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Publications by Guy A. Rouleau

Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations

American Journal of Human Genetics

English

A Stop Codon Mutation in SCN9A Causes Lack of Pain Sensation

Human Molecular Genetics

Molecular Biology

English

Genetic Predictors of Depressive Symptoms in Cardiac Patients

American Journal of Medical Genetics, Part B, Neuropsychiatric Genetics

Molecular Neuroscience

English

hnRNP A1 and a/B Interaction With PABPN1 in Oculopharyngeal Muscular Dystrophy

Canadian Journal of Neurological Sciences

English

LRRK2 Is Not a Significant Cause of Parkinson's Disease in French-Canadians

Canadian Journal of Neurological Sciences

English

Frequency of the Different Mutations Causing Spinocerebellar Ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a Large Group of Brazilian Patients

Arquivos de Neuro-Psiquiatria

Biological Psychiatry

English

Brain Glyceraldehyde-3-Phosphate Dehydrogenase Activity in Human Trinucleotide Repeat Disorders

Archives of Neurology

English

Three Families With Amyotrophic Lateral Sclerosis and Frontotemporal Dementia With Evidence of Linkage to Chromosome 9p

Archives of Neurology

English

Des Mutations Dans L’exonHSN2du gèneWNK1causent La Neuropathie Héréditaire Sensitive Et Autonomique De Type 2

Medecine/Sciences

Molecular Biology

English