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Researcher · Charles University · Czechia

Markéta Vlčková

Markéta Vlčková publishes mostly in Genetics, Molecular Biology and Biomedical Engineering, on topics such as Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders and Genomic variations and chromosomal abnormalities.

ORCID 0000-0002-1496-392X OpenAlex
World rank
#1,711,633
of 7,710,434 ranked researchers
Rank in Czechia
#3,534
of 39,303
Works
132
Citations
2.4k
Citations per work
18.5
h-index
23
i10-index 49Top 22% in Genetics (Biochemistry, Genetics and Molecular Biology)
Markéta Vlčková

What does Markéta Vlčková research?

Markéta Vlčková's work is mostly in Biochemistry, Genetics and Molecular Biology (43%), Medicine (11%), Engineering (7%).

Life Sciences: 57 works · 43.3% of their workBiochemistry, Genetics and Molecular Biology: 57 works · 43.3% of their workGenetics: 37 works · 27.8% of their workMolecular Biology: 20 works · 15.5% of their workEverything else: 52 works · 39.4% of their workHealth Sciences: 14 works · 10.7% of their workMedicine: 14 works · 10.7% of their workPsychiatry and Mental health: 8 works · 5.7% of their workPhysiology: 4 works · 2.8% of their workGenetics: 3 works · 2.2% of their workPhysical Sciences: 9 works · 6.6% of their workEngineering: 9 works · 6.6% of their workBiomedical Engineering: 9 works · 6.6% of their workTHEIR WORKMarkéta Vlčková132works
Life Sciences43%Physical Sciences7%Health Sciences11%

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 Biology5743.3%
  2. Everything else5239.4%
    1. Medicine1410.7%
    1. Engineering96.6%
  1. 1Genetics28% of their works
  2. 2Molecular Biology16% of their works
  3. 3Biomedical Engineering7% of their works
  4. 4Psychiatry and Mental health6% of their works
  5. 5Physiology3% of their works
  6. 6Genetics2% of their works

Research topics

Which keywords describe Markéta Vlčková's research?

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

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 18 words, with their numbers
  1. Genetic Variants321 topic
  2. Sequence Interpretation321 topic
  3. Neurodevelopmental Disorders252 topics
  4. Genetics242 topics
  5. Fragile X Syndrome231 topic
  6. Rett Syndrome231 topic
  7. Copy Number Variation191 topic
  8. Genomic Rearrangements191 topic
  9. Epilepsy181 topic
  10. Seizures181 topic
  11. Lab-on-a-Chip101 topic
  12. Poly(dimethylsiloxane)101 topic
  13. Biochemical Genetics71 topic
  14. Metabolic Disorders71 topic
  15. Autism Spectrum Disorders61 topic
  16. RNA methylation61 topic
  17. Social Skills Interventions61 topic
  18. m6A-seq61 topic

Where does Markéta Vlčková work?

Markéta Vlčková's main affiliation in the publication record is Charles University, Czechia.

How many publications and citations does Markéta Vlčková have?

OpenAlex counts 132 works and 2,438 citations for Markéta Vlčková, an h-index of 23, ranking #1,711,633 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

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