Alexis Brice

19PUBLICATIONS
285CO-AUTHORS
Neurology and neuromuscular diseasesAerospace structuresEpigenetics (incl. genome methylation and epigenomics)PharmacogenomicsMedical biochemistry - proteins and peptides (incl. medical proteomics)
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Publications (19)

|Oct 30, 2026
SNP rs11618521 modifies transcription factor NANOG-mediated expression of KPNA3 and the age at onset of spinocerebellar ataxia type 3.

|Sep 22, 2026
ATXN8OS Intermediate Expansion Acts as a Genetic Modifier in Spinocerebellar Ataxia Type 48 (SCA48/STUB1).

|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

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Frequent Collaborators

8 joint publications

Suzanne Lesage

7 joint publications

Alexandra Durr

6 joint publications

Dario R Alessi

5 joint publications

Aida M Bertoli-Avella