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Researcher · Statens Serum Institut · Denmark

Marie Bækvad‐Hansen

Marie Bækvad‐Hansen publishes mostly in Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health, on topics such as Genetic Associations and Epidemiology, Genetics and Neurodevelopmental Disorders and Epigenetics and DNA Methylation.

ORCID 0000-0002-5881-1776 OpenAlex
World rank
#39,508
of 7,710,434 ranked researchers
Rank in Denmark
#179
of 43,819
Works
164
Citations
29k
Citations per work
174.2
h-index
52
i10-index 106Top 4.3% in Genetics (Biochemistry, Genetics and Molecular Biology)
Marie Bækvad‐Hansen

What does Marie Bækvad‐Hansen research?

Marie Bækvad‐Hansen's work is mostly in Biochemistry, Genetics and Molecular Biology (40%), Medicine (19%), Psychology (4%).

Life Sciences: 66 works · 40.2% of their workBiochemistry, Genetics and Molecular Biology: 66 works · 40.2% of their workGenetics: 46 works · 28.3% of their workMolecular Biology: 20 works · 11.9% of their workEverything else: 61 works · 37.2% of their workHealth Sciences: 31 works · 18.9% of their workMedicine: 31 works · 18.9% of their workPediatrics, Perinatology and Child Health: 14 works · 8.4% of their workPsychiatry and Mental health: 10 works · 6.3% of their workPulmonary and Respiratory Medicine: 7 works · 4.2% of their workSocial Sciences: 6 works · 3.7% of their workPsychology: 6 works · 3.7% of their workClinical Psychology: 6 works · 3.7% of their workTHEIR WORKMarieBækvad‐Hansen164works
Life Sciences40%Health Sciences19%Social Sciences4%

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 Biology6640.2%
  2. Everything else6137.2%
    1. Medicine3118.9%
    1. Psychology63.7%
  1. 1Genetics28% of their works
  2. 2Molecular Biology12% of their works
  3. 3Pediatrics, Perinatology and Child Health8% of their works
  4. 4Psychiatry and Mental health6% of their works
  5. 5Pulmonary and Respiratory Medicine4% of their works
  6. 6Clinical Psychology4% of their works

Research topics

Which keywords describe Marie Bækvad‐Hansen's research?

The keywords of their largest research topics: Genetic Variation, Genome-Wide Association, Genetics, Fragile X Syndrome, Rett Syndrome, DNA Methylation, Histone Modification and Early-Life Conditions.

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
  1. Genetic Variation471 topic
  2. Genome-Wide Association471 topic
  3. Genetics252 topics
  4. Fragile X Syndrome231 topic
  5. Rett Syndrome231 topic
  6. DNA Methylation191 topic
  7. Histone Modification191 topic
  8. Early-Life Conditions161 topic
  9. Fetal Programming161 topic
  10. Autism Spectrum Disorders131 topic
  11. Genetic Variants131 topic
  12. Neurodevelopmental Disorders131 topic
  13. Sequence Interpretation131 topic
  14. Bipolar Spectrum Disorder121 topic
  15. Prevalence121 topic
  16. Biochemical Genetics111 topic
  17. Metabolic Disorders111 topic

Where does Marie Bækvad‐Hansen work?

Marie Bækvad‐Hansen's main affiliation in the publication record is Statens Serum Institut, Denmark.

How many publications and citations does Marie Bækvad‐Hansen have?

OpenAlex counts 164 works and 28,566 citations for Marie Bækvad‐Hansen, an h-index of 52, ranking #39,508 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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