Yeşim Parman
Yeşim Parman publishes mostly in Neurology, Cellular and Molecular Neuroscience and Molecular Biology, on topics such as Hereditary Neurological Disorders, Peripheral Neuropathies and Disorders and Myasthenia Gravis and Thymoma.
- World rank
- #967,890 of 7,710,434 ranked researchers
- Rank in Türkiye
- #3,301 of 117,622
- Works
- 221
- Citations
- 11k
- Citations per work
- 49.7
What does Yeşim Parman research?
Yeşim Parman's work is mostly in Medicine (26%), Neuroscience (20%), Biochemistry, Genetics and Molecular Biology (20%).
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 Sciences8839.8%
- Neuroscience4420.1%
- Biochemistry, Genetics and Molecular Biology4419.7%
- Everything else7533.8%
- Health Sciences5826.4%
- Medicine5826.4%
- 1Neurology22% of their works
- 2Cellular and Molecular Neuroscience15% of their works
- 3Molecular Biology14% of their works
- 4Cell Biology5% of their works
- 5Neurology5% of their works
- 6Physiology5% of their works
Research topics
- Hereditary Neurological Disorders
- Peripheral Neuropathies and Disorders
- Myasthenia Gravis and Thymoma
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Genetic Neurodegenerative Diseases
- Neurological diseases and metabolism
- Neurogenetic and Muscular Disorders Research
- Botulinum Toxin and Related Neurological Disorders
Which keywords describe Yeşim Parman's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Prognosis, Genetic Mutations, Treatment, Diagnosis, Charcot-Marie-Tooth Disease, Hereditary Spastic Paraplegia and Neurological Disorders.
- Botulinum Toxin
- SMN1
- Protein Aggregation
- Huntington's Disease
- Brain Iron Accumulation
- Myasthenia Gravis
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
- Neurological Disorders
- Charcot-Marie-Tooth Disease
- Treatment
- Prognosis
- Mitochondrial Dysfunction
- Genetic Mutations
- Diagnosis
- Hereditary Spastic Paraplegia
- Neuromuscular Junction
- Guillain-Barré Syndrome
- Thymic Tumors
- Cardiac Amyloidosis
- Neurodegeneration
- Transthyretin
- Spinal Muscular Atrophy
- Neurotoxins
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 23 words, with their numbers
- Mitochondrial Dysfunction1133 topics
- Prognosis943 topics
- Genetic Mutations852 topics
- Treatment803 topics
- Diagnosis642 topics
- Charcot-Marie-Tooth Disease571 topic
- Hereditary Spastic Paraplegia571 topic
- Neurological Disorders522 topics
- Neuromuscular Junction482 topics
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy361 topic
- Guillain-Barré Syndrome361 topic
- Myasthenia Gravis301 topic
- Thymic Tumors301 topic
- Brain Iron Accumulation281 topic
- Cardiac Amyloidosis281 topic
- Huntington's Disease281 topic
- Neurodegeneration281 topic
- Protein Aggregation281 topic
- Transthyretin281 topic
- SMN1181 topic
- Spinal Muscular Atrophy181 topic
- Botulinum Toxin161 topic
- Neurotoxins161 topic
Where does Yeşim Parman work?
Yeşim Parman's main affiliation in the publication record is Istanbul University, Türkiye.
How many publications and citations does Yeşim Parman have?
OpenAlex counts 221 works and 10,976 citations for Yeşim Parman, an h-index of 41, ranking #967,890 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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