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Matthew Nolan

4PUBLICATIONS

62CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Optical technologyCancer geneticsMolecular targets

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Publications (4)

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|Feb 05, 2026

Blocking RAN translation without altering repeat RNAs rescues <i>C9ORF72</i>-related ALS and FTD phenotypes.

Xin Jiang, Laure Schaeffer, Divya Patni

|Mar 17, 2021

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

Matthew Nolan, Paola Barbagallo, Martin R Turner

|May 05, 2017

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

Bradley N Smith, Simon D Topp, Claudia Fallini

|Sep 08, 2016

Pathogenesis of FUS-associated ALS and FTD: insights from rodent models.

Matthew Nolan, Kevin Talbot, Olaf Ansorge

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Frequent Collaborators

2 joint publications

Kevin Talbot

2 joint publications

Martin R Turner

1 joint publications

Bradley N Smith

1 joint publications

Simon D Topp

1 joint publications

Claudia Fallini

1 joint publications

Hideki Shibata

1 joint publications

Han-Jou Chen

1 joint publications

Claire Troakes

1 joint publications

Clotilde Lagier-Tourenne

1 joint publications

Nicola Ticozzi

Frequent Collaborators

2 joint publications

Kevin Talbot

2 joint publications

Martin R Turner

1 joint publications

Bradley N Smith

1 joint publications

Simon D Topp

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