Melanie Bahlo

77PUBLICATIONS
364CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Aboriginal and Torres Strait Islander artefactsEpigenetics (incl. genome methylation and epigenomics)Medical infection agents (incl. prions)Developmental genetics (incl. sex determination)
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Publications (77)

|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

|Nov 21, 2025
Novel, complex configurations of the MARCHF6 repeat expansion associated with progressive myoclonic epilepsy and familial adult myoclonic epilepsy.

Mark F Bennett, Mark A Corbett, Thessa Kroes

|Nov 19, 2025
Identification of novel vertebral development factors through UK Biobank candidate gene search and body imaging analysis.

Zhuopin Sun, Jiru Han, Liam G Fearnley

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Frequent Collaborators

15 joint publications

Ingrid E Scheffer

15 joint publications

Samuel F Berkovic

13 joint publications

Mark F Bennett

10 joint publications

Jacob Munro