Science Explorer Back to mapMap

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.

ORCID 0000-0002-6723-6865 OpenAlex
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
h-index
48
i10-index 103Top 3.6% in Neurology (Medicine)

What does Mathias Toft research?

Mathias Toft's work is mostly in Medicine (37%), Biochemistry, Genetics and Molecular Biology (26%), Neuroscience (19%).

Life Sciences45%Health Sciences37%

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
    1. Biochemistry, Genetics and Molecular Biology4625.6%
    2. Neuroscience3419.2%
    1. Medicine6636.6%
  1. Everything else3318.6%
  1. 1Neurology31% of their works
  2. 2Genetics14% of their works
  3. 3Molecular Biology11% of their works
  4. 4Neurology10% of their works
  5. 5Cellular and Molecular Neuroscience9% of their works
  6. 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.

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
  1. Parkinson's Disease1844 topics
  2. Neurodegeneration1763 topics
  3. Mitochondrial Dysfunction1482 topics
  4. Dopaminergic Neurons1382 topics
  5. Genetic Risk Factors1101 topic
  6. a-Synuclein1101 topic
  7. Genetic Mutations542 topics
  8. Brain Iron Accumulation381 topic
  9. Pantothenate Kinase381 topic
  10. Deep Brain Stimulation311 topic
  11. Subthalamic Nucleus311 topic
  12. NR4A2281 topic
  13. Nurr1281 topic
  14. Genetic Variation261 topic
  15. Genome-Wide Association261 topic
  16. Fragile X Syndrome161 topic
  17. Rett Syndrome161 topic
  18. Enzyme Replacement Therapy151 topic
  19. Lysosomal Storage Disorders151 topic
  20. Genetic Variants141 topic
  21. 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

Ask a question or share a note about Mathias Toft. Keep it to the research: no personal attacks, advertising or links. Any reader can report a post, which collapses it for everyone until it is opened.