Heidi R Fuller

8PUBLICATIONS
14CO-AUTHORS
Medical molecular engineering of nucleic acids and proteinsAutonomic nervous systemComputational neuroscience (incl. mathematical neuroscience and theoretical neuroscience)Gene and molecular therapyNeurology and neuromuscular diseases
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Publications (8)

|Nov 27, 2025
Characterising PMP22-Proximal Partners in a Schwann Cell Model of Charcot-Marie-Tooth Disease Type1A.

Ian Holt, Nicholas Emery, Monte A Gates

|Sep 28, 2024
State of the Art in Sub-Phenotyping Midbrain Dopamine Neurons.

Valentina Basso, Máté D Döbrössy, Lachlan H Thompson

|Mar 28, 2024
Increased NLRP1 mRNA and Protein Expression Suggests Inflammasome Activation in the Dorsolateral Prefrontal and Medial Orbitofrontal Cortex in Schizophrenia.

Ena Španić Popovački, Dora Vogrinc, Heidi R Fuller

|Jul 27, 2023
AAV9-mediated SMN gene therapy rescues cardiac desmin but not lamin A/C and elastin dysregulation in Smn2B/- spinal muscular atrophy mice.

Sharon J Brown, Darija Šoltić, Silvia A Synowsky

|Dec 23, 2022
Genotype-Phenotype Correlations in Human Diseases Caused by Mutations of LINC Complex-Associated Genes: A Systematic Review and Meta-Summary.

Emily C Storey, Heidi R Fuller

|Sep 09, 2022
The Proteome Signatures of Fibroblasts from Patients with Severe, Intermediate and Mild Spinal Muscular Atrophy Show Limited Overlap.

Sharon J Brown, Rachel A Kline, Silvia A Synowsky

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Frequent Collaborators

2 joint publications

Sharon J Brown

1 joint publications

Monte A Gates

1 joint publications

Rachel A Kline

1 joint publications

Peter Claus