Rune Weis Næraa
Rune Weis Næraa publishes mostly in Genetics, Molecular Biology and Developmental Biology, on topics such as Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities, Congenital limb and hand anomalies and Sexual Differentiation and Disorders.
- World rank
- #1,970,296 of 7,710,434 ranked researchers
- Rank in Denmark
- #14,910 of 43,819
- Works
- 28
- Citations
- 2.4k
- Citations per work
- 84.7
What does Rune Weis Næraa research?
Rune Weis Næraa's work is mostly in Biochemistry, Genetics and Molecular Biology (47%), Medicine (24%).
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 Sciences1347.2%
- Everything else828.6%
- Health Sciences724.2%
- Medicine724.2%
- 1Genetics23% of their works
- 2Molecular Biology13% of their works
- 3Developmental Biology11% of their works
- 4Endocrinology, Diabetes and Metabolism11% of their works
- 5Pediatrics, Perinatology and Child Health7% of their works
- 6Reproductive Medicine6% of their works
Research topics
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Congenital limb and hand anomalies
- Sexual Differentiation and Disorders
- Growth Hormone and Insulin-like Growth Factors
- Prenatal Screening and Diagnostics
- Sperm and Testicular Function
- Gender Studies in Language
- Chromosomal and Genetic Variations
Which keywords describe Rune Weis Næraa's research?
The keywords of their largest research topics: Sex Determination, X Chromosome Inactivation, Congenital Adrenal Hyperplasia, Genetic Heterogeneity, Limb Malformations, Steroid 21-Hydroxylase Deficiency, Aneuploidy Screening and IGF-1.
- Polyploidy
- Gender Stereotyping
- Sperm DNA Fragmentation
- Oxidative Stress
- IGF-1
- Steroid 21-Hydroxylase Deficiency
- Genetic Heterogeneity
- X Chromosome Inactivation
- Sex Determination
- Congenital Adrenal Hyperplasia
- Limb Malformations
- Aneuploidy Screening
- Insulin-like Growth Factors
- Prenatal Diagnosis
- Children's Literature
- Genome Evolution
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 16 words, with their numbers
- Sex Determination161 topic
- X Chromosome Inactivation161 topic
- Congenital Adrenal Hyperplasia81 topic
- Genetic Heterogeneity81 topic
- Limb Malformations81 topic
- Steroid 21-Hydroxylase Deficiency81 topic
- Aneuploidy Screening31 topic
- IGF-131 topic
- Insulin-like Growth Factors31 topic
- Oxidative Stress31 topic
- Prenatal Diagnosis31 topic
- Sperm DNA Fragmentation31 topic
- Children's Literature21 topic
- Gender Stereotyping21 topic
- Genome Evolution11 topic
- Polyploidy11 topic
Where does Rune Weis Næraa work?
Rune Weis Næraa's main affiliation in the publication record is Aarhus University Hospital, Denmark.
How many publications and citations does Rune Weis Næraa have?
OpenAlex counts 28 works and 2,372 citations for Rune Weis Næraa, an h-index of 14, ranking #1,970,296 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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