Author

Georgia Rouni

Alexander Fleming Biomedical Sciences Research Center

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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Cancer Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Vassiliki KostourouiD· 2 shared Alana R. CowelliD· 1 shared Anastasia Kotsoni· 1 shared Anastasios Klavdianos· 1 shared Benjamin T GoultiD· 1 shared Charikleia Moschou· 1 shared Christina Arapatzi· 1 shared Danit Oz-Levi· 1 shared

Activity by Year

2024-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCancer Biology

Vassiliki KostourouORCID

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2 papers

Recent·Most cited

A neural alternative splicing program controls cellular function and growth in Pancreatic Neuroendocrine tumours

Myrto Potiri, Charikleia Moschou, Zoi Erpapazoglou, Georgia Rouni, Anastasia Kotsoni, Margarita Andreadou, Anastasios Klavdianos, Melina Dragolia, Vasileios Ntafis, Joerg Schrader, Jonàs Juan‐Mateu, Skarlatos Dedos, Martina K. Samiotaki, Vassiliki Kostourou, Malgorzata Ewa Rogalska, Panagiota Kafasla

This study identifies an alternative splicing program regulated by SRRM3 that affects secretory function and neuronal characteristics in PanNETs, offering therapeutic targets.

Cell Reports · Jul 17, 2025Peer-reviewedCancer Biology

Talin1 dysfunction is genetically linked to systemic capillary leak syndrome.

Naama Elefant, Pinelopi Nikolopoulou, V Vassiliki Papadaki, Danit Oz-Levi, Georgia Rouni, Racheli Sion‐Sarid, William JS Edwards, Christina Arapatzi, Shira Yanovsky‐Dagan, Alana R. Cowell, Vardiella Meiner, Vladimir Vainstein, Sofia Grammenoudi, Doron Lancet, Benjamin T Goult, , Vassiliki Kostourou

The paper identifies a rare TLN1 splice-site variant in a familial SCLS case, linking Talin1 dysfunction to systemic capillary leak syndrome through disrupted endothelial barrier integrity.

JCI Insight · Dec 19, 2024Peer-reviewedGenetic & Genomic Medicine