Benjamin Durand
3PUBLICATIONS
106CO-AUTHORS
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Publications (3)
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|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
Elsa Leitão
2 joint publications
Gael Nicolas
1 joint publications
Sarah Baer
1 joint publications
Ilaria Parenti
1 joint publications
Alina Hesters
1 joint publications
Marta Gil-Salvador
1 joint publications
Laura Duffy
1 joint publications
Jennifer Kerkhof
1 joint publications
Julia Woestefeld
1 joint publications
Stylianos E Antonarakis
