Author

Frédéric Frénois

Université de LilleORCID 0000-0002-1405-0629Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:Hi-C· 1 Organism:mouse· 1 Research Focus:variant calling· 1

Frequent Co-Authors

Florence PetitiD· 2 shared Andrés HernándeziD· 1 shared Anne‐Sophie Jourdain· 1 shared Barbara R. PoberiD· 1 shared Boris KereniD· 1 shared Brigitte Gilbert‐DussardieriD· 1 shared Carol J. BultiD· 1 shared Caroline Thuillier· 1 shared

Activity by Year

2020-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 31 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Florence PetitORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Missense variants affecting the actin-binding domains of PLS3 cause X-linked congenital diaphragmatic hernia and body wall defects

Florence Petit, Mauro Longoni, Julie M. Wells, Richard S. Maser, Eric L. Bogenschutz, Matthew J. Dysart, Hannah T. M. Contreras, Frédéric Frénois, Barbara R. Pober, Robin Dawn Clark, Philip F. Giampietro, Hilger H. Ropers, Hao Hu, Marı́a Loscertales, Richard Wagner, , Frances A. High

The paper identifies missense variants in PLS3 causing X-linked congenital diaphragmatic hernia and body wall defects through genetic analysis and functional studies.

The American Journal of Human Genetics · Sep 25, 2023Peer-reviewedGenetic & Genomic Medicine

Lessons from the analysis of TAD boundary deletions in normal population

Thomas Smol, Jérôme Sigé, Caroline Thuillier, Frédéric Frénois, Perrine Brunelle, Mélanie Rama, Catherine Roche‐Lestienne, Sylvie Manouvrier‐Hanu, Florence Petit, Jamal Ghoumid

The paper analyzes TAD boundary deletions in the general population and finds that most TADs are not disrupted, with only a subgroup showing enrichment in disease genes.

bioRxiv · Apr 1, 2020 · PreprintGenomics