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Publications

Clinical trials in pediatric ALS: a TRICALS feasibility study.

Kliest T. et al, (2022), Amyotroph Lateral Scler Frontotemporal Degener, 1 - 8

Genetic testing in motor neurone disease.

Dharmadasa T. et al, (2022), Pract Neurol

The RNA-binding protein HuR is required for maintenance of the germinal centre response

Osma-Garcia IC. et al, (2021), Nature Communications, 12

Advancing Mechanistic Understanding and Biomarker Development in Amyotrophic Lateral Sclerosis.

Thompson AG. et al, (2021), Expert Rev Proteomics

Sequential inverse dysregulation of the RNA helicases DDX3X and DDX3Y facilitates MYC-driven lymphomagenesis.

Gong C. et al, (2021), Mol Cell, 81, 4059 - 4075.e11

Essential requirement for polypyrimidine tract binding proteins 1 and 3 in the maturation and maintenance of mature B cells in mice.

Monzón-Casanova E. et al, (2021), Eur J Immunol, 51, 2266 - 2273

RNA Binding Proteins As Regulators of Oxidative Stress Identified by a Targeted CRISPR-Cas9 Single Guide RNA Library

Turner DJ. and Turner M., (2021), CRISPR Journal, 4, 427 - 437

Non-neuronal cells in amyotrophic lateral sclerosis - from pathogenesis to biomarkers.

Vahsen BF. et al, (2021), Nat Rev Neurol

Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS-TDP.

Nolan M. et al, (2021), J Neurol Neurosurg Psychiatry

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

Dewan R. et al, (2021), Neuron, 109, 448 - 460.e4

To Zoom or Not to Zoom: The Should I Travel Index Revisited during the Coronavirus Disease Pandemic.

Rutkove SB. et al, (2021), Ann Neurol

Efficient homing of antibody-secreting cells to the bone marrow requires RNA-binding protein ZFP36L1

Saveliev A. et al, (2021), Journal of Experimental Medicine, 218

Spectrum, risk factors and outcomes of neurological and psychiatric complications of COVID-19: a UK-wide cross-sectional surveillance study.

Ross Russell AL. et al, (2021), Brain Commun, 3

Improving clinical trial outcomes in amyotrophic lateral sclerosis.

Kiernan MC. et al, (2020), Nat Rev Neurol

Detection and Quantification of Novel C-terminal TDP-43 Fragments in ALS-TDP.

Feneberg E. et al, (2020), Brain Pathol

Chitotriosidase as biomarker for early stage amyotrophic lateral sclerosis: A multicenter study

Steinacker P. et al, (2020), Amyotrophic lateral sclerosis & frontotemporal degeneration

Value of systematic genetic screening of patients with amyotrophic lateral sclerosis

Shepheard SR. et al, (2020), Journal of Neurology, Neurosurgery and Psychiatry

Methods for quantitative susceptibility and R2* mapping in whole post-mortem brains at 7T applied to amyotrophic lateral sclerosis.

Wang C. et al, (2020), Neuroimage, 222

Characterising neuropsychiatric disorders in patients with COVID-19 - Authors' reply.

Varatharaj A. et al, (2020), Lancet Psychiatry, 7, 934 - 935

Neuroimaging in primary lateral sclerosis

Pioro E. et al, (2020), Amyotrophic lateral sclerosis & frontotemporal degeneration

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