David Pellerin

14PUBLICATIONS
45CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Anthropological geneticsFlight dynamicsGene mappingNeurology and neuromuscular diseases
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Publications (14)

|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

|Dec 14, 2022
Deep Intronic FGF14 GAA Repeat Expansion in Late-Onset Cerebellar Ataxia.

David Pellerin, Matt C Danzi, Carlo Wilke

|Jan 24, 2020
Novel Recessive TNNT1 Congenital Core-Rod Myopathy in French Canadians.

David Pellerin, Asli Aykanat, Benjamin Ellezam

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Frequent Collaborators

7 joint publications

Matthis Synofzik

3 joint publications

Carlo Wilke

3 joint publications

Henry Houlden

2 joint publications

Guillemette Clément