Author

Sophie Ehresmann

CHU Sainte-Justine Research CenterORCID 0000-0002-4171-7222Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Molecular Biology· 1

Signature Assays, Organisms & Methods

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

Frequent Co-Authors

DDD study· 1 shared Elena GorettiiD· 1 shared Gilberto Duran-Bishop· 1 shared Jean-Francois LaurendeauiD· 1 shared Justine RousseauiD· 1 shared Kevin C.J. NixoniD· 1 shared Martin SauvageauiD· 1 shared Max H. StoneiD· 1 shared

Activity by Year

2018-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 20 mutual co-author links

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1 shared paperGenetics

DDD study

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2 papers

Recent·Most cited

Molecular BiologybioRxivPreprintApr 12, 2026

The lncRNA FENDRR fine-tunes FOXF1 protein levels through a negative feedback loop governing human embryonic lung fibroblast-to-myofibroblast transition

Jean-Francois Laurendeau, Sophie Mockly, Gilberto Duran-Bishop…·Martin Sauvageau

The paper identifies a negative feedback loop between lncRNA FENDRR and FOXF1 that regulates protein levels during fibroblast-to-myofibroblast transition in lung development.

DOI 10.64898/2026.04.10.716765

humanmouse

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GeneticsbioRxivPreprintSep 25, 2018

Identification of SMARCD1 as a syndromic intellectual disability gene that is required for memory and context-dependent regulation of neuronal genes in Drosophila

Kevin C.J. Nixon, Justine Rousseau, Max H. Stone…·DDD study

The paper identifies SMARCD1 mutations as a cause of intellectual disability and shows its role in regulating neuronal gene expression during development in Drosophila.

2 citations

Drosophilastatistical model

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