Snezana Maljevic

6PUBLICATIONS
14CO-AUTHORS
Neurology and neuromuscular diseasesInfant and child healthCellular nervous systemGene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)
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Publications (6)

|May 05, 2026
Disrupted inhibitory interneuron development in SCN1A Dravet syndrome revealed by patient-derived subpallial organoids.

|Apr 14, 2026
Antisense oligonucleotide-mediated knockdown therapy in two infants with severe KCNT1 epileptic encephalopathy.

Tojo Nakayama, Christelle M El Achkar, Lisseth E Burbano

|Mar 28, 2024
Variant-specific in vitro neuronal network phenotypes and drug sensitivity in SCN2A developmental and epileptic encephalopathy.

Linghan Jia, Melody Li, Svenja Pachernegg

|Dec 26, 2023
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

|Oct 25, 2017
Gain-of-function HCN2 variants in genetic epilepsy.

Melody Li, Snezana Maljevic, A Marie Phillips

|Jul 26, 2017
Models for discovery of targeted therapy in genetic epileptic encephalopathies.

Snezana Maljevic, Christopher A Reid, Steven Petrou

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Frequent Collaborators

2 joint publications

Christopher Reid

1 joint publications

Imran H Quraishi

1 joint publications

Jing Wu

1 joint publications

Yutaro Asami