Solveig Heide
10PUBLICATIONS
52CO-AUTHORS
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Publications (10)
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|Sep 15, 2025
Systematic analysis of snRNA genes reveals frequent RNU2-2 variants in dominant and recessive developmental and epileptic encephalopathies.Elsa Leitão, Amandine Santini, Benjamin Cogne
|Sep 04, 2025
A large cohort study of prenatal exome sequencing redefines diagnosis in fetal corpus callosum anomalies.Delphine Héron, Anna Gerasimenko, Lisa Frugère
|Jan 18, 2024
IRF2BPL Causes Mild Intellectual Disability Followed by Late-Onset Ataxia.Solveig Heide, Claire-Sophie Davoine, Paulina Cunha
|Oct 25, 2023
Further characterisation of ARX-related disorders in females due to inherited or de novo variants.Mathilde Gras, Solveig Heide, Boris Keren
|Oct 19, 2023
Loss-of-function variants in ZEB1 cause dominant anomalies of the corpus callosum with favourable cognitive prognosis.Solveig Heide, Emanuela Argilli, Stéphanie Valence
|Oct 21, 2022
Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severities.Lucie Pierron, Sophie Tezenas du Montcel, Anna Heinzmann
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Frequent Collaborators
2 joint publications
Caroline Nava
2 joint publications
Gaetan Lesca
1 joint publications
Karin Weiss
1 joint publications
Hayley P Lazar
1 joint publications
Alina Kurolap
1 joint publications
Ariel F Martinez
1 joint publications
Lior Cohen
1 joint publications
Boris Keren
1 joint publications
Christel Depienne
1 joint publications
Samantha A Schrier Vergano
