Author

Ivo Lieberam

King's College LondonORCID 0000-0003-3539-3054Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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

Frequent Co-Authors

Ariana P. GattiD· 2 shared Caoimhe KerinsiD· 2 shared Federica RiccioiD· 2 shared Guilherme NevesiD· 2 shared Juan BurroneiD· 2 shared Aimee CheesbroughiD· 1 shared Carolina Barcellos MachadoiD· 1 shared Christina E. ToomeyiD· 1 shared

Activity by Year

2023-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersNeuroscience

Ariana P. GattORCID

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3 papers

Recent·Most cited

NeuroscienceCommunications BiologyPeer-reviewedMay 19, 2026

ALS mutations do not alter perineuronal net formation in human stem cell-derived motor neurons

Caoimhe Kerins, Ivo Lieberam, Eileen Gentleman

The paper investigates whether ALS mutations affect PNN formation in human stem cell-derived motor neurons and finds no alteration in PNN-like structures or gene expression.

DOI 10.1038/s42003-026-10244-6

humanbulk RNA-seq

𝕏 PostBluesky

NeurosciencebioRxivPreprintOct 3, 2025

Increased HCN1 activity in human excitatory neurons drives excessive network bursting in Dravet syndrome

Federica Riccio, Guilherme Neves, Michelle Gottlieb-Marra…·Juan Burrone

The paper shows that increased HCN1 activity in excitatory neurons causes excessive network bursting in Dravet syndrome, suggesting HCN1 as a therapeutic target.

1 citation

humanelectronic health records

𝕏 PostBluesky

NeuroscienceCell ReportsPeer-reviewedNov 28, 2023

Pathogenic TDP-43 Disrupts Axon Initial Segment Structure and Neuronal Excitability in a Human iPSC Model of ALS

Peter Harley, Caoimhe Kerins, Ariana P. Gatt…·Ivo Lieberam

This study shows that TDP-43G298S mutations in human iPSC-derived motor neurons alter axon initial segment structure and neuronal excitability at different developmental stages.

41 citationstop 2%

humanelectronic health records

𝕏 PostBluesky