Benjamin Durand

4PUBLICATIONS
108CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (4)

|Mar 30, 2026
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.

Elsa Leitão, Amandine Santini, Benjamin Cogne

|Mar 30, 2026
Pathogenic variants in the cohesin loader subunit MAU2 underlie a distinct Cornelia de Lange Syndrome subtype.

Ilaria Parenti, Alina Hesters, Marta Gil-Salvador

|Jul 13, 2022
Neurocognitive and neurobehavioral characterization of two frequent forms of neurodevelopmental disorders: the DYRK1A and the Wiedemann-Steiner syndromes.

Benjamin Durand, Elise Schaefer, Pauline Burger

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Frequent Collaborators

2 joint publications

Sarah Baer

2 joint publications

Elsa Leitão

2 joint publications

Gael Nicolas

1 joint publications

Ilaria Parenti