Konstanze Hörtnagel
Konstanze Hörtnagel publishes mostly in Molecular Biology, Genetics and Cellular and Molecular Neuroscience, on topics such as Metabolism and Genetic Disorders, Genomics and Rare Diseases and Neurological diseases and metabolism.
- World rank
- #1,463,785 of 7,710,434 ranked researchers
- Rank in Germany
- #72,136 of 364,343
- Works
- 77
- Citations
- 4.4k
- Citations per work
- 57.0
What does Konstanze Hörtnagel research?
Konstanze Hörtnagel's work is mostly in Biochemistry, Genetics and Molecular Biology (42%), Neuroscience (11%), 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
- Life Sciences4457.0%
- Everything else3343.0%
- 1Molecular Biology21% of their works
- 2Genetics15% of their works
- 3Cellular and Molecular Neuroscience6% of their works
- 4Cell Biology6% of their works
- 5Neurology5% of their works
- 6Immunology4% of their works
Research topics
Which keywords describe Konstanze Hörtnagel's research?
The keywords of their largest research topics: Genetic Mutations, Mitochondrial Dysfunction, Biochemical Genetics, Brain Iron Accumulation, Epilepsy, Genetic Variants, Metabolic Disorders and Neurodegeneration.
- Skin Diseases
- RNA Editing
- Charcot-Marie-Tooth Disease
- Rett Syndrome
- Sequence Interpretation
- Neurodegeneration
- Genetic Variants
- Brain Iron Accumulation
- Mitochondrial Dysfunction
- Genetic Mutations
- Biochemical Genetics
- Epilepsy
- Metabolic Disorders
- Seizures
- Fragile X Syndrome
- ADAR Deaminases
- Hereditary Spastic Paraplegia
- Genomic Rearrangement
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 18 words, with their numbers
- Genetic Mutations213 topics
- Mitochondrial Dysfunction142 topics
- Biochemical Genetics81 topic
- Brain Iron Accumulation81 topic
- Epilepsy81 topic
- Genetic Variants81 topic
- Metabolic Disorders81 topic
- Neurodegeneration81 topic
- Seizures81 topic
- Sequence Interpretation81 topic
- Fragile X Syndrome71 topic
- Rett Syndrome71 topic
- ADAR Deaminases61 topic
- Charcot-Marie-Tooth Disease61 topic
- Hereditary Spastic Paraplegia61 topic
- RNA Editing61 topic
- Genomic Rearrangement51 topic
- Skin Diseases51 topic
Where does Konstanze Hörtnagel work?
Konstanze Hörtnagel's main affiliation in the publication record is CeGaT (Germany), Germany.
How many publications and citations does Konstanze Hörtnagel have?
OpenAlex counts 77 works and 4,390 citations for Konstanze Hörtnagel, an h-index of 26, ranking #1,463,785 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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