J. Roussel

发表

Molecular cloning and characterization of human RAI1, a gene associated with schizophrenia.

R. Joober, G. Rouleau, D. Rochefort, 2003, Genomics.

Inhibition of voltage-gated sodium channels by sumatriptan bioisosteres

G. Crescenzo, G. Lentini, C. Franchini, 2015, Front. Pharmacol..

Increased sodium channel use-dependent inhibition by a new potent analogue of tocainide greatly enhances in vivo antimyotonic activity

A. De Luca, F. Corbo, C. Franchini, 2017, Neuropharmacology.

Translational approach to address therapy in myotonia permanens due to a new SCN4A mutation

M. Lo Monaco, A. D’Amico, D. Conte Camerino, 2016, Neurology.

Transgenic expression of an expanded (GCG)13 repeat PABPN1 leads to weakness and coordination defects in mice

Simon E. Laganiere, J. Bouchard, B. Brais, 2005, Neurobiology of Disease.

CCM3 mutations are uncommon in cerebral cavernous malformations

C. Elger, D. Verlaan, A. Siegel, 2005, Neurology.

Ribosomal frameshifting on MJD-1 transcripts with long CAG tracts.

G. Rouleau, P. Dion, C. Gaspar, 2005, Human molecular genetics.

Postoperative Cognitive Dysfunction: An Updated Review

J. Roussel, L. Emory, A. Schubert, 2015 .

Neuron-Specific Expression of Mutant Superoxide Dismutase 1 in Transgenic Mice Does Not Lead to Motor Impairment

A. Pramatarova, J. Laganière, G. Rouleau, 2001, The Journal of Neuroscience.

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3

M. Dubé, D. Verlaan, G. Rouleau, 2006, Journal of Medical Genetics.

A novel locus for pure recessive hereditary spastic paraplegia maps to 10q22.1‐10q24.1

G. Rouleau, P. Cossette, J. Roussel, 2004, Annals of neurology.