Simon J. Kinder
- Molecular Biology top 10%
- Immunology top 10%
- Genetics top 10%
- Surgery
- Cell Biology top 10%
- Co-authors
- Patrick TamTania E. TsangAndrás NagyAlan G. BaxterDale I. GodfreyRon P. WeinbergerAnna‐Katerina HadjantonakisGabriel A. Quinlan
- Topics
- Congenital heart defects research (7 papers)Pluripotent Stem Cells Research (6 papers)Developmental Biology and Gene Regulation (6 papers)
- Partner nations
- AustraliaUnited StatesCanada
In The Last Decade
Simon J. Kinder
17 papers receiving 1.4k citations
Peers
Comparison fields: 5 of 84
- Molecular Biology 975
- Immunology 335
- Genetics 284
- Surgery 193
- Cell Biology 178
Countries citing papers authored by Simon J. Kinder
This map shows the geographic impact of Simon J. Kinder'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 Simon J. Kinder with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Simon J. Kinder more than expected).
Fields of papers citing papers by Simon J. Kinder
This network shows the impact of papers produced by Simon J. Kinder. 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 Simon J. Kinder. The network helps show where Simon J. Kinder may publish in the future.
Co-authorship network of co-authors of Simon J. Kinder
This figure shows the co-authorship network connecting the top 25 collaborators of Simon J. Kinder. A scholar is included among the top collaborators of Simon J. Kinder 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 Simon J. Kinder. Simon J. Kinder is excluded from the visualization to improve readability, since they are connected to all nodes in the network.
All Works
| # | Work | Indexed citations |
|---|---|---|
| 1 | 10 | |
| 2 | 5 | |
| 3 | 59 | |
| 4 | 38 | |
| 5 | Defects of the body plan of mutant embryos lacking Lim1, Otx2 or Hnf3beta activity. | 36 |
| 6 | 187 | |
| 7 | 33 | |
| 8 | 90 | |
| 9 | 12 | |
| 10 | Linkage analysis of systemic lupus erythematosus induced in diabetes-prone NOD mice by Mycobacterium bovis | 1 |
| 11 | Experimental analysis of the emergence of left-right asymmetry of the body axis in early postimplantation mouse embryos. | 12 |
| 12 | 74 | |
| 13 | 308 | |
| 14 | 44 | |
| 15 | 86 | |
| 16 | 207 | |
| 17 | 210 |
About Simon J. Kinder
Simon J. Kinder is a scholar working on Genetics, Immunology and Molecular Biology, having authored 17 papers that have together received 1.4k indexed citations. Recurring topics across this work include Congenital heart defects research (7 papers), Pluripotent Stem Cells Research (6 papers) and Developmental Biology and Gene Regulation (6 papers). The work is most often cited by research in Immunology (335 citations), Molecular Biology (975 citations) and Cell Biology (178 citations). Simon J. Kinder has collaborated with scholars based in Australia, United States and Canada. Frequent co-authors include Patrick Tam, Tania E. Tsang, András Nagy, Alan G. Baxter, Dale I. Godfrey, Ron P. Weinberger, Anna‐Katerina Hadjantonakis, Gabriel A. Quinlan, Richard R. Behringer and Roland Scollay. Their work appears in journals such as The Journal of Immunology, Development and Diabetes.
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.