Mark Corbett

26PUBLICATIONS
122CO-AUTHORS
Infant and child healthMedical infection agents (incl. prions)Cell and nuclear divisionEvolutionary computationMedical devices
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Publications (26)

|Oct 31, 2026
Genotype and phenotype analyses of 689 individuals with PCDH19-clustering epilepsy.

|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

|Mar 20, 2025
Optical genome mapping enables accurate testing of large repeat expansions.

Bart van der Sanden, Kornelia Neveling, Syukri Shukor

|Oct 04, 2024
Epigenomic newborn screening for conditions with intellectual disability and autistic features in Australian newborns.

Mohammed Alshawsh, Melissa Wake, Jozef Gecz

|Sep 28, 2024
CRISPR-mediated megabase-scale transgene de-duplication to generate a functional single-copy full-length humanized DMD mouse model.

Yu C J Chey, Mark A Corbett, Jayshen Arudkumar

|Feb 08, 2024
Compromised transcription-mRNA export factor THOC2 causes R-loop accumulation, DNA damage and adverse neurodevelopment.

Rudrarup Bhattacharjee, Lachlan A Jolly, Mark A Corbett

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Frequent Collaborators

22 joint publications

Jozef Gecz

9 joint publications

Clare L van Eyk

6 joint publications

Melanie Bahlo

5 joint publications

Jesia G Berry