Julie McGaughran

6PUBLICATIONS
120CO-AUTHORS
NeurogeneticsGene expression (incl. microarray and other genome-wide approaches)Cardiology (incl. cardiovascular diseases)Artificial life and complex adaptive systemsEpigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|Oct 16, 2025
NRL-associated autosomal recessive retinopathy: novel variants expanding the phenotype, natural history and a comprehensive literature search.

Marium Raza, Elisa E Cornish, Chris Ovens

|Aug 12, 2025
Titin-related familial dilated cardiomyopathy: factors associated with disease onset.

Renee Johnson, Robert A Fletcher, Stacey Peters

|Feb 12, 2025
Use of Advanced Echocardiographic Modalities to Discriminate Preclinical Hypertrophic Cardiomyopathy Mutation Carriers From Non-Carriers.

Ada K C Lo, Thomas Mew, Christina Mew

|Nov 26, 2024
Assessing the unmet needs of genomic testing in Australia: a geospatial exploration.

Sarah Casauria, Felicity Collins, Susan M White

|May 25, 2024
Reanalysis of genomic data in rare disease: current practice and attitudes among Australian clinical and laboratory genetics services.

Stephanie Best, Zoe Fehlberg, Christopher Richards

|Jan 09, 2023
Delineating the phenotype of RNU4ATAC-related spliceosomopathy.

Amanda Tabib, Christopher M Richmond, Julie McGaughran

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Frequent Collaborators

2 joint publications

Stephanie Best

2 joint publications

John J Atherton

2 joint publications

Mathew Wallis

1 joint publications

Amanda Tabib