Garth Nicholson
9PUBLICATIONS
66CO-AUTHORS
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Publications (9)
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|Oct 14, 2025
Pseudodominant Inheritance of Biallelic RFC1 Expansions-Revisiting the 3p22-p24 HSN1B Locus.Bianca R Grosz, Melina Ellis, Shuchi Trivedi
|Oct 17, 2024
Author Correction: A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.Andrea Cortese, Sarah J Beecroft, Stefano Facchini
|Jul 27, 2024
A CCG expansion in ABCD3 causes oculopharyngodistal myopathy in individuals of European ancestry.Andrea Cortese, Sarah J Beecroft, Stefano Facchini
|Jul 02, 2024
Author Correction: The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration.Sarah Opie-Martin, Alfredo Iacoangeli, Simon D Topp
|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
4 joint publications
Steve Vucic
4 joint publications
Ira W Deveson
4 joint publications
Igor Stevanovski
3 joint publications
Carolin Scriba
3 joint publications
Gianina Ravenscroft
3 joint publications
Marina L Kennerson
3 joint publications
Lyndal Henden
3 joint publications
Andrea Cortese
2 joint publications
Enrico Bugiardini
