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Guy A. Rouleau

Researcher at Montreal Neurological Institute and Hospital

Publications -  935
Citations -  75050

Guy A. Rouleau is an academic researcher from Montreal Neurological Institute and Hospital. The author has contributed to research in topics: Gene & Genome-wide association study. The author has an hindex of 129, co-authored 884 publications receiving 65892 citations. Previous affiliations of Guy A. Rouleau include Utrecht University & University of Helsinki.

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Expanding the differential diagnosis of inherited neuropathies with non‐uniform conduction: Andermann syndrome

Charles Marques Lourenço, +8 more
- 01 Mar 2012 - 
TL;DR: An 18‐year‐old girl, born from first cousins, that presented a late motor and psychological development, cerebellar ataxia, facial diplegia, abnormal eye movement, scoliosis, and corpus callosum agenesis, whose compound muscle action potentials were slowed and dispersed is presented.
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Autosomal Dominant Sensory Ataxia: A Neuroaxonal Dystrophy

Jeremy J. Moeller, +5 more
- 18 Mar 2008 - 
TL;DR: The major pathological process in ADSA is a neuroaxonal dystrophy most prominent in the dorsal columns and dorsal column nuclei, consistent with the clinical pattern of central sensory pathway degeneration.
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A novel locus for idiopathic generalized epilepsy in French-Canadian families maps to 10p11.

Peter Kinirons, +12 more
- 01 Mar 2008 - 
TL;DR: Genomewide linkage analysis for genes responsible for familial IGE in French‐Canadian pedigrees found one of the four larger IGE families provided a significant linkage result at marker D10S1426 on chromosome 10, suggesting an underlying genetic mechanism for the disease.
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Amyotrophic lateral sclerosis: new genes, new models, and new mechanisms.

Christine Vande Velde, +2 more
- 01 Sep 2011 - 
TL;DR: The focus of this piece is to highlight some of the more notable developments in the field and to encourage a re-appreciation for the superoxide dismutase 1 (SOD1) mouse models.
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Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.

Rhalena A. Thomas, +5 more
- 11 Mar 2016 - 
TL;DR: The protein NgR1 is encoded by RTN4R, a gene linked to schizophrenia, and it is reported that an LGI1–NgR1 signaling pathway may contribute to the development of schizophrenia.