Mathias Toft
Mathias Toft publishes mostly in Neurology, Genetics and Molecular Biology, on topics such as Parkinson's Disease Mechanisms and Treatments, Neurological diseases and metabolism and Neurological disorders and treatments.
- World rank
- #189,759 of 7,710,434 ranked researchers
- Rank in Norway
- #1,069 of 33,005
- Works
- 179
- Citations
- 12k
- Citations per work
- 68.7
What does Mathias Toft research?
Mathias Toft's work is mostly in Medicine (37%), Biochemistry, Genetics and Molecular Biology (26%), Neuroscience (19%).
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 Sciences8044.8%
- Biochemistry, Genetics and Molecular Biology4625.6%
- Neuroscience3419.2%
- Health Sciences6636.6%
- Medicine6636.6%
- Everything else3318.6%
- 1Neurology31% of their works
- 2Genetics14% of their works
- 3Molecular Biology11% of their works
- 4Neurology10% of their works
- 5Cellular and Molecular Neuroscience9% of their works
- 6Physiology5% of their works
Research topics
Which keywords describe Mathias Toft's research?
The keywords of their largest research topics: Parkinson's Disease, Neurodegeneration, Mitochondrial Dysfunction, Dopaminergic Neurons, a-Synuclein, Genetic Risk Factors, Genetic Mutations and Brain Iron Accumulation.
- Genetic Variants
- Enzyme Replacement Therapy
- Fragile X Syndrome
- Genetic Variation
- NR4A2
- Deep Brain Stimulation
- Brain Iron Accumulation
- a-Synuclein
- Dopaminergic Neurons
- Neurodegeneration
- Parkinson's Disease
- Mitochondrial Dysfunction
- Genetic Risk Factors
- Genetic Mutations
- Pantothenate Kinase
- Subthalamic Nucleus
- Nurr1
- Genome-Wide Association
- Rett Syndrome
- Lysosomal Storage Disorders
- Sequence Interpretation
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 21 words, with their numbers
- Parkinson's Disease1844 topics
- Neurodegeneration1763 topics
- Mitochondrial Dysfunction1482 topics
- Dopaminergic Neurons1382 topics
- Genetic Risk Factors1101 topic
- a-Synuclein1101 topic
- Genetic Mutations542 topics
- Brain Iron Accumulation381 topic
- Pantothenate Kinase381 topic
- Deep Brain Stimulation311 topic
- Subthalamic Nucleus311 topic
- NR4A2281 topic
- Nurr1281 topic
- Genetic Variation261 topic
- Genome-Wide Association261 topic
- Fragile X Syndrome161 topic
- Rett Syndrome161 topic
- Enzyme Replacement Therapy151 topic
- Lysosomal Storage Disorders151 topic
- Genetic Variants141 topic
- Sequence Interpretation141 topic
Where does Mathias Toft work?
Mathias Toft's main affiliation in the publication record is Oslo University Hospital, Norway.
How many publications and citations does Mathias Toft have?
OpenAlex counts 179 works and 12,291 citations for Mathias Toft, an h-index of 48, ranking #189,759 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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