Shannon Rego
- Genetics
- Molecular Biology
- Biomedical Engineering
- Cardiology and Cardiovascular Medicine
- General Health Professions
- Co-authors
- M SnyderDenis SalinsJessilyn DunnWenyu ZhouTracey McLaughlinSomalee DattaGao ZhouSophia Miryam Schüssler‐Fiorenza Rose
- Topics
- Genomics and Rare Diseases (12 papers)BRCA gene mutations in cancer (5 papers)Genomic variations and chromosomal abnormalities (4 papers)
- Partner nations
- United StatesPolandGermany
In The Last Decade
Shannon Rego
25 papers receiving 527 citations
Peers
Comparison fields: 5 of 112
- Genetics 137
- Molecular Biology 130
- Biomedical Engineering 78
- Cardiology and Cardiovascular Medicine 72
- General Health Professions 55
Countries citing papers authored by Shannon Rego
This map shows the geographic impact of Shannon Rego'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 Shannon Rego with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Shannon Rego more than expected).
Fields of papers citing papers by Shannon Rego
This network shows the impact of papers produced by Shannon Rego. 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 Shannon Rego. The network helps show where Shannon Rego may publish in the future.
Co-authorship network of co-authors of Shannon Rego
This figure shows the co-authorship network connecting the top 25 collaborators of Shannon Rego. A scholar is included among the top collaborators of Shannon Rego 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 Shannon Rego. Shannon Rego is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 1 | |
| 2 | 10 | |
| 3 | 1 | |
| 4 | 4 | |
| 5 | 6 | |
| 6 | 9 | |
| 7 | 6 | |
| 8 | 40 | |
| 9 | 1 | |
| 10 | 9 | |
| 11 | 4 | |
| 12 | 12 | |
| 13 | 26 | |
| 14 | 13 | |
| 15 | 12 | |
| 16 | 23 | |
| 17 | 25 | |
| 18 | 268 | |
| 19 | 12 | |
| 20 | 17 |
About Shannon Rego
Shannon Rego is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Pharmacy, having authored 25 papers that have together received 536 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (12 papers), BRCA gene mutations in cancer (5 papers) and Genomic variations and chromosomal abnormalities (4 papers). The work is most often cited by research in Genetics (137 citations), Applied Psychology (23 citations) and Cardiology and Cardiovascular Medicine (72 citations). Shannon Rego has collaborated with scholars based in United States, Poland and Germany. Frequent co-authors include M Snyder, Denis Salins, Jessilyn Dunn, Wenyu Zhou, Tracey McLaughlin, Somalee Datta, Gao Zhou, Sophia Miryam Schüssler‐Fiorenza Rose, Ryan Runge and Dalia Perelman. Their work appears in journals such as The Journal of Clinical Endocrinology & Metabolism, PLoS Biology and PLoS Genetics.
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.