Author

Pauline Romanet

InsermORCID 0000-0003-1775-9569Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cancer Biology· 1 Developmental Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Assay:bulk RNA-seq· 1 Research Focus:cancer & tumor microenvironment· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:statistical model· 1

Frequent Co-Authors

Anne BarlieriD· 3 shared Frédéric CastinettiiD· 2 shared Heather EtcheversiD· 2 shared Alexandra CsábiiD· 1 shared Ashutosh RaiiD· 1 shared Attila PatócsiD· 1 shared Barbara JarząbiD· 1 shared Carmen S. Martin· 1 shared

Activity by Year

2024-2026 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 38 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Anne BarlierORCID

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3 papers

Recent·Most cited

Familial medullary thyroid carcinoma secondary to an SLC30A9 intragenic deletion and translation reinitiation

Donato Iacovazzo, Federica Begalli, Oniz Suleyman, Márton Doleschall, Maria Alevizaki, Kevin E. Ashelford, Sherine Awad Mahmoud, Anne Barlier, Sayka Barry, Caroline E Brain, Claudia Cabrera, Frédéric Castinetti, Sabrina Chiloiro, Kevin Colclough, Alexandra Csábi, , Márta Korbonits

The paper identifies an SLC30A9 deletion causing familial medullary thyroid carcinoma through translation reinitiation and shows its oncogenic effects.

medRxiv · Feb 27, 2026 · PreprintGenetic & Genomic Medicine

Modeling corticotroph deficiency with pituitary organoids supports the functional role of NFKB2 in human pituitary differentiation

Thi Thom Mac, Teddy Fauquier, Nicolas Jullien, Pauline Romanet, Heather Etchevers, Anne Barlier, Frédéric Castinetti, Thierry Christian Brue

This study uses CRISPR/Cas9-edited human pituitary organoids to show that NFKB2 mutations impair corticotroph differentiation, confirming its role in ACTHD.

eLife · Nov 28, 2024Peer-reviewedDevelopmental Biology

Deconvoluted methylation profiles discriminate between closely related melanocytic nevi

Daniel Aldea, Nicolas Macagno, Elise Maréchal, Mathias Moreno, Pauline Romanet, Morgane Pertuit, Jérémy Garcia, N. Dégardin, S. Mallet, Isabelle James, Guillaume Captier, Anne Barlier, Heather Etchevers

The paper uses weighted whole-genome methylation analysis to distinguish between congenital and acquired melanocytic nevi.

Journal of Investigative Dermatology · Nov 9, 2024Peer-reviewedCancer Biology