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Mark Corbett

25PUBLICATIONS

121CO-AUTHORS

Medical infection agents (incl. prions)Cell and nuclear divisionEvolutionary computationMedical devicesMajor global burdens of disease

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Publications (25)

Sort by Publication Date:

|Nov 21, 2025

Novel, complex configurations of the <i>MARCHF6</i> 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

|Nov 17, 2023

Stuttering associated with a pathogenic variant in the chaperone protein cyclophilin 40.

Angela T Morgan, Thomas S Scerri, Adam P Vogel

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Frequent Collaborators

21 joint publications

Jozef Gecz

9 joint publications

Clare L van Eyk

6 joint publications

Melanie Bahlo

5 joint publications

Jesia G Berry

5 joint publications

Samuel F Berkovic

5 joint publications

Mark F Bennett

4 joint publications

Luís A Pérez-Jurado

4 joint publications

Christel Depienne

4 joint publications

Julien Buratti

3 joint publications

Mahalia S B Frank

Frequent Collaborators

21 joint publications

Jozef Gecz

9 joint publications

Clare L van Eyk

6 joint publications

Melanie Bahlo

5 joint publications

Jesia G Berry

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