Science Explorer Back to mapMap
Discussion
Researcher · Väestöliitto · Finland

Maarit M. Peippo

Maarit M. Peippo publishes mostly in Genetics, Molecular Biology and Surgery, on topics such as Genetics and Neurodevelopmental Disorders, Genomic variations and chromosomal abnormalities and Genomics and Rare Diseases.

OpenAlex
World rank
#1,932,604
of 7,710,434 ranked researchers
Rank in Finland
#11,705
of 37,370
Works
39
Citations
2.1k
Citations per work
53.4
h-index
20
i10-index 28Top 27% in Genetics (Biochemistry, Genetics and Molecular Biology)
Maarit M. Peippo

What does Maarit M. Peippo research?

Maarit M. Peippo's work is mostly in Biochemistry, Genetics and Molecular Biology (60%), Medicine (10%), Neuroscience (3%).

Life Sciences: 24 works · 62.5% of their workBiochemistry, Genetics and Molecular Biology: 23 works · 59.6% of their workGenetics: 14 works · 36.5% of their workMolecular Biology: 9 works · 23.1% of their workNeuroscience: 1 works · 2.9% of their workCognitive Neuroscience: 1 works · 2.9% of their workEverything else: 11 works · 27.0% of their workHealth Sciences: 4 works · 10.5% of their workMedicine: 4 works · 10.5% of their workSurgery: 2 works · 4.8% of their workPediatrics, Perinatology and Child Health: 1 works · 3.8% of their workPsychiatry and Mental health: 1 works · 1.9% of their workTHEIR WORKMaarit M. Peippo39works
Life Sciences62%Health Sciences10%

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 Biology2359.6%
    2. Neuroscience12.9%
  2. Everything else1127.0%
    1. Medicine410.5%
  1. 1Genetics36% of their works
  2. 2Molecular Biology23% of their works
  3. 3Surgery5% of their works
  4. 4Pediatrics, Perinatology and Child Health4% of their works
  5. 5Cognitive Neuroscience3% of their works
  6. 6Psychiatry and Mental health2% of their works

Research topics

Which keywords describe Maarit M. Peippo's research?

The keywords of their largest research topics: Fragile X Syndrome, Rett Syndrome, Neurodevelopmental Disorders, Copy Number Variation, Genetic Variants, Genomic Rearrangements, NF-?B Activation and Sequence Interpretation.

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 20 words, with their numbers
  1. Fragile X Syndrome121 topic
  2. Rett Syndrome121 topic
  3. Neurodevelopmental Disorders102 topics
  4. Copy Number Variation71 topic
  5. Genetic Variants71 topic
  6. Genomic Rearrangements71 topic
  7. NF-?B Activation72 topics
  8. Sequence Interpretation71 topic
  9. Genetics62 topics
  10. Epidemiology52 topics
  11. Proteasome41 topic
  12. Ubiquitin41 topic
  13. Autism Spectrum Disorders31 topic
  14. Enteric Nervous System31 topic
  15. Genomic Rearrangement31 topic
  16. Hirschsprung Disease31 topic
  17. Skin Diseases31 topic
  18. Social Skills Interventions31 topic
  19. Genetic Heterogeneity21 topic
  20. Limb Malformations21 topic

Where does Maarit M. Peippo work?

Maarit M. Peippo's main affiliation in the publication record is Väestöliitto, Finland.

How many publications and citations does Maarit M. Peippo have?

OpenAlex counts 39 works and 2,083 citations for Maarit M. Peippo, an h-index of 20, ranking #1,932,604 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.

Discussion

Ask a question or share a note about Maarit M. Peippo. Posts are plain text and can be reported.