Christelle Tesson

8PUBLICATIONS
112CO-AUTHORS
Pacific Peoples and disabilityMedical biochemistry - proteins and peptides (incl. medical proteomics)NeurogeneticsPharmacogenomics
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Publications (8)

|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

|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

|May 15, 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

|Jan 31, 2024
A pathogenic variant in RAB32 causes autosomal dominant Parkinson's disease and activates LRRK2 kinase.

Emil K Gustavsson, Jordan Follett, Joanne Trinh

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