Kerry Baldwin Jedele
- Co-authors
- Virginia V. MichelsElke Holinski‐FederRobert FeldtFrancisco J. PugaAlfons MeindlOliver BrandauBernd H. BelohradskySmith Rjh
- Topics
- Genetics and Neurodevelopmental Disorders (5 papers)Genomic variations and chromosomal abnormalities (2 papers)Genetic Neurodegenerative Diseases (2 papers)
- Cited by
- GeneticsImmunology
- Partner nations
- GermanyUnited StatesAustria
In The Last Decade
Kerry Baldwin Jedele
14 papers receiving 282 citations
Peers
Comparison fields: 5 of 48
- Genetics 150
- Molecular Biology 123
- Immunology 77
- Genetics 65
- Pulmonary and Respiratory Medicine 37
Countries citing papers authored by Kerry Baldwin Jedele
This map shows the geographic impact of Kerry Baldwin Jedele'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 Kerry Baldwin Jedele with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kerry Baldwin Jedele more than expected).
Fields of papers citing papers by Kerry Baldwin Jedele
This network shows the impact of papers produced by Kerry Baldwin Jedele. 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 Kerry Baldwin Jedele. The network helps show where Kerry Baldwin Jedele may publish in the future.
Co-authorship network of co-authors of Kerry Baldwin Jedele
This figure shows the co-authorship network connecting the top 25 collaborators of Kerry Baldwin Jedele. A scholar is included among the top collaborators of Kerry Baldwin Jedele 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 Kerry Baldwin Jedele. Kerry Baldwin Jedele is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 11 | |
| 2 | 39 | |
| 3 | 2 | |
| 4 | 43 | |
| 5 | 9 | |
| 6 | 87 | |
| 7 | 5 | |
| 8 | 6 | |
| 9 | 2 | |
| 10 | 17 | |
| 11 | 12 | |
| 12 | 42 | |
| 13 | 8 | |
| 14 | 5 |
About Kerry Baldwin Jedele
Kerry Baldwin Jedele is a scholar working on Genetics, Genetics and Neurology, having authored 14 papers that have together received 288 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (5 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (65 citations), Genetics (150 citations) and Immunology (77 citations). Kerry Baldwin Jedele has collaborated with scholars based in Germany, United States and Austria. Frequent co-authors include Virginia V. Michels, Elke Holinski‐Feder, Robert Feldt, Francisco J. Puga, Alfons Meindl, Oliver Brandau, Bernd H. Belohradsky, Smith Rjh, Michael Weiss and Mauno Vihinen. Their work appears in journals such as PEDIATRICS, The American Journal of Human Genetics and European Journal of Human 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.