Ástrós Skúladóttir
Ástrós Skúladóttir publishes mostly in Genetics, Neurology and Molecular Biology, on topics such as Genomics and Rare Diseases, Genetic Associations and Epidemiology and Genomic variations and chromosomal abnormalities.
- World rank
- #1,121,130 of 7,710,434 ranked researchers
- Rank in Iceland
- #434 of 2,050
- Works
- 26
- Citations
- 681
- Citations per work
- 26.2
What does Ástrós Skúladóttir research?
Ástrós Skúladóttir's work is mostly in Biochemistry, Genetics and Molecular Biology (32%), Medicine (17%), Neuroscience (12%).
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 Sciences1143.5%
- Everything else1039.2%
- Health Sciences417.3%
- Medicine417.3%
- 1Genetics20% of their works
- 2Neurology13% of their works
- 3Molecular Biology12% of their works
- 4Cellular and Molecular Neuroscience6% of their works
- 5Neurology6% of their works
- 6Rheumatology4% of their works
Research topics
Which keywords describe Ástrós Skúladóttir's research?
The keywords of their largest research topics: Mitochondrial Dysfunction, Genetic Variants, Sequence Interpretation, a-Synuclein, Alternative Splicing, Copy Number Variation, Fragile X Syndrome and Genetic Variation.
- Olfactory Dysfunction
- COVID-19
- Rett Syndrome
- Parkinson's Disease
- Genome-Wide Association
- Fragile X Syndrome
- Alternative Splicing
- Genetic Variants
- Mitochondrial Dysfunction
- Sequence Interpretation
- Copy Number Variation
- Genetic Variation
- Genomic Rearrangements
- RNA-Binding Proteins
- a-Synuclein
- Huntington's Disease
- Protein Aggregation
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 17 words, with their numbers
- Mitochondrial Dysfunction52 topics
- Genetic Variants41 topic
- Sequence Interpretation41 topic
- Alternative Splicing31 topic
- Copy Number Variation31 topic
- Fragile X Syndrome31 topic
- Genetic Variation31 topic
- Genome-Wide Association31 topic
- Genomic Rearrangements31 topic
- Parkinson's Disease31 topic
- RNA-Binding Proteins31 topic
- Rett Syndrome31 topic
- a-Synuclein31 topic
- COVID-1921 topic
- Huntington's Disease21 topic
- Olfactory Dysfunction21 topic
- Protein Aggregation21 topic
Where does Ástrós Skúladóttir work?
Ástrós Skúladóttir's main affiliation in the publication record is deCODE Genetics (Iceland), Iceland.
How many publications and citations does Ástrós Skúladóttir have?
OpenAlex counts 26 works and 681 citations for Ástrós Skúladóttir, an h-index of 13, ranking #1,121,130 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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