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Researcher · Statens Serum Institut · Denmark

Christine Søholm Hansen

Christine Søholm Hansen publishes mostly in Genetics, Molecular Biology and Psychiatry and Mental health, on topics such as Genetic Associations and Epidemiology, Epigenetics and DNA Methylation and Genetics and Neurodevelopmental Disorders.

ORCID 0000-0002-7518-4663 OpenAlex
World rank
#165,108
of 7,710,434 ranked researchers
Rank in Denmark
#1,080
of 43,819
Works
97
Citations
23k
Citations per work
237.4
h-index
39
i10-index 57Top 8.4% in Genetics (Biochemistry, Genetics and Molecular Biology)
Christine Søholm Hansen

What does Christine Søholm Hansen research?

Christine Søholm Hansen's work is mostly in Biochemistry, Genetics and Molecular Biology (52%), Medicine (12%), Neuroscience (6%).

Life Sciences: 56 works · 57.4% of their workBiochemistry, Genetics and Molecular Biology: 50 works · 51.8% of their workGenetics: 30 works · 31.0% of their workMolecular Biology: 17 works · 17.6% of their workClinical Biochemistry: 3 works · 3.2% of their workNeuroscience: 5 works · 5.6% of their workCognitive Neuroscience: 5 works · 5.6% of their workEverything else: 29 works · 30.1% of their workHealth Sciences: 12 works · 12.5% of their workMedicine: 12 works · 12.5% of their workPsychiatry and Mental health: 7 works · 7.4% of their workPediatrics, Perinatology and Child Health: 5 works · 5.1% of their workTHEIR WORKChristine SøholmHansen97works
Life Sciences57%Health Sciences12%

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 Biology5051.8%
    2. Neuroscience55.6%
  2. Everything else2930.1%
    1. Medicine1212.5%
  1. 1Genetics31% of their works
  2. 2Molecular Biology18% of their works
  3. 3Psychiatry and Mental health7% of their works
  4. 4Cognitive Neuroscience6% of their works
  5. 5Pediatrics, Perinatology and Child Health5% of their works
  6. 6Clinical Biochemistry3% of their works

Research topics

Which keywords describe Christine Søholm Hansen's research?

The keywords of their largest research topics: Genetic Variation, Genome-Wide Association, DNA Methylation, Genetics, Histone Modification, Neurodevelopmental Disorders, Fragile X 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 18 words, with their numbers
  1. Genetic Variation311 topic
  2. Genome-Wide Association311 topic
  3. DNA Methylation171 topic
  4. Genetics172 topics
  5. Histone Modification171 topic
  6. Neurodevelopmental Disorders152 topics
  7. Fragile X Syndrome131 topic
  8. Rett Syndrome131 topic
  9. Autism Spectrum Disorders91 topic
  10. Social Skills Interventions91 topic
  11. Bipolar Spectrum Disorder81 topic
  12. Prevalence81 topic
  13. Biochemical Genetics71 topic
  14. Early-Life Conditions71 topic
  15. Fetal Programming71 topic
  16. Metabolic Disorders71 topic
  17. Copy Number Variation61 topic
  18. Genomic Rearrangements61 topic

Where does Christine Søholm Hansen work?

Christine Søholm Hansen's main affiliation in the publication record is Statens Serum Institut, Denmark.

How many publications and citations does Christine Søholm Hansen have?

OpenAlex counts 97 works and 23,030 citations for Christine Søholm Hansen, an h-index of 39, ranking #165,108 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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