Paul B. Vrana
- Genetics top 2%
- Molecular Biology
- Pediatrics, Perinatology and Child Health top 5%
- Ecology, Evolution, Behavior and Systematics top 5%
- Ecology top 10%
- Co-authors
- Robert S. IngramS M TilghmanMichael J. O’NeillWard C. WheelerPaul G. MattesonMichael R. FelderRachel J. O’NeillTony del Rio
- Topics
- Genetic Syndromes and Imprinting (16 papers)Epigenetics and DNA Methylation (14 papers)Prenatal Screening and Diagnostics (10 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Paul B. Vrana
37 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 92
- Genetics 735
- Molecular Biology 649
- Pediatrics, Perinatology and Child Health 324
- Ecology, Evolution, Behavior and Systematics 169
- Ecology 132
Countries citing papers authored by Paul B. Vrana
This map shows the geographic impact of Paul B. Vrana'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 Paul B. Vrana with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Paul B. Vrana more than expected).
Fields of papers citing papers by Paul B. Vrana
This network shows the impact of papers produced by Paul B. Vrana. 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 Paul B. Vrana. The network helps show where Paul B. Vrana may publish in the future.
Co-authorship network of co-authors of Paul B. Vrana
This figure shows the co-authorship network connecting the top 25 collaborators of Paul B. Vrana. A scholar is included among the top collaborators of Paul B. Vrana 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 Paul B. Vrana. Paul B. Vrana 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 | 6 | |
| 3 | 15 | |
| 4 | 51 | |
| 5 | 21 | |
| 6 | 46 | |
| 7 | 18 | |
| 8 | 15 | |
| 9 | 7 | |
| 10 | 29 | |
| 11 | 9 | |
| 12 | 11 | |
| 13 | 71 | |
| 14 | 19 | |
| 15 | 22 | |
| 16 | 2 | |
| 17 | 146 | |
| 18 | 157 | |
| 19 | 11 | |
| 20 | 84 |
About Paul B. Vrana
Paul B. Vrana is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Ecology, Evolution, Behavior and Systematics, having authored 37 papers that have together received 1.2k indexed citations. Recurring topics across this work include Genetic Syndromes and Imprinting (16 papers), Epigenetics and DNA Methylation (14 papers) and Prenatal Screening and Diagnostics (10 papers). The work is most often cited by research in Genetics (735 citations), Pediatrics, Perinatology and Child Health (324 citations) and Paleontology (83 citations). Paul B. Vrana has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Robert S. Ingram, S M Tilghman, Michael J. O’Neill, Ward C. Wheeler, S M Tilghman, Paul G. Matteson, Michael R. Felder, Rachel J. O’Neill, Tony del Rio and John Fossella. Their work appears in journals such as Nature Genetics, PLoS ONE and Human Molecular 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.