Guy Armand Rouleau
Guy Armand Rouleau publishes mostly in Neurology, Molecular Biology and Genetics, on topics such as Amyotrophic Lateral Sclerosis Research, Genetic Neurodegenerative Diseases and Parkinson's Disease Mechanisms and Treatments.
- World rank
- #49,409 of 7,710,434 ranked researchers
- Rank in Canada
- #1,367 of 183,316
- Works
- 1,278
- Citations
- 97k
- Citations per work
- 76.0
What does Guy Armand Rouleau research?
Guy Armand Rouleau's work is mostly in Biochemistry, Genetics and Molecular Biology (30%), Medicine (26%), Neuroscience (11%).
Their six largest subfields, inside their fields and domains; the grey slice is everything else they publish. The interactive view splits every one of their works down to single topics.
The fields and subfields, with their numbers
- Life Sciences51840.5%
- Biochemistry, Genetics and Molecular Biology37829.6%
- Neuroscience13910.9%
- Everything else42833.5%
- Health Sciences33226.0%
- Medicine33226.0%
- 1Neurology16% of their works
- 2Molecular Biology16% of their works
- 3Genetics14% of their works
- 4Cellular and Molecular Neuroscience11% of their works
- 5Psychiatry and Mental health5% of their works
- 6Genetics5% of their works
Research topics
- Amyotrophic Lateral Sclerosis Research
- Genetic Neurodegenerative Diseases
- Parkinson's Disease Mechanisms and Treatments
- Neurogenetic and Muscular Disorders Research
- Genetics and Neurodevelopmental Disorders
- Hereditary Neurological Disorders
- Neurological diseases and metabolism
- Genetic Associations and Epidemiology
Which keywords describe Guy Armand Rouleau's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Neurodegeneration, Genetic Mutations, FUS/TLS, TDP-43, Huntington's Disease, Protein Aggregation and a-Synuclein.
- Genetic Variation
- Brain Iron Accumulation
- Charcot-Marie-Tooth Disease
- Fragile X Syndrome
- SMN1
- Parkinson's Disease
- Huntington's Disease
- FUS/TLS
- Neurodegeneration
- Mitochondrial Dysfunction
- Genetic Mutations
- TDP-43
- Protein Aggregation
- a-Synuclein
- Spinal Muscular Atrophy
- Rett Syndrome
- Hereditary Spastic Paraplegia
- Pantothenate Kinase
- Genome-Wide Association
Size is their works in the topics tagged with each word, from their 8 largest topics. Each links to the topic it comes from most. The words come from the keyword list OpenAlex gives each topic, not from the text of the papers, so a word can appear that none of the papers uses.
All 19 words, with their numbers
- Mitochondrial Dysfunction5314 topics
- Neurodegeneration4193 topics
- Genetic Mutations3503 topics
- FUS/TLS1751 topic
- TDP-431751 topic
- Huntington's Disease1731 topic
- Protein Aggregation1731 topic
- Parkinson's Disease1461 topic
- a-Synuclein1461 topic
- SMN11441 topic
- Spinal Muscular Atrophy1441 topic
- Fragile X Syndrome1381 topic
- Rett Syndrome1381 topic
- Charcot-Marie-Tooth Disease1141 topic
- Hereditary Spastic Paraplegia1141 topic
- Brain Iron Accumulation981 topic
- Pantothenate Kinase981 topic
- Genetic Variation951 topic
- Genome-Wide Association951 topic
Where does Guy Armand Rouleau work?
Guy Armand Rouleau's main affiliation in the publication record is McGill University, Canada.
How many publications and citations does Guy Armand Rouleau have?
OpenAlex counts 1,278 works and 97,105 citations for Guy Armand Rouleau, an h-index of 147, ranking #49,409 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised citation excellence (50%), output (30%) and citations (20%). Counts come from OpenAlex author records, which occasionally merge different people who share a name or split one person into several.
Papers, co-authors, who cited this work and researchers on the nearest topics have tabs of their own, above. Is this your page? Claim it with your ORCID iD, or request a correction or removal.
Discussion
Ask a question or share a note about Guy Armand Rouleau. Keep it to the research: no personal attacks, advertising or links. Any reader can report a post, which collapses it for everyone until it is opened.