Guerrot Anne Marie

7PUBLICATIONS
198CO-AUTHORS
Infant and child healthEpigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Epidemiological methodsPhotonics, optoelectronics and optical communications
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Publications (7)

|May 26, 2026
Burst-Suppression EEG in Early Infantile Developmental and Epileptic Encephalopathies: Phenotype, Genotype, and Outcome.

|Apr 09, 2026
Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies.

Amandine Santini, Angelo Tognon, Anne-Claire Richard

|Jan 28, 2026
Predictive value of seizure onset for gross motor dysfunction in individuals with pathogenic GABRB2 and GABRB3 variants.

Sebastian Ortiz, Leonardo Affronte, Chiara Bagliani

|Jul 23, 2025
The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome-SHS.

Charlène Daval, Nicolas Meunier-Beillard, Eléonore Viora-Dupont

|Mar 31, 2025
Parental germline mosaicism in genome-wide phased de novo variants: Recurrence risk assessment and implications for precision genetic counselling.

François Lecoquierre, Nathalie Drouot, Sophie Coutant

|Apr 16, 2024
Clinical phenotype of the PIK3R1-related vascular overgrowth syndrome.

Paul Kuentz, Camille Engel, Mathieu Laeng

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Frequent Collaborators

3 joint publications

François Lecoquierre

3 joint publications

Nicolas Chatron

3 joint publications

Gaetan Lesca

3 joint publications

Laurence Faivre