Dan Fults
- Molecular Biology top 10%
- Genetics top 2%
- Oncology top 10%
- Neurology top 5%
- Cancer Research top 10%
- Co-authors
- Carolyn A. PedoneRichard CawthonR. WhiteGregory A. ThomasDouglas L. BrockmeyerY LiFrank McCormickWade S. Samowitz
- Topics
- Glioma Diagnosis and Treatment (8 papers)RNA Research and Splicing (5 papers)RNA modifications and cancer (3 papers)
- Cited by
- GeneticsNeurologyCancer Research
- Partner nations
- United StatesSweden
In The Last Decade
Dan Fults
16 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 58
- Molecular Biology 772
- Genetics 467
- Oncology 335
- Neurology 288
- Cancer Research 280
Countries citing papers authored by Dan Fults
This map shows the geographic impact of Dan Fults'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 Dan Fults with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dan Fults more than expected).
Fields of papers citing papers by Dan Fults
This network shows the impact of papers produced by Dan Fults. 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 Dan Fults. The network helps show where Dan Fults may publish in the future.
Co-authorship network of co-authors of Dan Fults
This figure shows the co-authorship network connecting the top 25 collaborators of Dan Fults. A scholar is included among the top collaborators of Dan Fults 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 Dan Fults. Dan Fults is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 53 | |
| 2 | 19 | |
| 3 | 34 | |
| 4 | 4 | |
| 5 | 12 | |
| 6 | 51 | |
| 7 | Correlation of chromosome 17p loss with clinical outcome in medulloblastoma. | 47 |
| 8 | 2 | |
| 9 | 96 | |
| 10 | 37 | |
| 11 | 44 | |
| 12 | 343 | |
| 13 | p53 mutation and loss of heterozygosity on chromosomes 17 and 10 during human astrocytoma progression. | 268 |
| 14 | Allelotype of human malignant astrocytoma. | 146 |
| 15 | 5 | |
| 16 | Loss of heterozygosity for loci on chromosome 17p in human malignant astrocytoma. | 101 |
| 17 | 0 |
About Dan Fults
Dan Fults is a scholar working on Genetics, Neurology and Cancer Research, having authored 17 papers that have together received 1.3k indexed citations. Recurring topics across this work include Glioma Diagnosis and Treatment (8 papers), RNA Research and Splicing (5 papers) and RNA modifications and cancer (3 papers). The work is most often cited by research in Genetics (467 citations), Neurology (288 citations) and Cancer Research (280 citations). Dan Fults has collaborated with scholars based in United States and Sweden. Frequent co-authors include Carolyn A. Pedone, Richard Cawthon, R. White, Gregory A. Thomas, Douglas L. Brockmeyer, Y Li, Frank McCormick, Wade S. Samowitz, Robin Clark and Ken Ward. Their work appears in journals such as Cell, Brain Research and Journal of Neuropathology & Experimental 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.