List of works - Robin Highley

A clinicopathologic study of 11 rosette-forming meningiomas: a rare and potentially confusing pattern

scientific article published on 24 June 2015

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

scientific article

Antibody-negative neuromyelitis optica with heavy B-cell infiltration.

scientific article published in October 2009

Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy.

scientific article published on 6 May 2015

Asymmetry of the uncinate fasciculus: a post-mortem study of normal subjects and patients with schizophrenia.

scientific article published in November 2002

Brain haemosiderin in older people: pathological evidence for an ischaemic origin of magnetic resonance imaging (MRI) microbleeds

scientific article

C9ORF72 GGGGCC Expanded Repeats Produce Splicing Dysregulation which Correlates with Disease Severity in Amyotrophic Lateral Sclerosis

scientific article published on 27 May 2015

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

scientific article published on 24 July 2013

Combined fused in sarcoma-positive (FUS+) basophilic inclusion body disease and atypical tauopathy presenting with an amyotrophic lateral sclerosis/motor neurone disease (ALS/MND)-plus phenotype

scientific article published on 19 February 2019

Fiber content of the fornix in schizophrenia: lack of evidence for a primary limbic encephalopathy

scientific article published on 01 November 1999

Gamma-synuclein pathology in amyotrophic lateral sclerosis

scientific article

Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions

scientific article

Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones.

scientific article

Microglia in Motor Neuron Disease

scientific article published on 28 June 2020

Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusions.

scientific article published on 11 June 2015

Neuropathological characterization of a novel TANK binding kinase (TBK1) gene loss of function mutation associated with amyotrophic lateral sclerosis

scientific article published on 09 September 2019

Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.

scientific article published in April 2010

Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosis

scientific article published on 11 May 2020

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

scientific article published in May 2007

Pathological findings in a case of stiff person syndrome with anti-GAD antibodies

scientific article published on 24 May 2011

Schizophrenia and temporal lobe asymmetry. A post-mortem stereological study of tissue volume

scientific article published on 01 August 1999

Schizophrenia and the frontal lobes: post-mortem stereological study of tissue volume.

scientific article published in April 2001

Sex-dependent effects of schizophrenia: an MRI study of gyral folding, and cortical and white matter volume.

scientific article

Size of hippocampal pyramidal neurons in schizophrenia.

scientific article published in November 2003

TDP-43 pathology in the population: prevalence and associations with dementia and age.

scientific article published in January 2014

Temporal lobe epilepsy with and without psychosis: exploration of hippocampal pathology including that in subpopulations of neurons defined by their content of immunoreactive calcium-binding proteins

scientific article published on 01 May 2000

The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis

scientific article published on April 2015

List of works by Robin Highley

A clinicopathologic study of 11 rosette-forming meningiomas: a rare and potentially confusing pattern

ALS phenotypes with mutations in CHMP2B (charged multivesicular body protein 2B)

Antibody-negative neuromyelitis optica with heavy B-cell infiltration.

Antisense RNA foci in the motor neurons of C9ORF72-ALS patients are associated with TDP-43 proteinopathy.

Asymmetry of the uncinate fasciculus: a post-mortem study of normal subjects and patients with schizophrenia.

Brain haemosiderin in older people: pathological evidence for an ischaemic origin of magnetic resonance imaging (MRI) microbleeds

C9ORF72 GGGGCC Expanded Repeats Produce Splicing Dysregulation which Correlates with Disease Severity in Amyotrophic Lateral Sclerosis

C9ORF72 expansions, parkinsonism, and Parkinson disease: a clinicopathologic study.

Combined fused in sarcoma-positive (FUS+) basophilic inclusion body disease and atypical tauopathy presenting with an amyotrophic lateral sclerosis/motor neurone disease (ALS/MND)-plus phenotype

Fiber content of the fornix in schizophrenia: lack of evidence for a primary limbic encephalopathy

Gamma-synuclein pathology in amyotrophic lateral sclerosis

Gene expression signatures in motor neurone disease fibroblasts reveal dysregulation of metabolism, hypoxia-response and RNA processing functions

Loss of nuclear TDP-43 in amyotrophic lateral sclerosis (ALS) causes altered expression of splicing machinery and widespread dysregulation of RNA splicing in motor neurones.

Microglia in Motor Neuron Disease

Motor neurone disease/amyotrophic lateral sclerosis associated with intermediate-length CAG repeat expansions in Ataxin-2 does not have 1C2-positive polyglutamine inclusions.

Neuropathological characterization of a novel TANK binding kinase (TBK1) gene loss of function mutation associated with amyotrophic lateral sclerosis

Novel FUS/TLS mutations and pathology in familial and sporadic amyotrophic lateral sclerosis.

Oligodendrocyte pathology exceeds axonal pathology in white matter in human amyotrophic lateral sclerosis

Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations.

Pathological findings in a case of stiff person syndrome with anti-GAD antibodies

Schizophrenia and temporal lobe asymmetry. A post-mortem stereological study of tissue volume

Schizophrenia and the frontal lobes: post-mortem stereological study of tissue volume.

Sex-dependent effects of schizophrenia: an MRI study of gyral folding, and cortical and white matter volume.

Size of hippocampal pyramidal neurons in schizophrenia.

TDP-43 pathology in the population: prevalence and associations with dementia and age.

Temporal lobe epilepsy with and without psychosis: exploration of hippocampal pathology including that in subpopulations of neurons defined by their content of immunoreactive calcium-binding proteins

The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis