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Solveig Heide

10PUBLICATIONS

52CO-AUTHORS

NeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Infant and child healthDevelopmental genetics (incl. sex determination)Foetal development and medicine

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Publications (10)

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|Sep 15, 2025

Systematic analysis of snRNA genes reveals frequent <i>RNU2-2</i> 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

<i>IRF2BPL</i> Causes Mild Intellectual Disability Followed by Late-Onset Ataxia.

Solveig Heide, Claire-Sophie Davoine, Paulina Cunha

|Oct 25, 2023

Further characterisation of <i>ARX</i>-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 <i>ZEB1</i> 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

Frequent Collaborators

2 joint publications

Caroline Nava

2 joint publications

Gaetan Lesca

1 joint publications

Karin Weiss

1 joint publications

Hayley P Lazar

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