Camille Berges

4PUBLICATIONS
37CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Molecular targetsNeurogeneticsMedical infection agents (incl. prions)
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Publications (4)

|Jun 06, 2026
Novel Variants in PUS7 Associated With Intellectual Disability and Growth Retardation: Expanding the Clinical Spectrum in 13 Patients.

|Jan 10, 2026
Single-cell multiplex approaches deeply map ON-target CRISPR-genotoxicity and reveal its mitigation by palbociclib and long-term engraftment.

Julian Boutin, Sabrina Fayet, Victor Marin

|Jun 06, 2025
A novel heterozygous pathogenic variant in HEY2 led to a familial form of non-syndromic Tetralogy of Fallot.

Camille Bergès, Fanny Laffargue, Claire Dauphin

|Apr 09, 2024
Investigations of an individual with a Marfanoid habitus, mild intellectual disability, and severe social anxiety identifies PCDHGA5 as a candidate neurodevelopmental disorder gene.

Henri Margot, Adrien Pizano, Anouck Amestoy

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Frequent Collaborators

1 joint publications

Henri Margot

1 joint publications

Adrien Pizano

1 joint publications

Anouck Amestoy

1 joint publications

Didier Lacombe