Author

Tamar E. Sztal

Monash UniversityORCID 0000-0001-9745-3580Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Neuroscience· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:zebrafish· 3 Research Focus:cell type annotation· 1 Assay:electronic health records· 1 Organism:mouse· 1

Frequent Co-Authors

Robert J. Bryson‐RichardsoniD· 2 shared Adriana MessineoiD· 1 shared Alon M. DouekiD· 1 shared Augustin C.C. OgieriD· 1 shared Bang Viet BuiiD· 1 shared Charlotte GinesteiD· 1 shared Christophe Vilmen· 1 shared Clara LeeiD· 1 shared

Activity by Year

2018-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 24 mutual co-author links

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2 shared papersNeuroscience

Robert J. Bryson‐RichardsonORCID

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3 papers

Recent·Most cited

NeuroscienceDisease Models & MechanismsPeer-reviewedDec 16, 2021

Novel pre-clinical model for CDKL5 Deficiency Disorder

Rita J. Serrano, Clara Lee, Alon M. Douek…·Tamar E. Sztal

This study develops a zebrafish model for CDKL5 Deficiency Disorder to investigate disease mechanisms and screen for therapies.

13 citations

zebrafishexperimental assay

𝕏 PostBluesky

NeuroscienceInvestigative Ophthalmology & Visual SciencePeer-reviewedMar 22, 2021

Altered visual function in a larval zebrafish knockout of neurodevelopmental risk gene pdzk1

Jiaheng Xie, Patricia Regina Jusuf, Bang Viet Bui…·Patrick T. Goodbourn

This study investigates the role of pdzk1 in visual function using zebrafish knockouts, finding altered optomotor responses and ERG b-waves without major retinal structural changes.

6 citations

zebrafishelectronic health records

𝕏 PostBluesky

NeuroscienceScientific ReportsPeer-reviewedJul 25, 2018

L-tyrosine supplementation is not therapeutic for skeletal muscle dysfunction in zebrafish and mouse models of dominant skeletal muscle α-actin nemaline myopathy.

Adriana Messineo, Charlotte Gineste, Tamar E. Sztal…·Kristen J. Nowak

This study shows L-tyrosine supplementation does not improve skeletal muscle function in zebrafish and mouse models of nemaline myopathy caused by ACTA1 mutations.

27 citations

𝕏 PostBluesky