Fulya Akçimen
Fulya Akçimen publishes mostly in Neurology, Cellular and Molecular Neuroscience and Molecular Biology, on topics such as Parkinson's Disease Mechanisms and Treatments, Amyotrophic Lateral Sclerosis Research and Genetic Neurodegenerative Diseases.
- World rank
- #1,856,761 of 7,710,434 ranked researchers
- Rank in Canada
- #61,848 of 183,316
- Works
- 69
- Citations
- 1.1k
- Citations per work
- 16.6
What does Fulya Akçimen research?
Fulya Akçimen's work is mostly in Medicine (34%), Biochemistry, Genetics and Molecular Biology (22%), Neuroscience (21%).
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 Sciences3042.9%
- Biochemistry, Genetics and Molecular Biology1521.5%
- Neuroscience1521.4%
- Health Sciences2434.1%
- Medicine2434.1%
- Everything else1623.0%
- 1Neurology27% of their works
- 2Cellular and Molecular Neuroscience16% of their works
- 3Molecular Biology13% of their works
- 4Genetics9% of their works
- 5Genetics7% of their works
- 6Neurology5% of their works
Research topics
Which keywords describe Fulya Akçimen's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Neurodegeneration, Diagnostic Criteria, a-Synuclein, Parkinson's Disease, FUS/TLS, TDP-43 and Huntington's Disease.
- Sequence Interpretation
- Genetic Variants
- Restless Legs Syndrome
- Epidemiology
- Spinal Muscular Atrophy
- Genetic Mutations
- Huntington's Disease
- FUS/TLS
- Parkinson's Disease
- Neurodegeneration
- Mitochondrial Dysfunction
- Diagnostic Criteria
- a-Synuclein
- TDP-43
- Protein Aggregation
- SMN1
- Brain Iron Accumulation
- Pantothenate Kinase
- Charcot-Marie-Tooth Disease
- Hereditary Spastic Paraplegia
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 Dysfunction584 topics
- Neurodegeneration533 topics
- Diagnostic Criteria322 topics
- Parkinson's Disease231 topic
- a-Synuclein231 topic
- FUS/TLS211 topic
- TDP-43211 topic
- Huntington's Disease181 topic
- Protein Aggregation181 topic
- Genetic Mutations172 topics
- SMN1141 topic
- Spinal Muscular Atrophy141 topic
- Brain Iron Accumulation91 topic
- Epidemiology91 topic
- Pantothenate Kinase91 topic
- Restless Legs Syndrome91 topic
- Charcot-Marie-Tooth Disease81 topic
- Genetic Variants81 topic
- Hereditary Spastic Paraplegia81 topic
- Sequence Interpretation81 topic
Where does Fulya Akçimen work?
Fulya Akçimen's main affiliation in the publication record is McGill University, Canada.
How many publications and citations does Fulya Akçimen have?
OpenAlex counts 69 works and 1,146 citations for Fulya Akçimen, an h-index of 18, ranking #1,856,761 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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