Peter De Jonghe
Peter De Jonghe publishes mostly in Cellular and Molecular Neuroscience, Molecular Biology and Genetics, on topics such as Hereditary Neurological Disorders, Genetic Neurodegenerative Diseases and Neurological diseases and metabolism.
- World rank
- #69,066 of 7,710,434 ranked researchers
- Rank in Belgium
- #375 of 67,186
- Works
- 617
- Citations
- 37k
- Citations per work
- 60.8
What does Peter De Jonghe research?
Peter De Jonghe's work is mostly in Biochemistry, Genetics and Molecular Biology (33%), Neuroscience (24%), Medicine (9%).
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 Sciences35457.3%
- Biochemistry, Genetics and Molecular Biology20533.3%
- Neuroscience14824.0%
- Everything else20733.6%
- Health Sciences569.1%
- Medicine569.1%
- 1Cellular and Molecular Neuroscience19% of their works
- 2Molecular Biology17% of their works
- 3Genetics11% of their works
- 4Neurology9% of their works
- 5Cell Biology5% of their works
- 6Neurology5% of their works
Research topics
Which keywords describe Peter De Jonghe's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Genetic Mutations, Charcot-Marie-Tooth Disease, Hereditary Spastic Paraplegia, Neurodegeneration, Genetics, Huntington's Disease and Protein Aggregation.
- Metabolic Disorders
- Rett Syndrome
- TDP-43
- Sequence Interpretation
- Genetic Variants
- Pantothenate Kinase
- Protein Aggregation
- Genetics
- Hereditary Spastic Paraplegia
- Genetic Mutations
- Mitochondrial Dysfunction
- Charcot-Marie-Tooth Disease
- Neurodegeneration
- Huntington's Disease
- Brain Iron Accumulation
- Epilepsy
- Seizures
- FUS/TLS
- Fragile X Syndrome
- Biochemical Genetics
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.
All 20 words, with their numbers
- Mitochondrial Dysfunction3483 topics
- Genetic Mutations3113 topics
- Charcot-Marie-Tooth Disease1901 topic
- Hereditary Spastic Paraplegia1901 topic
- Neurodegeneration1252 topics
- Genetics1102 topics
- Huntington's Disease811 topic
- Protein Aggregation811 topic
- Brain Iron Accumulation771 topic
- Pantothenate Kinase771 topic
- Epilepsy621 topic
- Genetic Variants621 topic
- Seizures621 topic
- Sequence Interpretation621 topic
- FUS/TLS481 topic
- TDP-43481 topic
- Fragile X Syndrome441 topic
- Rett Syndrome441 topic
- Biochemical Genetics371 topic
- Metabolic Disorders371 topic
Where does Peter De Jonghe work?
Peter De Jonghe's main affiliation in the publication record is University of Antwerp, Belgium.
How many publications and citations does Peter De Jonghe have?
OpenAlex counts 617 works and 37,495 citations for Peter De Jonghe, an h-index of 102, ranking #69,066 of 7,710,434 researchers worldwide on the quality score.
Ranked on field-normalised 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.
Other researchers named Peter De Jonghe
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