Author

Manon Baudic

Centre National de la Recherche ScientifiqueORCID 0000-0001-6414-5012Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Developmental Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:cell-cell communication· 1 Assay:ChIP-seq· 1 Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Organism:mouse· 1

Frequent Co-Authors

Ahmad S. AminiD· 1 shared Alex LipoviD· 1 shared Alicia A Evans· 1 shared Ammar Al‐ChalabiiD· 1 shared Andrew A. GraceiD· 1 shared Andrew Michael GlazeriD· 1 shared Antoine LeenhardtiD· 1 shared Apichai KhongphatthanayothiniD· 1 shared

Activity by Year

2025-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Ahmad S. AminORCID

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 10, 2026

Whole-genome sequencing implicates rare, low-frequency and structural non-coding variation at the SCN5A locus in Brugada syndrome

Alex Lipov, Manon Baudic, Pierre Lindenbaum…·Connie R. Bezzina

This study identifies rare and low-frequency non-coding variants at the SCN5A locus associated with Brugada syndrome using whole-genome sequencing and functional assays.

DOI 10.64898/2026.07.07.26356386

humanwhole-genome sequencing

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Developmental BiologyDevelopmental CellPeer-reviewedJul 1, 2025

Structural perturbation of chromatin domains with multiple developmental regulators can severely impact gene regulation and development

Shreeta Chakraborty, Nina Wenzlitschke, Matthew J. Anderson…·Pedro P. Rocha

The paper shows that disrupting chromatin domain boundaries with multiple developmental regulators can cause severe gene dysregulation and developmental defects in mice.

22 citations

mouseDNA methylation

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