Garth Nicholson

11PUBLICATIONS
72CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Neurology and neuromuscular diseasesCell and nuclear divisionOptometryMedical infection agents (incl. prions)
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Publications (11)

|Sep 15, 2026
Characterising the motif composition and allele length distribution of ZFHX3 GGC repeat expansions in amyotrophic lateral sclerosis.

|Sep 12, 2026
The Charcot-Marie-Tooth Neuropathy (CMTX3) Complex Structural Variation Causes Differential SOX3 Spatiotemporal Expression.

|Oct 14, 2025
Pseudodominant Inheritance of Biallelic RFC1 Expansions-Revisiting the 3p22-p24 HSN1B Locus.

Bianca R Grosz, Melina Ellis, Shuchi Trivedi

|Jul 27, 2024
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.

Andrea Cortese, Sarah J Beecroft, Stefano Facchini

|Jun 11, 2024
A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing.

Bianca R Grosz, Jevin M Parmar, Melina Ellis

|Jan 23, 2024
Treatment with sodium butyrate induces autophagy resulting in therapeutic benefits for spinocerebellar ataxia type 3.

Maxinne Watchon, Katherine J Robinson, Luan Luu

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Frequent Collaborators

5 joint publications

Bianca R Grosz

5 joint publications

Steve Vucic

4 joint publications

Marina L Kennerson

4 joint publications

Lyndal Henden