# Guy A. Rouleau

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/guy-a-rouleau/

## Facts

| Field | Value |
| --- | --- |
| Citations | 96,358 |
| Field | Amyotrophic Lateral Sclerosis Research |
| h-index | 147 |
| i10-index | 766 |
| Last Known Institution | Montreal Neurological Institute and Hospital |
| OpenAlex ID | https://openalex.org/A5002628021 |
| ORCID iD | https://orcid.org/0000-0001-8403-1418 |
| Works | 1,277 |

## Researcher papers

Showing 12 of 17.

- [Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis](https://scholariq.org/papers/mutations-in-cu-zn-superoxide-dismutase-gene-are-associated-with-familial/)
- [Mutations in the <i>FUS/TLS</i> Gene on Chromosome 16 Cause Familial Amyotrophic Lateral Sclerosis](https://scholariq.org/papers/mutations-in-the-i-fus-tls-i-gene-on-chromosome-16-cause-familial-amyotrophic/)
- [TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis](https://scholariq.org/papers/tardbp-mutations-in-individuals-with-sporadic-and-familial-amyotrophic-lateral/)
- [Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways](https://scholariq.org/papers/exome-sequencing-in-amyotrophic-lateral-sclerosis-identifies-risk-genes-and/)
- [Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments](https://scholariq.org/papers/meta-analysis-of-shank-mutations-in-autism-spectrum-disorders-a-gradient-of/)
- [Narcolepsy is strongly associated with the T-cell receptor alpha locus](https://scholariq.org/papers/narcolepsy-is-strongly-associated-with-the-t-cell-receptor-alpha-locus/)
- [High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies](https://scholariq.org/papers/high-rate-of-recurrent-de-novo-mutations-in-developmental-and-epileptic/)
- [Interrogating the Genetic Determinants of Tourette’s Syndrome and Other Tic Disorders Through Genome-Wide Association Studies](https://scholariq.org/papers/interrogating-the-genetic-determinants-of-tourette-s-syndrome-and-other-tic/)
- [Exome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS](https://scholariq.org/papers/exome-wide-rare-variant-analysis-identifies-tuba4a-mutations-associated-with/)
- [Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture](https://scholariq.org/papers/partitioning-the-heritability-of-tourette-syndrome-and-obsessive-compulsive/)
- [<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations](https://scholariq.org/papers/i-sod1-i-i-ang-i-i-vapb-i-i-tardbp-i-and-i-fus-i-mutations-in-familial/)
- [NEK1 variants confer susceptibility to amyotrophic lateral sclerosis](https://scholariq.org/papers/nek1-variants-confer-susceptibility-to-amyotrophic-lateral-sclerosis/)

## Researcher topics

- [Amyotrophic Lateral Sclerosis Research](https://scholariq.org/topics/amyotrophic-lateral-sclerosis-research/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Parkinson's Disease Mechanisms and Treatments](https://scholariq.org/topics/parkinson-s-disease-mechanisms-and-treatments/)
- [Genetics and Neurodevelopmental Disorders](https://scholariq.org/topics/genetics-and-neurodevelopmental-disorders/)

## Researcher university

- [Montreal Neurological Institute and Hospital](https://scholariq.org/institutions/montreal-neurological-institute-and-hospital/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.