Author

Erlina S. Mohamed Syazwan

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

Frequent Co-Authors

Ingrid Eileen SchefferiD· 3 shared A. Marie PhillipsiD· 2 shared Chaseley E. McKenzieiD· 2 shared Christopher A. ReidiD· 2 shared Christopher SemsarianiD· 2 shared Ming S. SohiD· 2 shared Samuel Frank BerkoviciD· 2 shared Alibek KuanyshbekiD· 1 shared

Activity by Year

2021-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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3 shared papersNeuroscience

Ingrid Eileen SchefferORCID

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Author profile →

3 papers

Recent·Most cited

NeurosciencebioRxivPreprintMay 9, 2024

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

Cristiana Mattei, Miaomiao Mao, Sean Byars…·Snezana Maljevic

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

DOI 10.1101/2024.05.09.593441

humanscRNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintDec 10, 2023

Atenolol reduces cardiac-mediated mortality in a genetic mouse model of sudden unexpected death in epilepsy

Ming S. Soh, Alibek Kuanyshbek, Erlina S. Mohamed Syazwan…·Christopher A. Reid

This study shows that atenolol reduces cardiac-related mortality in a genetic mouse model of SUDEP by mitigating seizure and LQTS interactions.

DOI 10.1101/2023.12.10.570964

mousestatistical model

𝕏 PostBluesky

NeurosciencebioRxivPreprintMar 19, 2021

Loss-of-function variants in the cardiac Kv11.1 channel as a genetic biomarker for SUDEP

Ming S. Soh, Richard D. Bagnall, Mark F. Bennett…·Christopher A. Reid

The paper identifies loss-of-function KCNH2 variants as enriched in SUDEP patients compared to epilepsy controls, suggesting a genetic biomarker for SUDEP risk.

1 citation

humanwhole-exome sequencing

𝕏 PostBluesky