Lucie Pierron

4PUBLICATIONS
26CO-AUTHORS
NeurogeneticsComputational linguisticsFoetal development and medicineFamily and household studies
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Publications (4)

|Aug 12, 2026
BHLHE22 monoallelic and biallelic variants cause a neurodevelopmental disorder with agenesis of the corpus callosum, intellectual disability, abnormal muscle tone and movement abnormalities.

|May 22, 2026
A Patient-Reported Outcome Measure of Communication Difficulties in Friedreich Ataxia: COMATAX.

|Oct 21, 2022
Reproductive choices and intrafamilial communication in neurogenetic diseases with different self-estimated severities.

Lucie Pierron, Sophie Tezenas du Montcel, Anna Heinzmann

|Dec 10, 2020
Informing about genetic risk in families with Huntington disease: comparison of attitudes across two decades.

Lucie Pierron, Juliette Hennessy, Sophie Tezenas du Montcel

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Frequent Collaborators

2 joint publications

Alexandra Durr

1 joint publications

Sophie Tezenas du Montcel

1 joint publications

Solveig Heide

1 joint publications

Maresa Buchholz