Author

Andrew Smith

Macquarie UniversityORCID 0000-0002-9169-9202Unclaimed ORCID profile · follow to get notified of new preprints

Additional preprints under this name without ORCID

Andrew Smith2 papers · Cabrini Hospital

Biology Disciplines

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Genetic & Genomic Medicine· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Approach:statistical model· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Ian P. BlairiD· 2 shared Natalie GrimaiD· 2 shared Adam K. WalkeriD· 1 shared Alison L. HoganiD· 1 shared Cindy MaureliD· 1 shared Daniel S. O’ShaughnessyiD· 1 shared Dominic B. RoweiD· 1 shared Garth A. NicholsoniD· 1 shared

Activity by Year

2026-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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2 shared papersNeuroscience

Ian P. BlairORCID

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2 papers

Recent·Most cited

SFPQ dysregulation promotes TDP-43 pathology through a pathogenic feedback loop

Alison L. Hogan, Patrick Chiu, Natalie Grima, Sharlynn Wu, Grant Richter, Cindy Maurel, Madison A. Kane, Andrew Smith, Shu Yang, Adam K. Walker, Ian P. Blair, Marco Morsch

This study identifies SFPQ as a contributor to TDP-43 pathology through a bidirectional feedback loop, showing SFPQ dysregulation drives TDP-43 mislocalization and aggregation.

bioRxiv · Jul 25, 2026 · PreprintNeuroscience

Characterising the motif composition and allele length distribution of ZFHX3 GGC repeat expansions in amyotrophic lateral sclerosis

Zoe N. Zussa, Andrew Smith, Joke J.F.A. van Vugt, Daniel S. O’Shaughnessy, Natalie Grima, Sandrine Chan Moi Fat, Ian P. Blair, Dominic B. Rowe, Roger Pamphlett, Garth A. Nicholson, Matthew C. Kiernan, Wouter van Rheenen, Jan Herman Veldink, Kelly L. Williams, Lyndal Henden

This study examines ZFHX3 GGC repeat expansions in ALS and finds no association with disease risk, but identifies diverse repeat motif compositions.

medRxiv · Apr 13, 2026 · PreprintGenetic & Genomic Medicine