Author

Dominique Stoppa‐Lyonnet

InsermORCID 0000-0002-5438-8309Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:benchmark study· 1 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:chromatin & epigenetic regulation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

"Genetics and the General Public" FFGH Ethics Working Group· 1 shared Anna MinelloiD· 1 shared Anne Cambon‐ThomseniD· 1 shared Anne Vincent‐SalomoniD· 1 shared Antonio GalarretaiD· 1 shared Aura CarreiraiD· 1 shared Boris ChaumetteiD· 1 shared Célia CretolleiD· 1 shared

Activity by Year

2021-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

"Genetics and the General Public" FFGH Ethics Working Group

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 19, 2026

Knowledge and misconceptions of the French population regarding medical genetics: a survey of 3,000 respondents

Sandra Mercier, Francois Michael Petit, Micheline Misrahi…·"Genetics and the General Public" FFGH Ethics Working Group

This study surveys 3,000 French individuals to assess their knowledge and misconceptions about medical genetics, revealing limited understanding and significant gaps in awareness of genetic testing limitations and legal frameworks.

DOI 10.64898/2026.07.17.26358259

benchmark study

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Cancer BiologyNature CommunicationsPeer-reviewedDec 10, 2025

A recurrent pathogenic BRCA2 truncating variant reveals a role for BRCA2-PCAF complex in modulating NF-κB-driven transcription

Anna Minello, Jesús Gómez-Escudero, Sree Rama Chaitanya Sridhara…·Aura Carreira

The paper investigates a BRCA2 truncating variant's effect on NF-κB-driven transcription by showing it disrupts the BRCA2-PCAF complex, reducing histone acetylation and impairing cell migration.

2 citations

humanbulk RNA-seq

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GeneticsPLoS Computational BiologyPeer-reviewedMar 18, 2021

Biological networks and GWAS: comparing and combining network methods to understand the genetics of familial breast cancer susceptibility in the GENESIS study

Héctor Climente-González, Christine Lonjou, Fabienne Lesueur…·GENESIS study group

The paper compares six network methods using GWAS data from the GENESIS study to identify breast cancer susceptibility genes, finding that network approaches improve results over standard GWAS.

13 citations

humanGWAS summary statistics

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