Laura I. Rudaks
Hospital Rd
Concord, NSW 2139, Australia
Concord, NSW 2139, Australia
Last Updated: 09/26/2026
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Found 19 publications
MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel Insights.
MDSGene Systematic Review of Common Forms of Dominant Hereditary Spastic Paraplegia: Novel Insights.
Journal: Movement disorders clinical practice
Published: December 24, 2025
Targeted long-read sequencing enables comprehensive analysis of the genetic and epigenetic landscape of inherited myopathies.
Journal: Nature communications
Published: November 17, 2025
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.
Journal: Annals of neurology
Published: August 25, 2025
Barriers to clinical genetic testing in movement disorders.
Journal: Current opinion in neurology
Published: May 21, 2025
Climate change and neurology: A survey of neurologists in Australia and New Zealand.
Journal: Journal of the neurological sciences
Published: January 31, 2025
Targeted Long-Read Sequencing as a Single Assay Improves the Diagnosis of Spastic-Ataxia Disorders.
Journal: Annals of clinical and translational neurology
Published: December 26, 2024
Long-read sequencing for diagnosis of genetic myopathies.
Journal: BMJ neurology open
Published: November 25, 2024
An Update on the Adult-Onset Hereditary Cerebellar Ataxias: Novel Genetic Causes and New Diagnostic Approaches.
Journal: Cerebellum (London, England)
Published: May 07, 2024
Reply to: Comment to "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies".
Reply to: Comment to "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies".
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: April 16, 2024
SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies.
Journal: Movement disorders : official journal of the Movement Disorder Society
Published: January 17, 2024
Genome sequencing reanalysis increases the diagnostic yield in dystonia.
Journal: Parkinsonism & related disorders
Published: January 14, 2024
Expert commentary for fragile X premutation mimicking late onset hereditary spastic paraplegia.
Journal: Parkinsonism & related disorders
Published: December 13, 2023
Last Updated: 09/26/2026