A/Prof Snezana Maljevic
Honorary Principal Fellow
Florey Department of Neuroscience and Mental Health
93 Scholarly works
3 Projects
HIGHLIGHTS
2026
Journal article
Antisense oligonucleotide-mediated knockdown therapy in two infants with severe KCNT1 epileptic encephalopathy
DOI: 10.1038/s41591-026-04314-92026
Journal article
Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoids
DOI: 10.1002/epi.702672025
Journal article
KV7.2 channel dysfunction delays neuronal maturation and undermines early network development in a hiPSC model of KCNQ2-DEE
DOI: 10.1016/j.nbd.2025.1071202025
Journal article
An iPSC line (FINi102-A) carrying a heterozygous R950Q variant in KCNT1 from a boy with early-onset epilepsy
DOI: 10.1016/j.scr.2025.1038262025
Journal article
Three-Dimensional Morphological Characterisation of Human Cortical Organoids Using a Customised Image Analysis Workflow
DOI: 10.3390/organoids40100012024
Research grants (other domestic)
Utilizing Early Neurogenesis Disruption to Establish Genotype Phenotype Correlations in SYNGAP1 Disorders
2017
Research Grant
Detection of Somatic Mutations in Sporadic Epilepsies
RECENT SCHOLARLY WORKS
2025
Journal article
Developmental dysfunction in a preclinical model of Kcnq2 developmental and epileptic encephalopathy
DOI: 10.1016/j.nbd.2024.1067822024
Journal article
Variant-specific in vitro neuronal network phenotypes and drug sensitivity in SCN2A developmental and epileptic encephalopathy
DOI: 10.1111/jnc.161032024
Journal article
Slc35a2 mosaic knockout impacts cortical development, dendritic arborisation, and neuronal firing
DOI: 10.1016/j.nbd.2024.1066572024
Journal article
Standardizing a method for functional assessment of neural networks in brain organoids
DOI: 10.1016/j.jneumeth.2024.1101782024
Journal article
Genetic or Pharmacological Ablation of Acid-Sensing Ion Channel 1a (ASIC1a) Is Not Neuroprotective in a Mouse Model of Spinal Cord Injury
DOI: 10.1089/neu.2022.0295
RECENT PROJECTS
2017
Research Grant
Detection of Somatic Mutations in Sporadic Epilepsies