Suzanne Sindi
- Molecular Biology
- Genetics top 10%
- Plant Science
- Cancer Research
- Neurology top 10%
- Co-authors
- Benjamin J. RaphaelTricia R. SerioAli BashirElena HelmanSusanne DiSalvoHsin-Ta WuAaron DerdowskiCourtney L. Klaips
- Topics
- Genomic variations and chromosomal abnormalities (19 papers)Genomics and Phylogenetic Studies (18 papers)Prion Diseases and Protein Misfolding (16 papers)
- Cited by
- GeneticsMolecular BiologyNeurology
- Partner nations
- United StatesGermanyFrance
In The Last Decade
Suzanne Sindi
69 papers receiving 986 citations
Peers
Comparison fields: 5 of 126
- Molecular Biology 639
- Genetics 326
- Plant Science 100
- Cancer Research 82
- Neurology 76
Countries citing papers authored by Suzanne Sindi
This map shows the geographic impact of Suzanne Sindi'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 Suzanne Sindi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Suzanne Sindi more than expected).
Fields of papers citing papers by Suzanne Sindi
This network shows the impact of papers produced by Suzanne Sindi. 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 Suzanne Sindi. The network helps show where Suzanne Sindi may publish in the future.
Co-authorship network of co-authors of Suzanne Sindi
This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne Sindi. A scholar is included among the top collaborators of Suzanne Sindi 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 Suzanne Sindi. Suzanne Sindi is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 0 | |
| 2 | 1 | |
| 3 | 1 | |
| 4 | 12 | |
| 5 | 31 | |
| 6 | 11 | |
| 7 | 6 | |
| 8 | 3 | |
| 9 | 19 | |
| 10 | 2 | |
| 11 | 49 | |
| 12 | 52 | |
| 13 | 3 | |
| 14 | 10 | |
| 15 | 12 | |
| 16 | 1 | |
| 17 | 6 | |
| 18 | 4 | |
| 19 | 34 | |
| 20 | 86 |
About Suzanne Sindi
Suzanne Sindi is a scholar working on Genetics, Neurology and Modeling and Simulation, having authored 76 papers that have together received 995 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (19 papers), Genomics and Phylogenetic Studies (18 papers) and Prion Diseases and Protein Misfolding (16 papers). The work is most often cited by research in Genetics (326 citations), Molecular Biology (639 citations) and Neurology (76 citations). Suzanne Sindi has collaborated with scholars based in United States, Germany and France. Frequent co-authors include Benjamin J. Raphael, Tricia R. Serio, Ali Bashir, Elena Helman, Susanne DiSalvo, Hsin-Ta Wu, Aaron Derdowski, Courtney L. Klaips, Karin Leiderman and Janice Villali. Their work appears in journals such as Science, Journal of Biological Chemistry and Nature Communications.
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.