Courtney Sebold
- Genetics top 5%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 10%
- Plant Science
- Neurology
- Co-authors
- Daniel E. HaleJannine D. CodyPatricia HeardBridgette SoileauLouise O’DonnellErika CarterAnnice HillBrian P. Perry
- Topics
- Genomic variations and chromosomal abnormalities (18 papers)Genetics and Neurodevelopmental Disorders (9 papers)Genomics and Rare Diseases (7 papers)
- Partner nations
- United StatesCanadaKosovo
In The Last Decade
Courtney Sebold
26 papers receiving 538 citations
Peers
Comparison fields: 5 of 56
- Genetics 437
- Molecular Biology 216
- Pediatrics, Perinatology and Child Health 141
- Plant Science 97
- Neurology 75
Countries citing papers authored by Courtney Sebold
This map shows the geographic impact of Courtney Sebold'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 Courtney Sebold with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Courtney Sebold more than expected).
Fields of papers citing papers by Courtney Sebold
This network shows the impact of papers produced by Courtney Sebold. 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 Courtney Sebold. The network helps show where Courtney Sebold may publish in the future.
Co-authorship network of co-authors of Courtney Sebold
This figure shows the co-authorship network connecting the top 25 collaborators of Courtney Sebold. A scholar is included among the top collaborators of Courtney Sebold based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Courtney Sebold. Courtney Sebold is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 6 | |
| 2 | 3 | |
| 3 | 57 | |
| 4 | 10 | |
| 5 | 46 | |
| 6 | 7 | |
| 7 | 39 | |
| 8 | 32 | |
| 9 | 0 | |
| 10 | 50 | |
| 11 | 42 | |
| 12 | 14 | |
| 13 | 43 | |
| 14 | 1 | |
| 15 | 2 | |
| 16 | 31 | |
| 17 | 10 | |
| 18 | 29 | |
| 19 | 19 | |
| 20 | 15 |
About Courtney Sebold
Courtney Sebold is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Rheumatology, having authored 27 papers that have together received 616 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (18 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Genomics and Rare Diseases (7 papers). The work is most often cited by research in Genetics (437 citations), Pediatrics, Perinatology and Child Health (141 citations) and Neurology (75 citations). Courtney Sebold has collaborated with scholars based in United States, Canada and Kosovo. Frequent co-authors include Daniel E. Hale, Jannine D. Cody, Patricia Heard, Bridgette Soileau, Louise O’Donnell, Erika Carter, Annice Hill, Brian P. Perry, Jack L. Lancaster and Gretchen Schneider. Their work appears in journals such as Journal of Adolescent Health, Human Genetics and Genetics in Medicine.
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.