Raissa Relator
Raissa Relator publishes mostly in Genetics, Molecular Biology and Computer Vision and Pattern Recognition, on topics such as Genetics and Neurodevelopmental Disorders, Epigenetics and DNA Methylation and Genomics and Rare Diseases.
- World rank
- #1,225,106 of 7,710,434 ranked researchers
- Rank in Canada
- #41,564 of 183,316
- Works
- 63
- Citations
- 981
- Citations per work
- 15.6
What does Raissa Relator research?
Raissa Relator's work is mostly in Biochemistry, Genetics and Molecular Biology (63%), Computer Science (14%), Medicine (2%).
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 Sciences4063.4%
- Everything else1320.4%
- Physical Sciences914.5%
- Computer Science914.5%
- Health Sciences11.7%
- Medicine11.7%
- 1Genetics37% of their works
- 2Molecular Biology26% of their works
- 3Computer Vision and Pattern Recognition8% of their works
- 4Artificial Intelligence5% of their works
- 5Signal Processing2% of their works
- 6Surgery2% of their works
Research topics
Which keywords describe Raissa Relator's research?
The keywords of their largest research topics: DNA Methylation, Fragile X Syndrome, Rett Syndrome, Epigenetic Reprogramming, Histone Modification, Genetic Variants, Sequence Interpretation and Genomic Imprinting.
- Feature Matching
- Dimensionality Reduction
- Chromatin Remodeling
- Copy Number Variation
- Genomic Imprinting
- Genetic Variants
- Epigenetic Reprogramming
- Fragile X Syndrome
- DNA Methylation
- Rett Syndrome
- Histone Modification
- Sequence Interpretation
- Parental Influence
- Genomic Rearrangements
- SWI/SNF Complexes
- Face Recognition
- Local Descriptors
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 17 words, with their numbers
- DNA Methylation292 topics
- Fragile X Syndrome201 topic
- Rett Syndrome201 topic
- Epigenetic Reprogramming191 topic
- Histone Modification191 topic
- Genetic Variants171 topic
- Sequence Interpretation171 topic
- Genomic Imprinting101 topic
- Parental Influence101 topic
- Copy Number Variation91 topic
- Genomic Rearrangements91 topic
- Chromatin Remodeling61 topic
- SWI/SNF Complexes61 topic
- Dimensionality Reduction51 topic
- Face Recognition51 topic
- Feature Matching41 topic
- Local Descriptors41 topic
Where does Raissa Relator work?
Raissa Relator's main affiliation in the publication record is London Health Sciences Centre, Canada.
How many publications and citations does Raissa Relator have?
OpenAlex counts 63 works and 981 citations for Raissa Relator, an h-index of 16, ranking #1,225,106 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.
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
Ask a question or share a note about Raissa Relator. Posts are plain text and can be reported.