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Sébastien Moutton

20PUBLICATIONS

218CO-AUTHORS

Gene expression (incl. microarray and other genome-wide approaches)Epigenetics (incl. genome methylation and epigenomics)Cross-sectional analysisNeurology and neuromuscular diseasesGenome structure and regulation

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Publications (20)

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|Sep 22, 2025

Further phenotypical delineation of DLG3-related neurodevelopmental disorders.

Marlène Malbos, Thierry Gautier, Amelle Shillington

|Sep 04, 2025

A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies.

Delphine Héron, Anna Gerasimenko, Lisa Frugère

|Dec 31, 2024

RICTOR variants are associated with neurodevelopmental disorders.

Raphael Carapito, Anne Molitor, Lisa Pavinato

|May 27, 2024

Expectations, needs and mid-term outcomes in people accessing to secondary findings from ES: 1st French mixed study (FIND Study).

Eléonore Viora-Dupont, Françoise Robert, Aline Chassagne

|Mar 10, 2023

Mechanism of KMT5B haploinsufficiency in neurodevelopment in humans and mice.

Sarah E Sheppard, Laura Bryant, Rochelle N Wickramasekara

|Feb 09, 2023

The clinical and genetic spectrum of autosomal-recessive TOR1A-related disorders.

Afshin Saffari, Tracy Lau, Homa Tajsharghi

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Frequent Collaborators

8 joint publications

Ange-Line Bruel

8 joint publications

Antonio Vitobello

6 joint publications

Christophe Philippe

6 joint publications

Frédéric Tran-Mau-Them

5 joint publications

Laurence Faivre

5 joint publications

Christel Thauvin-Robinet

5 joint publications

Sophie Nambot

4 joint publications

Anne-Sophie Denommé-Pichon

3 joint publications

Caroline Racine

3 joint publications

Arthur Sorlin

Frequent Collaborators

8 joint publications

Ange-Line Bruel

8 joint publications

Antonio Vitobello

6 joint publications

Christophe Philippe

6 joint publications

Frédéric Tran-Mau-Them

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