Alexis Brice

Centre National de la Recherche Scientifique — France

Medicine · Health Sciences

154h-index115.4kcitations1.2kworks7.32yr avg
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Research Topics

Parkinson's Disease Mechanisms and Treatments(373), Genetic Neurodegenerative Diseases(342), Neurological diseases and metabolism(272), Mitochondrial Function and Pathology(239), Hereditary Neurological Disorders(167)

Publications1.1k total

TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
npj Parkinson s Disease·2025· 2 citedOpen Access
Italian intersocietal recommendations for restructuring the diagnostic-therapeutic pathway for the implementation and appropriate use of anti-amyloid monoclonal antibodies in Alzheimer’s disease
Repository of the University of Primorsk (University of Primorska)·2025Open Access
Should ITSN1 be considered as a Mendelian Parkinson’s disease gene? Description of three novel families
npj Parkinson s Disease·2025Open Access
Parkinson’s disease and multiple system atrophy are gateways to <i>RFC1</i> -related disorders
2025Open Access
Classification of GBA1 variants and their impact on Parkinson’s disease: an in silico score analysis
npj Parkinson s Disease·2025· 3 citedOpen Access
Late-onset cerebellar ataxia in three European patients with repeat expansions in RFC1 and FGF14: a case series
Journal of Neurology·2025· 2 cited
Expanding the clinical spectrum of <i>RAB3A</i> : from cerebellar ataxia to spastic paraplegia
Brain·2025· 1 citedOpen Access
Impact of Y chromosome loss on the risk of Parkinson's disease and progression
EBioMedicine·2025· 2 citedOpen Access
Linking polygenic risk scores to dopaminergic neuron loss using neuromelanin-sensitive imaging
Brain·2025
Usage of an Alternative Translation Start Site in <i>PRKN</i> mutation carriers: Key to Later-Onset Parkinson’s Disease and a Novel Therapeutic Target
2025Open Access
The FGF14-SCA27B GAA•TTC Repeat Shows a Marked Somatic Expansion Bias in the Cerebellum (S4.004)
Neurology·2025
The LRRK2 p.L1795F variant causes Parkinson’s disease in the European population
npj Parkinson s Disease·2025· 3 citedOpen Access
Quelles sont les causes d’ataxies cérébelleuses héréditaires avec downbeat nystagmus ?
Revue Neurologique·2025
How is familial idiopathic scoliosis transmitted? Analysis of 26 pedigrees
Orthopaedics & Traumatology Surgery & Research·2025
Copy Number Variation and Haplotype Analysis of <scp>17q21.31</scp> Reveals Increased Risk Associated with Progressive Supranuclear Palsy and Gene Expression Changes in Neuronal Cells
Movement Disorders·2025· 1 citedOpen Access
Exploration of Neurodegenerative Diseases Using Long‐Read Sequencing and Optical Genome Mapping Technologies
Movement Disorders·2025· 6 citedOpen Access
La maladie de Parkinson : de la génétique aux thérapies ciblées
Comptes Rendus Biologies·2025· 3 citedOpen Access
Analysis of short tandem repeats linked to polyglutamine diseases from whole-genome sequencing reveals intermediate alleles of <i>HTT</i> associated with an early disease onset in <i>C9orf72</i> carriers
Brain Communications·2025Open Access
Proteomic analysis reveals distinct cerebrospinal fluid signatures across genetic frontotemporal dementia subtypes
Florence Research (University of Florence)·2025
Correction: Whole-genome sequencing analysis reveals new susceptibility loci and structural variants associated with progressive supranuclear palsy
Molecular Neurodegeneration·2024· 2 citedOpen Access
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Frequent Co-authors

Alexandra Dürr(21), Nicholas Wood(13), Suzanne Lesage(12), Thomas Gasser(12), John Hardy(11), Peter Heutink(10), Yves Agid(9), Manu Sharma(8), Giovanni Stévanin(8), María Martínez(7), Jean‐Christophe Corvol(7), Michael A. Nalls(7), Vincenzo Bonifati(6), Jean‐Louis Mandel(6), Joshua Shulman(6), Andrew Singleton(6), Dena G. Hernandez(6), José Brás(5), Claudia Schulte(5), J. Raphael Gibbs(5)