Camille Verebi

11PUBLICATIONS
34CO-AUTHORS
Developmental genetics (incl. sex determination)Gene mappingFood properties (incl. characteristics and health benefits)Terahertz physicsPolymerisation mechanisms
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Publications (11)

|Sep 18, 2026
Extending the ATP9A-Related Phenotypic Spectrum: Indication of Schizophrenia Susceptibility.

|Jul 06, 2026
Autosomal Dominant Missense DAG1 Variant Linked to Mild-Moderate LGMD R16.

|May 12, 2026
Fragmentomics features of cell free DNA in eating disorders.

|Aug 13, 2025
The Value of Enhancing Sonographic Phenotyping to Improve the Diagnostic Yield of Noninvasive Prenatal Diagnosis (NIPD) for Achondroplasia.

Camille Verebi, Victor Gravrand, Claire Guerini

|Apr 14, 2025
Variants in CAPN3 Causing Autosomal Dominant Limb-Girdle Muscular Dystrophy Combined With Calpain-3 Deficiency.

Thomas Krag, Emily Nasho, Lauren Brady

|Dec 26, 2024
SMCHD1 genetic variants in type 2 facioscapulohumeral dystrophy and challenges in predicting pathogenicity and disease penetrance.

Laurène Gérard, Mégane Delourme, Charlotte Tardy

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Frequent Collaborators

3 joint publications

Juliette Nectoux

3 joint publications

Thierry Bienvenu

2 joint publications

Edoardo Malfatti

1 joint publications

Sophie Brouillet