David Pellerin

17PUBLICATIONS
62CO-AUTHORS
Genetics not elsewhere classifiedCondensed matter characterisation technique developmentGene expression (incl. microarray and other genome-wide approaches)Anthropological geneticsFlight dynamics
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Publications (17)

|Oct 23, 2026
Very Low Frequency of SCA27B Among Undiagnosed Cerebellar Ataxia Patients in Peru.

|Sep 29, 2026
Structural Brain and Spinal Cord Signature of Spinocerebellar Ataxia 27B: A Multisite MRI-Based Study.

|May 24, 2026
Frequency and phenotype of GAA-FGF14 disease in bilateral vestibulopathy syndromes: insights from repeat expansion carriers, including a case of co-occurrence with RFC1-related CANVAS.

|Feb 25, 2025
Involvement of the Superior Cerebellar Peduncles in GAA-FGF14 Ataxia.

Shihan Chen, Catherine Ashton, Rawan Sakalla

|Sep 12, 2024
Clinical, Radiological and Pathological Features of a Large American Cohort of Spinocerebellar Ataxia (SCA27B).

Widad Abou Chaar, Anirudh N Eranki, Hannah A Stevens

|Jul 03, 2023
Intronic FGF14 GAA repeat expansions are a common cause of ataxia syndromes with neuropathy and bilateral vestibulopathy.

David Pellerin, Carlo Wilke, Andreas Traschütz

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Frequent Collaborators

7 joint publications

Matthis Synofzik

3 joint publications

Carlo Wilke

3 joint publications

Bernard Brais

3 joint publications

Henry Houlden