Sandrina Weber
Sandrina Weber publishes mostly in Neurology, Genetics and Molecular Biology, on topics such as Parkinson's Disease Mechanisms and Treatments, Neurological disorders and treatments and Genomics and Rare Diseases.
- World rank
- #648,106 of 7,710,434 ranked researchers
- Rank in Germany
- #31,909 of 364,343
- Works
- 39
- Citations
- 1.2k
- Citations per work
- 30.4
What does Sandrina Weber research?
Sandrina Weber's work is mostly in Medicine (43%), Biochemistry, Genetics and Molecular Biology (19%), Neuroscience (13%).
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 Sciences1743.3%
- Medicine1743.3%
- Life Sciences1332.6%
- Everything else924.1%
- 1Neurology43% of their works
- 2Genetics10% of their works
- 3Molecular Biology10% of their works
- 4Cellular and Molecular Neuroscience7% of their works
- 5Neurology4% of their works
- 6Sensory Systems3% of their works
Research topics
- Parkinson's Disease Mechanisms and Treatments
- Neurological disorders and treatments
- Genomics and Rare Diseases
- Genetics and Neurodevelopmental Disorders
- Genetic Neurodegenerative Diseases
- Olfactory and Sensory Function Studies
- Botulinum Toxin and Related Neurological Disorders
- Amyotrophic Lateral Sclerosis Research
Which keywords describe Sandrina Weber's research?
The keywords of their largest research topics: Parkinson's Disease, Mitochondrial Dysfunction, Neurodegeneration, a-Synuclein, Dopaminergic Neurons, Neurological Disorders, Deep Brain Stimulation and Subthalamic Nucleus.
- TDP-43
- Protein Aggregation
- Neurotoxins
- Fragile X Syndrome
- COVID-19
- Sequence Interpretation
- Subthalamic Nucleus
- a-Synuclein
- Dopaminergic Neurons
- Mitochondrial Dysfunction
- Parkinson's Disease
- Neurodegeneration
- Neurological Disorders
- Deep Brain Stimulation
- Genetic Variants
- Botulinum Toxin
- FUS/TLS
- Huntington's Disease
- Olfactory Dysfunction
- Rett 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 20 words, with their numbers
- Parkinson's Disease372 topics
- Mitochondrial Dysfunction232 topics
- Neurodegeneration232 topics
- Dopaminergic Neurons201 topic
- Neurological Disorders202 topics
- a-Synuclein201 topic
- Deep Brain Stimulation171 topic
- Subthalamic Nucleus171 topic
- Genetic Variants61 topic
- Sequence Interpretation61 topic
- Botulinum Toxin31 topic
- COVID-1931 topic
- FUS/TLS31 topic
- Fragile X Syndrome31 topic
- Huntington's Disease31 topic
- Neurotoxins31 topic
- Olfactory Dysfunction31 topic
- Protein Aggregation31 topic
- Rett Syndrome31 topic
- TDP-4331 topic
Where does Sandrina Weber work?
Sandrina Weber's main affiliation in the publication record is Paracelsus Elena Klinik Kassel, Germany.
How many publications and citations does Sandrina Weber have?
OpenAlex counts 39 works and 1,187 citations for Sandrina Weber, an h-index of 15, ranking #648,106 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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