Sabrina Sayah

5PUBLICATIONS
39CO-AUTHORS
Computational linguisticsNeurogeneticsNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)
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Publications (5)

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

|Dec 19, 2025
Sequence Variants in Small CAG Repeat Expansions of the <i>HTT</i> Gene and Disease Onset and Progression in Huntington Disease.

Anna Heinzmann, Emilien Petit, Jessica Dawson

|Aug 20, 2025
Prevalence, Severity, and Progression of Cerebellar Cognitive-Affective Syndrome in Patients With Spinocerebellar Ataxias.

Emilien Petit, Daniel López Domínguez, Cecilia Marelli

|Jun 08, 2023
Huntington's Disease with Small CAG Repeat Expansions.

Anna Heinzmann, Sabrina Sayah, François-Xavier Lejeune

|Nov 17, 2021
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.

Marie Coutelier, Maxime Jacoupy, Alexandre Janer

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Frequent Collaborators

4 joint publications

Alexandra Durr

3 joint publications

Anna Heinzmann

2 joint publications

Jennifer Faber

2 joint publications

Giulia Coarelli