User profiles for "author:Peter McColgan"

Peter McColgan

University College London
Verified email at qub.ac.uk
Cited by 4004

Huntington's disease: a clinical review

P McColgan, SJ Tabrizi - European journal of neurology, 2018 - Wiley Online Library
Huntington's disease (HD) is a fully penetrant neurodegenerative disease caused by a
dominantly inherited CAG trinucleotide repeat expansion in the huntingtin gene on …

Towards the identification of blood biomarkers for acute stroke in humans: a comprehensive systematic review

N Hasan, P McColgan, P Bentley… - British journal of …, 2012 - Wiley Online Library
WHAT IS ALREADY KNOWN ABOUT THIS SUBJECT Stroke is the largest single cause of
disability in the UK. While tests based upon biomarkers have been around for decades …

The human motor cortex microcircuit: insights for neurodegenerative disease

P McColgan, J Joubert, SJ Tabrizi… - Nature Reviews …, 2020 - nature.com
The human motor cortex comprises a microcircuit of five interconnected layers with different
cell types. In this Review, we use a layer-specific and cell-specific approach to integrate …

C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies

DJ Hensman Moss, M Poulter, J Beck, J Hehir… - Neurology, 2014 - AAN Enterprises
Objective: In many cases where Huntington disease (HD) is suspected, the genetic test for
HD is negative: these are known as HD phenocopies. A repeat expansion in the C9orf72 …

[HTML][HTML] Biological and clinical characteristics of gene carriers far from predicted onset in the Huntington's disease Young Adult Study (HD-YAS): a cross-sectional …

RI Scahill, P Zeun, K Osborne-Crowley… - The Lancet …, 2020 - thelancet.com
Background Disease-modifying treatments are in development for Huntington's disease;
crucial to their success is to identify a timepoint in a patient's life when there is a measurable …

Large-scale DCMs for resting-state fMRI

A Razi, ML Seghier, Y Zhou, P McColgan… - Network …, 2017 - direct.mit.edu
This paper considers the identification of large directed graphs for resting-state brain
networks based on biophysical models of distributed neuronal activity, that is, effective …

The Addenbrooke's Cognitive Examination for the differential diagnosis and longitudinal assessment of patients with parkinsonian disorders

T Rittman, BC Ghosh, P McColgan… - Journal of Neurology …, 2013 - jnnp.bmj.com
Objective Differentiating idiopathic Parkinson's disease from atypical parkinsonian
syndromes is challenging, especially in the early stages. We assessed whether the Revised …

[HTML][HTML] Brain regions showing white matter loss in Huntington's disease are enriched for synaptic and metabolic genes

P McColgan, S Gregory, KK Seunarine, A Razi… - Biological …, 2018 - Elsevier
Background The earliest white matter changes in Huntington's disease are seen before
disease onset in the premanifest stage around the striatum, within the corpus callosum, and …

Selective vulnerability of Rich Club brain regions is an organizational principle of structural connectivity loss in Huntington's disease

P McColgan, KK Seunarine, A Razi, JH Cole… - Brain, 2015 - academic.oup.com
Huntington's disease can be predicted many years before symptom onset, and thus makes
an ideal model for studying the earliest mechanisms of neurodegeneration. Diffuse patterns …

Can neuroimaging predict dementia in Parkinson's disease?

JH Lanskey, P McColgan, AE Schrag… - Brain, 2018 - academic.oup.com
Dementia in Parkinson's disease affects 50% of patients within 10 years of diagnosis but
there is wide variation in severity and timing. Thus, robust neuroimaging prediction of …