Daphne J. Smits
- Co-authors
- Tjakko J. van HamGrazia M.S. ManciniRachel SchotMartina WilkeAntonio RomitoBrahim TabarkiA. James BarkovichMarjolein H. G. Dremmen
- Topics
- Congenital heart defects research (2 papers)Genomic variations and chromosomal abnormalities (2 papers)Genomics and Rare Diseases (1 paper)
- Partner nations
- NetherlandsUnited StatesAustralia
In The Last Decade
Daphne J. Smits
5 papers receiving 26 citations
Peers
Comparison fields: 5 of 24
- Molecular Biology 12
- Neurology 8
- Cell Biology 7
- Physiology 6
- Genetics 5
Countries citing papers authored by Daphne J. Smits
This map shows the geographic impact of Daphne J. Smits'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 Daphne J. Smits with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daphne J. Smits more than expected).
Fields of papers citing papers by Daphne J. Smits
This network shows the impact of papers produced by Daphne J. Smits. 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 Daphne J. Smits. The network helps show where Daphne J. Smits may publish in the future.
Co-authorship network of co-authors of Daphne J. Smits
This figure shows the co-authorship network connecting the top 25 collaborators of Daphne J. Smits. A scholar is included among the top collaborators of Daphne J. Smits 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 Daphne J. Smits. Daphne J. Smits 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 | 0 | |
| 3 | 8 | |
| 4 | 1 | |
| 5 | 9 | |
| 6 | 7 |
About Daphne J. Smits
Daphne J. Smits is a scholar working on Genetics, Genetics and Physiology, having authored 6 papers that have together received 26 indexed citations. Recurring topics across this work include Congenital heart defects research (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genomics and Rare Diseases (1 paper). The work is most often cited by research in Aging (1 citation), Neurology (8 citations) and Genetics (5 citations). Daphne J. Smits has collaborated with scholars based in Netherlands, United States and Australia. Frequent co-authors include Tjakko J. van Ham, Grazia M.S. Mancini, Rachel Schot, Martina Wilke, Antonio Romito, Brahim Tabarki, A. James Barkovich, Marjolein H. G. Dremmen, Herma C. van der Linde and Rob Willemsen. Their work appears in journals such as Human Genetics, Disease Models & Mechanisms and European Journal of Paediatric Neurology.
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.