Author

Camille Engel

Centre National de la Recherche ScientifiqueORCID 0000-0003-1531-7628Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 2 Organism:human· 2 Assay:bulk RNA-seq· 1 Approach:machine learning (classical)· 1 Approach:statistical model· 1

Frequent Co-Authors

Amélie PitoniD· 2 shared Jean‐Louis MandeliD· 2 shared Nathalie Drouot· 2 shared Vera M. KalscheueriD· 2 shared Agnès Rastetter· 1 shared Alexander P.A. StegmanniD· 1 shared Alma Kuechler· 1 shared Angélique QuartieriD· 1 shared

Activity by Year

2022-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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2 shared papersGenetics

Amélie PitonORCID

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2 papers

Recent·Most cited

GeneticsMolecular PsychiatryPeer-reviewedNov 29, 2023

Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome

Jérémie Courraud, Camille Engel, Angélique Quartier…·Amélie Piton

This study investigates the molecular consequences of PQBP1 deficiency in Renpenning syndrome by analyzing gene expression and protein interactions, identifying dysregulated genes and a novel UPF3B isoform.

10 citations

humanbulk RNA-seq

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Genetic & Genomic MedicineNature CommunicationsPeer-reviewedNov 2, 2022

Systematic analysis and prediction of genes associated with disorders on chromosome X

Elsa Leitão, Christopher Schröder, Ilaria Parenti…·Christel Depienne

The paper systematically analyzes chrX genes to predict disease associations, identifying 235 genes likely involved in disorders and reporting damaging variants in CDK16 and TRPC5 in patients with intellectual disability or autism.

48 citationstop 2%

humanmachine learning (classical)

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