Céline Bonnet

15PUBLICATIONS
82CO-AUTHORS
Cancer geneticsCardiology (incl. cardiovascular diseases)Epigenetics (incl. genome methylation and epigenomics)Gene expression (incl. microarray and other genome-wide approaches)Gene and molecular therapy
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Publications (15)

|Jul 10, 2026
Continuous Intrajejunal Levodopa-Carbidopa Infusion in Parkinson's Disease Associated with 22q11.2 Deletion Syndrome: A Case Series.

|Jul 01, 2026
Hyperhomocysteinemia and Vitamin B Deficiency as Potential Aggravating Factors in Huntington's Disease: A Prospective Monocentric Study.

|May 25, 2026
Distinct Neuropsychiatric Profiles Associated With 17p11.2 Deletions and RAI1 Variants in Smith-Magenis Syndrome.

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

Shihan Chen, Catherine Ashton, Rawan Sakalla

|Jun 27, 2024
A common flanking variant is associated with enhanced stability of the FGF14-SCA27B repeat locus.

David Pellerin, Giulia F Del Gobbo, Madeline Couse

|Jun 27, 2024
Expanding the genetic and clinical spectrum of Tatton-Brown-Rahman syndrome in a series of 24 French patients.

Hortense Thomas, Tom Alix, Émeline Renard

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Frequent Collaborators

3 joint publications

Matthis Synofzik

3 joint publications

Henry Houlden

2 joint publications

Albin Blanc

2 joint publications

Catherine Ashton