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Evan Reid

8PUBLICATIONS

79CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Gene mappingPeripheral nervous systemNeurology and neuromuscular diseasesEnvironmental epidemiology

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Publications (8)

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|Apr 03, 2026

Blood-based RNA-Seq of 5412 individuals with rare disease identifies new candidate diagnoses in the National Genomic Research Library.

Jenny Lord, Alistair T Pagnamenta, Letizia Vestito

|May 15, 2024

Unravelling undiagnosed rare disease cases by HiFi long-read genome sequencing.

Wouter Steyaert, Lydia Sagath, German Demidov

|Feb 26, 2021

Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in <i>HPDL</i>.

Neil V Morgan, Bryndis Yngvadottir, Mary O'Driscoll

|Nov 06, 2020

Protrudin functions from the endoplasmic reticulum to support axon regeneration in the adult CNS.

Veselina Petrova, Craig S Pearson, Jared Ching

|Oct 07, 2019

ESCRT-III-associated proteins and spastin inhibit protrudin-dependent polarised membrane traffic.

James W Connell, Rachel J Allison, Catherine E Rodger

|Aug 08, 2018

BMP- and neuropilin 1-mediated motor axon navigation relies on spastin alternative translation.

Nicolas Jardin, François Giudicelli, Daniel Ten Martín

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Frequent Collaborators

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Rachel Allison

1 joint publications

James R Edgar

1 joint publications

Guy Pearson

1 joint publications

Tania Rizo

1 joint publications

Sven Günther

1 joint publications

Fiamma Berner

1 joint publications

Jennifer Hague

1 joint publications

Jürgen Winkler

1 joint publications

Jennifer Lippincott-Schwartz

1 joint publications

Christian Beetz

Frequent Collaborators

1 joint publications

Rachel Allison

1 joint publications

James R Edgar

1 joint publications

Guy Pearson

1 joint publications

Tania Rizo

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