Taïeb Chkili
Taïeb Chkili publishes mostly in Neurology, Molecular Biology and Cellular and Molecular Neuroscience, on topics such as Peripheral Neuropathies and Disorders, Glycogen Storage Diseases and Myoclonus and Hereditary Neurological Disorders.
- World rank
- #6,025,890 of 7,710,434 ranked researchers
- Rank in Morocco
- #8,389 of 14,526
- Works
- 55
- Citations
- 1k
- Citations per work
- 18.8
What does Taïeb Chkili research?
Taïeb Chkili's work is mostly in Medicine (21%), Biochemistry, Genetics and Molecular Biology (17%), Neuroscience (14%).
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
- Everything else2647.9%
- Life Sciences1731.1%
- Health Sciences1221.0%
- Medicine1221.0%
- 1Neurology14% of their works
- 2Molecular Biology11% of their works
- 3Cellular and Molecular Neuroscience9% of their works
- 4Rheumatology7% of their works
- 5Genetics6% of their works
- 6Neurology5% of their works
Research topics
Which keywords describe Taïeb Chkili's research?
The keywords of their largest research topics: Genetic Mutations, Mitochondrial Dysfunction, Neurodegeneration, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Glycogen, Guillain-Barré Syndrome, Metabolism and Charcot-Marie-Tooth Disease.
- Reactive Oxygen Species
- Mitochondria
- Fragile X Syndrome
- Brain Iron Accumulation
- Huntington's Disease
- Charcot-Marie-Tooth Disease
- Guillain-Barré Syndrome
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
- Mitochondrial Dysfunction
- Genetic Mutations
- Neurodegeneration
- Glycogen
- Metabolism
- Hereditary Spastic Paraplegia
- Protein Aggregation
- Pantothenate Kinase
- Genomic Imprinting
- Parental Influence
- Rett Syndrome
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
- Genetic Mutations214 topics
- Mitochondrial Dysfunction184 topics
- Neurodegeneration122 topics
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy81 topic
- Glycogen81 topic
- Guillain-Barré Syndrome81 topic
- Metabolism81 topic
- Charcot-Marie-Tooth Disease61 topic
- Hereditary Spastic Paraplegia61 topic
- Huntington's Disease51 topic
- Protein Aggregation51 topic
- Brain Iron Accumulation41 topic
- Pantothenate Kinase41 topic
- Fragile X Syndrome31 topic
- Genomic Imprinting31 topic
- Mitochondria31 topic
- Parental Influence31 topic
- Reactive Oxygen Species31 topic
- Rett Syndrome31 topic
Where does Taïeb Chkili work?
Taïeb Chkili's main affiliation in the publication record is Hôpital 20 Août, Morocco.
How many publications and citations does Taïeb Chkili have?
OpenAlex counts 55 works and 1,035 citations for Taïeb Chkili, an h-index of 14, ranking #6,025,890 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
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