Kāri Stefánsson
Kāri Stefánsson publishes mostly in Genetics, Molecular Biology and Cardiology and Cardiovascular Medicine, on topics such as Genetic Associations and Epidemiology, Genomics and Rare Diseases and Epigenetics and DNA Methylation.
- World rank
- #77 of 7,710,434 ranked researchers
- Rank in Iceland
- #2 of 2,050
- Works
- 1,140
- Citations
- 211k
- Citations per work
- 184.9
What does Kāri Stefánsson research?
Kāri Stefánsson's work is mostly in Biochemistry, Genetics and Molecular Biology (44%), Medicine (9%), Immunology and Microbiology (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 Sciences53446.8%
- Everything else50444.2%
- Health Sciences1039.0%
- Medicine1039.0%
- 1Genetics28% of their works
- 2Molecular Biology16% of their works
- 3Cardiology and Cardiovascular Medicine3% of their works
- 4Physiology3% of their works
- 5Immunology3% of their works
- 6Surgery3% of their works
Research topics
Which keywords describe Kāri Stefánsson's research?
The keywords of their largest research topics: Genetic Variation, Genome-Wide Association, Haplotype Mapping, Genetic Variants, Sequence Interpretation, DNA Methylation, Histone Modification and Copy Number Variation.
- BRCA1
- Genome-wide Association Studies
- RNA methylation
- Fragile X Syndrome
- Copy Number Variation
- DNA Methylation
- Genetic Variants
- Genome-Wide Association
- Genetic Variation
- Haplotype Mapping
- Sequence Interpretation
- Histone Modification
- Genomic Rearrangements
- Rett Syndrome
- m6A-seq
- Quantitative Trait Loci
- BRCA2
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
- Genetic Variation3582 topics
- Genome-Wide Association3221 topic
- Haplotype Mapping3221 topic
- Genetic Variants861 topic
- Sequence Interpretation861 topic
- DNA Methylation671 topic
- Histone Modification671 topic
- Copy Number Variation641 topic
- Genomic Rearrangements641 topic
- Fragile X Syndrome461 topic
- Rett Syndrome461 topic
- RNA methylation371 topic
- m6A-seq371 topic
- Genome-wide Association Studies361 topic
- Quantitative Trait Loci361 topic
- BRCA1331 topic
- BRCA2331 topic
Where does Kāri Stefánsson work?
Kāri Stefánsson's main affiliation in the publication record is deCODE Genetics (Iceland), Iceland.
How many publications and citations does Kāri Stefánsson have?
OpenAlex counts 1,140 works and 210,729 citations for Kāri Stefánsson, an h-index of 221, ranking #77 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.
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