Martino Montomoli
Martino Montomoli publishes mostly in Genetics, Molecular Biology and Psychiatry and Mental health, on topics such as Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders and Epilepsy research and treatment.
- World rank
- #431,397 of 7,710,434 ranked researchers
- Rank in Italy
- #11,735 of 242,206
- Works
- 45
- Citations
- 2.3k
- Citations per work
- 50.0
What does Martino Montomoli research?
Martino Montomoli's work is mostly in Biochemistry, Genetics and Molecular Biology (62%), Medicine (15%), Neuroscience (3%).
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 Sciences2964.6%
- Everything else920.8%
- Health Sciences714.6%
- Medicine714.6%
- 1Genetics38% of their works
- 2Molecular Biology19% of their works
- 3Psychiatry and Mental health11% of their works
- 4Clinical Biochemistry4% of their works
- 5Pediatrics, Perinatology and Child Health4% of their works
- 6Cellular and Molecular Neuroscience3% of their works
Research topics
Which keywords describe Martino Montomoli's research?
The keywords of their largest research topics: Genetic Variants, Sequence Interpretation, Fragile X Syndrome, Rett Syndrome, Epilepsy, Seizures, Copy Number Variation and Genomic Rearrangements.
- RNA Editing
- m6A-seq
- RNA methylation
- Metabolic Disorders
- Genomic Rearrangements
- Seizures
- Rett Syndrome
- Sequence Interpretation
- Genetic Variants
- Fragile X Syndrome
- Epilepsy
- Copy Number Variation
- Biochemical Genetics
- Mitochondria
- Reactive Oxygen Species
- ADAR Deaminases
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 16 words, with their numbers
- Genetic Variants231 topic
- Sequence Interpretation231 topic
- Fragile X Syndrome161 topic
- Rett Syndrome161 topic
- Epilepsy141 topic
- Seizures141 topic
- Copy Number Variation61 topic
- Genomic Rearrangements61 topic
- Biochemical Genetics51 topic
- Metabolic Disorders51 topic
- Mitochondria51 topic
- RNA methylation51 topic
- Reactive Oxygen Species51 topic
- m6A-seq51 topic
- ADAR Deaminases41 topic
- RNA Editing41 topic
Where does Martino Montomoli work?
Martino Montomoli's main affiliation in the publication record is Meyer Children's Hospital, Italy.
How many publications and citations does Martino Montomoli have?
OpenAlex counts 45 works and 2,251 citations for Martino Montomoli, an h-index of 23, ranking #431,397 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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