Maarten J. Titulaer
Maarten J. Titulaer publishes mostly in Neurology, Psychiatry and Mental health and Genetics, on topics such as Autoimmune Neurological Disorders and Treatments, Peripheral Neuropathies and Disorders and Myasthenia Gravis and Thymoma.
- World rank
- #33,609 of 7,710,434 ranked researchers
- Rank in Netherlands
- #637 of 107,149
- Works
- 233
- Citations
- 26k
- Citations per work
- 112.6
What does Maarten J. Titulaer research?
Maarten J. Titulaer's work is mostly in Medicine (57%), Biochemistry, Genetics and Molecular Biology (5%), Immunology and Microbiology (4%).
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
- Health Sciences13457.3%
- Medicine13457.3%
- Everything else7030.1%
- Life Sciences2912.6%
- 1Neurology47% of their works
- 2Psychiatry and Mental health6% of their works
- 3Genetics5% of their works
- 4Epidemiology5% of their works
- 5Immunology4% of their works
- 6Cellular and Molecular Neuroscience4% of their works
Research topics
- Autoimmune Neurological Disorders and Treatments
- Peripheral Neuropathies and Disorders
- Myasthenia Gravis and Thymoma
- Genetics and Neurodevelopmental Disorders
- Epilepsy research and treatment
- Multiple Sclerosis Research Studies
- Immunodeficiency and Autoimmune Disorders
- Neuroscience and Neuropharmacology Research
Which keywords describe Maarten J. Titulaer's research?
The keywords of their largest research topics: Neurological Disorders, Autoantibodies, Immunotherapy, Cognitive Impairment, Diagnostic Criteria, Anti-NMDA Receptor Encephalitis, Paraneoplastic Syndromes and Prognosis.
- Synaptic Plasticity
- Primary Immunodeficiency
- Neuromyelitis Optica
- Seizures
- Rett Syndrome
- Thymic Tumors
- Dendritic Spines
- Guillain-Barré Syndrome
- Prognosis
- Anti-NMDA Receptor Encephalitis
- Cognitive Impairment
- Autoantibodies
- Neurological Disorders
- Immunotherapy
- Diagnostic Criteria
- Paraneoplastic Syndromes
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
- Genetic Mutations
- Myasthenia Gravis
- Fragile X Syndrome
- Epilepsy
- Multiple Sclerosis
- Immune Dysregulation
- Neurotransmission
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 24 words, with their numbers
- Neurological Disorders2743 topics
- Autoantibodies2272 topics
- Immunotherapy2272 topics
- Cognitive Impairment2042 topics
- Diagnostic Criteria2042 topics
- Anti-NMDA Receptor Encephalitis1871 topic
- Paraneoplastic Syndromes1871 topic
- Prognosis1132 topics
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy731 topic
- Guillain-Barré Syndrome731 topic
- Genetic Mutations442 topics
- Dendritic Spines432 topics
- Myasthenia Gravis401 topic
- Thymic Tumors401 topic
- Fragile X Syndrome291 topic
- Rett Syndrome291 topic
- Epilepsy251 topic
- Seizures251 topic
- Multiple Sclerosis171 topic
- Neuromyelitis Optica171 topic
- Immune Dysregulation151 topic
- Primary Immunodeficiency151 topic
- Neurotransmission141 topic
- Synaptic Plasticity141 topic
Where does Maarten J. Titulaer work?
Maarten J. Titulaer's main affiliation in the publication record is Erasmus MC, Netherlands.
How many publications and citations does Maarten J. Titulaer have?
OpenAlex counts 233 works and 26,228 citations for Maarten J. Titulaer, an h-index of 65, ranking #33,609 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.
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