Katarzyna Bryc
Katarzyna Bryc publishes mostly in Genetics, Molecular Biology and Neurology, on topics such as Genetic Associations and Epidemiology, Forensic and Genetic Research and Parkinson's Disease Mechanisms and Treatments.
- World rank
- #11,518 of 7,710,434 ranked researchers
- Rank in United States
- #3,974 of 1,627,098
- Works
- 114
- Citations
- 20k
- Citations per work
- 172.0
What does Katarzyna Bryc research?
Katarzyna Bryc's work is mostly in Biochemistry, Genetics and Molecular Biology (46%), Medicine (13%).
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 Sciences5346.4%
- Everything else4741.0%
- Health Sciences1412.6%
- Medicine1412.6%
- 1Genetics35% of their works
- 2Molecular Biology11% of their works
- 3Neurology4% of their works
- 4Surgery3% of their works
- 5Epidemiology3% of their works
- 6Physiology3% of their works
Research topics
- Genetic Associations and Epidemiology
- Forensic and Genetic Research
- Parkinson's Disease Mechanisms and Treatments
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genetics and Neurodevelopmental Disorders
- Race, Genetics, and Society
- Epigenetics and DNA Methylation
Which keywords describe Katarzyna Bryc's research?
The keywords of their largest research topics: Population Genetics, Genetic Variation, Genome-Wide Association, Haplotype Mapping, Mendelian Randomization, Marker-Assisted Selection, Ancient DNA and Genomic Analysis.
- Histone Modification
- Rett Syndrome
- Genetics
- Quantitative Trait Loci
- Genomic Selection
- a-Synuclein
- Genomic Analysis
- Marker-Assisted Selection
- Haplotype Mapping
- Genetic Variation
- Population Genetics
- Genome-Wide Association
- Mendelian Randomization
- Ancient DNA
- Parkinson's Disease
- Genome-wide Association Studies
- Plant Breeding
- Fragile X Syndrome
- Race
- DNA Methylation
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 20 words, with their numbers
- Population Genetics563 topics
- Genetic Variation492 topics
- Genome-Wide Association492 topics
- Haplotype Mapping411 topic
- Mendelian Randomization411 topic
- Marker-Assisted Selection162 topics
- Ancient DNA141 topic
- Genomic Analysis141 topic
- Parkinson's Disease111 topic
- a-Synuclein111 topic
- Genome-wide Association Studies81 topic
- Genomic Selection81 topic
- Plant Breeding81 topic
- Quantitative Trait Loci81 topic
- Fragile X Syndrome71 topic
- Genetics71 topic
- Race71 topic
- Rett Syndrome71 topic
- DNA Methylation61 topic
- Histone Modification61 topic
Where does Katarzyna Bryc work?
Katarzyna Bryc's main affiliation in the publication record is 23andMe (United States), United States.
How many publications and citations does Katarzyna Bryc have?
OpenAlex counts 114 works and 19,604 citations for Katarzyna Bryc, an h-index of 54, ranking #11,518 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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