Stefan Presslauer
Stefan Presslauer publishes mostly in Pathology and Forensic Medicine, Neurology and Molecular Biology, on topics such as Multiple Sclerosis Research Studies, Peripheral Neuropathies and Disorders and Amyloidosis: Diagnosis, Treatment, Outcomes.
- World rank
- #1,333,902 of 7,710,434 ranked researchers
- Rank in Austria
- #8,079 of 43,330
- Works
- 16
- Citations
- 1.7k
- Citations per work
- 105.0
What does Stefan Presslauer research?
Stefan Presslauer's work is mostly in Medicine (57%), Biochemistry, Genetics and Molecular Biology (14%), Neuroscience (5%).
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 Sciences957.2%
- Medicine957.2%
- Everything else423.7%
- Life Sciences319.1%
- 1Pathology and Forensic Medicine24% of their works
- 2Neurology24% of their works
- 3Molecular Biology14% of their works
- 4Neurology5% of their works
- 5Rheumatology5% of their works
- 6Physiology5% of their works
Research topics
- Multiple Sclerosis Research Studies
- Peripheral Neuropathies and Disorders
- Amyloidosis: Diagnosis, Treatment, Outcomes
- Advanced Biosensing Techniques and Applications
- Neurological diseases and metabolism
- Parkinson's Disease Mechanisms and Treatments
- Systemic Lupus Erythematosus Research
- Genetics and Neurodevelopmental Disorders
Which keywords describe Stefan Presslauer's research?
The keywords of their largest research topics: Diagnostic Criteria, Multiple Sclerosis, Neuromyelitis Optica, Diagnosis, Treatment, Chronic Inflammatory Demyelinating Polyradiculoneuropathy, Guillain-Barré Syndrome and Mitochondrial Dysfunction.
- Rett Syndrome
- a-Synuclein
- Systemic Lupus Erythematosus
- Parkinson's Disease
- High-Throughput Analysis
- Brain Iron Accumulation
- Genetic Mutations
- Mitochondrial Dysfunction
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy
- Diagnosis
- Multiple Sclerosis
- Diagnostic Criteria
- Neuromyelitis Optica
- Treatment
- Guillain-Barré Syndrome
- Neurodegeneration
- Antiphospholipid Syndrome
- Cardiac Amyloidosis
- Pantothenate Kinase
- Protein Microarrays
- Transthyretin
- Fragile X Syndrome
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 22 words, with their numbers
- Diagnostic Criteria112 topics
- Multiple Sclerosis91 topic
- Neuromyelitis Optica91 topic
- Diagnosis82 topics
- Treatment82 topics
- Chronic Inflammatory Demyelinating Polyradiculoneuropathy61 topic
- Guillain-Barré Syndrome61 topic
- Mitochondrial Dysfunction42 topics
- Neurodegeneration42 topics
- Genetic Mutations32 topics
- Antiphospholipid Syndrome21 topic
- Brain Iron Accumulation21 topic
- Cardiac Amyloidosis21 topic
- High-Throughput Analysis21 topic
- Pantothenate Kinase21 topic
- Parkinson's Disease21 topic
- Protein Microarrays21 topic
- Systemic Lupus Erythematosus21 topic
- Transthyretin21 topic
- a-Synuclein21 topic
- Fragile X Syndrome11 topic
- Rett Syndrome11 topic
Where does Stefan Presslauer work?
Stefan Presslauer's main affiliation in the publication record is Wilhelminen Hospital, Austria.
How many publications and citations does Stefan Presslauer have?
OpenAlex counts 16 works and 1,680 citations for Stefan Presslauer, an h-index of 11, ranking #1,333,902 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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