Hildigunnur Katrínardóttir
Hildigunnur Katrínardóttir publishes mostly in Genetics, Molecular Biology and Pulmonary and Respiratory Medicine, on topics such as Genomics and Rare Diseases, Genetic Associations and Epidemiology and Connective tissue disorders research.
- World rank
- #2,631,860 of 7,710,434 ranked researchers
- Rank in Iceland
- #996 of 2,050
- Works
- 20
- Citations
- 2k
- Citations per work
- 100.5
What does Hildigunnur Katrínardóttir research?
Hildigunnur Katrínardóttir's work is mostly in Biochemistry, Genetics and Molecular Biology (55%), Medicine (21%).
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 Sciences1154.7%
- Everything else524.5%
- Health Sciences420.8%
- Medicine420.8%
- 1Genetics40% of their works
- 2Molecular Biology15% of their works
- 3Pulmonary and Respiratory Medicine9% of their works
- 4Surgery4% of their works
- 5Cardiology and Cardiovascular Medicine4% of their works
- 6Physiology4% of their works
Research topics
Which keywords describe Hildigunnur Katrínardóttir's research?
The keywords of their largest research topics: Genetic Variants, Sequence Interpretation, Genetic Variation, Genome-Wide Association, Ehlers-Danlos Syndrome, Fragile X Syndrome, Marfan Syndrome and Rett Syndrome.
- Ubiquitin
- Proteasome
- Histone Modification
- DNA Methylation
- Rett Syndrome
- Fragile X Syndrome
- Genome-Wide Association
- Sequence Interpretation
- Genetic Variants
- Genetic Variation
- Ehlers-Danlos Syndrome
- Marfan Syndrome
- Copy Number Variation
- Genomic Rearrangements
- Obstructive Sleep Apnea
- Sleep-Disordered Breathing
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 Variants61 topic
- Sequence Interpretation61 topic
- Genetic Variation41 topic
- Genome-Wide Association41 topic
- Ehlers-Danlos Syndrome31 topic
- Fragile X Syndrome31 topic
- Marfan Syndrome31 topic
- Rett Syndrome31 topic
- Copy Number Variation21 topic
- DNA Methylation21 topic
- Genomic Rearrangements21 topic
- Histone Modification21 topic
- Obstructive Sleep Apnea21 topic
- Proteasome21 topic
- Sleep-Disordered Breathing21 topic
- Ubiquitin21 topic
Where does Hildigunnur Katrínardóttir work?
Hildigunnur Katrínardóttir's main affiliation in the publication record is deCODE Genetics (Iceland), Iceland.
How many publications and citations does Hildigunnur Katrínardóttir have?
OpenAlex counts 20 works and 2,009 citations for Hildigunnur Katrínardóttir, an h-index of 9, ranking #2,631,860 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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