Melanie Bahlo

79PUBLICATIONS
374CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Central nervous systemGene expression (incl. microarray and other genome-wide approaches)Aboriginal and Torres Strait Islander artefactsMedical infection agents (incl. prions)
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Publications (79)

|Nov 03, 2026
Disentangling the Genetic Relationship Between Sleep and Epilepsy.

|Oct 18, 2026
Genetic architecture of MRI-derived cervical spinal cord morphology reveals sensory-motor axis and systemic disease associations.

|Sep 24, 2026
Unravelling the genetic basis of stuttering: GWAS meta-analysis highlights link with rare speech disorders.

|Sep 18, 2026
SLC7A6OS Founder Mutation: A Rare Cause of Progressive Myoclonus Epilepsy Dated to 1100 Years Ago.

|May 07, 2026
Genome sequencing boosts diagnostic yield for the developmental and epileptic encephalopathies.

|Dec 08, 2025
HTRA1/lncRNA HTRA1-AS1 dominates in age-related macular degeneration reticular pseudodrusen genetic risk with no complement involvement.

Samaneh Farashi, Carla J Abbott, Brendan R E Ansell

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Frequent Collaborators

16 joint publications

Ingrid E Scheffer

16 joint publications

Samuel F Berkovic

13 joint publications

Mark F Bennett

10 joint publications

Jacob Munro