG2, in paediatric brain tumors.

K. Ashkan, A. King, L. Donovan, 2014, Anticancer research.

Aluminium in brain tissue in autism.

A. King, C. Exley, M. Mold, 2018, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Inherited prion disease with 5-OPRI

S. Mead, J. Collinge, S. Joiner, 2007, Neurology.

Mutations in ANXA11 cause familial and sporadic amyotrophic lateral sclerosis

F. Baas, J. Belleroche, A. Al-Chalabi, 2017 .

Optineurin inclusions occur in a minority of TDP-43 positive ALS and FTLD-TDP cases and are rarely observed in other neurodegenerative disorders

T. Hortobágyi, C. Shaw, C. Troakes, 2011, Acta Neuropathologica.

p62 positive, TDP-43 negative, neuronal cytoplasmic and intranuclear inclusions in the cerebellum and hippocampus define the pathology of C9orf72-linked FTLD and MND/ALS

T. Hortobágyi, A. Al-Chalabi, C. Shaw, 2011, Acta Neuropathologica.

Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation

S. Mead, J. Collinge, T. Révész, 2009, Journal of Neurology, Neurosurgery & Psychiatry.

F. Muntoni, N. Dlamini, A. King, 2015, Neuromuscular Disorders.

The Identification of Aluminum in Human Brain Tissue Using Lumogallion and Fluorescence Microscopy

C. Troakes, A. King, C. Exley, 2016, Journal of Alzheimer's disease : JAD.

Mixed tau, TDP-43 and p62 pathology in FTLD associated with a C9ORF72 repeat expansion and p.Ala239Thr MAPT (tau) variant

C. Shaw, C. Troakes, S. Al-Sarraj, 2013, Acta Neuropathologica.

Neuropathology of the hippocampus in FTLD‐Tau with Pick bodies: a study of the BrainNet Europe Consortium

T. Hortobágyi, H. Budka, C. Troakes, 2013, Neuropathology and applied neurobiology.

Simulated surgical-type cerebral biopsies from post-mortem brains allows accurate neuropathological diagnoses in the majority of neurodegenerative disease groups

C. Troakes, S. Al-Sarraj, K. Ashkan, 2013, Acta neuropathologica communications.

Ubiquitinated, p62 immunopositive cerebellar cortical neuronal inclusions are evident across the spectrum of TDP‐43 proteinopathies but are only rarely additionally immunopositive for phosphorylation‐dependent TDP‐43

C. Troakes, S. Al-Sarraj, A. King, 2011, Neuropathology : official journal of the Japanese Society of Neuropathology.

ALS-FUS pathology revisited: singleton FUS mutations and an unusual case with both a FUS and TARDBP mutation

C. Shaw, C. Troakes, S. Al-Sarraj, 2015, Acta Neuropathologica Communications.

Assessment of the degree of asymmetry of pathological features in neurodegenerative diseases. What is the significance for brain banks?

C. Troakes, S. Al-Sarraj, A. King, 2015, Journal of Neural Transmission.

A pathologically confirmed case of combined amyotrophic lateral sclerosis with C9orf72 mutation and multiple system atrophy

C. Troakes, A. King, Yuan Kai Lee, 2022, Neuropathology : official journal of the Japanese Society of Neuropathology.

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

P. Lantos, S. Mead, J. Collinge, 2006, Brain : a journal of neurology.

Investigation of variant Creutzfeldt-Jakob disease and other human prion diseases with tonsil biopsy samples

J Collinge, P. Lantos, M. Rossor, 1999, The Lancet.

Pathogenic Huntingtin Repeat Expansions in Patients with Frontotemporal Dementia and Amyotrophic Lateral Sclerosis.

Timothy A. Miller, Sonja W. Scholz, Jennifer E. Phillips-Cremins, 2020, Neuron.

Unusual neuropathological features and increased brain aluminium in a resident of Camelford, UK

C. Troakes, S. Al-Sarraj, A. Hodges, 2017, Neuropathology and applied neurobiology.

Mitochondrial abnormalities and low grade inflammation are present in the skeletal muscle of a minority of patients with amyotrophic lateral sclerosis; an observational myopathology study

S. Bates, S. Al-Sarraj, V. Meininger, 2014, Acta neuropathologica communications.

Phenotypic variability in the brains of a family with a prion disease characterized by a 144‐base pair insertion in the prion protein gene

P. Lantos, M. Rossor, S. Mead, 2003, Neuropathology and applied neurobiology.

TMCC2 Associates with Alzheimer’s Disease Pathology in the Human Brain

C. Troakes, G. Tear, A. King, 2021, bioRxiv.

M. Ashworth, A. King, R. Sofat, 2020, Journal of inherited metabolic disease.

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene in and for Therapeutic

Timothy A. Miller, Denis C. Bauer, Shankaracharya, 2018 .

Clinical and neuroanatomical signatures of tissue pathology in frontotemporal lobar degeneration

Nick C. Fox, Sebastien Ourselin, Jason D. Warren, 2011, Brain : a journal of neurology.

Aluminium in Brain Tissue in Multiple Sclerosis

C. Linhart, A. King, C. Exley, 2018, International Journal of Environmental Research and Public Health.

Spontaneous epidural spinal haematoma in children caused by vascular malformations

A. King, I. Bodi, C. Chandler, 2016, European Spine Journal.

Aluminium in brain tissue in familial Alzheimer's disease.

C. Troakes, A. King, C. Exley, 2017, Journal of trace elements in medicine and biology : organ of the Society for Minerals and Trace Elements.

Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium

Andrew King, Isidro Ferrer, Istvan Bodi, 2008, Brain pathology.

Genome-wide Analyses Id entify KIF 5 A as a Novel ALS Gene Highlights

Sonja W. Scholz, Janel O. Johnson, D. Hernandez, 2018 .

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Annelot M. Dekker, Robert H. Brown, F. Baas, 2016, Nature Genetics.

Clinical and neuropathological features of X-linked spinal muscular atrophy (SMAX2) associated with a novel mutation in the UBA1 gene

T. Jacques, Amanda J Murphy, N. Dlamini, 2013, Neuromuscular Disorders.

The genetics and neuropathology of amyotrophic lateral sclerosis

A. Al-Chalabi, C. Troakes, S. Al-Sarraj, 2012, Acta Neuropathologica.

A comparative clinical, pathological, biochemical and genetic study of fused in sarcoma proteinopathies.

Nick C Fox, M. Rossor, N. Quinn, 2011, Brain : a journal of neurology.

Heterogeneous Nuclear Ribonucleoprotein E2 (hnRNP E2) Is a Component of TDP-43 Aggregates Specifically in the A and C Pathological Subtypes of Frontotemporal Lobar Degeneration

T. Hortobágyi, C. Shaw, C. Troakes, 2019, Journal of the Neurological Sciences.

Staging/typing of Lewy body related α-synuclein pathology: a study of the BrainNet Europe Consortium

Andrew King, Isidro Ferrer, Nikolaos Kavantzas, 2009, Acta Neuropathologica.

Primary intracerebral INI1-deficient rhabdoid tumor with CD34 immunopositivity in a young adult

F. Vergani, A. King, I. Bodi, 2018, Surgical neurology international.

Abnormal TDP‐43 expression is identified in the neocortex in cases of dementia pugilistica, but is mainly confined to the limbic system when identified in high and moderate stages of Alzheimer's disease

C. Troakes, S. Al-Sarraj, A. King, 2010, Neuropathology : official journal of the Japanese Society of Neuropathology.

The Increased Densities, But Different Distributions, of Both C3 and S100A10 Immunopositive Astrocyte-Like Cells in Alzheimer’s Disease Brains Suggest Possible Roles for Both A1 and A2 Astrocytes in the Disease Pathogenesis

C. Troakes, A. King, Shalmai Jones, 2020, Brain sciences.

TDP‐43 is consistently co‐localized with ubiquitinated inclusions in sporadic and Guam amyotrophic lateral sclerosis but not in familial amyotrophic lateral sclerosis with and without SOD1 mutations

T. Hortobágyi, C. Shaw, S. Al-Sarraj, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Expression of the candidate invasion suppressor gene, nm23, in human brain tumors

A. King, G. Pilkington, K. O’Neill, 1998 .

Clusterin expression is upregulated following acute head injury and localizes to astrocytes in old head injury

C. Troakes, S. Al-Sarraj, A. King, 2017, Neuropathology : official journal of the Japanese Society of Neuropathology.

ATRX immunohistochemistry can help refine ‘not elsewhere classified’ categorisation for grade II/III gliomas

S. Al-Sarraj, K. Ashkan, A. King, 2019, British journal of neurosurgery.

Co-deletion of 1p/19q is Strongly Correlated with a High Level of MGMT Promoter Methylation in High Grade Gliomas as Revealed by Pyrosequencing

S. Al-Sarraj, K. Ashkan, R. Beaney, 2014 .

Plasma p-tau181 accurately predicts Alzheimer’s disease pathology at least 8 years prior to post-mortem and improves the clinical characterisation of cognitive decline

K. Blennow, D. Aarsland, C. Troakes, 2020, Acta Neuropathologica.

Simulated surgical-type cerebral biopsies from post-mortem brains allows accurate neuropathological diagnoses in the majority of neurodegenerative disease groups

C. Troakes, S. Al-Sarraj, K. Ashkan, 2013, Acta neuropathologica communications.

Expression of MMP-2 and -9 in short-term cultures of meningioma: influence of histological subtype.

A. King, G. Pilkington, T. Van Meter, 2003, International journal of molecular medicine.

Comparative gene expression profiling of ADAMs, MMPs, TIMPs, EMMPRIN, EGF-R and VEGFA in low grade meningioma.

R. Selway, A. King, G. Pilkington, 2016, International journal of oncology.

A distinct clinical, neuropsychological and radiological phenotype is associated with progranulin gene mutations in a large UK series.

Andrew King, Nick C Fox, Tamas Revesz, 2008, Brain : a journal of neurology.

Stratified gene expression analysis identifies major amyotrophic lateral sclerosis genes

J. D. Macklis, J. Powell, A. Al-Chalabi, 2015, Neurobiology of Aging.

Vascular cognitive impairment neuropathology guidelines (VCING): the contribution of cerebrovascular pathology to cognitive impairment.

T. Hortobágyi, J. Attems, D. Mann, 2016, Brain : a journal of neurology.

Comparison of clinical and neuropathological diagnoses of neurodegenerative diseases in two centres from the Brains for Dementia Research (BDR) cohort

D. Aarsland, C. Troakes, S. Al-Sarraj, 2019, Journal of Neural Transmission.

Inter-laboratory comparison of neuropathological assessments of β-amyloid protein: a study of the BrainNet Europe consortium

I. Ferrer, H. Budka, S. Al-Sarraj, 2008, Acta Neuropathologica.

Frontotemporal lobar degeneration with ubiquitinated tau‐negative inclusions and additional α‐synuclein pathology but also unusual cerebellar ubiquitinated p62‐positive, TDP‐43‐negative inclusions

C. Shaw, S. Al-Sarraj, A. King, 2009, Neuropathology : official journal of the Japanese Society of Neuropathology.

Interlaboratory Comparison of Assessments of Alzheimer Disease-Related Lesions: A Study of the BrainNet Europe Consortium

I. Ferrer, J. Hauw, H. Budka, 2006, Journal of neuropathology and experimental neurology.

Neuropathologic variation in frontotemporal dementia due to the intronic tau 10+16 mutation

P. Lantos, M. Rossor, N. Cairns, 2002, Neurology.

Extended post-mortem delay times should not be viewed as a deterrent to the scientific investigation of human brain tissue: a study from the Brains for Dementia Research Network Neuropathology Study Group, UK

D. Lett, J. Attems, D. Mann, 2016, Acta Neuropathologica.

The Neuropathological Diagnosis of Alzheimer’s Disease—The Challenges of Pathological Mimics and Concomitant Pathology

C. Troakes, A. King, I. Bodi, 2020, Brain sciences.

Control tissue in brain banking: the importance of thorough neuropathological assessment

C. Troakes, S. Al-Sarraj, A. King, 2015, Journal of Neural Transmission.

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.

The need to unify neuropathological assessments of vascular alterations in the ageing brain Multicentre survey by the BrainNet Europe consortium

K. Jellinger, T. Hortobágyi, J. Attems, 2012, Experimental Gerontology.

Lack of Correlation Between Immunohistochemical Expression of SPARC and Invasion in Different Grades of Meningiomas

A. King, G. Pilkington, A. Martin, 2020, AntiCancer Research.

Assessment of &agr;-Synuclein Pathology: A Study of the BrainNet Europe Consortium

I. Ferrer, H. Budka, S. Al-Sarraj, 2008, Journal of neuropathology and experimental neurology.

Atypical progressive supranuclear palsy presenting as primary lateral sclerosis

S. Al-Sarraj, A. King, Olimpia E Curran, 2013, Journal of the Neurological Sciences.

Adult parasellar capillary haemangioma with intrasellar extension.

S. Al-Sarraj, Atul Kumar, A. King, 2019, World neurosurgery.

H3 G34-mutant high-grade gliomas: integrated clinical, imaging and pathological characterisation of a single-centre case series

F. Vergani, K. Ashkan, A. King, 2023, Acta Neurochirurgica.

Aluminium in Brain Tissue in Multiple Sclerosis

C. Linhart, A. King, C. Exley, 2018, International journal of environmental research and public health.

NEK1 variants confer susceptibility to amyotrophic lateral sclerosis

Annelot M. Dekker, F. Baas, T. Meitinger, 2016, Nature Genetics.

Genome-wide analyses as part of the international FTLD-TDP whole-genome sequencing consortium reveals novel disease risk factors and increases support for immune dysfunction in FTLD

C. Geula, M. Mesulam, J. Grafman, 2019, Acta Neuropathologica.

Clusterin expression is upregulated following acute head injury and localizes to astrocytes in old head injury

C. Troakes, S. Al-Sarraj, A. King, 2017, Neuropathology : official journal of the Japanese Society of Neuropathology.