Pauline Le Tanno

5PUBLICATIONS
48CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene mappingAdolescent healthDevelopmental genetics (incl. sex determination)Infant and child health
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Publications (5)

|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

|Feb 24, 2026
Phenotypic description of a large French series of individuals with Potocki-Lupski syndrome.

Alicia Coudert, Pauline Le Tanno, William Dufour

|Nov 23, 2024
An Extended Phenotype of PPP1R13L Cardiocutaneous Syndrome.

Alicia Coudert, Julien Thevenon, Quentin Testard

|Oct 17, 2024
Exome Sequencing Detects Uniparental Disomy of Chromosome 4 Revealing a LARP7 Pathogenic Variant Responsible for Alazami Syndrome: A Case Report.

Amélie Buisine-Sbraggia, Julien Thevenon, Kevin Yauy

|Dec 08, 2021
Diagnostic workup in children with arthrogryposis: description of practices from a single reference centre, comparison with literature and suggestion of recommendations.

Pauline Le Tanno, Xenia Latypova, John Rendu

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Frequent Collaborators

3 joint publications

Klaus Dieterich

2 joint publications

Willems Marjolaine

2 joint publications

Alicia Coudert

2 joint publications

Laurence Faivre