Sara Caylor
Impact in
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- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- BRCA gene mutations in cancer
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- Metabolism and Genetic Disorders
Papers in
- Genetics 3
- Genomics and Rare Diseases 3
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- Congenital heart defects research 1
- CRISPR and Genetic Engineering 1
- Co-authors
- David Dimmock (4 shared papers)Stephen F. Kingsmore (3 shared papers)Michelle M. Clark (3 shared papers)Julie A. Cakici (3 shared papers)Cinnamon S. Bloss (2 shared papers)Christina Clarke (2 shared papers)Shareef Nahas (1 shared paper)John J. Nigro (1 shared paper)
- Journals
- Clinical Therapeutics (1 paper)The American Journal of Human Genetics (1 paper)npj Genomic Medicine (1 paper)Children (1 paper)
- Partner nations
- United States
In The Last Decade
Sara Caylor
4 papers receiving 138 citations
Peers
Comparison fields: 5 of 27
- Genetics 109
- Clinical Biochemistry 16
- Pediatrics, Perinatology and Child Health 34
- Cancer Research 18
- Pathology and Forensic Medicine 14
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 22 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 | 66 | |
| 2 | 2021 | 49 | |
| 3 | 2023 | 17 | |
| 4 | 2023 | 7 |
About Sara Caylor
Sara Caylor is a scholar working on Genetics, Molecular Biology, Public Health, Environmental and Occupational Health, Pediatrics, Perinatology and Child Health and Epidemiology, having authored 4 papers that have together received 139 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (3 papers), Ethics in Clinical Research (2 papers), Congenital heart defects research (1 paper), Williams Syndrome Research (1 paper), Congenital Heart Disease Studies (1 paper), Cancer Genomics and Diagnostics (1 paper), CRISPR and Genetic Engineering (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (109 citations), Clinical Biochemistry (16 citations), Pediatrics, Perinatology and Child Health (34 citations), Cancer Research (18 citations) and Pathology and Forensic Medicine (14 citations). Sara Caylor has collaborated with scholars based in United States. Frequent co-authors include David Dimmock, Stephen F. Kingsmore, Michelle M. Clark, Julie A. Cakici, Cinnamon S. Bloss, Christina Clarke, Shareef Nahas, John J. Nigro, Nathaly M. Sweeney and Shimul Chowdhury. Their work appears in journals such as Clinical Therapeutics, The American Journal of Human Genetics, npj Genomic Medicine 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.