Ahmed Bouhouche
Ahmed Bouhouche publishes mostly in Cellular and Molecular Neuroscience, Molecular Biology and Neurology, on topics such as Hereditary Neurological Disorders, Neurological diseases and metabolism and Genetic Neurodegenerative Diseases.
- World rank
- #1,993,561 of 7,710,434 ranked researchers
- Rank in Morocco
- #1,641 of 14,526
- Works
- 78
- Citations
- 2.6k
- Citations per work
- 32.8
What does Ahmed Bouhouche research?
Ahmed Bouhouche's work is mostly in Neuroscience (29%), Biochemistry, Genetics and Molecular Biology (21%), Medicine (16%).
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 Sciences3950.5%
- Neuroscience2329.4%
- Biochemistry, Genetics and Molecular Biology1621.1%
- Everything else2633.0%
- Health Sciences1316.5%
- Medicine1316.5%
- 1Cellular and Molecular Neuroscience19% of their works
- 2Molecular Biology13% of their works
- 3Neurology11% of their works
- 4Neurology10% of their works
- 5Genetics8% of their works
- 6Physiology6% of their works
Research topics
Which keywords describe Ahmed Bouhouche's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Genetic Mutations, Neurodegeneration, Charcot-Marie-Tooth Disease, Hereditary Spastic Paraplegia, Brain Iron Accumulation, Pantothenate Kinase and Parkinson's Disease.
- Sequence Interpretation
- RNA Editing
- Enzyme Replacement Therapy
- Spinal Muscular Atrophy
- a-Synuclein
- Protein Aggregation
- Parkinson's Disease
- Brain Iron Accumulation
- Charcot-Marie-Tooth Disease
- Genetic Mutations
- Mitochondrial Dysfunction
- Neurodegeneration
- Hereditary Spastic Paraplegia
- Pantothenate Kinase
- Huntington's Disease
- Dopaminergic Neurons
- SMN1
- ADAR Deaminases
- Lysosomal Storage Disorders
- Genetic Variants
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.
All 20 words, with their numbers
- Mitochondrial Dysfunction704 topics
- Genetic Mutations452 topics
- Neurodegeneration332 topics
- Charcot-Marie-Tooth Disease241 topic
- Hereditary Spastic Paraplegia241 topic
- Brain Iron Accumulation211 topic
- Pantothenate Kinase211 topic
- Parkinson's Disease182 topics
- Huntington's Disease131 topic
- Protein Aggregation131 topic
- Dopaminergic Neurons121 topic
- a-Synuclein121 topic
- SMN171 topic
- Spinal Muscular Atrophy71 topic
- ADAR Deaminases61 topic
- Enzyme Replacement Therapy61 topic
- Lysosomal Storage Disorders61 topic
- RNA Editing61 topic
- Genetic Variants51 topic
- Sequence Interpretation51 topic
Where does Ahmed Bouhouche work?
Ahmed Bouhouche's main affiliation in the publication record is Mohammed V University, Morocco.
How many publications and citations does Ahmed Bouhouche have?
OpenAlex counts 78 works and 2,555 citations for Ahmed Bouhouche, an h-index of 21, ranking #1,993,561 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised 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.
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