Author

Cristiana Mattei

The University of Melbourne

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 3 Approach:experimental assay· 3 Organism:human· 3 Assay:scRNA-seq· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:drug response / drug discovery· 1

Frequent Co-Authors

Sean ByarsiD· 3 shared Snezana MaljeviciD· 3 shared Steven PetrouiD· 3 shared Ingrid Eileen SchefferiD· 2 shared Miaomiao MaoiD· 2 shared Alex Nemiroff· 1 shared Ben RolloiD· 1 shared Christopher A. ReidiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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3 shared papersNeuroscience

Sean ByarsORCID

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

SYNGAP1 haploinsufficiency disrupts early neurodevelopment and accelerates intrinsic neuronal maturation in human patient-derived models

Montanna Waters, Lucas Teasdale, Sean Byars, Cristiana Mattei, Nessia Eve Roseno, Dmitry A. Ovchinnikov, Ingrid Eileen Scheffer, Heath Pardoe, Steven Petrou, Snezana Maljevic

This study investigates SYNGAP1 haploinsufficiency in human patient-derived models, showing disrupted early neurodevelopment and accelerated neuronal maturation.

bioRxiv · Jul 16, 2026 · PreprintNeuroscience

Emerging neurodevelopmental mechanisms in patient induced pluripotent stem cells-derived spheroids modelling SCN1A Dravet Syndrome

Cristiana Mattei, Miaomiao Mao, Sean Byars, Erlina S. Mohamed Syazwan, Megan Oliva, Timothy J Karle, Kay Richards, Ingrid Eileen Scheffer, Steven Petrou, Snezana Maljevic

This study uses patient-derived iPSC spheroids to model SCN1A Dravet Syndrome, revealing dysregulated developmental processes and predicting drug response to fenfluramine.

bioRxiv · May 9, 2024 · PreprintNeuroscience

Distinctive in vitro phenotypes in iPSC-derived neurons from patients with gain- and loss-of-function SCN2A developmental and epileptic encephalopathy

Miaomiao Mao, Cristiana Mattei, Ben Rollo, Sean Byars, Claire Cuddy, Géza Berecki, Jacqueline Heighway, Svenja Pachernegg, Trevelyan R. Menheniott, Danielle Apted, Linghan Jia, Kelley Dalby, Alex Nemiroff, Saul Alator Mullen, Christopher A. Reid, , Steven Petrou

This study compares iPSC-derived neurons from patients with gain- and loss-of-function SCN2A variants, finding distinct electrophysiological and transcriptomic changes associated with different disease presentations.

bioRxiv · Feb 14, 2023 · PreprintNeuroscience