Elizabeth S. Noblin
Elizabeth S. Noblin publishes mostly in Genetics, Molecular Biology and Surgery, on topics such as Genetic Associations and Epidemiology, Parkinson's Disease Mechanisms and Treatments and Genetics and Neurodevelopmental Disorders.
- World rank
- #20,773 of 7,710,434 ranked researchers
- Rank in United States
- #7,570 of 1,627,098
- Works
- 78
- Citations
- 10k
- Citations per work
- 134.5
What does Elizabeth S. Noblin research?
Elizabeth S. Noblin's work is mostly in Biochemistry, Genetics and Molecular Biology (34%), Medicine (17%).
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
- Everything else3849.3%
- Life Sciences2633.6%
- Health Sciences1317.1%
- Medicine1317.1%
- 1Genetics23% of their works
- 2Molecular Biology10% of their works
- 3Surgery6% of their works
- 4Neurology4% of their works
- 5Epidemiology4% of their works
- 6Rheumatology3% of their works
Research topics
- Genetic Associations and Epidemiology
- Parkinson's Disease Mechanisms and Treatments
- Genetics and Neurodevelopmental Disorders
- Bioinformatics and Genomic Networks
- Genomic variations and chromosomal abnormalities
- Nonmelanoma Skin Cancer Studies
- Genetic Mapping and Diversity in Plants and Animals
- Epigenetics and DNA Methylation
Which keywords describe Elizabeth S. Noblin's research?
The keywords of their largest research topics: Genetic Variation, Genome-Wide Association, Haplotype Mapping, a-Synuclein, Parkinson's Disease, Fragile X Syndrome, Gene Set Enrichment Analysis and Protein-Protein Interaction Networks.
- Histone Modification
- DNA Methylation
- Nonmelanoma Skin Cancer
- Copy Number Variation
- Protein-Protein Interaction Networks
- Fragile X Syndrome
- Parkinson's Disease
- Genome-Wide Association
- Genetic Variation
- Haplotype Mapping
- a-Synuclein
- Gene Set Enrichment Analysis
- Rett Syndrome
- Genomic Rearrangements
- Skin Cancers
- Genome-wide Association Studies
- Quantitative Trait Loci
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
- Genetic Variation272 topics
- Genome-Wide Association241 topic
- Haplotype Mapping241 topic
- Parkinson's Disease81 topic
- a-Synuclein81 topic
- Fragile X Syndrome51 topic
- Gene Set Enrichment Analysis51 topic
- Protein-Protein Interaction Networks51 topic
- Rett Syndrome51 topic
- Copy Number Variation41 topic
- Genomic Rearrangements41 topic
- Nonmelanoma Skin Cancer41 topic
- Skin Cancers41 topic
- DNA Methylation31 topic
- Genome-wide Association Studies31 topic
- Histone Modification31 topic
- Quantitative Trait Loci31 topic
Where does Elizabeth S. Noblin work?
Elizabeth S. Noblin's main affiliation in the publication record is 23andMe (United States), United States.
How many publications and citations does Elizabeth S. Noblin have?
OpenAlex counts 78 works and 10,490 citations for Elizabeth S. Noblin, an h-index of 42, ranking #20,773 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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