Sara Caylor
Impact in
-
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
Papers in
- Genetics 3
- Genomics and Rare Diseases 3
- Animal Genetics and Reproduction 1
-
- CRISPR and Genetic Engineering 1
- Congenital heart defects research 1
- Co-authors
- David Dimmock (4 shared papers)Stephen F. Kingsmore (3 shared papers)Julie A. Cakici (3 shared papers)Michelle M. Clark (3 shared papers)Christina Clarke (2 shared papers)Cinnamon S. Bloss (2 shared papers)Charlotte A. Hobbs (1 shared paper)Nathaly M. Sweeney (1 shared paper)
- Journals
- npj Genomic Medicine (1 paper)Clinical Therapeutics (1 paper)The American Journal of Human Genetics (1 paper)Children (1 paper)
- Partner nations
- United States
In The Last Decade
Sara Caylor
4 papers receiving 147 citations
Peers
Comparison fields: 5 of 25
- Genetics 105
- Clinical Biochemistry 12
- Cancer Research 15
- Pediatrics, Perinatology and Child Health 17
- Pathology and Forensic Medicine 13
Countries citing papers authored by Sara Caylor
This map shows the geographic impact of Sara Caylor's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sara Caylor with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sara Caylor more than expected).
Fields of papers citing papers by Sara Caylor
This network shows the impact of papers produced by Sara Caylor. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sara Caylor. The network helps show where Sara Caylor may publish in the future.
Co-authors
The 21 scholars most cited alongside Sara Caylor, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2020 | 69 | |
| 2 | 2021 | 53 | |
| 3 | 2023 | 18 | |
| 4 | 2023 | 8 |
About Sara Caylor
Sara Caylor is a scholar working on Genetics, Molecular Biology, Epidemiology, Public Health, Environmental and Occupational Health and Developmental Neuroscience, having authored 4 papers that have together received 148 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Williams Syndrome Research (1 paper), Cancer Genomics and Diagnostics (1 paper), Animal Genetics and Reproduction (1 paper), Ethics in Clinical Research (1 paper), CRISPR and Genetic Engineering (1 paper), Congenital heart defects research (1 paper) and Congenital Heart Disease Studies (1 paper). The work is most often cited by research in Genetics (105 citations), Clinical Biochemistry (12 citations), Cancer Research (15 citations), Pediatrics, Perinatology and Child Health (17 citations) and Pathology and Forensic Medicine (13 citations). Sara Caylor has collaborated with scholars based in United States. Frequent co-authors include David Dimmock, Stephen F. Kingsmore, Julie A. Cakici, Michelle M. Clark, Christina Clarke, Cinnamon S. Bloss, Charlotte A. Hobbs, Nathaly M. Sweeney, Narayanan Veeraraghavan and Yan Ding. Their work appears in journals such as npj Genomic Medicine, Clinical Therapeutics, The American Journal of Human Genetics and Children.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.