Alexis Brice

17PUBLICATIONS
276CO-AUTHORS
Neurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)PharmacogenomicsMedical biochemistry - proteins and peptides (incl. medical proteomics)Medical infection agents (incl. prions)
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Publications (17)

|Apr 15, 2026
Variants in the proteasome regulator PSMF1 cause a phenotypic spectrum from parkinsonism to perinatal lethality.

|Mar 08, 2025
Copy Number Variation and Haplotype Analysis of 17q21.31 Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells.

Hui Wang, Timothy S Chang, Beth A Dombroski

|Feb 13, 2025
[Parkinson's disease: from genetics to targeted therapies].

Guillaume Cogan, 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

|Aug 01, 2024
The parkin V380L variant is a genetic modifier of Machado-Joseph disease with impact on mitophagy.

Jonasz J Weber, Leah Czisch, Priscila Pereira Sena

|Jul 10, 2024
Association of Body Mass Index and Parkinson Disease: A Bidirectional Mendelian Randomization Study.

Cloé Domenighetti, Pierre-Emmanuel Sugier, Ashwin Ashok Kumar Sreelatha

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Frequent Collaborators

8 joint publications

Suzanne Lesage

6 joint publications

Dario R Alessi

5 joint publications

Aida M Bertoli-Avella

5 joint publications

Hermann Steller