Author

Barbara Morone

Institute of Genetics and Biophysics

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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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Research Focus:differential expression· 2 Approach:experimental assay· 2 Research Focus:gene regulatory network inference· 2 Organism:human· 2 Assay:ChIP-seq· 1 Assay:DNA methylation· 1 Approach:statistical model· 1

Frequent Co-Authors

Floriana Della RagioneiD· 2 shared Maria Rosaria MatarazzoiD· 2 shared Maria StrazzulloiD· 2 shared Salvatore FiorinielloiD· 2 shared Andrea RiccioiD· 1 shared Claudia AngeliniiD· 1 shared Claudio PignataiD· 1 shared Francesco CecereiD· 1 shared

Activity by Year

2023-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 40 mutual co-author links

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2 shared papersGenetics

Floriana Della RagioneORCID

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2 papers

Recent·Most cited

A novel iPSC-based model of ICF syndrome subtype 2 recapitulates the molecular phenotype of ZBTB24 deficiency

Vincenzo Lullo, Francesco Cecere, Saveria Batti, Sara Allegretti, Barbara Morone, Salvatore Fioriniello, Laura Pisapia, Rita Genesio, Floriana Della Ragione, Giuliana Giardino, Claudio Pignata, Andrea Riccio, Maria Rosaria Matarazzo, Maria Strazzullo

The paper develops an iPSC model of ICF2 syndrome to study ZBTB24 deficiency's effects on DNA methylation and cellular function.

Frontiers in Immunology · Jul 8, 2024Peer-reviewedGenetics

The rescue of epigenomic abnormalities in ICF1 patient iPSCs following DNMT3B correction is incomplete at a residual fraction of H3K4me3-enriched regions

Varsha Poondi Krishnan, Barbara Morone, Shir Toubiana, Monika Krzak, Salvatore Fioriniello, Floriana Della Ragione, Maria Strazzullo, Claudia Angelini, Sara Selig, Maria Rosaria Matarazzo

The study corrects DNMT3B mutations in ICF1 iPSCs and finds that while most hypomethylated regions are restored, some regions remain hypomethylated and show increased H3K4me3 and CTCF motifs.

Genome Research · Feb 1, 2023Peer-reviewedGenomics