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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.

OpenAlex
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%).

Life Sciences55%Health Sciences21%

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
    1. Biochemistry, Genetics and Molecular Biology1154.7%
  1. Everything else524.5%
    1. Medicine420.8%
  1. 1Genetics40% of their works
  2. 2Molecular Biology15% of their works
  3. 3Pulmonary and Respiratory Medicine9% of their works
  4. 4Surgery4% of their works
  5. 5Cardiology and Cardiovascular Medicine4% of their works
  6. 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.

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
  1. Genetic Variants61 topic
  2. Sequence Interpretation61 topic
  3. Genetic Variation41 topic
  4. Genome-Wide Association41 topic
  5. Ehlers-Danlos Syndrome31 topic
  6. Fragile X Syndrome31 topic
  7. Marfan Syndrome31 topic
  8. Rett Syndrome31 topic
  9. Copy Number Variation21 topic
  10. DNA Methylation21 topic
  11. Genomic Rearrangements21 topic
  12. Histone Modification21 topic
  13. Obstructive Sleep Apnea21 topic
  14. Proteasome21 topic
  15. Sleep-Disordered Breathing21 topic
  16. 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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