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Publications by Bertrand Fontaine

NR1H3 p.Arg415Gln Is Not Associated to Multiple Sclerosis Risk

English

Expression of P2X7R mRNA in Mouse Astrocytes and Microglia

Molecular Psychiatry

Molecular Neuroscience

Molecular Biology

English

Loss of Paraplegin Drives Spasticity Rather Than Ataxia in a Cohort of 241 Patients With SPG7

English

Determination of the Real Effect of Genes Identified in GWAS: The Example of IL2RA in Multiple Sclerosis

European Journal of Human Genetics

English

Brian Hears: Online Auditory Processing Using Vectorization Over Channels

Frontiers in Neuroinformatics

Computer Science Applications

Biomedical Engineering

English

Sound Envelope Extraction in Cochlear Nucleus Neurons: Modulation Filterbank and Cellular Mechanism

BMC Neuroscience

Molecular Neuroscience

English

A New Locus for Autosomal Dominant Pure Spastic Paraplegia, on Chromosome 2q24-Q34

American Journal of Human Genetics

English

Hereditary Spastic Paraplegia SPG13 Is Associated With a Mutation in the Gene Encoding the Mitochondrial Chaperonin Hsp60

American Journal of Human Genetics

English

Atlastin1 Mutations Are Frequent in Young-Onset Autosomal Dominant Spastic Paraplegia

Archives of Neurology

English