Christelle Tesson

8PUBLICATIONS
112CO-AUTHORS
Neurology and neuromuscular diseasesPacific Peoples and disabilityGene mappingMedical biochemistry - proteins and peptides (incl. medical proteomics)Neurogenetics
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Publications (8)

|Jun 23, 2025
Screening of Hidden Pathogenic Structural Variants in PRKN.

Kensuke Daida, Guillaume Cogan, Christelle Tesson

|Jan 23, 2025
A PARK7 Mutation-Induced Early-Onset Parkinson's Disease in a Moroccan Family: Expanding the Geographic Spectrum.

Hicham El Otmani, Christelle Tesson, Alexis Brice

|Sep 23, 2024
Confirmation of RAB32 Ser71Arg Involvement in Parkinson's Disease.

Guillaume Cogan, Christelle Tesson, Christine Brefel-Courbon

|Aug 16, 2024
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from early-onset Parkinson's disease to perinatal lethality and disrupt mitochondrial function.

Francesca Magrinelli, Christelle Tesson, Plamena R Angelova

|Jun 29, 2024
Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's Disease.

Guillaume Cogan, Kensuke Daida, Kimberley J Billingsley

|May 15, 2024
Long-read sequencing unravels the complexity of structural variants in <i>PRKN</i> in two individuals with early-onset Parkinson's disease.

Guillaume Cogan, Kensuke Daida, Kimberley J Billingsley

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Frequent Collaborators

5 joint publications

Guillaume Cogan

4 joint publications

Alexis Brice

3 joint publications

Dario R Alessi

3 joint publications

Cornelis Blauwendraat